Skip to main content
Nutrients logoLink to Nutrients
. 2016 Jun 7;8(6):351. doi: 10.3390/nu8060351

Maternal Dietary Patterns and Pregnancy Outcome

Xuyang Chen 1,2,, Diqi Zhao 1,2,, Xun Mao 1,2,, Yinyin Xia 2,3, Philip N Baker 2,4, Hua Zhang 1,2,*
PMCID: PMC4924192  PMID: 27338455

Abstract

Maternal nutritional status during pregnancy will affect the outcomes for the mother and the baby. Many analyses of the relationship between diet and outcome are often based on a single or a few food items or nutrients. However, foods are not consumed in isolation and dietary patterns can be used to assess the whole diet consumed. The use of dietary pattern analysis to understand nutritional intake and pregnancy outcome is becoming more and more popular. Many published studies have showed the association between maternal dietary patterns and pregnancy outcome. This review examined articles about the relationship between maternal dietary patterns and pregnancy outcome. As a modifiable factor, dietary patterns may be more applicable to clinical and pregnant health interventions.

Keywords: dietary patterns, diet, pregnancy, maternal outcome, offspring outcome

1. Introduction

Nutritional status during pregnancy will affect the outcomes for the mother and the baby, but the evidence for a beneficial effect of specific nutritional supplements for women of reproductive age is inconclusive [1,2,3]. Thus, identifying what foods should be eaten, in what quantities, and even how often these foods should be eaten, remain important questions—the answers will enable accurate nutritional assessment and facilitate appropriate counseling in pregnancy.

Many analyses of the relationship between diet and an outcome are based on a single or a few food items or nutrients. Examples such as a high consumption of saturated fatty acids [4,5], total carbohydrates and soft drinks [6,7,8] and a low intake of polyunsaturated fatty acids [9,10] have been associated with increased risk of gestational diabetes mellitus (GDM). The calcium supplementation has been found to decrease preeclampsia [11] and result in fewer preterm births [12]. However, foods are not consumed in isolation and people eat foods containing a mix of nutrients and nonnutrients. Moreover, the individual nutrient approach does not take biological complexity resulting from interactions between nutrients into consideration. For this reason, methods that identify patterns of food intake instead of looking at single food have become popular and are being used to examine potential disease risk prediction [13].

Dietary patterns study the whole diet and provide a simple but helpful, comprehensive and complimentary approach way to deliver meaningful results to the respective population [14]. Dietary patterns have potential to be used as a valid tool in assessing the relationship between diet and pregnancy outcomes [15].

2. Methods

The purpose of this review is to examine articles about maternal dietary patterns before or during their pregnancies and pregnancy outcome. For this purpose, a PubMed Central search was conducted up to November 2015. The terms used to search abstracts were (dietary pattern or diet or dietary) AND (pregnancy or pregnant women or infant or offspring). This review included studies of dietary patterns and pregnancy outcome meeting the following criteria: studies based on dietary patterns rather than any single food and studies relating diet during pregnancy with health outcomes in the mother and the infant. The PubMed Central search strategy yielded a total amount of 2927 articles. After applying the inclusion criteria by screening titles and abstracts, 54 articles were selected.

3. Dietary Patterns Assessment

The information obtained from food frequency questionnaires (FFQs) can be used to assess dietary patterns. Use of the FFQs has shown the validity of identifying maternal dietary patterns and of studying the relationship between dietary patterns [14]. FFQs have become the most common measure of diet to obtain dietary patterns.

Two different approaches for observing overall dietary exposure were evident in the published literature. One approach is based on the popular hypotheses and guidance about the role of nutrients in disease prevention, and the diet is evaluated in accordance with this guidance (Table 1). In this approach, the diet assessed for certain foods or nutrient characteristics, and then the score resulting from the particular dietary exposure is the variable.

Table 1.

Studies reporting dietary patterns based on the popular hypotheses and guidance about the role of nutrients in disease prevention.

Reference Dietary Patterns Assessment Food Distinct Nutrients
Chavarro, J.E., et al. [20] FFQ a (items NA b)
“Fertility diet” score
High “fertility diet” score was characterized by a higher intake of monounsaturated fat, vegetable protein, high-fiber, low-glycemic carbohydrates, high fat dairy products, nonheme iron intake and higher frequency of multivitamin use, but a lower intake of trans fat and animal protein. Multivitamins, vegetable protein and the amount and quality of carbohydrates.
Bao, W., et al. [21] FFQ (items NA)
Low-carbohydrate dietary patterns scores
Higher scores consumed more heme iron, red meat, poultry, and high fat dairy but less total calories, dietary fiber, magnesium, vitamin C, vitamin E, low-fat dairy, fruit, vegetables, whole grains, and sugar-sweetened beverages. Fat, protein, carbohydrate, heme iron and nitrite.
Karamanos, B., et al. [22] 78 questions dietary questionnaire Mediterranean Diet Index Evaluated diet for intake of bread, cereals, legumes, vegetables, fruits, meat, fish, eggs, the ratio of olive oil to animal fat, potatoes, cheese and dairy products. trans fatty acids, fiber, antioxidants, polyphenols and magnesium.
Asemi, Z., et al. [23,24] Dietary Approaches to Stop Hypertension Rich in fruits, vegetables, whole grains and low-fat dairy products, and contained lower amounts of saturated fats, cholesterol and refined grains with a total of 2400 mg Na/day Dietary fiber, phytoestrogens, cholesterol, potassium, magnesium, folic acid.
Tobias, D.K., et al. [25,26] FFQ (items NA)
Alternate Mediterranean Diet
Dietary Approaches to Stop Hypertension
Alternate Healthy Eating Index
High intakes of fruit, vegetables, nuts, legumes, soy, fish, seafood, whole grains, moderate alcohol and higher MUFA:SFA c, but low intakes of red and processed meats.
High intakes of fruit, vegetables, nuts, legumes, soy, fish, seafood, whole grains and low-fat dairy, but low intakes of red, processed meats, sweetened beverages and sodium.
High intakes of fruit, vegetables, nuts, legumes, soy, fish, seafood, cereal fiber, moderate alcohol, multivitamin use and higher white: red meat ratio and PUFA:SFA d, but low intakes of trans fat.
Antioxidants and photochemicals, dietary fiber, saturated fat, heme iron, nitrosamines and micronutrients such as magnesium and vitamin C.
Mikkelsen, T.B., et al. [27] 360-items FFQ
Mediterranean-type diet
Consumption of fish twice a week or more (lunch or dinner), intake of olive or rape seed oil, high consumption of fruits and vegetables (5 a day or more), meat (other than poultry and fish) at most twice a week, and at most 2 cups of coffee a day. Higher carbohydrate, vitamin C, folate, α-tocopherol, magnesium, calcium, iron and vitamin D intake and lower sugar, alcohol and cholesterol.
Haugen, M., et al. [28] 255-items FFQ
Mediterranean-type diet
Intake of at least 5 vegetables/fruits per day, 2 servings of fish or more per week, olive or canola oil for cooking and dressings, no more than 2 servings of red meat per week, and no more than 2 cups of coffee per day. Higher intake of vitamin C, folate and fiber and lower intake of fat and saturated fat.
Saunders, L., et al. [29] 214-items FFQ
The Mediterranean scale
Evaluated diet for intake of beneficial components (vegetables, legumes, fruits and nuts, cereals, fish and dairy products), components presumably detrimental (meat, poultry and alcohol) and fat. Vitamins C, E and n-3 PUFA.
Timmermans, S., et al. [30] 293-items FFQ
Adherence to the Mediterranean diet
Higher intakes of pasta, rice, vegetable oils, fish, vegetables and alcohol, and lower intakes of meat, potatoes and fatty sauces. Vegetable protein, carbohydrate polymers, fiber, folate, vitamin B12 and a favourable ratio of unsaturated: saturated lipids.
Chatzi, L., et al. [31] 42-items FFQ
Mediterranean Diet Score
Evaluated diet for intake of vegetables, legumes, fruits and nuts, cereal, fish, dairy products and meat. Antioxidant compounds (vitamin C, E, phenolic acids, phytic acid, carotenoids, selenium, flavonoids) and n-3 PUFA.
de Batlle, J., et al. [32] 70-items FFQ
Mediterranean diet score
A greater adherence to a Mediterranean dietary pattern is a high intake of vegetables, fruits and nuts, legumes, fish and cereals, and a low intake of dairy products, meat and junk food and fat. High ω-3/ω-6 fatty acid ratio and low salt content.
Castro-Rodriguez, J.A., et al. [33] The environmental questionnaire included questions on the consumption of certain foods based on the International Study of Asthma and Allergies in Childhood Phase III
Mediterranean diet score
Evaluated diet for intake of fruit, fish (oily and white), vegetables (including salads), legumes, cereals, pasta, rice, potatoes, meat, milk and fast food. Low in SFA and high in carbohydrates, fiber, antioxidants, MUFA and n-3 PUFA.
Chatzi, L., et al. [34] 100-items FFQ in Spain
250-items FFQ in Greece
Mediterranean diet score
Evaluated diet for intake of beneficial components (vegetables, legumes, fruits and nuts, cereals, fish and seafood, and dairy products), components presumably detrimental (meat, including all types of meat) and fat. Low in SFA and high in carbohydrates, fiber, antioxidants, MUFA and n-3 PUFA.
Lange, N.E., et al. [35] 166-items FFQ Mediterranean diet score
Alternate Healthy Eating Index
Evaluated diet for intake of beneficial components (dairy, fish, fruit, legumes, nuts, vegetables, unsaturated-to-saturated fat ratio, and whole grains) and components presumably detrimental (red and processed meats). NA
Evaluated diet for intake of vegetables; fruit; ratio of white to red meat; fiber; transfat; ratio of polyunsaturated to saturated fatty acids; and folate, calcium, and iron from foods. NA
Lombardi, C., et al. [36] 72-items FFQ
Two a priori dietary scores
One capturing a diet high in fruits and vegetables and low in red and cured meats and one capturing a diet high in fruits and vegetables and low in fried foods and sweets. Folate, vitamin B6, α-carotene, lutein/zeaxanthin, acrylamide and nitrates.

a FFQ: food frequency questionnaire; b NA: not available; c MUFA: monounsaturated fatty acid; SFA: saturated fatty acid; d PUFA: polyunsaturated fatty acid.

The alternative approach is data driven, using statistical analyses that seek to minimize bias (Table 2). In epidemiologic studies, statistical analyses play a central role in nutritional epidemiology and are used to promote objectivity in the conclusions drawn [16]. Statistical methods like factor analysis or cluster analysis are common a posteriori approaches to the identification of dietary patterns [13].

Table 2.

Studies reporting dietary patterns derived from statistical analyses.

Reference Dietary Assessment Dietary Patterns Food Distinct Nutrients
Vujkovic, M., et al. [37] 195-items FFQ a Health conscious–low Processed High intakes of fruits, vegetables, whole grains, fish, and legumes, but low intakes of mayonnaise, snacks, and meat products. NA c
PCA b Mediterranean High intakes of vegetable oil, fish, legumes, and vegetables but low intakes of snacks. Vitamin B6 and fatty acids.
Toledo, E., et al. [38] 136-items FFQ Western-type High consumption of processed and unprocessed red meat, fast food, whole fat dairy products, commercial bakery, potatoes, eggs, refined grains, sauces, processed meals, and sugar-sweetened soda. Carbohydrates, protein and trans unsaturated fat.
PCA Mediterranean-type High consumption of vegetables, fish, fruits, poultry, low-fat dairy products, and olive oil. Iron intake, polyunsaturated fatty acids, B vitamins and folic acid.
Zhang, C., et al. [39] 133-items FFQ Western High intake of red meat, sweets, processed meat, refined grain products, French fries and pizza. Saturated fatty acids and cholesterol nitrites and haem iron.
PCA Prudent High intake of fruit, green leafy vegetables, poultry and fish. NA
Tryggvadottir, E.A., et al. [40] 4-day weighed food record PCA Prudent Positive for seafood, eggs, vegetables, fruit and berries, vegetable oils, nuts and seeds, pasta, breakfast cereals, and coffee and tea, and negative for soft drinks and French fries. Polyunsaturated fatty acids.
He, J.R., et al. [41] 67-items FFQ Vegetable pattern Evaluated intake of root vegetables, beans, mushrooms, melon vegetables, seaweed, other legumes, fruits, leafy and cruciferous vegetables, processed vegetables, nuts, and cooking oil. Dietary fiber.
PCA Protein-rich pattern Evaluated intake of poultry, red meat, animal organ meat, grains (mainly refined), processed meat, fish, soups, leafy and cruciferous vegetables, and eggs. NA
Prudent pattern Evaluated intake of dairy products, nuts, eggs, fish, soups, fruits, and infrequent intake of processed meat, sugar-sweetened beverages, and processed vegetables. NA
Sweets and seafood pattern Evaluated intake of Cantonese desserts, mollusks and shellfish, and sugar-sweetened beverages and low intakes of grains (mainly refined) and leafy and cruciferous vegetables. NA
Schoenaker, D.A., et al. [42] 101-items FFQ Meats, snacks and sweets High consumption of red and processed meat, cakes, sweet biscuits, fruit juice, chocolate and pizza. Sugar and saturated fat.
PCA Mediterranean-style High factor loadings for vegetables, legumes, nuts, tofu, rice, pasta, rye bread, red wine and fish. Dietary fiber, magnesium, Vitamin E
and other antioxidants.
Fruit and low-fat dairy Positively correlated with fruits and low fat dairy including yoghurt, low-fat cheese and skimmed milk. NA
Cooked vegetables High consumption of carrots, peas, cooked potatoes, cauliflower and pumpkin. NA
Schoenaker, D.A., et al. [43] 101-items FFQ Meat, high-fat, and sugar High consumption of meat, processed meat, cakes, sweet biscuits, chocolate, meat pies, and pizza. NA
PCA Mediterranean-style High consumption of vegetables, legumes, nuts, tofu, rice, pasta, rye bread, red wine, and fish. Vitamin E, dietary fiber, magnesium, and PUFA d.
Fruit and low-fat dairy High consumption of fruit, yogurt, low-fat cheese, and skim milk. NA
Cooked vegetable High consumption of carrots, peas, cooked potatoes, cauliflower, and pumpkin. NA
Brantsaeter, A.L., et al. [44] 255-items FFQ Vegetable High positive loadings on vegetables, cooking oil, olive oil, fruits and berries, rice, and chicken. Folate, Vitamin B6, fiber, Vitamin C, β-carotene, tocopherol, potassium, and magnesium.
PCA Processed food High positive loadings on processed meat products, white bread, French fries, salty snacks, and sugar-sweetened drinks and high negative loadings on oily fish, high-fiber breakfast cereals, and lean fish. SFA e, added sugar and sodium.
Potato and fish High positive loadings on cooked potatoes, processed fish, lean fish, fish spread and shellfish, and margarine. Sodium, fiber, folate, and tocopherol.
Cakes and sweets High loadings on cakes, waffles and pancakes, buns, ice cream, sweet biscuits, sweets, and chocolate. SFA and added sugar.
Timmermans, S., et al. [45] 293-items FFQ Mediterranean High intake of vegetables, vegetable oils, pasta, rice, fish, and legumes, moderate intake of alcohol, and low intake of sweets. Vegetable protein, carbohydrates polymers, fiber, folate, Vitamin B1 and a favorable ratio of unsaturated to saturated lipids.
PCA Traditional High intake of meat and potatoes, and low intake of fruit, nonalcoholic drinks, fish, and bread. Animal protein and saturated lipids.
Eshriqui, I., et al. [46] 82-items FFQ Healthy High intake of milk, dairy products, fruit, fruit juice, green vegetables and legumes, fish, cakes and cookies-crackers and tea. Fatty acids, fiber, magnesium, potassium, calcium, flavonoids and antioxidants.
PCA Common-Brazilian High intake of rice, beans, vegetable spices, eggs and bread and fats. NA
Processed High intake of meats, candies And sugar, pasta, roots and tubers, fast food and snacks, sausages and deli meats, soft drinks, and was inversely related to beef and coffee. NA
Chatzi, L., et al. [47] 250-items FFQ Western Mainly comprised meat and meat products, potatoes, sugar and sweets, cereals, fats except olive oil, salty snacks, eggs, beverages and sauces. NA
PCA Health conscious Mainly comprised vegetables, fruit, nuts, pulses, fish and seafood, olive oil and dairy products. Vitamins C, E, carotenoids, Se Flavonoids, α- tocopherol, PUFA and polyphenols.
Vaz Jdos, S., et al. [48] 43-items FFQ Health conscious High intake of salad, fruit, fruit juice, rice, pasta, oat/bran based breakfast cereal, fish, pulses, cheese, non-white bread. Vitamin B12 and n-3 PUFA.
Traditional High intake of vegetables, red meat, poultry. NA
PCA Processed High intake of meat pies, sausages, burgers, fried foods, pizza, chips, white bread, eggs, baked beans. NA
Confectionery High intake of chocolate, sweets, biscuits, cakes, puddings. NA
Vegetarian High intake of meat substitutes, pulses, nuts, herbal tea and high negative loadings for red meat and poultry. NA
Vilela, A.A., et al. [49,50] 82-items FFQ Common-Brazilian Consisted of rice, beans, vegetable spices, and meats and eggs. n-3 PUFA.
PCA Healthy Comprised dairy products, fruits and fruit juices, green vegetables and legumes, candies, fish, cakes and cookies/crackers, noodles, pasta, roots and tubers, and tea. Flavonoids, vitamins, minerals and n-3 PUFA.
Processed High intake of bread, fat, fast food and snacks, sugar, sausages and deli meats, soft drinks, and coffee. Fat and carbohydrates.
Okubo, H., et al. [51] 150-items FFQ Healthy High intake of green and yellow vegetables, seaweeds, white vegetables, potatoes, fish, fruits, shellfish and sea products. Vitamins B2, B6, B12, folate, total n-3
PUFA, DHA and EPA f.
Factor analysis Western High intake of vegetable oil, beef and pork, salt-containing seasonings, processed meat, chicken and eggs. Total n-3 PUFA.
Japanese High intake of rice, miso soup, sea products, fish and pickled vegetables. Total n-3 PUFA, DHA and EPA.
Englund-Ogge, L., et al. [52] 255-items FFQ Prudent High intake of raw and cooked vegetables, salad, onion/leek/garlic, fruit and berries, nuts, vegetables oils, water as beverage, whole grain cereals, poultry, and fiber rich bread, low intake of processed meat products (hot dogs, hamburgers, and so on), white bread, and pizza/tacos. Folic acid, dietary fibre, β carotene, potassium, and ascorbic acid.
PCA Western High intake of salty snacks, chocolate and sweets, cakes, French fries, white bread, ketchup, sugar sweetened drinks, processed meat products, and pasta, low intake of lean fish and fiber rich bread. Total fat, saturated fat, and added sugar.
Traditional High intake of boiled potatoes, fish products, gravy, lean fish, margarine, rice pudding, low fat milk, an cooked vegetables, low intake of poultry and pizza/tacos. Potassium, magnesium, protein and dietary fiber.
Rasmussen, M.A., et al. [53] 360-items FFQ Vegetables/Prudent High in cabbage, onion, mushroom, corn, salad, tomato, vegetables other and legumes NA
Western High in potatoes, french fries, bread white, pork, beef veal, meat mixed, meat cold and dressing sauce. NA
Nordic High in bread dark, fruit nordic, banana, fruit dried, sweet spread and hard cheese. NA
PCA Seafood High in fish lean, fish oily, fish cold, lamb, egg and vegetables other. n-3 fatty acids.
Alcohol High in wine, beer, liquor, soya and root. NA
Candy High in bread white, french fries, margarine, sweet spread, candy, sugar cakes, dessert dairy and chocolate. NA
Rice/Pasta/Poultry High in pasta, rice and poultry NA
Grieger, J.A., et al. [54] 100-items FFQ High-protein/fruit High in fish, meat, chicken, fruit, and some whole grains. Long-chain ω-3 PUFAs, protein, niacin equivalents, cholesterol, zinc, iron, and sodium.
PCA High-fat/sugar/takeaway High in takeaway foods, potato chips, refined grains. Saturated fat, α-linolenic acid, total fat, energy, carbohydrate and MUFAs.
Vegetarian-type High in vegetables, legumes, whole grains. Fiber, dietary folate and Vitamin A.
Cole, Z.A., et al. [55] 100-items FFQ PCA Prudent diet High intakes of fruit and vegetables, whole meal bread, rice, and pasta, yogurt, and breakfast cereals and low intakes of chips and roast potatoes, sugar, white bread, processed meat, crisps, tinned vegetables, and soft drinks. Protein and calcium.
Petersen, S.B., et al. [56] 360-items FFQ Prudent High in vegetables, legumes, root, fruit, corn and low in meat, french fries, margarine, white bread, candy/snack. NA
Alcohol High in alcohol, soy, root, soft drinks, berries and low in pasta/rice, yogurt, poultry, cheese, bread. NA
PCA Western High in meat, potatoes, white bread, egg, margarine and low in vegetables, fruit, breakfast, cereals, nuts, water. NA
Nordic High in dark bread, nordic fruit, cheese, banana, cakes and low in french fries, candy/snack, soft drinks, processed meat, desserts. NA
Shellfish High in fish, shellfish, lamb, oils, egg and low in soft drinks, diet, candy/snack, low-fat milk, coffee, white bread. NA
Sweets High in white bread, cakes, margarine, french fries, soft drinks, sugar and low in Low-fat milk, cabbage, fruits, fish, legumes. NA
Traditional High in poultry, meat, low-fat milk, meat, water and low in full fat milk, coffee, butter, potatoes, white bread. NA
Knudsen, V.K., et al. [57] 360-items FFQ Western High intake of high-fat dairy, refined grains, processed and red meat, animal fat (butter and lard), potatoes, sweets, beer, coffee and high-energy drinks. Saturated fats and trans fatty acids.
PCA Health conscious High intake of fruits, vegetables, fish, poultry, breakfast cereals, vegetable juice and water. Vitamins and minerals.
Intermediate Low-fat dairy and fruit Juice, consumption of the remaining food groups was in between western and health conscious. NA
Thompson, J.M., et al. [58] 71-items FFQ Junk High intake of ice cream, sweet biscuits, scones, cakes, sweetened cereal, crisps, pies, lollies, chocolate bars, ice blocks and milo (chocolate energy drink). NA
PCA Traditional High intake of apples/pears, citrus fruit, kiwifruit/feijoas, bananas, green vegetables, root vegetables, peas/maize, dairy food/yogurt and water. NA
Fusion High intake of fruits, fried rice/noodles, boiled rice/pasta, fish/shellfish, milk and negative loading for tea/coffee, sherry/wine and hard cheeses. NA
Okubo, H., et al. [59] 150-items FFQ Meat and eggs High intake of beef and pork, processed meat, chicken, eggs, butter and dairy products. NA
K-means cluster analysis Wheat products High intake of bread, confectioneries, fruit and vegetable juice, and soft drinks. NA
Rice, fish and vegetables High intake of rice, potatoes, nuts, pulses, fruits, green and yellow vegetables, white vegetables, mushrooms, seaweeds, Japanese and Chinese tea, fish, shellfish, sea products, miso soup and salt-containing seasoning. NA
Northstone, K., et al. [60] 44-items FFQ Health conscious High intake of salad, fruit, rice, pasta, breakfast cereals, fish, eggs, pulses, fruit juices, poultry and non-white bread. NA
Traditional High intake of green vegetables and root vegetables, potatoes, peas and to some extent red meat and poultry. NA
PCA Processed High intake of high-fat processed foods, such as meat pies, sausages and burgers, fried foods, pizza, chips and crisps. NA
Confectionery High intake of confectionery and other foods with high sugar content such as chocolate, sweets, biscuits, cakes and other puddings. NA
Vegetarian High intake of meat substitutes, pulses, nuts and herbal tea and low intake of red meat and poultry. NA
Coelho Nde, L., et al. [61] 29-items FFQ Prudent pattern High intake of milk, yogurt, cheese, fruit and fresh-fruit juice, cracker, and chicken/beef/fish/liver. NA
PCA Traditional High intake of beans, rice, vegetables, breads, butter/margarine and sugar. NA
Western High intake of potato/cassava/yams, macaroni, flour/farofa/grits, pizza/hamburger/deep fried pastries, soft drinks/cool drinks and pork/sausages/egg. NA
Snack pattern High intake of sandwich cookie, salty snacks, chocolate, and chocolate drink mix. High simple carbohydrates, lipids and low amounts of protein and micronutrients.
Bouwland-Both, M.I., et al. [62] 293-items FFQ Mediterranean High intakes of vegetables, legumes, pasta/rice, dairy, fish/shellfish, vegetable oils, alcohol, nonsweetened nonalcoholic beverages and low intakes of processed meat. NA
PCA Energy-rich High intakes of bread/breakfast cereals, margarine, nuts, snacks/sweets and nonsweetened nonalcoholic beverages and low intakes of sweetened, nonalcoholic beverages. Total fat, protein, Vitamin B6 and carbohydrate.
Western High intakes of potatoes, pasta/rice, dairy, fresh meat, processed meat, margarine and alcohol and low intakes of nuts, fish/shellfish. NA
Colon-Ramos, U., et al. [63] 111-items FFQ Healthy High intakes of vegetables, fruits, non-fried fish and chicken, and water. Protein and carbohydrate.
Processed High intakes of processed meat, fast food items, snacks, sweets, and soft drinks. Transfats and total grains.
Southern High intakes of cooked cereals, peaches, corn, fried fish, beans, greens, pig’s feet, neck bones oxtails, tongue, pork. NA
PCA Southern-processed High intakes of total fat, total sugar, iron, zinc, sodium, and meats, and low intake of whole grains. Total fat, total sugar, iron, zinc and sodium.
Healthy-Southern High intakes of fiber, folate, egg-meat equivalents, oils, vegetables (including dark green and orange vegetables, and tomatoes, excluding legumes and potatoes) and fruits (including fruit juice). Fiber and folate.
Healthy-processed High intakes of nuts, seeds, whole grains, and dairy, as well as highly refined foods that are higher in simple sugars and fat. Simple sugars and fat.
Mixed Reflects foods from all of the other patterns together. NA
Miyake, Y., et al. [64] 150-items FFQ Healthy High intake of green and yellow vegetables, seaweed, mushrooms, white vegetables, pulses, potatoes, fish, sea products, fruit, and shellfish. Linoleic acid, DHA, α-linolenic acid, calcium, Vitamin D, β-carotene and Vitamin E.
Factor analysis Western High intake of vegetable oil, salt-containing seasonings, beef and pork, processed meat, eggs, chicken, and white vegetables. Linoleic acid, α-linolenic acid, β-carotene and Vitamin E.
Japanese High intake of rice, miso soup, sea products, and fish. DHA, calcium, Vitamins D and E.
Shaheen, S.O., et al. [65] 111-items FFQ Health conscious High intake of salad, fruit, fruit juices, rice, pasta, oat/bran based breakfast cereals, fish, pulses, cheese, non-white bread. Protein, Mg, Fe, Zn, Na, K, niacin, fiber, thiamine, Vitamins B6, C, and folate.
Traditional High intake of vegetables, red meat, poultry. Carotene, K, Vitamins B6 and C.
PCA Processed High intake of meat pies, sausages, burgers, fried foods, pizza, chips, crisps, white bread, eggs, baked beans. Monounsaturated and saturated fats,
protein, carbohydrates and Na.
Vegetarian High intake of meat substitutes, pulses, nuts, herbal tea and low in poultry and red meat. NA
Confectionery High intake of chocolate, sweets, biscuits, cakes, puddings. Sugar.
Lange, N.E., et al. [35] 166-items FFQ Prudent High in vegetables, fruit, legumes, fish, poultry, eggs, salad dressing, and whole grains. NA
PCA Western High in red and processed meats, sugar-sweetened beverages, NA
French fries, high-fat dairy products, desserts, butter, and refined grains.
Grieger, J.A., et al. [66] 100-items FFQ High protein/fruit High in fish, meat, chicken, fruit. Long-chain n-3 PUFA, protein, cholesterol and Zn.
PCA High fat/sugar/takeaway High in takeaway foods, crisps, refined grains. Total fat, α-linolenic acid, SFA and Na.
Vegetarian-type High in vegetables, fruit, soya milk, whole grains. Fiber, dietary folate and Vitamin A.
Steenweg-de Graaff, J., et al. [67] 293-items FFQ Mediterranean High intake of vegetables, fish & shellfish, vegetable oil, fruit, and eggs, and relatively low in processed meat. Antioxidants and ω-3 fatty acids.
PCA Traditionally Dutch High intakes of fresh and processed meat, potatoes, margarines and low intake of soy and diet products. Saturated fat and ω-6 fatty acids.
Confectionary High intakes of cakes, sugar & confectionary products, tea, cereals, fruit, dairy products. Sugar and fat.
Vujkovic, M., et al. [68] 178-items FFQ Western High intakes of organ meat, red meat, processed meat, pizza, legumes, potatoes, French fries, condiments, and mayonnaise, but low intakes of fruits. Higher saturated fats, cholesterol monounsaturated and polyunsaturated fats and lower total proteins, carbohydrates, fiber, β-carotene, ascorbic acid, thiamin, riboflavin and pyridoxine.
PCA Prudent High intakes of fish, garlic, nuts, and vegetables and a higher frequency of hot meals per day. Higher polyunsaturated fats, fiber, Carotene, Vitamin B12 and folate.
Vujkovic, M., et al. [69] 200-items FFQ PCA Mediterranean High intakes of vegetables, fruit, legumes, vegetable oil, cereal products, alcohol and fish and low intakes of potatoes and sugar and confectionary. Higher serum and red blood cell folate, serum vitamin B12 and lower plasma homocysteine.
de Kort, C.A., et al. [70] 28-items FFQ Health conscious High intakes of fresh fruit and vegetables, dried fruit, fresh or frozen fish, soya products, pulses, olive oil and organic food. NA
Cluster analysis Mixed High intakes of dairy products, all types of frozen or tinned products, meat, poultry and organ meats (offal). NA
Non-health conscious Low intakes of yoghurt, cheese, eggs, fruit and vegetables, fish, beans and pulses, olive oil and organic food. NA
Sotres-Alvarez, D., et al. [71] 58-items FFQ Prudent High intakes of yogurt, reduced-fat milk, whole-wheat bread, fortified cereal, fish, fruits and vegetables and low in chili peppers, avocados and beef by-product. Almost all micronutrients except choline, iron, and Vitamins E, B6, and B12.
LCA g Mexican High intakes of fruits, vegetables, salsa, chili peppers, avocados, refried beans, tortillas, and chicken or beef by-products (liver, tongue) and low in reduced-fat milk, spinach and low-calorie soda. High carbohydrates, choline, iron, Vitamins E, B6,B12 and fiber and low saturated fat, total fat, and folic acid.
Western High intakes of frankfurters, bacon, French fries, white bread, potato chips and regular soda and low in fruits and vegetables. Transfat and caffeine.
Low-calorie Western The same as Western just 273 fewer calories than women in the Western on average. Transfat and caffeine.
Musselman, J.R., et al. [72] 21-items FFQ Western diet High intakes of processed meats and packaged snack foods. NA
PCA Fruits and vegetables High intakes of carrots, fruits, juices, green salads, and cruciferous vegetables. NA
Proteins High intakes of eggs, bacon, pork, and fried chicken. NA
Healthful High intakes of skim/low-fat milk and other vegetables and low in whole milk, processed foods, and fried chicken. NA

a FFQ: food frequency questionnaire; b PCA: Principal Component Analysis; c NA: not available; d PUFA: polyunsaturated fatty acid; e SFA: saturated fatty acid; f DHA: docosahexaenoic acid; EPA: eicosapentaenooic acid; g LCA: Latent Class Analysis.

Factor analysis can be considered a pattern detection method that reduces the number of dietary variables by finding correlated dietary variables. Most published studies that have used factor analysis to describe dietary patterns have used principal components analysis (PCA). The PCA is used to reduce a large amount of detailed information into a smaller set of interpretable factors that have the characteristic of explaining the largest amount of variability in the specific patterns [16].

Cluster analysis is a subject-oriented method with the objective of joining together variables placed into different nonoverlapping groups on the basis of some shared characteristics. Members of a cluster tend to be similar but distinct members of another cluster [17].

Another analytical approach in reflecting complex relationships between diet and disease is latent class analysis (LCA). LCA is useful to study unobserved heterogeneity characterized by several unidentified groups that behave differently. Thus group membership is an unobserved random variable and individuals have a predicted probability for belonging to each class, which reflects the uncertainty of class membership [18]. However, it has rarely been used due to its complexity, making it difficult to interpret and apply the results.

In addition, there is clear evidence of social confounders associated with the dietary patterns. Social factors, such as educational levels, financial difficulties and age, need to be accounted for in studies using dietary patterns [19].

4. Results

4.1. Infertility

Infertility is defined as the failure to achieve a clinical pregnancy after 12 months or more of regular unprotected sexual intercourse [73]. Its prevalence rates range from 6.9% to 9.3% in developing nations and from 3.5% to 16.7% in developed nations [74].

From the Nurses’ Health Study II a prospective cohort study, a diet score was calculated based on variables previously found to predict ovulatory disorder infertility. This ‘fertility diet’ was found to have favorable effects on fertility and was associated with a 69% lower risk of ovulatory disorder infertility (95% CI 29%–86%) [20]. In a Dutch cohort of couples seeking to conceive by means of vitro fertilization or intracytoplasmic sperm injection, researchers found that a preconception Mediterranean diet contributed to successful pregnancy with a 40% increased probability (OR 1.4, 95% CI 1.0–1.9) [37]. Similar results were obtained in a Spain nested case-control study; a greater adherence to the Mediterranean-type dietary pattern enhanced fertility (OR 0.56, 95% CI 0.35–0.95) [38].

4.2. Gestational Diabetes Mellitus

Gestational diabetes mellitus is characterized as glucose intolerance is first diagnosed during pregnancy, is one of the most common pregnancy complications, and has serious, long-term consequences for both mother and baby [75].

A prospective study included 13,110 American women who were free of cancer, cardiovascular disease, type 2 diabetes and history of GDM and reported at least one singleton pregnancy between 1992 and 1998 in the Nurses’ Health Study II. This study found that the Western dietary pattern high in red and processed meat was positively associated with the risk of GDM (OR 1.63, 95% CI 1.20–2.21), however, a prudent dietary pattern high in fruit, green leafy vegetables and fish was negatively associated [39]. Another prospective study included 21,411 singleton pregnancies in the Nurses’ Health Study II between 1991 and 2001 and reported that a pre-pregnancy low-carbohydrate dietary pattern with high protein and fat from animal food sources was positively associated with the risk of GDM (OR 1.36, 95% CI 1.13–1.64), whereas association for a pre-pregnancy low-carbohydrate dietary pattern with high protein and fat from vegetable food sources was not found [21].

In a study in 10 Mediterranean countries, the GDM was interpreted both by the American Diabetes Association (ADA) 2010 and the more stringent International Association of the Diabetes and Pregnancy Study Groups (IADPSG) 2012 criteria which require only one abnormal glucose value, instead of two, for the diagnosis. Adherence to a Mediterranean dietary pattern was associated with better glucose tolerance and a lower incidence of GDM (8.0% vs. 12.3%, OR = 0.618, by ADA_2010 and 24.3% vs. 32.8%, OR = 0.655, by IADPSG_2012 criteria) [22]. Another study concluded that a prudent dietary pattern in pregnancy was associated with decreased risk of GDM (OR 0.54, 95% CI 0.30–0.98), especially among women who were either overweight or obese pre-pregnancy (OR 0.31, 95% CI 0.13–0.75) [40]. In China, He et al. found that the vegetable dietary pattern was significantly associated with a lower risk of GDM (RR 0.79, 95% CI 0.64–0.97), while the sweets and seafood pattern was associated with increased risk of GDM (RR 1.23, 95% CI 1.02–1.49) [41]. In an Australian population-based prospective cohort study, a Mediterranean-style dietary pattern pre-pregnancy was inversely associated with GDM risk (RR 0.85, 95% CI 0.76–0.98), moreover, a dietary pattern of meats, snacks and sweets was associated with higher GDM risk (RR 1.38, 95% CI 1.02–1.86) [42].

A randomized clinical trial aimed at identifying the effects of the Dietary Approaches to Stop Hypertension (DASH) diet (rich in fruits, vegetables, whole grains and low-fat dairy products, and contained lower amounts of saturated fats, cholesterol and refined grains with a total of 2400 mg Na/day) on glucose tolerance and lipid profiles in GDM found that in pregnant women with GDM, the DASH eating pattern for four weeks resulted in beneficial effects on glucose tolerance and lipid profiles compared with a control diet [23]. The same authors demonstrated that consumption of the DASH diet by pregnant women with GDM had beneficial effects on fasting plasma glucose, serum insulin levels, Homeostasis Model of Assessment-Insulin Resistance score, plasma total antioxidant capacity, and total glutathione levels [24].

The results from the Nurses’ Health Study II indicated that healthy dietary patterns including the alternate Mediterranean Diet (aMED), DASH, and alternate Healthy Eating Index (aHEI) were significantly associated with a lower risk of GDM (aMED:RR 0.76, 95% CI 0.60–0.95; DASH:RR 0.66, 95% CI 0.53–0.82; aHEI:RR 0.54, 95% CI 0.43–0.68) [25]. Moreover, they observed increased adherence to the aMED, DASH, and aHEI dietary patterns with a lower risk of type 2 diabetes mellitus (T2DM) in this large prospective study of women with a history of GDM (aMED:RR 0.60, 95% CI 0.44–0.82; DASH:RR 0.54, 95% CI 0.39–0.73; aHEI:RR 0.43, 95% CI 0.31–0.59) [26]. All three dietary patterns include a high intake of fruit, vegetables, nuts, legumes, soy, fish, seafood, whole grains and low intake of red and processed meats. aMED includes moderate alcohol and higher ratio of monounsaturated fatty acid to saturated fatty acid (MUFA:SFA). aHEI also includes moderate alcohol, in addition to multivitamin use, higher ratio of polyunsaturated fatty acid to saturated fatty acid (PUFA:SFA) and lower intakes of transfat. DASH assesses high intakes of low-fat dairy, lower sweetened beverages and sodium.

4.3. Hypertensive Disorders of Pregnancy

Hypertensive disorders of pregnancy (HDPs), including gestational hypertension and preeclampsia, are obstetric complications [43]. The frequency of preeclampsia ranges between 2% and 7% in healthy nulliparous women. Preeclampsia is associated with adverse health outcomes (maternal mortality, perinatal deaths, preterm birth, and intrauterine growth restriction) for both the mother and child [76].

Research in nulliparous pregnant Norwegian women, found that a dietary pattern characterized by high intake of vegetables, plant foods and vegetable oils resulted in a lower risk of preeclampsia (OR 0.72, 95% CI 0.62–0.85), whereas a dietary pattern characterized by a high consumption of meat, sweet drinks, and snacks increased the risk (OR 1.21, 95% CI 1.03–1.42) [44]. In a prospective cohort study, researchers showed that low adherence to a Mediterranean-style dietary pattern and high adherence to a traditional dietary pattern during pregnancy were positively associated with higher blood pressure during pregnancy, but were not associated with gestational hypertension or preeclampsia outcomes [45]. In a population-based study of Australian women, pre-pregnancy consumption of a Mediterranean-style dietary pattern was associated with lower risk of developing HDPs (RR 0.58, 95% CI 0.42–0.81) [43].

In contrast to the above studies, in a Brazilian cohort, investigators did not observe associations between dietary patterns and prospective changes in blood pressure during pregnancy and the early postpartum period. The difference may be explained on the basis that this study only included healthy pregnant women and excluded those who developed hypertension or preeclampsia. The investigators hypothesized that the powerful mechanisms involved in maternal hemodynamic adaptations, such as the integrity of endothelium, were not disrupted in normotensive pregnant women, and maintained blood pressure despite the different dietary intakes [46].

4.4. Depressive Symptoms

The prevalence of depressive symptoms during pregnancy varies from 8% to 26% around the world [77]. Depressive symptoms have been associated with adverse outcomes for both mother and fetus, such as insufficient weight gain, premature birth, low birth weight, obstetric complications, and postpartum depression [78,79,80,81].

From a ‘Rhea’ cohort study in Crete, Greece, intake of the ‘health-conscious’ pattern comprised vegetables, fruit, nuts, pulses, fish and seafood, olive oil and dairy products led to a protective effect against depressive symptoms in postpartum women (RR 0.51, 95% CI 0.25–1.05) [47]. Another study found that traditional (OR 0.84, 95% CI 0.73–0.97) and health-conscious (OR 0.77, 95% CI 0.65–0.93) dietary patterns were associated with protective effects on symptoms of anxiety whereas there was an increased possibility of anxiety symptoms with the vegetarian pattern (OR 1.25, 95% CI 1.08–1.44) [48]. This is due to the reduced animal sources meat and fish in the vegetarian pattern; meat is the richest source of Vitamin B12 and fish is the main source of long-chain essential n-3 PUFA, especially docosahexaenoic acid (DHA; 22:6n-3). These nutrients are known to be necessary components for optimal neurological function [82]. The direction of causality between observed association between the vegetarian diet and increased maternal anxiety requires further exploration. In a prospective cohort of Brazilian women, researchers found that a pre-pregnancy healthy pattern (the common-Brazilian or healthy patterns) was inversely associated with depressive symptoms throughout pregnancy, even to early postpartum [49,50].

In the Osaka Maternal and Child Health Study, researchers hypothesized that a dietary pattern high in the main food sources of nutrients that are potentially protective against postpartum-depressive symptoms would be related to a lower risk of postpartum depression. However, there was no association between dietary patterns and the risk of depressive symptoms [51].

4.5. Preterm Birth

Preterm birth, defined as delivery before 37 weeks or 259 days of gestation occurs in about 10% of pregnancies globally, is significantly associated with neonatal mortality and morbidity, and has long-term adverse consequences for health [83,84].

In Denmark, a Mediterranean diet during pregnancy was associated with reduced risk of preterm birth (OR 0.61, 95% CI 0.35–1.05) [27]. Results from a large prospective cohort study in Norway, showed that a “traditional” dietary pattern or a “prudent” dietary pattern during pregnancy was associated with a reduced risk of preterm birth, 9% (OR 0.91, 95% CI 0.83–0.99) and 12% (OR 0.88, 95% CI 0.80–0.97) respectively [52]. In another large, prospective cohort of close to 60,000 Danish women followed during pregnancy, researchers found that a high intake of Western-type diet led to an increased risk of preterm birth (OR 1.30, 95% CI 1.13–1.49), while a seafood diet had a modestly protective effect (OR 0.90, 95% CI 0.72–1.11) [53]. Moreover, a study of the association between preconception dietary patterns and preterm birth demonstrated that a high-protein/fruit pattern reduced the likelihood of induced preterm birth (OR 0.31, 95% CI 0.13–0.72) and a high-fat/sugar/takeaway was positively associated with preterm birth (OR 1.54, 95% CI 1.10–2.15) and shorter gestational ages [54]. In contrast, in other studies there was no association between Mediterranean diet adherence during pregnancy and the risk of preterm birth [28,29], although a mother-child cohort study found that adherence to the Mediterranean diet was associated with a lower risk of preterm birth, specifically in overweight and obese women (OR 0.7, 95% CI 0.6–0.9) [29].

4.6. Fetal Growth

The baby’s health outcome is the single issue that a mother cares most about. Fetal growth is an important determinant of future health and development [85,86,87].

A high adherence to a maternal prudent diet (characterized by a high intakes of fruit and vegetables, whole meal bread, rice, and pasta, yogurt, and breakfast cereals and low intakes of chips and roast potatoes, sugar, white bread, processed meat, crisps, tinned vegetables, and soft drinks) was found to be associated with greater offspring bone size and bone mineral density; this study suggested that maternal dietary pattern during pregnancy was an independent determinant of bone mineral accrual in the offspring [55]. Through a prospective study of the Danish National Birth Cohort, researchers indicated that the maternal Western diet was positively associated with offspring forearm fractures (hazard ratio 1.11, 95% CI 1.01–1.23) [56].

Four studies have observed the relationship between maternal dietary patterns during pregnancy and subsequent small for gestational age (SGA) infants. A Danish study has found that the Western diet led to a significantly higher risk of having a SGA infant and lower birth weight [57]. In New Zealand, Thompson et al. found that the ‘traditional’ diet in early pregnancy was associated with a lower risk of having a SGA infant (OR 0.86, 95% CI 0.75–0.99) [58]. A Dutch study indicated that high adherence to a Mediterranean dietary pattern was associated with decreased risk of SGA [30]. In Japan, pregnant women in the ‘wheat products’ pattern had significantly higher probabilities of having a SGA infant (multivariate OR 5.2, 95% CI 1.1–24.4) [59].

Studies conducted in UK and Brazil both found a positive association between dietary pattern and birth weight, a ‘health conscious’ pattern in UK and a snack dietary pattern in Brazil [60,61]. Moreover, another study from the Netherlands suggested that high adherence to an energy-rich dietary pattern was associated with increased crown–rump length in the first trimester [62].

In contrast, two studies found that no dietary pattern was significantly associated with any of the birth outcomes [29,63]. An adherence to Mediterranean diet was not significantly associated with the risk of delivering an infant with fetal growth restriction [29]. No dietary pattern was significantly associated with any of the birth outcomes, the mixed dietary patterns may provide antagonistic relationships between foods and nutrients that result in null associations with birth outcomes [63].

4.7. Asthma

The prevalence of asthma and allergies in children has been increasing globally during the last few decades [88].

Four studies have examined the relationship between a maternal Mediterranean diet during pregnancy and asthma or other atopic conditions in children. Two studies found a protective effect of a high level of adherence to a Mediterranean diet during pregnancy against childhood atopic conditions at ages 6–7 years [31,32]. However, the other two studies suggested that a Mediterranean diet during pregnancy was not associated with infantile wheeze and eczema [33,34].

A Japanese study examined three maternal dietary patterns (Healthy, Western, and Japanese). The maternal Western pattern during pregnancy may have had a preventive effect against wheeze in offspring (OR 0.59, 95% CI 0.35–0.98), however, neither the Healthy diet nor Japanese diet during pregnancy was related to wheeze or eczema in offspring [64]. Two other studies investigated the association between maternal dietary patterns during pregnancy and wheeze, but none of the maternal dietary patterns was meaningfully associated with wheeze in the offspring [35,65].

A further study investigated the relationship between maternal diet and maternal asthma control during pregnancy. This study found pre-pregnancy dietary patterns influenced maternal asthma control [66].

4.8. Others

A small number of studies have investigated the association between dietary patterns and other pregnancy/offspring outcomes.

There are two global domains of child problem behavior: internalizing problems consist of emotionally reactive, anxious/depressed symptoms, somatic complaints and symptoms of being withdrawn; externalizing problems consist of attention problems and aggressive behavior. Both high adherence to the traditionally Dutch diet characterized by a high intakes of fresh and processed meat, potatoes, margarines and low intake of soy and diet products (OR 1.11, 95% CI 1.03–1.21) and low adherence to the Mediterranean diet (OR 0.90, 95% CI 0.83–0.97) during pregnancy are significantly associated with an increased risk of childhood externalizing problems; there were no associations between dietary patterns and child internalizing problems [67].

There are some studies of the congenital defect about babies. In contrast to the prudent diet (characterized by a high intakes of fish, garlic, nuts, and vegetables and a higher frequency of hot meals per day) users, mothers with the high adherence to the Western diet increased the risk of having an offspring with a cleft lip or cleft palate approximately two fold (OR 1.9, 95% CI 1.2–3.1) [68]. The Mediterranean dietary pattern seemed to have a protective effect in reducing the risk of offspring being affected by spine bifida [69]. A more ‘Non-health conscious’ maternal food pattern was associated with an increased risk of hypospadias in baby boys (OR 1.54, 95% CI 1.06–2.26) [70]. Women who adhered to a prudent dietary pattern, even when folate supplementation was administered, may have lower risk of neural tube defects (NTDs) and some heart defects [71].

When cancer in offspring was studies, Musselman et al. found that higher adherence to a diet that is high in fruits and vegetables was associated with a lower likelihood of childhood germ cell tumors (OR 0.83, 95% CI 0.69–0.99) [72]. A case-control study provided preliminary evidence that a diet higher in fruit and lower in fried foods and cured meats during pregnancy may decrease the risk of unilateral retinoblastoma in offspring (OR 0.75, 95% CI 0.61–0.92) [36].

5. Conclusions

The validity of identifying maternal dietary patterns and of studying the relationship between dietary patterns using FFQs has been demonstrated [14]. The majority of studies in this review used FFQs rather than diet scores to obtain a comprehensive account of dietary information. However, there are inevitable misclassifications in dietary intake; this is likely to bias the magnitude of the observed effects towards the null hypothesis. Moreover, as most of the diet information was obtained from memory, limitations of recall bias are also inevitable.

In a mother–child ‘Rhea’ cohort in Crete, Greece, two dietary patterns during pregnancy were identified using principal component analysis: ‘health conscious’ and ‘Western’. The ‘Western’ dietary pattern comprised mainly meat and meat products, potatoes, sugar and sweets, cereals, fats except olive oil, salty snacks, eggs, beverages and sauces [47]. In contrast, the Western pattern in a Japan study was characterized by low consumption of soft drinks and sweets [64]. The Western pattern in Greece may thus have been more extreme than the Western pattern in Japan. This is just one example of different dietary patterns in the different studies having the same name. In contrast, some patterns that have similar content have an alternative name in different studies. There is a variety of names for the ‘Mediterranean Diet’, such as Mediterranean-type diet, Mediterranean Diet Index, alternate Mediterranean Diet and Mediterranean Diet Score. Confusingly, the main diet content are similar, but the methods for calculation are subtly different, and dietary criteria to define the Mediterranean Diet was used for some studies [27,28] while much research used the method of scoring according to the consumption of various foodstuffs [22,25,26,29,30,31,32,33,34,35]. Therefore, a comparison between various research studies is both difficult and challenging and formal development of taxonomy and classification is required.

This review has highlighted many research studies of dietary patterns associated with pregnancy outcome, however, some pregnancy outcomes have yet to be investigated, such as intrahepatic cholestasis of pregnancy.

In addition, low-glycemic-index (GI) diet has also impact on pregnancy outcomes [89,90,91]. In recent years, low-GI diet has received increased interest from the public and researchers as an important strategy in GDM management [92]. However, low-GI diet mainly focuses on the glycemic index of food and its carbohydrate content, not the overall diet. We did not include it in our review. Also, there is a comprehensive evaluation of GI and pregnancy outcomes [92].

The studies detailed above highlight the importance of emphasising healthy dietary choices in preconception counseling to optimise not only reproductive outcomes but also general maternal health. Current guidelines of preconception care emphasise that nutrition and certain lifestyle factors play an important role in pregnancy. This review finds evidence that, for European countries, the Mediterranean diet is a relatively healthy diet. Importantly, the diets with higher intake of fruits, vegetables, legumes and fish have positive pregnancy outcomes in general and this conclusive evidence should be communicated to women specifically. As a modifiable factor, diet is a key area for intervention in pregnant women, but the precise content of the intervention is yet to be elucidated.

Acknowledgments

This work was supported by the National Natural Science Foundation of China (Hua Zhang, grant numbers 81370732, 81571453), (Yinyin Xia, grant number 81502777); the Natural Science Foundation Project of CQ CSTC (Yinyin Xia, grant number 2012jjA10070, 2015jcyjA10032); and the Science-Technology Research Program of the CQ Municipal Commission of Education (Yinyin Xia, grant number KJ1400231).

Abbreviations

The following abbreviations are used in this manuscript:

GDM gestational diabetes mellitus
FFQs food frequency questionnaires
PCA principal components analysis
LCA Latent Class Analysis
DASH Dietary Approaches to Stop Hypertension
aMED alternate Mediterranean Diet
aHEI alternate Healthy Eating Index
MUFA:SFA the ratio of monounsaturated fatty acid to saturated fatty acid
PUFA:SFA the ratio of polyunsaturated fatty acid to saturated fatty acid
DHA docosahexaenoic acid
EPA eicosapentaenooic acid
T2DM Type 2 diabetes mellitus
HDPs Hypertensive disorders of pregnancy
SGA small for gestational age
NTDs neural tube defects
GI glycemic-index

Author Contributions

XC, DZ and XM: were involved in writing the manuscript and contributed to critical revision of the manuscript; YX, PB and HZ had primary responsibility for final content.

Conflicts of Interest

The authors declare no conflict of interest.

References

  • 1.Bhutta Z.A., Das J.K., Rizvi A., Gaffey M.F., Walker N., Horton S., Webb P., Lartey A., Black R.E., The Lancet Nutrition Interventions Review Group et al. Evidence-based interventions for improvement of maternal and child nutrition: What can be done and at what cost? Lancet. 2013;382:452–477. doi: 10.1016/S0140-6736(13)60996-4. [DOI] [PubMed] [Google Scholar]
  • 2.Black R.E., Victora C.G., Walker S.P., Bhutta Z.A., Christian P., de Onis M., Ezzati M., Grantham-McGregor S., Katz J., Martorell R., et al. Maternal and child undernutrition and overweight in low-income and middle-income countries. Lancet. 2013;382:427–451. doi: 10.1016/S0140-6736(13)60937-X. [DOI] [PubMed] [Google Scholar]
  • 3.Rush D. Nutrition and maternal mortality in the developing world. Am. J. Clin. Nutr. 2000;72:212S–240S. doi: 10.1093/ajcn/72.1.212S. [DOI] [PubMed] [Google Scholar]
  • 4.Bo S., Menato G., Lezo A., Signorile A., Bardelli C., De Michieli F., Massobrio M., Pagano G. Dietary fat and gestational hyperglycaemia. Diabetologia. 2001;44:972–978. doi: 10.1007/s001250100590. [DOI] [PubMed] [Google Scholar]
  • 5.Park S., Kim M.Y., Baik S.H., Woo J.T., Kwon Y.J., Daily J.W., Park Y.M., Yang J.H., Kim S.H. Gestational diabetes is associated with high energy and saturated fat intakes and with low plasma visfatin and adiponectin levels independent of prepregnancy BMI. Eur. J. Clin. Nutr. 2013;67:196–201. doi: 10.1038/ejcn.2012.207. [DOI] [PubMed] [Google Scholar]
  • 6.Saldana T.M., Siega-Riz A.M., Adair L.S. Effect of macronutrient intake on the development of glucose intolerance during pregnancy. Am. J. Clin. Nutr. 2004;79:479–486. doi: 10.1093/ajcn/79.3.479. [DOI] [PubMed] [Google Scholar]
  • 7.Chen L., Hu F.B., Yeung E., Willett W., Zhang C. Prospective study of pre-gravid sugar-sweetened beverage consumption and the risk of gestational diabetes mellitus. Diabetes Care. 2009;32:2236–2241. doi: 10.2337/dc09-0866. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Ley S.H., Hanley A.J., Retnakaran R., Sermer M., Zinman B., O’Connor D.L. Effect of macronutrient intake during the second trimester on glucose metabolism later in pregnancy. Am. J. Clin. Nutr. 2011;94:1232–1240. doi: 10.3945/ajcn.111.018861. [DOI] [PubMed] [Google Scholar]
  • 9.Ying H., Wang D.F. Effects of dietary fat on onset of gestational diabetes mellitus. Zhonghua Fu Chan Ke Za Zhi. 2006;41:729–731. [PubMed] [Google Scholar]
  • 10.Jing X., Qiao R., Li M., Liu X., Kang D., Huang C. Gestational diabetes mellitus and the lifestyle and dietary structure of pregnant women: A case-control study. Wei Sheng Yan Jiu. 2010;39:209–211. [PubMed] [Google Scholar]
  • 11.Hofmeyr G.J., Lawrie T.A., Atallah A.N., Duley L., Torloni M.R. Calcium supplementation during pregnancy for preventing hypertensive disorders and related problems. Cochrane Database Syst. Rev. 2014;6:CD001059. doi: 10.1002/14651858.CD001059.pub4. [DOI] [PubMed] [Google Scholar]
  • 12.Villar J., Abdel-Aleem H., Merialdi M., Mathai M., Ali M.M., Zavaleta N., Purwar M., Hofmeyr J., Nguyen T.N., Campodonico L., et al. World health organization randomized trial of calcium supplementation among low calcium intake pregnant women. Am. J. Obstet Gynecol. 2006;194:639–649. doi: 10.1016/j.ajog.2006.01.068. [DOI] [PubMed] [Google Scholar]
  • 13.Hu F.B. Dietary pattern analysis: A new direction in nutritional epidemiology. Curr. Opin. Lipidol. 2002;13:3–9. doi: 10.1097/00041433-200202000-00002. [DOI] [PubMed] [Google Scholar]
  • 14.Loy S.L., Jan Mohamed H.J.B. Relative validity of dietary patterns during pregnancy assessed with a food frequency questionnaire. Int. J. Food Sci. Nutr. 2013;64:668–673. doi: 10.3109/09637486.2013.787398. [DOI] [PubMed] [Google Scholar]
  • 15.Northstone K., Emmett P.M., Rogers I. Dietary patterns in pregnancy and associations with nutrient intakes. Br. J. Nutr. 2008;99:406–415. doi: 10.1017/S0007114507803977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Martinez M.E., Marshall J.R., Sechrest L. Invited commentary: Factor analysis and the search for objectivity. Am. J. Epidemiol. 1998;148:17–19. doi: 10.1093/oxfordjournals.aje.a009552. [DOI] [PubMed] [Google Scholar]
  • 17.Hoffman K., Schulze M.B., Boeing H., Altenburg H.P. Dietary patterns: Report of an international workshop. Public Health Nutr. 2002;5:89–90. doi: 10.1079/PHN2001252. [DOI] [PubMed] [Google Scholar]
  • 18.Sotres-Alvarez D., Herring A.H., Siega-Riz A.M. Latent class analysis is useful to classify pregnant women into dietary patterns. J. Nutr. 2010;140:2253–2259. doi: 10.3945/jn.110.124909. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Northstone K., Emmett P., Rogers I. Dietary patterns in pregnancy and associations with socio-demographic and lifestyle factors. Eur. J. Clin. Nutr. 2008;62:471–479. doi: 10.1038/sj.ejcn.1602741. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Chavarro J.E., Rich-Edwards J.W., Rosner B.A., Willett W.C. Diet and lifestyle in the prevention of ovulatory disorder infertility. Obstet Gynecol. 2007;110:1050–1058. doi: 10.1097/01.AOG.0000287293.25465.e1. [DOI] [PubMed] [Google Scholar]
  • 21.Bao W., Bowers K., Tobias D.K., Olsen S.F., Chavarro J., Vaag A., Kiely M., Zhang C. Prepregnancy low-carbohydrate dietary pattern and risk of gestational diabetes mellitus: A prospective cohort study. Am. J. Clin. Nutr. 2014;99:1378–1384. doi: 10.3945/ajcn.113.082966. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Karamanos B., Thanopoulou A., Anastasiou E., Assaad-Khalil S., Albache N., Bachaoui M., Slama C.B., El Ghomari H., Jotic A., Lalic N., et al. Relation of the mediterranean diet with the incidence of gestational diabetes. Eur. J. Clin. Nutr. 2014;68:8–13. doi: 10.1038/ejcn.2013.177. [DOI] [PubMed] [Google Scholar]
  • 23.Asemi Z., Tabassi Z., Samimi M., Fahiminejad T., Esmaillzadeh A. Favourable effects of the dietary approaches to stop hypertension diet on glucose tolerance and lipid profiles in gestational diabetes: A randomised clinical trial. Br. J. Nutr. 2013;109:2024–2030. doi: 10.1017/S0007114512004242. [DOI] [PubMed] [Google Scholar]
  • 24.Asemi Z., Samimi M., Tabassi Z., Sabihi S.S., Esmaillzadeh A. A randomized controlled clinical trial investigating the effect of dash diet on insulin resistance, inflammation, and oxidative stress in gestational diabetes. Nutrition. 2013;29:619–624. doi: 10.1016/j.nut.2012.11.020. [DOI] [PubMed] [Google Scholar]
  • 25.Tobias D.K., Zhang C., Chavarro J., Bowers K., Rich-Edwards J., Rosner B., Mozaffarian D., Hu F.B. Prepregnancy adherence to dietary patterns and lower risk of gestational diabetes mellitus. Am. J. Clin. Nutr. 2012;96:289–295. doi: 10.3945/ajcn.111.028266. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Tobias D.K., Hu F.B., Chavarro J., Rosner B., Mozaffarian D., Zhang C. Healthful dietary patterns and type 2 diabetes mellitus risk among women with a history of gestational diabetes mellitus. Arch. Intern. Med. 2012;172:1566–1572. doi: 10.1001/archinternmed.2012.3747. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Mikkelsen T.B., Osterdal M.L., Knudsen V.K., Haugen M., Meltzer H.M., Bakketeig L., Olsen S.F. Association between a mediterranean-type diet and risk of preterm birth among Danish women: A prospective cohort study. Acta Obstet. Gynecol. Scand. 2008;87:325–330. doi: 10.1080/00016340801899347. [DOI] [PubMed] [Google Scholar]
  • 28.Haugen M., Meltzer H.M., Brantsaeter A.L., Mikkelsen T., Osterdal M.L., Alexander J., Olsen S.F., Bakketeig L. Mediterranean-type diet and risk of preterm birth among women in the norwegian mother and child cohort study (Moba): A prospective cohort study. Acta Obstet. Gynecol. Scand. 2008;87:319–324. doi: 10.1080/00016340801899123. [DOI] [PubMed] [Google Scholar]
  • 29.Saunders L., Guldner L., Costet N., Kadhel P., Rouget F., Monfort C., Thome J.P., Multigner L., Cordier S. Effect of a mediterranean diet during pregnancy on fetal growth and preterm delivery: Results from a French Caribbean mother-child cohort study (Timoun) Paediatr. Perinat Epidemiol. 2014;28:235–244. doi: 10.1111/ppe.12113. [DOI] [PubMed] [Google Scholar]
  • 30.Timmermans S., Steegers-Theunissen R.P., Vujkovic M., den Breeijen H., Russcher H., Lindemans J., Mackenbach J., Hofman A., Lesaffre E.E., Jaddoe V.V., et al. The mediterranean diet and fetal size parameters: The generation R study. Br. J. Nutr. 2012;108:1399–1409. doi: 10.1017/S000711451100691X. [DOI] [PubMed] [Google Scholar]
  • 31.Chatzi L., Torrent M., Romieu I., Garcia-Esteban R., Ferrer C., Vioque J., Kogevinas M., Sunyer J. Mediterranean diet in pregnancy is protective for wheeze and atopy in childhood. Thorax. 2008;63:507–513. doi: 10.1136/thx.2007.081745. [DOI] [PubMed] [Google Scholar]
  • 32.De Batlle J., Garcia-Aymerich J., Barraza-Villarreal A., Anto J.M., Romieu I. Mediterranean diet is associated with reduced asthma and rhinitis in Mexican children. Allergy. 2008;63:1310–1316. doi: 10.1111/j.1398-9995.2008.01722.x. [DOI] [PubMed] [Google Scholar]
  • 33.Castro-Rodriguez J.A., Garcia-Marcos L., Sanchez-Solis M., Perez-Fernandez V., Martinez-Torres A., Mallol J. Olive oil during pregnancy is associated with reduced wheezing during the first year of life of the offspring. Pediatr. Pulmonol. 2010;45:395–402. doi: 10.1002/ppul.21205. [DOI] [PubMed] [Google Scholar]
  • 34.Chatzi L., Garcia R., Roumeliotaki T., Basterrechea M., Begiristain H., Iniguez C., Vioque J., Kogevinas M., Sunyer J., INMA study group et al. Mediterranean diet adherence during pregnancy and risk of wheeze and eczema in the first year of life: Inma (Spain) and rhea (Greece) mother-child cohort studies. Br. J. Nutr. 2013;110:2058–2068. doi: 10.1017/S0007114513001426. [DOI] [PubMed] [Google Scholar]
  • 35.Lange N.E., Rifas-Shiman S.L., Camargo C.A., Gold D.R., Gillman M.W., Litonjua A.A. Maternal dietary pattern during pregnancy is not associated with recurrent wheeze in children. J. Allergy Clin. Immunol. 2010;126:250–255. doi: 10.1016/j.jaci.2010.05.009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Lombardi C., Ganguly A., Bunin G.R., Azary S., Alfonso V., Ritz B., Heck J.E. Maternal diet during pregnancy and unilateral retinoblastoma. Cancer Causes Control. 2015;26:387–397. doi: 10.1007/s10552-014-0514-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Vujkovic M., de Vries J.H., Lindemans J., Macklon N.S., van der Spek P.J., Steegers E.A., Steegers-Theunissen R.P. The preconception mediterranean dietary pattern in couples undergoing in vitro fertilization/intracytoplasmic sperm injection treatment increases the chance of pregnancy. Fertil Steril. 2010;94:2096–2101. doi: 10.1016/j.fertnstert.2009.12.079. [DOI] [PubMed] [Google Scholar]
  • 38.Toledo E., Lopez-del Burgo C., Ruiz-Zambrana A., Donazar M., Navarro-Blasco I., Martinez-Gonzalez M.A., de Irala J. Dietary patterns and difficulty conceiving: A nested case-control study. Fertil Steril. 2011;96:1149–1153. doi: 10.1016/j.fertnstert.2011.08.034. [DOI] [PubMed] [Google Scholar]
  • 39.Zhang C., Schulze M.B., Solomon C.G., Hu F.B. A prospective study of dietary patterns, meat intake and the risk of gestational diabetes mellitus. Diabetologia. 2006;49:2604–2613. doi: 10.1007/s00125-006-0422-1. [DOI] [PubMed] [Google Scholar]
  • 40.Tryggvadottir E.A., Medek H., Birgisdottir B.E., Geirsson R.T., Gunnarsdottir I. Association between healthy maternal dietary pattern and risk for gestational diabetes mellitus. Eur. J. Clin. Nutr. 2016;70:237–242. doi: 10.1038/ejcn.2015.145. [DOI] [PubMed] [Google Scholar]
  • 41.He J.R., Yuan M.Y., Chen N.N., Lu J.H., Hu C.Y., Mai W.B., Zhang R.F., Pan Y.H., Qiu L., Wu Y.F., et al. Maternal dietary patterns and gestational diabetes mellitus: A large prospective cohort study in China. Br. J. Nutr. 2015;113:1292–1300. doi: 10.1017/S0007114515000707. [DOI] [PubMed] [Google Scholar]
  • 42.Schoenaker D.A., Soedamah-Muthu S.S., Callaway L.K., Mishra G.D. Pre-pregnancy dietary patterns and risk of gestational diabetes mellitus: Results from an Australian population-based prospective cohort study. Diabetologia. 2015;58:2726–2735. doi: 10.1007/s00125-015-3742-1. [DOI] [PubMed] [Google Scholar]
  • 43.Schoenaker D.A., Soedamah-Muthu S.S., Callaway L.K., Mishra G.D. Prepregnancy dietary patterns and risk of developing hypertensive disorders of pregnancy: Results from the Australian longitudinal study on women’s health. Am. J. Clin. Nutr. 2015;102:94–101. doi: 10.3945/ajcn.114.102475. [DOI] [PubMed] [Google Scholar]
  • 44.Brantsaeter A.L., Haugen M., Samuelsen S.O., Torjusen H., Trogstad L., Alexander J., Magnus P., Meltzer H.M. A dietary pattern characterized by high intake of vegetables, fruits, and vegetable oils is associated with reduced risk of preeclampsia in nulliparous pregnant Norwegian women. J. Nutr. 2009;139:1162–1168. doi: 10.3945/jn.109.104968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Timmermans S., Steegers-Theunissen R.P., Vujkovic M., Bakker R., den Breeijen H., Raat H., Russcher H., Lindemans J., Hofman A., Jaddoe V.W., et al. Major dietary patterns and blood pressure patterns during pregnancy: The generation R study. Am. J. Obstet. Gynecol. 2011;205:337.e1–337.e12. doi: 10.1016/j.ajog.2011.05.013. [DOI] [PubMed] [Google Scholar]
  • 46.Eshriqui I., Vilela A.A., Rebelo F., Farias D.R., Castro M.B., Kac G. Gestational dietary patterns are not associated with blood pressure changes during pregnancy and early postpartum in a Brazilian prospective cohort. Eur. J. Nutr. 2016;55:21–32. doi: 10.1007/s00394-014-0819-4. [DOI] [PubMed] [Google Scholar]
  • 47.Chatzi L., Melaki V., Sarri K., Apostolaki I., Roumeliotaki T., Georgiou V., Vassilaki M., Koutis A., Bitsios P., Kogevinas M. Dietary patterns during pregnancy and the risk of postpartum depression: The mother-child ‘rhea’ cohort in Crete, Greece. Public Health Nutr. 2011;14:1663–1670. doi: 10.1017/S1368980010003629. [DOI] [PubMed] [Google Scholar]
  • 48.Vaz Jdos S., Kac G., Emmett P., Davis J.M., Golding J., Hibbeln J.R. Dietary patterns, n-3 fatty acids intake from seafood and high levels of anxiety symptoms during pregnancy: Findings from the Avon longitudinal study of parents and children. PLoS ONE. 2013;8:351. doi: 10.1371/journal.pone.0067671. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Vilela A.A., Farias D.R., Eshriqui I., Vaz Jdos S., Franco-Sena A.B., Castro M.B., Olinto M.T., Machado S.P., Moura da Silva A.A., Kac G. Prepregnancy healthy dietary pattern is inversely associated with depressive symptoms among pregnant Brazilian women. J. Nutr. 2014;144:1612–1618. doi: 10.3945/jn.114.190488. [DOI] [PubMed] [Google Scholar]
  • 50.Vilela A.A., Pinto T.J., Rebelo F., Benaim C., Lepsch J., Dias-Silva C.H., Castro M.B., Kac G. Association of prepregnancy dietary patterns and anxiety symptoms from midpregnancy to early postpartum in a prospective cohort of Brazilian women. J. Acad. Nutr. Diet. 2015;115:1626–1635. doi: 10.1016/j.jand.2015.01.007. [DOI] [PubMed] [Google Scholar]
  • 51.Okubo H., Miyake Y., Sasaki S., Tanaka K., Murakami K., Hirota Y., Osaka Maternal and Child Health Study Group Dietary patterns during pregnancy and the risk of postpartum depression in Japan: The Osaka maternal and child health study. Br. J. Nutr. 2011;105:1251–1257. doi: 10.1017/S0007114510004782. [DOI] [PubMed] [Google Scholar]
  • 52.Englund-Ogge L., Brantsaeter A.L., Sengpiel V., Haugen M., Birgisdottir B.E., Myhre R., Meltzer H.M., Jacobsson B. Maternal dietary patterns and preterm delivery: Results from large prospective cohort study. BMJ. 2014;348:g1446. doi: 10.1136/bmj.g1446. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 53.Rasmussen M.A., Maslova E., Halldorsson T.I., Olsen S.F. Characterization of dietary patterns in the Danish national birth cohort in relation to preterm birth. PLoS ONE. 2014;9:351. doi: 10.1371/journal.pone.0093644. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.Grieger J.A., Grzeskowiak L.E., Clifton V.L. Preconception dietary patterns in human pregnancies are associated with preterm delivery. J. Nutr. 2014;144:1075–1080. doi: 10.3945/jn.114.190686. [DOI] [PubMed] [Google Scholar]
  • 55.Cole Z.A., Gale C.R., Javaid M.K., Robinson S.M., Law C., Boucher B.J., Crozier S.R., Godfrey K.M., Dennison E.M., Cooper C. Maternal dietary patterns during pregnancy and childhood bone mass: A longitudinal study. J. Bone Miner Res. 2009;24:663–668. doi: 10.1359/jbmr.081212. [DOI] [PubMed] [Google Scholar]
  • 56.Petersen S.B., Rasmussen M.A., Olsen S.F., Vestergaard P., Molgaard C., Halldorsson T.I., Strom M. Maternal dietary patterns during pregnancy in relation to offspring forearm fractures: Prospective study from the Danish national birth cohort. Nutrients. 2015;7:2382–2400. doi: 10.3390/nu7042382. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 57.Knudsen V.K., Orozova-Bekkevold I.M., Mikkelsen T.B., Wolff S., Olsen S.F. Major dietary patterns in pregnancy and fetal growth. Eur. J. Clin. Nutr. 2008;62:463–470. doi: 10.1038/sj.ejcn.1602745. [DOI] [PubMed] [Google Scholar]
  • 58.Thompson J.M., Wall C., Becroft D.M., Robinson E., Wild C.J., Mitchell E.A. Maternal dietary patterns in pregnancy and the association with small-for-gestational-age infants. Br. J. Nutr. 2010;103:1665–1673. doi: 10.1017/S0007114509993606. [DOI] [PubMed] [Google Scholar]
  • 59.Okubo H., Miyake Y., Sasaki S., Tanaka K., Murakami K., Hirota Y., Osaka Maternal and Child Health Study Group Maternal dietary patterns in pregnancy and fetal growth in Japan: The Osaka maternal and child health study. Br. J. Nutr. 2012;107:1526–1533. doi: 10.1017/S0007114511004636. [DOI] [PubMed] [Google Scholar]
  • 60.Northstone K., Ness A.R., Emmett P.M., Rogers I.S. Adjusting for energy intake in dietary pattern investigations using principal components analysis. Eur. J. Clin. Nutr. 2008;62:931–938. doi: 10.1038/sj.ejcn.1602789. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 61.Coelho N.D.L.P., Cunha D.B., Esteves A.P., Lacerda E.M., Theme Filha M.M. Dietary patterns in pregnancy and birth weight. Rev. Saude Publica. 2015;49:62. doi: 10.1590/S0034-8910.2015049005403. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62.Bouwland-Both M.I., Steegers-Theunissen R.P., Vujkovic M., Lesaffre E.M., Mook-Kanamori D.O., Hofman A., Lindemans J., Russcher H., Jaddoe V.W., Steegers E.A. A periconceptional energy-rich dietary pattern is associated with early fetal growth: The generation R study. BJOG. 2013;120:435–445. doi: 10.1111/1471-0528.12086. [DOI] [PubMed] [Google Scholar]
  • 63.Colon-Ramos U., Racette S.B., Ganiban J., Nguyen T.G., Kocak M., Carroll K.N., Volgyi E., Tylavsky F.A. Association between dietary patterns during pregnancy and birth size measures in a diverse population in Southern US. Nutrients. 2015;7:1318–1332. doi: 10.3390/nu7021318. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 64.Miyake Y., Okubo H., Sasaki S., Tanaka K., Hirota Y. Maternal dietary patterns during pregnancy and risk of wheeze and eczema in Japanese infants aged 16–24 months: The osaka maternal and child health study. Pediatr. Allergy Immunol. 2011;22:734–741. doi: 10.1111/j.1399-3038.2011.01176.x. [DOI] [PubMed] [Google Scholar]
  • 65.Shaheen S.O., Northstone K., Newson R.B., Emmett P.M., Sherriff A., Henderson A.J. Dietary patterns in pregnancy and respiratory and atopic outcomes in childhood. Thorax. 2009;64:411–417. doi: 10.1136/thx.2008.104703. [DOI] [PubMed] [Google Scholar]
  • 66.Grieger J.A., Grzeskowiak L.E., Wood L.G., Clifton V.L. Asthma control in pregnancy is associated with pre-conception dietary patterns. Public Health Nutr. 2016;19:332–338. doi: 10.1017/S1368980015001226. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 67.Steenweg-de Graaff J., Tiemeier H., Steegers-Theunissen R.P., Hofman A., Jaddoe V.W., Verhulst F.C., Roza S.J. Maternal dietary patterns during pregnancy and child internalising and externalising problems. The generation R study. Clin. Nutr. 2014;33:115–121. doi: 10.1016/j.clnu.2013.03.002. [DOI] [PubMed] [Google Scholar]
  • 68.Vujkovic M., Ocke M.C., van der Spek P.J., Yazdanpanah N., Steegers E.A., Steegers-Theunissen R.P. Maternal Western dietary patterns and the risk of developing a cleft lip with or without a cleft palate. Obstet. Gynecol. 2007;110:378–384. doi: 10.1097/01.AOG.0000268799.37044.c3. [DOI] [PubMed] [Google Scholar]
  • 69.Vujkovic M., Steegers E.A., Looman C.W., Ocke M.C., van der Spek P.J., Steegers-Theunissen R.P. The maternal mediterranean dietary pattern is associated with a reduced risk of spina bifida in the offspring. BJOG. 2009;116:408–415. doi: 10.1111/j.1471-0528.2008.01963.x. [DOI] [PubMed] [Google Scholar]
  • 70.de Kort C.A., Nieuwenhuijsen M.J., Mendez M.A. Relationship between maternal dietary patterns and hypospadias. Paediatr. Perinat Epidemiol. 2011;25:255–264. doi: 10.1111/j.1365-3016.2011.01194.x. [DOI] [PubMed] [Google Scholar]
  • 71.Sotres-Alvarez D., Siega-Riz A.M., Herring A.H., Carmichael S.L., Feldkamp M.L., Hobbs C.A., Olshan A.F., The National Birth Defects Prevention Study Maternal dietary patterns are associated with risk of neural tube and congenital heart defects. Am. J. Epidemiol. 2013;177:1279–1288. doi: 10.1093/aje/kws349. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 72.Musselman J.R., Jurek A.M., Johnson K.J., Linabery A.M., Robison L.L., Shu X.O., Ross J.A. Maternal dietary patterns during early pregnancy and the odds of childhood germ cell tumors: A children’s oncology group study. Am. J. Epidemiol. 2011;173:282–291. doi: 10.1093/aje/kwq365. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 73.Practice Committee of tAmerican Society for Reproductive Medicine Definitions of infertility and recurrent pregnancy loss. Fertil. Steril. 2008;90:S60. doi: 10.1016/j.fertnstert.2008.08.065. [DOI] [PubMed] [Google Scholar]
  • 74.Boivin J., Bunting L., Collins J.A., Nygren K.G. International estimates of infertility prevalence and treatment-seeking: Potential need and demand for infertility medical care. Hum. Reprod. 2007;22:1506–1512. doi: 10.1093/humrep/dem046. [DOI] [PubMed] [Google Scholar]
  • 75.Reece E.A., Leguizamon G., Wiznitzer A. Gestational diabetes: The need for a common ground. Lancet. 2009;373:1789–1797. doi: 10.1016/S0140-6736(09)60515-8. [DOI] [PubMed] [Google Scholar]
  • 76.Sibai B., Dekker G., Kupferminc M. Pre-eclampsia. Lancet. 2005;365:785–799. doi: 10.1016/S0140-6736(05)71003-5. [DOI] [PubMed] [Google Scholar]
  • 77.Shakeel N., Eberhard-Gran M., Sletner L., Slinning K., Martinsen E.W., Holme I., Jenum A.K. A prospective cohort study of depression in pregnancy, prevalence and risk factors in a multi-ethnic population. BMC Pregnancy Childbirth. 2015;15:351. doi: 10.1186/s12884-014-0420-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 78.Kinsella M.T., Monk C. Impact of maternal stress, depression and anxiety on fetal neurobehavioral development. Clin. Obstet Gynecol. 2009;52:425–440. doi: 10.1097/GRF.0b013e3181b52df1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 79.Marcus S.M. Depression during pregnancy: Rates, risks and consequences—Motherisk update 2008. Can. J. Clin. Pharmacol. 2009;16:e15–e22. [PubMed] [Google Scholar]
  • 80.Dunkel Schetter C., Tanner L. Anxiety, depression and stress in pregnancy: Implications for mothers, children, research, and practice. Curr. Opin. Psychiatry. 2012;25:141–148. doi: 10.1097/YCO.0b013e3283503680. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 81.Broekman B.F., Chan Y.H., Chong Y.S., Kwek K., Cohen S.S., Haley C.L., Chen H., Chee C., Rifkin-Graboi A., Gluckman P.D., et al. The influence of anxiety and depressive symptoms during pregnancy on birth size. Paediatr. Perinat Epidemiol. 2014;28:116–126. doi: 10.1111/ppe.12096. [DOI] [PubMed] [Google Scholar]
  • 82.Hibbeln J.R., Davis J.M. Considerations regarding neuropsychiatric nutritional requirements for intakes of omega-3 highly unsaturated fatty acids. Prostaglandins Leukot Essent Fatty Acids. 2009;81:179–186. doi: 10.1016/j.plefa.2009.06.005. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 83.Beck S., Wojdyla D., Say L., Betran A.P., Merialdi M., Requejo J.H., Rubens C., Menon R., Van Look P.F. The worldwide incidence of preterm birth: A systematic review of maternal mortality and morbidity. Bull World Health Organ. 2010;88:31–38. doi: 10.2471/BLT.08.062554. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 84.Pennell C.E., Jacobsson B., Williams S.M., Buus R.M., Muglia L.J., Dolan S.M., Morken N.H., Ozcelik H., Lye S.J., PREBIC Genetics Working Group et al. Genetic epidemiologic studies of preterm birth: Guidelines for research. Am. J. Obstet Gynecol. 2007;196:107–118. doi: 10.1016/j.ajog.2006.03.109. [DOI] [PubMed] [Google Scholar]
  • 85.Barker D.J. Maternal nutrition, fetal nutrition, and disease in later life. Nutrition. 1997;13:807–813. doi: 10.1016/S0899-9007(97)00193-7. [DOI] [PubMed] [Google Scholar]
  • 86.Zadik Z. Maternal nutrition, fetal weight, body composition and disease in later life. J. Endocrinol. Investig. 2003;26:941–945. doi: 10.1007/BF03345248. [DOI] [PubMed] [Google Scholar]
  • 87.Harding J.E. The nutritional basis of the fetal origins of adult disease. Int. J. Epidemiol. 2001;30:15–23. doi: 10.1093/ije/30.1.15. [DOI] [PubMed] [Google Scholar]
  • 88.Braman S.S. The global burden of asthma. Chest. 2006;130:4S–12S. doi: 10.1378/chest.130.1_suppl.4S. [DOI] [PubMed] [Google Scholar]
  • 89.Walsh J.M., McGowan C.A., Mahony R., Foley M.E., McAuliffe F.M. Low glycaemic index diet in pregnancy to prevent macrosomia (rolo study): Randomised control trial. BMJ. 2012;345:e5605. doi: 10.1136/bmj.e5605. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 90.Horan M.K., McGowan C.A., Gibney E.R., Donnelly J.M., McAuliffe F.M. Maternal diet and weight at 3 months postpartum following a pregnancy intervention with a low glycaemic index diet: Results from the rolo randomised control trial. Nutrients. 2014;6:2946–2955. doi: 10.3390/nu6072946. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 91.Horan M.K., McGowan C.A., Gibney E.R., Donnelly J.M., McAuliffe F.M. Maternal low glycaemic index diet, fat intake and postprandial glucose influences neonatal adiposity—Secondary analysis from the rolo study. Nutr. J. 2014;13:78. doi: 10.1186/1475-2891-13-78. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 92.McGowan C.A., McAuliffe F.M. The influence of maternal glycaemia and dietary glycaemic index on pregnancy outcome in healthy mothers. Br. J. Nutr. 2010;104:153–159. doi: 10.1017/S0007114510000425. [DOI] [PubMed] [Google Scholar]

Articles from Nutrients are provided here courtesy of Multidisciplinary Digital Publishing Institute (MDPI)

RESOURCES