Abstract
Objective
Elderly people may be at particular risk of Zn deficiency due to an increased prevalence of malnutrition. The aim of the present study was to evaluate the Zn status in community-living elderly people at risk of malnutrition.
Design
Cross-sectional population-based survey. Individuals at risk of malnutrition were identified by the Malnutrition Universal Screening Tool. Zn status was assessed by measuring serum Zn. Logistic regression was performed to evaluate the association between the risk of malnutrition and Zn deficiency.
Setting
Municipality of Tromsø, Norway.
Subjects
Random sample of 743 men and 778 women aged 65–87 years.
Results
Zn deficiency was found in 10·1 % of the participants, including 13·1 % of the men and 7·3 % of the women. Among the men and women at risk of malnutrition, 31·0 % and 12·7 %, respectively, had Zn deficiency. In a model adjusted for age, gender, serum albumin and smoking status, Zn deficiency was positively associated with the risk of malnutrition (OR=2·2; 95 % CI 1·3, 3·6).
Conclusions
Overall, Zn deficiency was found in one out of ten community-living elderly people and was associated with the risk of malnutrition. Our results encourage the assessment of Zn status in elderly people at risk of malnutrition, with a special emphasis on elderly men.
Keywords: Zinc deficiency, Elderly people, Malnutrition, Malnutrition Universal Screening Tool, Mental distress
Zn is an essential micronutrient present in all body tissues and fluids. It is contained in a large number of enzymes. Second only to Fe, Zn is the most abundant trace element in man( 1 ). Mild Zn deficiency may be associated with impaired taste and smell, reduced immunity and increased risk of pneumonia( 2 , 3 ). In cases of severe Zn deficiency, skin lesions, anaemia, diarrhoea, anorexia, decreased lymphocyte function, impaired visual function and mental retardation may be observed( 4 ). An increased risk of depression in individuals with Zn deficiency has been previously reported( 5 ). At present, community-based research on the impact of Zn deficiency on mental health is scarce.
Important causes of reduced body Zn include a low intake of Zn-containing foods and a decreased absorption of Zn due to intestinal malabsorption( 2 ). Meat is a good source of Zn. Additionally, plant-based foods contain Zn. However, phytate in many plants reduces the bioavailability of Zn from those plants. Worldwide, Zn deficiency is regarded as a significant contributor to the disease burden, especially among children in developing countries( 6 ). In the developed part of the world, elderly people may be at particular risk for Zn deficiency due to an increased prevalence of malnutrition( 7 ). However, previous studies from Belgium and the UK exploring the relationship between malnutrition and Zn deficiency in elderly individuals have yielded conflicting results( 8 , 9 ).
Moreover, previous studies addressing Zn status in the general population of elderly men and women have mostly included a limited number of participants; only a few larger population-based studies of Zn status in elderly people have been conducted. The prevalence of Zn deficiency has been found to be between 6 and 15 %( 10 ).
Therefore, in the present study, we aimed to evaluate both the Zn status and the association between Zn deficiency and risk of malnutrition in a large sample of community-living elderly individuals.
Methods
Study population
The Tromsø Study is a population-based health study of the population of Tromsø, a town with 70 000 inhabitants in northern Norway( 11 ). The 6th survey of the Tromsø Study was conducted between October 2007 and December 2008( 12 ). We restricted our analysis to participants between 65 and 87 years of age, and all inhabitants in this age group (n 6098) were invited. A total of 4017 men and women participated by going to a study centre for data collection, yielding an overall participation rate of 66 % (4017/6098). Serum from all participating individuals was frozen, and serum Zn and albumin were later analysed in a random selection of 1765 individuals. The blood collection tubes were free of trace elements and the needles were of standard type. Information on weight loss, height or weight was missing for 200 individuals. Due to laboratory technical problems, forty-four samples were discarded. Consequently, a population of 1521 men and women was included in the present analysis.
Zinc and albumin analysis
Non-fasting venous blood samples were collected for the measurement of Zn and albumin using trace-metal-free tubes to avoid contamination. The samples were frozen and stored at −70°C, and the serum Zn was analysed later using flame atomic absorption at a wavelength of 213·9 nm (Perkin Elmer AAnalyst 800 Atomic Absorption Spectrophotometer). Serum Zn concentrations have diurnal variations, with the highest values present in the morning and slightly reduced values present after food intake later in the day( 13 ). The International Zinc Nutrition Consultative Group recommended different serum Zn cut-off values according to gender (men or women), fasting state (non-fasting or fasting) and time of measurement (AM or PM)( 13 ). In the present study, the participants visited the research centre between 8 am and 5:30 pm. According to the International Zinc Nutrition Consultative Group guidelines, we applied the non-fasting AM or PM cut-off values for men and women depending on attendance time, i.e. cut-offs of 10·7 μmol/l (AM) and 9·3 μmol/l (PM) for men and 10·1 μmol/l (AM) and 9·0 μmol/l (PM) for women. Zn deficiency was defined as a serum Zn level below these cut-off values.
Because a large proportion of Zn in the serum is bound to albumin( 13 ), an additional assessment of the serum albumin was necessary using the bromocresol green method (Hitachi Modular P, Roche). The lower reference for serum albumin was 34·0 g/l.
Nutritional assessment
Height and weight were measured without shoes and in light clothing. BMI was calculated as weight divided by the square of height (kg/m2). The participants were asked if they had involuntarily lost weight during the last 6 months and, if so, how many kilograms they had lost. The weight loss was grouped as below 5 %, between 5 % and 10 % or above 10 % of body weight prior to weight loss. Based on both BMI and degree of weight loss, we categorised each individual as being at low, medium or high risk of malnutrition, according to the Malnutrition Universal Screening Tool (MUST; Fig. 1). This tool also has an acute disease component (associated with a lack of nutritional intake for >5 d) that, in our analyses, was set to zero because all of the participants presented at the research centre and were thus regarded as not acutely ill. The weight loss question in the present study was slightly modified to address weight loss over a time span of the ‘last 6 months’, but this encompass the time span of the ‘last 3−6 months’ in the original ‘MUST’ tool. The British Society of Parenteral and Enteral nutrition (www.bapen.org.uk) developed the ‘MUST’ tool( 14 ) and it is one of the nutritional screening instruments recommended by the European Society for Parenteral and Enteral nutrition for use in non-institutionalised elderly( 15 ).
Fig. 1.
The Malnutrition Universal Screening Tool (MUST) is composed of a BMI score, a weight-loss score and an acute illness component. The risk of malnutrition can be assessed based on the sum of these scores. The ‘MUST’ tool is reproduced here with the kind permission of BAPEN (British Association for Parenteral and Enteral Nutrition). For further information on ‘MUST’ and management guidelines, see www.bapen.org.uk
Mental health, sociodemographic characteristics and lifestyle factors
We also aimed to study the association between Zn deficiency and mental health. The Hopkins Symptoms Check List-10 (SCL-10) was utilised to assess mental health distress. The SCL-10 is a self-administered instrument that primarily explores symptoms of anxiety and depression( 16 ). The ten items of the SCL-10 were part of the self-administered questionnaire that was included in the invitation to participate in the survey. The questionnaire was collected at the research centre. A higher SCL-10 score indicates a greater number of symptoms (score ranging between 1·0 and 4·0).
An important source of Zn in the Western diet is meat( 17 ). Frequency of meat intake during the preceeding week, smoking habits and sociodemographic variables were also obtained from the self-administered questionnaires.
Statistical analysis
Differences between both men and women and participants according to Zn status were analysed using the t test, χ 2 test or Mann–Whitney U test. The associations between risk of malnutrition (medium and high risk combined) and Zn deficiency were analysed using logistic regression, yielding odds ratio estimates with 95 % confidence intervals. The odds ratio estimates were adjusted for age, smoking status and serum albumin. The SCL-10 score was positively skewed, and the median SCL-10 values with 25–75 % interquartile range are reported. Two-sided P values <0·05 were considered statistically significant. The analyses were performed using the statistical software package IMB SPSS Statistics version 19·0.
Each participant provided written informed consent. The study was conducted according to the guidelines of the Declaration of Helsinki.
Results
A total of 743 men and 778 women were included in the analysis. A risk of malnutrition (medium and high risk combined) was found in 8·0 % of the participants, more often in women (10·4 %) than in men (5·5 %). BMI did not differ between men and women; however, former smoking was more common in men than in women (Table 1).
Table 1.
Characteristics of participating elderly men and women, the Tromsø Study, 2007–2008*
| All (n 1521) | Men (n 743) | Women (n 778) | |||||
|---|---|---|---|---|---|---|---|
| Mean, %, median or range | sd, n or IQR | Mean, %, median or range | sd, n or IQR | Mean, %, median or range | sd, n or IQR | P value† | |
| Age (years), mean and sd | 71·9 | 5·6 | 71·3 | 5·3 | 72·4 | 5·8 | <0·01‡ |
| Smoking status, % and n | |||||||
| Never smoked | 35·5 | 528 | 22·8 | 167 | 47·8 | 361 | |
| Previous smoker | 49·4 | 736 | 62·2 | 456 | 37·0 | 280 | <0·01§ |
| Current smoker | 15·1 | 225 | 15·0 | 110 | 15·2 | 115 | |
| Nutritional status | |||||||
| BMI (kg/m2), mean and sd | 26·9 | 4·1 | 27·0 | 3·5 | 26·9 | 4·6 | 0·89‡ |
| Medium/high risk of malnutrition, % and n | 8·0 | 122 | 5·5 | 41 | 10·4 | 81 | <0·01§ |
| Laboratory values | |||||||
| Serum Zn (μmol/l), mean and sd | 11·9 | 1·8 | 11·9 | 1·8 | 11·9 | 1·7 | 0·94‡ |
| Serum Zn (μmol/l), range | 4·8–20·0 | 4·8–18·3 | 7·6–20·0 | ||||
| Serum Zn deficiency, % and n | 10·1 | 154 | 13·1 | 97 | 7·3 | 57 | <0·01§ |
| Albumin (g/l), mean and sd | 45·1 | 2·3 | 45·3 | 2·2 | 44·8 | 2·3 | <0·01‡ |
| Mental health score | |||||||
| SCL-10 score, median and IQR | 1·1 | 1·0–1·3 | 1·1 | 1·0–1·3 | 1·2 | 1·1–1·5 | <0·01|| |
IQR, interquartile range; SCL-10, Hopkins Symptoms Check List-10.
There are minor differences in the number of evaluated individuals due to variations in missing values on the self-administered questionnaire regarding smoking.
P value for differences between men and women.
P value from the t test.
P value from the χ 2 test.
P value from the Mann–Whitney U test.
The mean serum Zn value was 11·9 μmol/l in both men and women (range 4·8–20 μmol/l; Table 1). The prevalence of Zn deficiency was 10·1 % among all participants, with rates of 13·1 % in men and 7·3 % in women. Among participants at risk of malnutrition, Zn deficiency was found in 31·7 % of the men and 12·3 % of the women (Fig. 2). With increasing age, Zn deficiency was more prevalent in both men and women (Table 2). The mean albumin level was 45·1 g/l (range 35·7–51·9 g/l) and the albumin level was slightly lower in Zn-deficient individuals (Table 3).
Fig. 2.
Zinc deficiency, given as % and (n/N, the number of subjects with zinc deficiency/number of subjects in the group) for all men and women, as well as for low and medium/high risk categories of malnutrition, the Tromsø Study, 2007–2008
Table 2.
Prevalence of zinc deficiency in different age categories of elderly men and women, the Tromsø Study, 2007–2008
| All | Men | Women | ||||
|---|---|---|---|---|---|---|
| Age range (years) | Prevalence (%) | n/N * | Prevalence (%) | n/N * | Prevalence (%) | n/N * |
| 64–71 | 8·9 | 75/843 | 12·0† | 53/441 | 5·5 | 22/402 |
| 72–78 | 9·4 | 43/456 | 12·0 | 26/217 | 7·1 | 17/239 |
| 79–87 | 16·2 | 36/222 | 21·2 | 18/85 | 13·1 | 18/137 |
| P value† | 0·005 | 0·07 | 0·005 | |||
Number of subjects with Zn deficiency/number of subjects in the age group.
P value for linear by linear association between age categories.
Table 3.
Characteristics of the participating elderly men and women* according to zinc status, the Tromsø Study, 2007–2008
| Men (n 743) | Women (n 778) | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Zn status | Zn status | |||||||||
| Zn-deficient (n 97) | Zn-normal (n 646) | Zinc-deficient (n 57) | Zn-normal (n 721) | |||||||
| Mean, % or median | sd, n or IQR | Mean, % or median | sd, n or IQR | P value† | Mean, % or median | sd, n or IQR | Mean, % or median | sd, n or IQR | P value† | |
| Age (years), mean and sd | 72·2 | 5·9 | 71·2 | 5·2 | 0·02‡ | 74·7 | 6·5 | 72·2 | 5·7 | 0·07‡ |
| Single marital status, % and n | 26·8 | 26 | 22·4 | 145 | 0·41§ | 63·2 | 36 | 49·8 | 359 | 0·07§ |
| Smoking status, % and n | ||||||||||
| Never | 27·7 | 26 | 22·1 | 141 | 56·4 | 31 | 47·1 | 330 | ||
| Previous | 58·5 | 55 | 62·8 | 401 | 0·48§ | 30·9 | 17 | 37·5 | 263 | 0·41§ |
| Current | 13·8 | 13 | 15·2 | 97 | 12·7 | 7 | 15·4 | 108 | ||
| Nutritional status, % and n | ||||||||||
| Medium/high risk of malnutrition | 13·4 | 13 | 4·3 | 28 | 0·01§ | 17·5 | 10 | 9·8 | 17 | 0·07§ |
| Nutritional intake, % and n | ||||||||||
| Meat intake ≤3 times/week | 20·2 | 18 | 18·8 | 114 | 0·85§ | 34·7 | 17 | 28·1 | 181 | 0·41§ |
| Mental health | ||||||||||
| SCL-10 score, median and IQR | 1·1 | 1·0–1·3 | 1·1 | 1·0–1·2 | 0·93|| | 1·2 | 1·1–1·5 | 1·2 | 1·1–1·4 | 0·77|| |
| Supplementary laboratory values | ||||||||||
| Albumin (g/l), mean and sd | 44·3 | 2·4 | 45·5 | 2·2 | <0·05‡ | 43·6 | 2·7 | 44·9 | 2·2 | <0·05‡ |
IQR, interquartile range; SCL-10, Hopkins Symptoms Check List-10.
There are minor differences in the number of evaluated individuals due to variations in missing values on the self-administered questionnaire regarding smoking.
P value for differences between groups.
P value from the t test.
P value from the χ 2 test.
P value from the Mann–Whitney U test.
The association between Zn deficiency and risk of malnutrition was further analysed using logistic regression. Zn deficiency was positively associated with the risk of malnutrition both in a model adjusted for gender only (OR=2·6; 95 % CI 1·6, 4·2) and in a model adjusted for gender, age, smoking status and serum albumin (OR=2·2; 95 % CI 1·3, 3·6).
The reported weekly frequency of meat intake was not lower in the participants with Zn deficiency (Table 3). Mental health distress, as assessed by the SCL-10 score, was reported more frequently by women than by men (Table 1). However, no significant differences in mental health distress were found between the two categories of Zn status in men or women (Table 3).
Discussion
In this population-based study of elderly men and women, we found that, based on a low serum Zn concentration, one out of ten individuals had Zn deficiency. However, in elderly men at risk of malnutrition, one out of three had Zn deficiency. In women, the corresponding proportion was lower, but the value was still significantly increased compared with that in women not at risk of malnutrition.
Prevalence of zinc deficiency in elderly individuals
Previous studies of Zn status in elderly individuals largely explored smaller populations and various cut-offs for Zn deficiency have been applied. A Norwegian study of home-living elderly individuals revealed that four out of ninety-seven participants had serum Zn levels below 8 μmol/l( 18 ). In a European multicentre study that included 853 elderly individuals from Italy, Greece, Germany, France and Poland, a slightly higher cut-off (11·0 μmol/l) was used, resulting in the classification of 31 % of the participants as Zn-deficient( 5 ). Applying the same cut-off value to the present study sample would have revealed a similar Zn deficiency prevalence rate (28 %).
In the present study, the prevalence of Zn deficiency increased significantly with increasing age (Table 2). Some previous studies of Zn deficiency compared the old and oldest old, but most studies included a small number of participants. In the ZENITH study of 387 participants from France, the UK and Italy, the prevalence of Zn deficiency was similar between old and oldest old individuals( 19 ). However, in another study from Italy, the oldest old had significantly lower levels of plasma Zn compared with the old( 20 ). This age-associated increase in Zn deficiency may be explained by several factors, including both an age-related decline in the absorptive capacity of the small bowel and a general decline in energy and food intake in the oldest old( 10 ).
Risk of malnutrition and zinc deficiency
The relationship between the risk of malnutrition and serum Zn was previously explored in a study of fifty hospitalised patients using the Mini Nutritional Assessment tool( 8 ). In that study, no association was found between Zn status and the risk of malnutrition. A population-based study of elderly individuals using the ‘MUST’ tool showed lower mean Zn values in individuals at risk of malnutrition( 9 ). However, the proportion of malnourished elderly individuals with Zn deficiency was not estimated.
Several mechanisms may explain the observed associations between malnutrition and Zn deficiency. First, Zn deficiency may produce altered taste and smell, resulting in reduced appetite and consequent weight loss and malnutrition( 21 ). Second, a reduced intake of Zn-containing food in malnourished elderly individuals may result in reduced body Zn. In Western diets, meat (beef and pork) is the most important source of Zn, contributing approximately 50 % of the total Zn intake( 17 ).
The recommendations for the intake of Zn are similar for elderly and other adult individuals. In the present study, no association was found between the reported intake of meat per day and Zn deficiency. However, more detailed information regarding the intake of Zn-containing foods was not available; in general, it may be difficult to obtain valid data concerning food habits from self-administered questionnaires( 22 ).
One strength of the present study is the strictly population-based design and the relatively large study population. The Tromsø Study includes populations from both urban and rural areas and may be regarded as relatively homogeneous with respect to both ethnicity and living conditions. The external validity (to other countries) of our results regarding the association between risk of malnutrition and Zn deficiency in community-living elderly individuals may, of course, be questioned, but it is likely that the positive relationship between the two variables that we demonstrate is generalisable. There is, however, a need for more studies in diverse populations which may confirm or refute our conclusions.
A potential problem is the assessment of Zn status by serum Zn as only a small proportion of the body Zn is present in the serum pool. The assessment of Zn status is challenging and several biomarkers and methods have been suggested, such as the measurement of Zn in hair, erythrocytes and serum or plasma. However, serum (or plasma) Zn is the recommended method for the assessment of Zn status in larger populations( 23 , 24 ). The optimal indicator of individual Zn status has not been identified and caution should be used when applying serum (or plasma) Zn in an individual setting.
Furthermore, we did not collect information about sources of Zn such as micronutrient supplementation containing Zn and the consumption of Zn-fortified foods. Participation in the study required the ability to fill out a self-administered questionnaire and to visit a research centre. These requirements may have led to a bias in the sampling because elderly people with cognitive decline or mental illness may have been less willing to participate in the study. The blood collection tubes were free of trace elements, but the needles were of standard type. Thus, the needles may have introduced contamination with Zn and increased the plasma Zn concentration.
The level of serum Zn may be related to that of serum albumin. The majority of Zn in the serum is bound to albumin and it has been proposed that a reduction of Zn-binding sites in hypoalbuminaemia may influence the serum Zn level. However, a reduced Zn status may also inhibit albumin synthesis( 25 ). Although albumin is not a reliable marker of nutritional status, a reduction in serum albumin can be observed in some patients with malnutrition. This reduction may be explained by coexisting comorbidity and inflammation( 26 ). We therefore compared serum albumin levels between the low and normal Zn groups. The albumin levels were lower in both men and women with Zn deficiency. However, no individuals exhibited an albumin level below 35 g/l, which is regarded as the cut-off value defining a significant effect of albumin level on serum Zn concentration( 13 ). Moreover, the inclusion of albumin in the model of the relationship between Zn deficiency and malnutrition only slightly changed the odds ratio estimate.
No significantly high levels of Zn were detected in this study sample. High levels of serum Zn occur only during supplementation with Zn( 13 ) and in Norway, supplements containing significant amounts of Zn are primarily obtained by prescription. No data on supplement consumption was available in the present study.
Zn is not often analysed in clinical practice, as other micronutrients are more closely associated with specific functions. As an example, Fe and folate are required for Hb production, the deficiency of which can be manifested by anaemia and is thus more easily detected. In contrast, Zn is necessary for general metabolism and manifestations of any deficiency may therefore be more elusive than those associated with other micronutrients( 25 ).
Impact of zinc deficiency
The impact of mild to moderate Zn deficiency has not been fully explored. Previous research has provided evidence for the impairment of the T-lymphocyte balance due to such deficiency, resulting in an impaired immune system and moderate Zn deficiencies in elderly men and women( 27 ). Studies of nursing home residents suggested an increased level of pneumonia in Zn-deficient individuals and a reduction in the risk of pneumonia following Zn supplementation( 28 ).
Furthermore, some studies have linked Zn deficiency to depression and other psychiatric disorders, mostly based on studies of psychiatric in- and out-patients( 29 , 30 ). We used the SCL-10 instrument for the assessment of psychiatric symptoms. This instrument has been widely used in epidemiological studies including elderly people. The SCL-10 captures symptoms of both anxiety and depression, which often appear together as comorbid disorders( 16 ). However, in the present study, we found no association between Zn deficiency and symptoms of anxiety or depression in community-living elderly individuals.
Conclusion
In this population-based study, we found Zn deficiency to be associated with the risk of malnutrition. Overall, Zn deficiency was found in one out of ten community-living elderly people. Although caution should be taken when applying serum (or plasma) Zn as an indicator of individual Zn status, our results support a special attention on Zn deficiency in elderly people at risk of malnutrition, particularly elderly men.
Acknowledgements
Financial support: This study was supported by a research grant from the Northern Regional Health Authority (grant number 778-08). The funder had no role in the design, analysis or writing of this article. The Tromsø 6 study was carried out by The University of Tromsø, Department of Community Medicine. Conflict of interest: None. Authorship: J.-M.K., O.G. and J.F. were responsible for the initial design of the study. J.-M.K. performed the analysis and wrote the first draft of the paper. All authors contributed to the critical revision of the article and approved the final version to be published. Ethics of human subject participation: Each participant provided written informed consent prior to inclusion in the study. The Tromsø 6 study was approved by the Regional Board of Research Ethics in Northern Norway (http://helseforskning.etikkom.no/xnet/public/side?p_dim=11928; approval number 200605174-12/IAY/400). The study was performed in accordance with the ethical standards of the 1964 Declaration of Helsinki.
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