Background
Girls in the United States are experiencing earlier pubertal onset and sexual development than in the past [
1]. Girls who undergo earlier puberty are at higher risk of emotional and behavioral problems including depression, eating disorders, substance use, early initiation of sexual behavior, teen pregnancy, and sexual abuse [
2‐
7]. They are also at increased risk for serious health conditions later in life, including reproductive cancers and cardiovascular disease [
2,
8]. Prepubertal obesity has been associated with earlier pubertal development, but does not fully explain the overall decline in the age of pubertal onset as this trend has been observed in girls of varying body mass index (BMI) [
1]. We recently reported that African American girls experience substantially earlier pubertal onset than non-Hispanic White or Asian girls. We found that the median age of breast onset was 8.8 years in African American girls, compared to 9.7 years in White girls [
1]. This difference in age is particularly striking given that just a century ago African American girls experienced later menarche than their non-Hispanic White counterparts [
9]. Racial/ethnic differences in age of pubertal onset may lead to worse health outcomes for racial/ethnic minorities in the US; thus, understanding these differences is crucial to efforts to narrow racial/ethnic health disparities.
Infant nutrition, including breastfeeding, may offer a partial explanation for racial/ethnic disparities in age of pubertal onset. Studies show that African American mothers are the least likely to initiate breastfeeding [
10,
11]. One study found that only 47.9% of African American children were ever breastfed, compared with 74% of non-Hispanic Whites and 71.5% of Hispanics, among those born to US-born parents [
10]. When examining breastfeeding practices at 6 months, breastfeeding rates were similarly substantially lower in the African American group, at 21.3%, compared with non-Hispanic Whites (39%), and Hispanics (32.3%) [
10]. Because of the known association between lack of breastfeeding and obesity as well as the association between childhood obesity and early puberty, [
1,
12] differences in breastfeeding practices may at least partially contribute to the observed disparities in pubertal timing among different racial/ethnic groups.
Few studies have examined the association between breastfeeding and timing of puberty, and most were small and/or had racially/ethnically homogenous cohorts [
13‐
21]. We thus conducted a population-based study using a large, racially/ethnically diverse cohort of girls and prospectively-collected, clinical data on pubertal development to investigate whether breastfeeding is associated with the timing of pubertal onset. We hypothesized that girls who were breastfed for longer durations would experience later pubertal onset compared to those who were not breastfed. We also examined the role of prepubertal BMI in the relationship between breastfeeding and timing of puberty. Lastly, we explored whether there are differences in the strengths of the associations among different race/ethnic groups.
Methods
Participants
The study was conducted within Kaiser Permanente Northern California (KPNC), a large integrated health care delivery system that serves a socio-demographically and ethnically diverse population of over 4.2 million in Northern California. Using the KPNC clinical and administrative databases, including its electronic health record (EHR) system, we identified a cohort of mother-daughter pairs who met the following eligibility criteria. All girls were born at a KPNC medical facility between 2004 and 2006 and were followed through March 31, 2018. Girls were included if they had continuous KPNC membership, defined as KPNC health insurance with no coverage gap > 90 days during the follow-up period, to minimize missing data. We included mother-daughter pairs where the mother did not have extreme BMI (< 15 kg/m2 or > 60 kg/m2) and had attended at least 1 postnatal pediatrician checkup when their daughter was < 6 months and at least another checkup at ≥6 months. Additionally, girls were required to have had at least one measured prepubertal BMI and one pubertal stage (breast and/or pubic hair) assessment as described below.
Girls with medical conditions known to influence pubertal development, such as adrenal tumors, or premature birth (< 37 weeks gestation) were excluded. Additionally, underage mothers (< 18 years) were excluded as they may be at greater risk for depression [
22] and preterm delivery [
23], both of which may influence pubertal development. Likewise, multiple births were excluded because of their association with low birthweight and preterm delivery [
24]. Lastly, we excluded pairs that were missing important covariates such as maternal age at delivery and race/ethnicity.
A total of 3331 mother-daughter pairs were included in the analysis after excluding 45 who had conditions affecting pubertal development, 382 premature births, 182 multiple births, 22 underage mothers, and 28 pairs with missing information on important covariates. All data were drawn from KPNC EHR. The study was approved by the KPNC Institutional Review Board.
Measurements
Exposure variable (breastfeeding duration)
KPNC members with newborn babies are strongly encouraged to attend “Well Baby/Child” visits to discuss and assess their child’s health and growth trajectory with their pediatricians from birth to adolescence. These visits are accompanied by health questionnaires asking questions on nutrition, safety, parenting behaviors, household circumstances, and other topics pertaining to the child’s health and wellbeing. Within the first year after birth, parents are encouraged to come to these well-baby checkups at the following intervals: birth-1 week, 2–4 weeks, 2 months, 4 months, 6 months, and 9–10 months. During these checkups, parents or caregivers are asked “Do you feed your baby breastmilk?” We categorized breastfeeding practice as: “breastfed for ≥6 months” if the response was “Yes” at ≥6 months after birth; “breastfed for <6 months” if the response was “Yes” at <6 months and “No” at ≥6 months checkup; and “not breastfed” if the response was “No” to the breastfeeding questions at both <6 months and ≥6 months. The 6-month cutoff was selected in accordance with the World Health Organization (WHO) breastfeeding guidelines, which recommend that infants are breastfed for at least 6 months [
25].
Outcomes
Pubertal stage for breast and pubic hair development was assessed by physical exam using the 5-level Tanner stages developed by Marshall and Tanner [
26]. Beginning in 2010, documentation of Tanner stages in the KNPC EHR became a routine part of pediatric checkups. KPNC pediatricians determine girls’ breast Tanner staging using palpation and visual inspection, and pubic hair Tanner staging using visual inspection. KPNC pediatricians are trained to assess Tanner stages for all children age 6+ years during each well-child check-up exam, which are due every 1–2 years. Although KPNC encourages all pediatricians to conduct Tanner assessment and enter the data in the EHR, some pediatricians skip the assessments due to lack of time, refusal by the patients, or obvious full maturation. In our cohort the number of pediatric check-ups with a recorded Tanner Stage ranged from 1 to 7 with a median of 2 (SD: 0.9).
In this study, our primary outcome was the timing of transition from Tanner Stage 1 (prepubertal) to Tanner Stage 2 and above, which characterizes the physical and clinical onset of pubertal development. We have measured and confirmed the validity of using Tanner-staging data from the KPNC EHR, as described elsewhere [
27]. Thelarche is defined as onset of breast development and pubarche is onset of pubic hair development.
Covariates
Girl’s prepubertal BMI was identified from clinic visits in the time window within 60 days prior to or after the last known Tanner Stage 1 assessment. Percentiles and z-scores were calculated using age- and sex-specific CDC year 2000 standard population distributions [
28]. We assessed the role of prepubertal BMI in secondary analyses using continuous prepubertal BMI percentiles.
We accounted for potential confounding using several sociodemographic variables and maternal characteristics that have been associated with breastfeeding practice and pubertal development in girls [
1,
10,
16,
29‐
32]. Maternal race/ethnicity was categorized as ‘African American’, ‘Hispanic’, ‘Asian/Pacific Islander’, and ‘non-Hispanic White’. Socioeconomic status, particularly income, is a strong predictor of pubertal outcomes, however is not collected routinely by KPNC health practitioners. Thus, we used maternal education (high school or less, some college, 4-year college, and graduate school) as a proxy for socioeconomic status. Maternal age at delivery was measured in years, and parity was categorized as ‘0’, ‘1,’, and ‘2+’. All covariates were obtained from the KPNC EHR.
Statistical analyses
We analyzed the association between breastfeeding and age at onset of puberty using Weibull regression, an accelerated failure time and proportional hazards regression model that accommodates left, right, and interval censoring. A subject was considered left-censored if they had already transitioned to Tanner Stage 2+ at the time of the first (baseline) Tanner stage exam and right-censored if they had not transitioned to Tanner Stage 2+ by the time of the last exam or had only one assessment at Tanner Stage 1. Weibull regression analyses provided two estimates of the association of an exposure variable with the outcome of time to puberty onset: the time ratio (TR) and the hazard ratio (HR). TR estimates represent the ratio of the median time to event for a given level of the exposure variable (e.g., not breastfed) in relation to its reference level (e.g., breastfed ≥6 months). Clinically important confounders including maternal age at delivery, race/ethnicity, education, and parity were included in all models. Due to theoretical or empirical associations with breastfeeding and/or pubertal timing, birthweight was also tested as a potential covariate but was not included in the final models because its inclusion did not substantially change effect estimates.
In secondary analyses, we assessed the role of girl’s prepubertal BMI (percentile) by comparing the effect estimates for breastfeeding before and after inclusion of this variable. Effect modification by maternal race/ethnicity was also examined using a cross-product term of mother’s race/ethnicity and breastfeeding. Although the test for interaction was not statistically significant, we conducted and presented the results from the stratified analyses by race/ethnicity. All analyses were conducted using SAS version 9.4 (SAS Institute, Cary, NC).
Discussion
In this multiethnic cohort of U.S. mother-daughter pairs, we found that breastfeeding is associated with timing of pubertal onset. Girls who were not breastfed are at increased risk of earlier breast and pubic hair onset compared with girls who breastfed for ≥6 months. Adjustment of the models with childhood BMI partially attenuated the associations, but they remained significant. Lastly, we observed that the association between breastfeeding and timing of thelarche may vary by race/ethnicity. There are several potential mechanisms explaining our observations.
The WHO guidelines on breastfeeding recommend that infants be exclusively breastfed for the first 6 months of life in order to ensure optimal health benefits for both mother and baby [
25]. One of the known benefit of breastfeeding is lower risk of childhood obesity, which in turn is known to be associated with pubertal timing [
1,
12]. These associations may be explained by the regulatory role of insulin in fat cell formation. Lucas et al. found that 6-day-old term infants that are formula-fed have significantly higher levels of blood insulin compared with breastfed infants. Insulin plays an important role in fat deposition by inhibiting lipolysis, the biological mechanism used to break down fats and other lipids. As a result, breastfed infants were found to have less body fat compared with formula-fed infants [
33]. Additionally, breast milk has two regulatory hormones, leptin and ghrelin, which are involved in food intake and body weight regulation [
34]. Breastfed infants also have more control over their energy intake compared with formula-fed infants and may be less likely to overeat [
35]. Thus, breastfeeding provides a balance of nutrients and bioactive substances necessary to maintain healthy levels of fat. Although we do not have direct measures of adiposity or body composition, our results demonstrating the role of child prepubertal BMI suggest that obesity or higher fat may partially influence the association between breastfeeding and earlier pubertal onset. However, the significant association even after adjustment for pre-pubertal BMI suggest that there may also be other pathways explaining the associations between breastfeeding and pubertal timing.
Psychosocial factors may also explain the observed associations. The evolutionary-developmental theory of reproductive development postulates that early childhood experiences, such as infant-parent attachment, regulate reproductive development later in life [
36]. One study found that infants with insecure infant-parent attachment had earlier pubertal onset compared with infants with secure attachment [
36]. Infant-parent attachment security has been shown to have a positive association with breastfeeding duration and could mediate the relationship between breastfeeding and pubertal onset [
37]. It is also possible that this relationship was confounded by maternal factors that are inversely associated with breastfeeding. For example, mothers with maternal depression and/or partner/marital stress may be less likely to initiate breastfeeding [
38,
39]. Likewise, daughters raised in households affected by maternal depression or familial stress may be more likely to experience earlier pubertal timing [
40]. Thus, not breastfeeding may be a proxy for maternal stress and depression, leading to earlier onset of daughters’ puberty. In this case, psychosocial interventions focusing on improving maternal mental health and wellness could potentially mitigate adverse health outcomes, such as earlier pubertal onset, in offspring later in life.
Our findings are consistent with the two existing studies that have examined breastfeeding and pubertal onset. We have recently conducted a study using a U.S.-based multiethnic cohort of 1237 girls and reported that girls who were predominantly breastfed were less likely to experience earlier thelarche compared with girls who were formula-fed (HR: 0.74; 95%CI: 0.59–0.94) [
13]. Similarly, a study using a cohort of 219 Korean boys and girls found that being breastfed for at least 6 months compared with not being breastfed was inversely associated with earlier pubertal onset (odds ratio [OR]: 0.27; 95% CI: 0.11–0.66) [
14]. Comparable results have been found in relation to menarche. Al-Sahab et al. found that an increase in 1 month of exclusive breastfeeding was associated with later menarche (HR: 0.94; 95% CI: 0.90–0.98) [
17]. Similarly, another study showed that formula-fed girls were more than twice as likely to have experienced earlier menarche compared with breastfed girls [
19]. Our results extend the existing knowledge by examining racial/ethnic differences. Although the test for interaction was not statistically significant, our data suggest that the strengths of the associations may vary by race/ethnicity. In our data, we observed particularly strong associations amongst African American girls. This may be partially due to the presence of greater variability in breastfeeding practice and duration amongst African Americans, as observed in Kale et al. [
13], and warrants further investigation using a larger cohort given the known racial/ethnic disparities in the timing of pubertal onset. If racial/ethnic differences in these associations truly exist, such knowledge would help the design of future interventions involving breastfeeding and psychosocial support to reduce the risk of early puberty, thereby reducing ever-widening racial/ethnic health disparities.
There are several limitations to this study to be considered. First, reliance on data from the EHR and other clinical sources meant that detailed data were not available on potentially relevant factors. For example, although we were able to identify clear groups of mothers according to breastfeeding practices, our measure was relatively crude, and we were unable to provide more precise estimates of breastfeeding duration or exclusivity in our cohort. However, because of the availability of EHR data, including prospectively-collected pubertal stage data assessed objectively by pediatricians and clinically measured BMI, we were able to examine the associations of breastfeeding and pubertal onset in a large number of girls. Second, we did not have information on potential confounders or mediating factors such as girls’ body composition, maternal psychosocial factors such as stress or depression, parenting styles and breast milk composition. Lastly, we were only able to examine these associations amongst girls due to funding constraints. Early-life risk factors for pubertal onset are vastly understudied in boys. These are exciting areas for future research, and results from future studies may shed more light on the racial/ethnic differences in the timing of pubertal onset. Despite these limitations, our study extended the knowledge in the area of risk factors of early puberty by using a diverse and large cohort of mother-daughter pairs, enabling us to explore racial/ethnic differences, which had never been done in previous studies.
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