Abstract
Background
The protection of breastfeeding against respiratory tract infections in the first year of life has often been suggested. Few studies examined the effect of breastfeeding on respiratory tract infections after infancy.
Objective
To examine the association between breastfeeding with lower respiratory tract infections (LRTI) and upper respiratory tract infections (URTI) after infancy up to 4 years of age (n = 5322).
Methods
This study was embedded in The Generation R study, a Dutch population-based prospective cohort study from fetal life until young adulthood. Information on breastfeeding duration (never; <3 months; 3–6 months; ≥6 months) and dose (never; partially until 4 months; predominantly until 4 months) were collected by questionnaire at 2, 6, and 12 months of age. Information on doctor attendance for LRTI and URTI were obtained by questionnaire at 2, 3, and 4 years of age.
Results
Breastfeeding for 6 months or longer was significantly associated with a reduced risk of LRTI up to 4 years of age (aOR: 0.71; 95% CI: 0.51–0.98). Similar ORs for LRTI were found with breastfeeding for less than 3 months and 3–6 months. Although in the same direction, weaker ORs were found for URTI and breastfeeding duration. The same trend was found for partial and predominant breastfeeding until 4 months and LRTI and URTI.
Conclusion
Breastfeeding duration for 6 months or longer is associated with a reduced risk of LRTI in pre-school children. These findings are compatible with the hypothesis that the protective effect of breastfeeding for respiratory tract infections persist after infancy therefore supporting current recommendations for breastfeeding for at least 6 months.
Introduction
Infectious diseases, including respiratory tract infections, are a leading cause of morbidity and hospitalization in infants and children.[1, 2] There is much epidemiological evidence for the benefits of breastfeeding against a wide range of infections and illnesses.[3, 4] Breast milk contains various antimicrobial substances, anti-inflammatory components and factors that promote immune development.[4, 5] It enhances the immature immune system of the infant and strengthens defense mechanisms against infectious and other agents during the breastfeeding period.[4–7] Exclusive breastfeeding for the first 6 months of life with breastfeeding along with complementary feeding thereafter is recommended by the World Health Organization (WHO).[8] The benefits have been found to be dose-dependent and related to the duration of breastfeeding.[3, 4] The protection of exclusive and prolonged breastfeeding against respiratory tract infections in the first year of life has often been suggested and also found in The Generation R Study.[3, 4, 9, 10] But, not all studies found breastfeeding exclusivity and duration to reduce the occurrence of respiratory tract infections.[11, 12] It is suggested that the influences of breast milk on the infant’s immune system may persist beyond the breastfeeding period, as it not only provides passive immunity but also maturation of the immune system in the long run.[13, 14] Since breastfeeding might protect against diseases in adulthood such as type 1 diabetes and inflammatory bowel disease [3, 4, 15] a prolonged protection against respiratory tract infections after the first year of life seems plausible. However, only few studies have examined the effect of breastfeeding on respiratory tract infections after infancy and reported inconsistent results.[16–21]
The aim of this study was to examine the association between breastfeeding and lower and upper respiratory tract infections after infancy up to 4 years of age.
Subjects and methods
Participants and study design
This study was embedded in the Generation R study, a population-based prospective cohort study from fetal life until young adulthood and has been described in detail previously.[22] In total, 9778 mothers with a delivery date from April 2002 through January 2006 enrolled in the study. Consent for postnatal follow-up was provided by 7893 participants (S1 Fig). The study was approved by the medical ethical review board of the Erasmus Medical Center, Rotterdam, the Netherlands.
Respiratory tract infections
Data on respiratory tract infections was obtained by postal parent-reported questionnaires at the age of 2, 3 and 4 years. Parents were asked whether their child had suffered from a respiratory tract infection in the previous year and had visited a doctor for the infectious disease. Information on upper respiratory tract infections was obtained by asking parents whether their child had suffered from a serious cold, ear infection or throat infection. Information on lower respiratory tract infections was obtained by asking parents whether their child had pneumonia or bronchitis. Upper and lower respiratory tract infections were defined as present or absent in the second, third and fourth year of life. Questionnaire response rates were 76%, 69% and 73% at the age of 2, 3 and 4 years respectively. No information was available for the number of episodes or severity of these infections.
Breastfeeding
Data on breastfeeding were collected by a combination of delivery reports and postnatal postal questionnaires at the age of 2, 6 and 12 months. By questionnaire the mothers were asked whether they had ever breastfed their child and at which age (in months) the child had stopped receiving breast milk. The duration of breastfeeding was categorized as (I) never breastfed, (II) breastfed for less than 3 months, (III) breastfed for 3–6 months, and (IV) breastfed for 6 months and longer. The majority of infants had stopped receiving breast milk before the age of 12 months, only 3 infants thereafter. An approximation of breastfeeding exclusivity was defined on the basis of parent reports of the child’s age at which solid foods were first introduced, including the introduction of formula feeding. Predominant breastfeeding was defined as receiving breastfeeding without any other infant formula, milk or solid foods.[23] Breastfeeding dose was categorized as (I) never breastfed, (II) partially breastfed until 4 months, and (III) predominantly breastfed until 4 months. Partial breastfeeding was defined as receiving both breast milk and infant formula and/or solid foods. Questionnaire response rates were 82%, 73% and 72% at the age 2, 6 and 12 months respectively.
Covariates
Information on potential confounders, including mode of delivery, gender and gestational age, were obtained from obstetric records assessed in mid-wife practices and hospital registries.[22] Additional information was obtained by a combination of prenatal and postnatal questionnaires completed by both parents. The questionnaires included information on maternal age, maternal educational level, maternal marital status, maternal ethnicity, household income per month, maternal BMI before pregnancy, any maternal smoking during pregnancy, any maternal alcohol use during pregnancy, parity and parental history of asthma or atopy. Ethnicity of the mother was defined as follows: if both parents were born in The Netherlands, the ethnicity of the mother was defined as Dutch; if one of the parents was born in another country than The Netherlands, that country applied; if parents were born in different countries other than The Netherlands, the country of the mother applied.[24] Ethnicity of the mother was categorized into Western (Dutch, European, American-Western, Asian-Western) and non-Western (American non-Western, Asian non Western, African, Turkish, Cape Verdean, Moroccan, Dutch Antillean, Surinamese, Oceania, and Indonesian). Maternal educational level was defined as follows; low: no education, primary school or less than 3 years of secondary school, mid: more than 3 years of secondary school, higher vocational training or bachelor's degree, and high: academic education.[25] Household income per month was categorized into two income-groups using the approximate monthly general labour income during the inclusion period of this study as cut off point (≤ € 2200 and > € 2200).[26] Postnatal questionnaire completed by the mother at the child’s age of 6 months included information on smoke exposure of the child inside and outside the home. Environmental smoking was defined as maternal smoking, smoking of mother or anybody else at home in the presence of the child and smoking in any other places in the presence of the child at the age of 6 months. Postnatal questionnaires completed by the mother at age 12 months included information on vitamin D supplementation in the previous 6 months and questionnaires at age 12 and 24 months included information on day-care attendance.
Population for analyses
Children whose parents did not provide informed consent for the use of postnatal questionnaire data (n = 1885) and children without information on respiratory tract infections at ages 2 to 4 years (n = 2015) were excluded from the analysis. To prevent clustering, only one child per family within the Generation R cohort was included by random selection (n = 556 excluded). To reduce attrition bias, variables with missing values were multiple imputed (20 imputations) based on the correlation between the variable with missing values with other maternal and child characteristics (S1 Table).[27] Consequently data of 5322 children were available after multiple imputation for statistical analyses (S1 Fig).
Statistical methods
First, independent Student’s t test and chi-square test were performed to test for differences in characteristics between the 4 groups of breastfeeding duration. Second, logistic regression analyses by using generalized estimating equations (GEE) were performed. Regression analysis by GEE assesses the association between two variables by correction for the within subject's dependence as a result of the repeated observations on lower and upper respiratory tract infections (age 2, 3 and 4 years) since repeated measurements within one individual are frequently correlated.[28] An unstructured working correlation structure was used in the GEE analyses as adjustment for the dependency between the repeated measurements, since the within-subject correlation coefficient for lower and upper respiratory tract infections between the three time points were different (r = 0.13–0.32). Logistic regression analysis with GEE was performed with lower respiratory tract infections and upper respiratory tract infections as dependent variables and breastfeeding as independent variable. All analyses were adjusted for the age (time) at which observations of illness were assessed to account for potential confounding by age as well as clustering of repeated measurement. The selection of potential confounders was performed by the alteration in odds ratio (OR) and kept in the multivariable model in case of an alteration of ≥ 10% in OR.[29] The pooled results of the 20 imputed datasets were reported in this paper as odds ratio’s (OR’s) and 95% confidence intervals (95% CIs). A P-value < 0 .05 was considered as statistically significant. The statistical analyses were carried out by using SPSS 22.0 for Windows (SPSS Inc, Chicago, IL).
Results
Study population
Maternal and child characteristics are presented in Table 1 and S1 Table. Out of 5322 children, 14% had suffered from at least one episode of lower respiratory tract infection in the second year of life, 8% in the third year and 6% in the fourth year of life (Table 2). At least one episode of upper respiratory tract infection was reported for 44% of children in the second year of life, 36% in the third year and 31% in the fourth year of life (Table 2).
Table 1. Maternal and child characteristics (n = 5322).
Breastfeeding duration¶ | |||||||||
---|---|---|---|---|---|---|---|---|---|
Characteristics | Never | < 3 months | 3–6 months | ≥ 6 months | |||||
n = 5322 | n = 893 (17%) | n = 1602 (30%) | n = 1093 (21%) | n = 1734 (32%) | |||||
Number—% or mean ± SD | Number—% or mean ± SD | Number—% or mean ± SD | Number—% or mean ± SD | ||||||
Maternal characteristics | |||||||||
Maternal age—Mean (SD) | * | * | |||||||
30.7 | 5.1 | 30.3 | 4.9 | 31.5 | 4.6 | 31.8 | 4.8 | ||
Educational level – n (%) | * | * | |||||||
Low | 230 | 26 | 384 | 24 | 129 | 12 | 262 | 15 | |
Mid | 496 | 55 | 881 | 55 | 566 | 52 | 856 | 49 | |
High | 167 | 19 | 337 | 21 | 398 | 36 | 616 | 36 | |
Ethnicity – n (%) | * | ||||||||
Western | 623 | 70 | 1057 | 66 | 786 | 72 | 1186 | 68 | |
Non-Western | 270 | 30 | 545 | 34 | 307 | 28 | 548 | 32 | |
Household income per month – n (%) | * | ||||||||
≤ 2200 euro | 385 | 43 | 648 | 40 | 332 | 30 | 710 | 41 | |
>2200 euro | 508 | 57 | 954 | 60 | 761 | 70 | 1024 | 59 | |
Marital status – n (%) | * | ||||||||
No partner | 105 | 12 | 185 | 12 | 88 | 8 | 157 | 9 | |
Married/ Living together | 788 | 88 | 1417 | 88 | 1005 | 92 | 1577 | 91 | |
Maternal BMI before pregnancy (kg/m2)—mean (SD) | * | * | |||||||
23.9 | 4.3 | 23.9 | 4.4 | 23.1 | 3.6 | 23.1 | 3.6 | ||
Child exposure to smoke – n (%) | * | * | * | ||||||
Never | 471 | 53 | 929 | 58 | 699 | 64 | 1224 | 70 | |
Prenatal smoking, no environmental smoking | 51 | 6 | 115 | 7 | 77 | 7 | 113 | 7 | |
Prenatal smoking and environmental smoking | 198 | 22 | 340 | 21 | 154 | 14 | 160 | 9 | |
Environmental smoking, no prenatal smoking | 173 | 19 | 218 | 14 | 163 | 15 | 237 | 14 | |
Alcohol use during pregnancy – n (%) | * | * | |||||||
Never | 454 | 51 | 724 | 45 | 356 | 33 | 741 | 43 | |
Drank alcohol during pregnancy | 439 | 49 | 878 | 55 | 737 | 67 | 993 | 57 | |
Parental history of asthma or atopy – n (%) | * | * | |||||||
No | 462 | 52 | 833 | 52 | 581 | 53 | 840 | 48 | |
Yes | 432 | 48 | 769 | 48 | 512 | 47 | 894 | 52 | |
Parity – n (%) | * | * | * | ||||||
0 | 468 | 52 | 1037 | 65 | 677 | 62 | 947 | 55 | |
≥1 | 426 | 48 | 565 | 35 | 416 | 38 | 787 | 45 | |
Caesarean section – n (%) | * | * | * | ||||||
No | 742 | 83 | 1357 | 85 | 943 | 86 | 1547 | 89 | |
Yes | 152 | 17 | 245 | 15 | 150 | 14 | 186 | 11 | |
Child characteristics | |||||||||
Male – n (%) | |||||||||
464 | 52 | 818 | 51 | 554 | 51 | 832 | 48 | ||
Gestational age at birth – n (%) | * | * | * | ||||||
<37 weeks | 52 | 6 | 88 | 5 | 61 | 6 | 72 | 4 | |
≥37 weeks | 842 | 94 | 1514 | 95 | 1032 | 94 | 1662 | 96 | |
Vitamin D supplementation age 6–12 months – n (%) | * | * | |||||||
No | 450 | 50 | 941 | 59 | 657 | 60 | 786 | 45 | |
Yes | 444 | 50 | 661 | 41 | 436 | 40 | 948 | 55 | |
Day care attendance first 2 years – n (%) | * | * | |||||||
No | 248 | 28 | 369 | 23 | 213 | 19 | 423 | 24 | |
Yes | 646 | 72 | 1233 | 77 | 880 | 81 | 1311 | 76 |
* Significantly different from breastfeeding ≥ 6 months, P < 0.05
¶ Missing data for breastfeeding duration before multiple imputation n: 1083 (20%)
Table 2. Prevalence of lower and upper respiratory tract infections (n = 5322).
Outcome | Age 2 | Age 3 | Age 4 | |||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Original data | Multiple imputed | Original data | Multiple imputed | Original data | Multiple imputed | |||||||
n | % | n | % | n | % | n | % | n | % | n | % | |
LRTI | ||||||||||||
No | 4019 | 87 | 4591 | 86 | 3952 | 93 | 4884 | 92 | 4071 | 95 | 5011 | 94 |
Yes | 594 | 13 | 732 | 14 | 316 | 7 | 438 | 8 | 201 | 5 | 311 | 6 |
Missing | 709 | 13 | 1054 | 20 | 1050 | 20 | ||||||
URTI | ||||||||||||
No | 2598 | 57 | 2954 | 56 | 2788 | 66 | 3412 | 64 | 3073 | 72 | 3666 | 69 |
Yes | 1970 | 43 | 2368 | 44 | 1442 | 34 | 1910 | 36 | 1211 | 28 | 1656 | 31 |
Missing | 754 | 14 | 1092 | 21 | 1038 | 20 |
Duration of breastfeeding and respiratory tract infections
Compared to children who were never breastfed, breastfeeding for 6 months or longer was significantly associated with a decreased risk of lower respiratory tract infections after infancy up to 4 years of age (aOR: 0.71; 95% CI: 0.51–0.98) (Table 3) (S2 Table). Similar ORs for lower respiratory tract infections were found with breastfeeding for less than 3 months and breastfeeding for 3–6 months but this was not statistically significant (aOR: 0.75; 95% CI: 0.56–1.00 and aOR: 0.78; 95% CI: 0.53–1.13) (Table 3) (S2 Table). Although in the same direction, weaker ORs were found for upper respiratory tract infections and breastfeeding for less than 3 months, 3–6 months or 6 months and longer after adjustment for confounding variables (aOR: 0.86; 95% CI: 0.70–1.04 for less than 3 months, aOR: 0.91; 95% CI: 0.73–1.12 for 3–6 months and aOR: 0.85; 95% CI: 0.69–1.05 for 6 months and longer) (Table 3) (S2 Table). The effects of the duration of breastfeeding on respiratory tract infections did not differ between the ages of 2, 3 and 4 years (pinteraction >0.23 for lower and upper respiratory tract infections).
Table 3. Association between breastfeeding duration and lower and upper respiratory tract infections up to age 4 years (n = 5322).
Lower respiratory tract infections | Upper respiratory tract infections | ||||
---|---|---|---|---|---|
Breastfeeding | Univariate model | Multivariable model 1 | Univariate model | Multivariable model 1 | |
n (%) | OR (95% CI) | aOR (95% CI) a | OR (95% CI) | aOR (95% CI) a | |
Never | 893 (17%) | Reference | Reference | Reference | Reference |
< 3 months | 1602 (30%) | 0.75 (0.56–1.02) | 0.75 (0.56–1.00) | 0.87 (0.71–1.06) | 0.86 (0.70–1.04) |
3–6 months | 1093 (21%) | 0.72 (0.48–1.06) | 0.78 (0.53–1.13) | 0.80 (0.64–1.00) | 0.91 (0.73–1.12) |
≥ 6 months | 1734 (32%) | 0.63 (0.46–0.87) | 0.71 (0.51–0.98) | 0.78 (0.62–0.98) | 0.85 (0.69–1.05) |
OR: Odds Ratio; 95% confidence interval. OR’s are compared to never-breastfed.
a Adjusted for caesarean section, maternal age, marital status, maternal ethnicity, maternal educational level, household income per month, maternal BMI before pregnancy, smoke exposure child, alcohol use during pregnancy, gender child, vitamin D supplementation age 6–12 months, day-care attendance in the first two years of life, gestational age at birth, parity and parental history of asthma or atopy.
Dose of breastfeeding and respiratory tract infections
Partial breastfeeding until 4 months was significantly associated with a decreased risk of lower respiratory tract infections after infancy up to age 4 years (OR: 0.76; 95% CI: 0.59–0.99). However, the association did not remain significant after adjustment for confounders (aOR: 0.78; 95% CI: 0.59–1.02) (Table 4) (S3 Table). The same trend was found for predominant breastfeeding but not statistically significant (Table 4). Before multiple imputation, predominant breastfeeding was associated with lower respiratory tract infections (S3 Table). Although partial breastfeeding until 4 months and predominant breastfeeding until 4 months was not significantly associated with upper respiratory tract infections, the effect estimates were found to be in the same direction (aOR: 0.89; 95% CI: 0.72–1.10 and aOR: 0.93; 95% CI: 0.72–1.20) (Table 4) (S3 Table). The effects of breastfeeding dose on respiratory tract infections did not differ between the ages of 2, 3 and 4 years (pinteraction >0.59 for upper and lower respiratory tract infections).
Table 4. Association between exclusive breastfeeding and lower and upper respiratory tract infections up to age 4 years (n = 5322).
Lower respiratory tract infections | Upper respiratory tract infections | ||||
---|---|---|---|---|---|
Breastfeeding | Univariate model | Multivariable model 1 | Univariate model | Multivariable model 1 | |
n (%) | OR (95% CI) | aOR (95% CI) a | OR (95% CI) | aOR (95% CI) a | |
Never | 862 (16%) | Reference | Reference | Reference | Reference |
Partially until 4 months | 2870(54%) | 0.76 (0.59–0.99) | 0.78 (0.59–1.02) | 0.87 (0.72–1.05) | 0.89 (0.72–1.10) |
Predominantly until 4 months | 1590 (30%) | 0.66 (0.44–1.00) | 0.72 (0.48–1.09) | 0.84 (0.65–1.08) | 0.93 (0.72–1.20) |
OR: Odds Ratio; 95% confidence interval. OR’s are compared to never-breastfed.
a Adjusted for caesarean section, maternal age, marital status, maternal ethnicity, maternal educational level, household income per month, maternal BMI before pregnancy, smoke exposure child, alcohol use during pregnancy, gender child, vitamin D supplementation age 6–12 months, day-care attendance in the first two years of life, gestational age at birth, parity and parental history of asthma or atopy.
Discussion
In this population-based prospective birth cohort study we found children who were breastfed for 6 months or longer to have a reduced risk of lower respiratory tract infections after infancy. For breastfeeding for less than 3 months and 3–6 months similar direction of the effect estimates were found. Also, similar direction of the effect estimates were found for the association between the duration and dose of breastfeeding and upper respiratory tract infections but not significant.
Various studies, including a previous study within our cohort, found exclusive breastfeeding for 6 months to be protective for the development of respiratory tract infections in infancy, thereby supporting the recommendation of the WHO.[10, 19, 30] Our study found breastfeeding for 6 months or longer to be associated with a reduced risk for lower respiratory tract infections after infancy till the age of 4 years. Contrary to our findings, a prospective longitudinal study found that breastfeeding duration, including breastfeeding longer than 6 months, was not associated with pneumonia or lung infection in 6 year old children.[17] However, the association was only examined in children who initiated breastfeeding whereas we also included children who were never breastfed. In agreement with our findings on breastfeeding dose, Li et al [17] did not find breastfeeding exclusivity to be associated with lower respiratory tract infections. As for upper respiratory tract infections, we did not observe a significant association among children who were breastfed (duration and dose) compared to those who were never breastfed. Similarly, Chantry et al [19] found full breastfeeding for less than 6 months not to be associated with an increased risk of recurrent upper respiratory tract infections and recurrent otitis media in children 6–72 months of age. Li et al [17] also found no association between breastfeeding, including duration and exclusivity, and colds or upper respiratory tract infections among 6 year old children. The possibility that the protective effect of breastfeeding might wear off after breastfeeding cessation has previously been suggested.[31–33] Other studies that did find breastfeeding to be associated with a reduced risk of upper respiratory tract infections after infancy mainly focused on otitis media and mostly before the age of 3 years.[20, 34, 35] Some studies examined the effect of breastfeeding on respiratory tract infections in general. A Japanese study reported breastfeeding duration for 6–7 months to be borderline significantly associated with a reduced risk of hospitalization for respiratory tract infections between the age of 18–30 months.[21] Respiratory tract infections for which hospitalization is needed are often more serious and mainly infections of the lower respiratory tract [2, 36] which might explain the discrepancy between these latter results and those from our study. Conversely, another study did not find a protective effect of breastfeeding for all acute respiratory illness in children 1–6 years [20] which might be due to an overrepresentation of upper respiratory tract infections since these symptoms are more common in childhood.[2] The WHO definition of exclusive breastfeeding allows for ORS, drops and syrups but no other food or drink, not even water.[23] Therefore, this study examined the effect of predominant breastfeeding defined as no infant formula, milk or solid foods. This study cannot examine the effect of predominant breastfeeding per month neither for the duration of 6 months or longer due to small group size. The majority of mothers in the Netherlands do not continue breastfeeding after the age of 4 months.[37] Thus, our study precludes conclusions on the effect of exclusive breastfeeding for 6 months as defined by the WHO. In line with our findings, a birth cohort study from Hong Kong did not find exclusive and partial breastfeeding for 3 months to be associated with a reduced risk for hospital admissions for respiratory tract infections after the age of 6 months up to age 8 years.[16] However, Yamakawa et al.[21] did find exclusive breastfeeding at 6–7 months of age to be significantly associated with hospitalization for respiratory tract infections between the age of 18–42 months. Also, Li et al.[17] reported exclusive breastfeeding for 6 months and longer, compared to breastfeeding between 0 to 4 months, to be significantly associated with a reduced odds for ear, throat, and sinus infection at age 6 years.
We performed multiple imputation to account for bias associated with missing data. Children with and without questionnaire data differed in socioeconomic background, ethnicity, and a selection towards a relative more healthy study population seems to be present.[22] However, this would only affect the interpretation of our results if the association between breastfeeding and respiratory infections was different for children without questionnaire data compared with those with questionnaire data, which is unlikely. For the analyses on breastfeeding duration ≥6 months and lower respiratory tract infections, results were comparable in the original data (aOR: 0.56; 95% CI: 0.32–0.99) and after the multiple imputation procedure (aOR: 0.71; 95% CI: 0.51–0.98). However, for the analyses on predominant breastfeeding and lower respiratory tract infections the estimate in the original data analysis (aOR: 0.53; 95% CI: 0.30–0.93) slightly weakened after the imputation procedure (aOR: 0.72; 95% CI: 0.48–1.09). This would suggest that the missing data was not completely random and affected the uncertainty of the effect estimates for predominant breastfeeding.
An important strength of this study is the large study population drawn from the general population. On the basis of previous findings in our cohort, respiratory illnesses are socially patterned and related to several mother and child characteristics.[38] Our study design provided information on multiple potential confounders and allowed for follow-up into childhood. However, due to the observational nature of our study, residual confounding cannot be fully excluded. In addition, the prospective design made it possible to obtain information on breastfeeding at multiple time points during infancy therefore limiting recall bias. Whereas other studies examined the effect of respiratory tract infections in general, or focused on specific infections,[20, 21, 34, 35] we examined the effect of breastfeeding on the development of lower and upper respiratory tract infections separately.
A weakness may be that the diagnosis of respiratory tract infection was obtained by parent-reported questionnaires at yearly intervals. The questions used to obtain information on respiratory infections were comparable to other studies. Parents were asked whether their child had suffered from a respiratory tract infection and whether they had visited a doctor for this infection since physician diagnosis is more accurate. However, this could have led to misclassification of the outcome as parents may not be able to distinguish between lower and upper respiratory tract infections and children who had not visited a doctor may even so have suffered from a respiratory tract infection. However, since the outcome was measured after the breastfeeding period we do not expect such misclassification to be differential and to have influenced the effect of the duration or dose of breastfeeding. Also, our study did not have information on the number of episodes of infection. Li et al.[17] found a relation between two or more visits to the physician and breastfeeding duration and exclusivity.
Several long-term effects of breastfeeding on the offspring have been reported.[3–5, 15] Different mechanisms for the stimulation of the immune response by breastfeeding have been suggested, among others transfer of anti-idiotypic antibodies and lymphocytes.[6, 13] However, the mechanism by which breastfeeding might add to a long-term protection remain unclear.
In conclusion, this study showed that breastfeeding duration for 6 months or longer is associated with a reduced risk of lower respiratory tract infections in pre-school children. These findings are compatible with the hypothesis that the protective effect of the duration of breastfeeding for respiratory tract infections persist after infancy therefore supporting current WHO recommendations for breastfeeding for at least 6 months also in industrialized countries.
Supporting information
Acknowledgments
The Generation R Study is conducted by the Erasmus Medical Center in close collaboration with the School of Law and Faculty of Social Sciences of the Erasmus University Rotterdam, the Municipal Health Service–Rotterdam Metropolitan Area, the Rotterdam Homecare Foundation, and the Stichting Trombosedienst & Artsenlaboratorium Rijnmond. We acknowledge the contributions of children and parents, general practitioners, hospitals and midwives in Rotterdam.
Data Availability
All relevant data are within the paper and its Supporting Information files.
Funding Statement
This phase of the Generation R Study was supported by the Erasmus Medical Center, the Erasmus University Rotterdam, the Netherlands Organization for Health Research and Development (Zon Mw) and Europe Container terminals B.V. The funders had no role in the design of the study, the data collection and analyses, the interpretation of data, or the preparation of, review of, and decision to submit the manuscript.
References
- 1.Walker CL, Rudan I, Liu L, Nair H, Theodoratou E, Bhutta ZA, et al. Global burden of childhood pneumonia and diarrhoea. Lancet. 2013;381(9875): 1405–16. 10.1016/S0140-6736(13)60222-6 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Hasegawa K, Tsugawa Y, Cohen A, Camargo CA Jr. Infectious Disease-related Emergency Department Visits Among Children in the United States. Pediatr Infect Dis J. 2015;34(7): 681–5. 10.1097/INF.0000000000000704 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Hörnell A, Lagström H, Lande B, Thorsdottir I. Breastfeeding, introduction of other foods and effects on health: a systematic literature review for the 5th Nordic Nutrition Recommendations. Food Nutr Res. 2013;12;57. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.ESPGHAN Committee on Nutrition, Agostoni C, Braegger C, Decsi T, Kolacek S, Koletzko B, et al. Breast-feeding: A commentary by the ESPGHAN Committee on Nutrition. J Pediatr Gastroenterol Nutr. 2009;49(1): 112–25. 10.1097/MPG.0b013e31819f1e05 [DOI] [PubMed] [Google Scholar]
- 5.Hanson LA. Session 1: Feeding and infant development breast-feeding and immune function. Proc Nutr Soc. 2007;66(3): 384–96. 10.1017/S0029665107005654 [DOI] [PubMed] [Google Scholar]
- 6.Hanson LA, Korotkova M, Lundin S, Håversen L, Silfverdal SA, Mattsby-Baltzer I, et al. The transfer of immunity from mother to child. Ann N Y Acad Sci. 2003;987: 199–206. [DOI] [PubMed] [Google Scholar]
- 7.Jansen MA, van den Heuvel D, van Zelm MC, Jaddoe VW, Hofman A, de Jongste JC, et al. Decreased Memory B Cells and Increased CD8 Memory T Cells in Blood of Breastfed Children: The Generation R Study. PLoS One. 2015;18;10(5): e0126019 10.1371/journal.pone.0126019 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.World Health Organization. The optimal duration of exclusive breastfeeding: report of the expert consultation. Geneva: World Health Organization; March 28–30, 2001. Available: http://www.who.int/nutrition/publications/optimal_duration_of_exc_bfeeding_report_eng.pdf. Accessed February 20 2016.
- 9.Duijts L, Ramadhani MK, Moll HA. Breastfeeding protects against infectious diseases during infancy in industrialized countries. A systematic review. Matern Child Nutr. 2009;5(3): 199–210. 10.1111/j.1740-8709.2008.00176.x [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Duijts L, Jaddoe VW, Hofman A, Moll HA. Prolonged and exclusive breastfeeding reduces the risk of infectious diseases in infancy. Pediatrics. 2010; 126(1): e18–25. 10.1542/peds.2008-3256 [DOI] [PubMed] [Google Scholar]
- 11.Rebhan B, Kohlhuber M, Schwegler U, Fromme H, Abou-Dakn M, Koletzko BV. Breastfeeding duration and exclusivity associated with infants' health and growth: data from a prospective cohort study in Bavaria, Germany. Acta Paediatr. 2009;98(6): 974–80. [DOI] [PubMed] [Google Scholar]
- 12.Kramer MS, Chalmers B, Hodnett ED, Sevkovskaya Z, Dzikovich I, Shapiro S, et al. Promotion of Breastfeeding Intervention Trial (PROBIT): a randomized trial in the Republic of Belarus. JAMA. 2001;285(4): 413–20. [DOI] [PubMed] [Google Scholar]
- 13.Hanson LA. Breastfeeding provides passive and likely long-lasting active immunity. Ann Allergy Asthma Immunol. 1998;81(6): 523–33; quiz 533–4, 537. 10.1016/S1081-1206(10)62704-4 [DOI] [PubMed] [Google Scholar]
- 14.Hanson LA. The mother-offspring dyad and the immune system. Acta Paediatr. 2000;89(3): 252–8. [PubMed] [Google Scholar]
- 15.Schack-Nielsen L, Michaelsen KF. Breast feeding and future health. Curr Opin Clin Nutr Metab Care. 2006;9(3): 289–96. 10.1097/01.mco.0000222114.84159.79 [DOI] [PubMed] [Google Scholar]
- 16.Tarrant M, Kwok MK, Lam TH, et al. Schooling CM . Breast-feeding and childhood hospitalizations for infections. Epidemiology. 2010;21(6): 847–54. [DOI] [PubMed] [Google Scholar]
- 17.Li R, Dee D, Li CM, Hoffman HJ, Grummer-Strawn LM. Breastfeeding and risk of infections at 6 years. Pediatrics. 2014;134 Suppl 1: S13–20. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Prietsch SO, Fischer GB, César JA, Lempek BS, Barbosa LV, Zogbi L, et al. Acute lower respiratory illness in under-five children in Rio Grande, Rio Grande do Sul State, Brazil: prevalence and risk factors. Cad Saude Publica. 2008;24(6): 1429–38. [DOI] [PubMed] [Google Scholar]
- 19.Chantry CJ, Howard CR, Auinger P. Full breastfeeding duration and associated decrease in respiratory tract infection in US children. Pediatrics. 2006;117(2): 425–32. 10.1542/peds.2004-2283 [DOI] [PubMed] [Google Scholar]
- 20.Hatakka K, Piirainen L, Pohjavuori S, Poussa T, Savilahti E, Korpela R. Factors associated with acute respiratory illness in day care children. Scand J Infect Dis. 2010;42(9): 704–11. 10.3109/00365548.2010.483476 [DOI] [PubMed] [Google Scholar]
- 21.Yamakawa M, Yorifuji T, Kato T, Inoue S, Tokinobu A, Tsuda T, et al. Long-Term Effects of Breastfeeding on Children's Hospitalization for Respiratory Tract Infections and Diarrhea in Early Childhood in Japan. Matern Child Health J. 2015;19(9): 1956–65. 10.1007/s10995-015-1703-4 [DOI] [PubMed] [Google Scholar]
- 22.Jaddoe VW, van Duijn CM, Franco OH, van der Heijden AJ, van Iizendoorn MH, de Jongste JC, et al. The Generation R Study: design and cohort update 2012. Eur J Epidemiol. 2012;27(9): 739–56. 10.1007/s10654-012-9735-1 [DOI] [PubMed] [Google Scholar]
- 23.Indicators for Assessing Breast-Feeding Practices. Geneva, Switzerland: World Health Organization; WHO Document WHO/CDD/SER 1991; 91:14. [Google Scholar]
- 24.Swertz O, Duimelaar P, Thijssen J. Migrants in the Netherlands 2004. Voorburg/Heerlen: Statistics Netherlands, 2004. [Google Scholar]
- 25.Statistics, Netherlands. Dutch Standard Classification of Education 2003. Voorburg/Heerlen: Statistics Netherlands, 2004. [Google Scholar]
- 26.Statistics, Netherlands. Welfare in the Netherlands. Income, welfare and spending of households and individuals. Den Haag/Heerlen: Statistics Netherlands, 2012. [Google Scholar]
- 27.Sterne JA, White IR, Carlin JB, Spratt M, Royston P, Kenward MG, et al. Multiple imputation for missing data in epidemiological and clinical research: potential and pitfalls. BMJ. 2009;338: b2393 10.1136/bmj.b2393 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Twisk JW. Longitudinal data analysis. A comparison between generalized estimating equations and random coefficient analysis. Eur J Epidemiol. 2004;19(8): 769–76. [DOI] [PubMed] [Google Scholar]
- 29.Mickey RM, Greenland S. The impact of confounder selection criteria on effect estimation. Am J Epidemiol. 1989;129(1): 125–37. [DOI] [PubMed] [Google Scholar]
- 30.Ladomenou F, Moschandreas J, Kafatos A, Tselentis Y, Galanakis E. Protective effect of exclusive breastfeeding against infections during infancy: a prospective study. Arch Dis Child. 2010;95(12): 1004–8. 10.1136/adc.2009.169912 [DOI] [PubMed] [Google Scholar]
- 31.Fisk CM, Crozier SR, Inskip HM, Godfrey KM, Cooper C, Roberts GC, et al. Breastfeeding and reported morbidity during infancy: findings from the Southampton Women's Survey. Matern Child Nutr. 2011;7(1): 61–70. 10.1111/j.1740-8709.2010.00241.x [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Quigley MA, Kelly YJ, Sacker A. Breastfeeding and hospitalization for diarrheal and respiratory infection in the United Kingdom Millennium Cohort Study. Pediatrics. 2007;119(4): e837–42. 10.1542/peds.2006-2256 [DOI] [PubMed] [Google Scholar]
- 33.Sassen ML, Brand R, Grote JJ. Breast-feeding and acute otitis media. Am J Otolaryngol. 1994;15(5): 351–7. [DOI] [PubMed] [Google Scholar]
- 34.Hetzner NM, Razza RA, Malone LM, Brooks-Gunn J. Associations among feeding behaviors during infancy and child illness at two years. Matern Child Health J. 2009;13(6): 795–805. 10.1007/s10995-008-0401-x [DOI] [PubMed] [Google Scholar]
- 35.Pukander J, Luotonen J, Timonen M, Karma P. Risk factors affecting the occurrence of acute otitis media among 2-3-year-old urban children. Acta Otolaryngol. 1985;100(3–4): 260–5. [DOI] [PubMed] [Google Scholar]
- 36.Craig JC, Williams GJ, Jones M, Codarini M, Macaskill P, Hayen A, et al. The accuracy of clinical symptoms and signs for the diagnosis of serious bacterial infection in young febrile children: prospective cohort study of 15 781 febrile illnesses. BMJ. 2010;20;340: c1594. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.Lanting CI, Van Wouwe JP, Reijneveld SA. Infant milk feeding practices in the Netherlands and associated factors. Acta Paediatr. 2005;94(7): 935–42. 10.1080/08035250510036723 [DOI] [PubMed] [Google Scholar]
- 38.Gabriele C, Silva LM, Arends LR, Raat H, Moll HA, Hofman A, Jaddoe VW, de Jongste JC. Early respiratory morbidity in a multicultural birth cohort: the Generation R Study. Eur J Epidemiol. 2012;27(6):453–62. 10.1007/s10654-012-9675-9 [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
All relevant data are within the paper and its Supporting Information files.