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. Author manuscript; available in PMC: 2015 Dec 1.
Published in final edited form as: Int J Obes (Lond). 2015 Mar 16;39(6):939–944. doi: 10.1038/ijo.2015.25

Even transient rapid infancy weight gain is associated with higher BMI in young adults and earlier menarche

Burak Salgin 1,2, Shane A Norris 3, Philippa Prentice 1, John M Pettifor 3, Linda M Richter 3,4, Ken K Ong 1,5, David B Dunger 1,3
PMCID: PMC4471108  EMSID: EMS62499  PMID: 25771929

Abstract

Background

Early postnatal rapid “catch-up” weight gain has been consistently associated with subsequent higher obesity risk and earlier pubertal development. In many low- and middle-income countries, infancy catch-up weight gain is transient and often followed by growth faltering. We explored the hypothesis that even transient catch-up weight gain during infancy is associated with later obesity risk and earlier puberty.

Methods

2352 (1151 male, 1201 female) black South African children in the Birth to Twenty (Bt20) prospective birth cohort study (Johannesburg-Soweto) underwent serial measurements of body size and composition from birth to age 18 years. At age 18 years, whole-body fat mass and fat-free mass were determined using dual energy x-ray absorptiometry. Pubertal development was assessed by the research team between ages 9 and 10 years, and recorded annually from age 11 years using a validated self-assessment protocol.

Results

Catch-up weight gain from birth to age 1 year, despite being followed by growth faltering between ages 1 and 2 years, was associated greater mid-upper arm circumference (p=0.04) and skin fold thickness (p=0.048) at age 8 years, and with higher weight (p<0.001) and BMI (p=0.001) at age 18 years after adjustment for sex, age, smoking during pregnancy, birth order, gestational age, formula-milk feeding and household socio-economic status. Infancy catch-up weight gain was also associated with younger age at menarche in girls (p<0.001). This association persisted after adjustment for smoking during pregnancy, birth order, gestational age, formula-milk feeding and household socio-economic status (p=0.005).

Conclusion

Transient catch-up weight gain from birth to age 1 year among children born in a low-income area of South Africa was associated with earlier menarche and greater adiposity in early adulthood. This observation suggests that modifiable determinants of rapid infancy weight gain may be targeted in order to prevent later obesity and consequences of earlier puberty in girls.

Keywords: Catch-up weight gain, rapid infancy growth, menarche, obesity

Introduction

Childhood obesity has been shown to track into adult life and confer a higher risk of cardiovascular disease and all-cause mortality 1-4. Strategies to prevent the development of obesity may therefore benefit from interventions that are implemented in early life. This in turn requires a better understanding of biological factors that underlie the development of childhood overweight and obesity.

In high-resource settings, rapid “catch-up” weight gain during the first two postnatal years has consistently been associated with obesity in children and adults 5-9. In addition, rapid infancy weight gain has been associated with earlier menarche with younger age at menarche as a robust marker of increased risk of adult obesity 10-18.

However, in many low- and middle-income countries infancy catch-up weight gain is transient and tends to be followed by growth faltering from around the age at weaning due to environmental factors and changes in feeding practice 19-21. We therefore explored the hypothesis that even transient early postnatal catch-up weight gain is associated with later obesity risk and earlier puberty in a developing middle-income country.

Methods

Study population

Birth to Twenty (Bt20) is a prospective birth cohort study of 3,273 singleton births between late April 1990 and early June 1990, who continued residence within the metropolitan area of Johannesburg-Soweto, South Africa, for at least six months after delivery. At that time, Johannesburg-Soweto covered approximately 100 square miles and had close to 3.5 million inhabitants living in various forms of housing, including 400,000 informal housing units.

Children were enrolled into the Bt20 cohort through public antenatal and delivery clinics and hospitals. No children was excluded based on gestational age or birth weight. Study participants were demographically representative of the study area population for black, Asian and mixed ancestry backgrounds. White subjects were underrepresented as private clinics were not targeted during the recruitment strategy. The recruitment process and cohort characteristics are described in more detail elsewhere 22, 23. All subjects of the current study were of black South African origin. Ethical approval was obtained from the University of the Witwatersrand Committee for Research and Human Subjects. A parent provided signed consent and verbal assent was obtained from each child.

Assessments of body size, body composition and pubertal development

Birth weight was obtained from hospital records. Birth length data were not available. Experienced research assistants measured weight and length during home visits at age 1 year and 2 years. Weight and standing height were measured by research assistants in a data collection site at ages 4, 5, 8, 13, 15 and 18 years. Mid-upper arm circumference (MUAC) as a general marker of nutritional status and triceps and subscapular skinfold thickness as estimates of fat mass were additional measurements at age 8 years. At age 18 years, dual energy x-ray absorptiometry (DEXA) (Hologic QDR 4500A) was used to measure whole-body fat and fat-free mass. A trained member of the research team assessed pubertal development between ages 9 and 10 years using the Sexual Maturation Scale (SMS) by Tanner 24, 25. Subsequent determination of pubertal development was based on annual self-assessments according to the SMS and supported by drawings, descriptions and a tutorial. We have previously shown a high concordance between these self-assessments and assessments undertaken by a healthcare professional in the same population 26. Female subjects and their parents were asked to recall age at menarche in full years on an annual basis from age 9 years.

Calculations

Body mass index (BMI) was calculated as weight/height2 in kilogram per square metre. Sex- and age-adjusted standard deviation scores (SDS) for weight, height and BMI were calculated as SDS = (subject’s measurement - population mean) / (population SD) in the LMSgrowth program version 2.12 (Medical Research Council, UK) using World Health Organization standards. Measurements of triceps and subscapular skinfold thickness were added together to create the sum of skinfolds in millimetres. DEXA-derived measurements of whole-body fat mass were corrected for height (ratio of whole-body fat mass to height) and for whole-body fat-free mass (ratio of whole-body fat mass to fat-free mass). Infancy weight gain was calculated as the change in weight SDS from birth to age 1 year. Gain in weight SDS greater than 0.67 (equivalent to a change in weight e.g from 9th to 25th centile) was taken to indicate catch-up weight gain 27. Downward change in weight SDS less than −0.67 between birth and age 1 year was defined as “catch-down” weight gain 27. The remaining children showed “no rapid change” in weight SDS during infancy.

Statistics

Data were analysed for normality using the Kolmogorov-Smirnov test and log-transformed to a normal distribution to allow use of analysis of variance to assess differences between boys and girls and across subjects with different patterns of weight gain during infancy. Post-hoc analyses using the Bonferroni correction were employed to test body size and composition between subjects of different patterns of infancy weight gain. Mean values for body size and composition and age at menarche were adjusted for several covariates as indicated. Weight and height from birth to age 18 years were also assessed using repeated-measures analysis for women stratified according to age at menarche. Significance was set to p<0.05. Analyses were performed using SPSS for Windows version 19. Data are means (standard deviation) unless stated otherwise.

Results

Cohort characteristics

Cohort characteristics are summarised in Table 1. The mean gestational age was 38.1 weeks (range 26-44 weeks, 61 subjects with gestational age <33 weeks) and the mean birth weight was 3064 grams (range 1000-4920 grams, 78 subjects with a birth weight <2000 grams). Data on 1613 out of the original 2352 subjects were available at age 18 years. The average birth weight was <0 SDS according to WHO growth standards (Table 1, Figure 1A). Weight gain till age 1 year was relatively fast in both boys and girls (Figure 1A). Girls age 1 year showed a trend towards higher weight SDS than boys (p=0.06; Table 1, Figure 1A) whilst height SDS (p=0.8; Table 1, Figure 1B) and BMI SDS (p=0.1; Table 1, Figure 1C) were similar.

Table 1.

Body size and composition of male and female subjects from birth to age 18 years.

Male n=1151 Female n=1201 p-value
Birth
Weight (kg) 3.11 (0.54) 3.02 (0.50) <0.001
Weight SDS −0.55 (1.20) −0.53 (1.19) 0.9
Age 1 year
Weight (kg) 9.3 (1.2) 9.2 (1.2) 0.001
Weight SDS −0.17 (1.11) −0.09 (1.04) 0.06
Height (cm) 73.8 (3.0) 73.2 (2.9) <0.001
Height SDS −0.54 (1.21) −0.52 (1.12) 0.8
BMI (kg/m2) 17.2 (1.8) 17.2 (1.8) 0.6
BMI SDS 0.27 (1.24) 0.38 (1.18) 0.1
Age 8 years
Weight (kg) 24.8 (4.1) 24.3 (4.4) 0.01
Weight SDS −0.49 (1.11) −0.54 (1.05) 0.3
Height (cm) 124.7 (5.9) 123.7 (6.0) 0.001
Height SDS −0.66 (1.01) −0.79 (0.97) 0.04
BMI (kg/m2) 15.8 (1.8) 15.8 (2.1) 0.4
BMI SDS −0.12 (1.02) −0.12 (0.98) 0.9
MUAC (cm) 17.8 (1.8) 18.0 (2.0) 0.2
Sum of skin folds (mm) 13.7 (4.8) 16.2 (5.8) <0.001
Age 18 years
Weight (kg) 59.7 (11.7) 58.9 (12.1) 0.1
Weight SDS −1.05 (1.35) −0.04 (1.28) <0.001
Height (cm) 167.0 (8.9) 163.3 (8.7) <0.001
Height SDS −1.17 (1.18) 0.02 (1.28) <0.001
BMI (kg/m2) 21.4 (4.0) 22.1 (4.6) 0.001
BMI SDS −0.33 (1.24) 0.05 (1.15) <0.001
Fat mass (kg) 8.4 (5.0) 19.1 (7.6) <0.001
Percentage fat mass (%) 13.9 (5.6) 32.4 (6.6) <0.001
Fat mass/height (kg/m) 5.1 (3.0) 11.7 (4.6) <0.001
Fat-free mass (kg) 49.6 (6.1) 38.1 (5.3) <0.001
Fat mass/fat-free mass 0.66 (0.19) 1.04 (0.52) <0.001

Data are means (SD).

Figure 1.

Figure 1

Weight SDS (A), height SDS (B) and BMI SDS (C) in male and female subjects from birth to age 18 years. Data are means ± standard error. ■ = male. ● = female.

Weight and height gain slowed between ages 1 and 2 years in boys and girls (Figure 1A and 1B). At age 8 years, girls had similar weight SDS (p=0.3; Table 1, Figure 1A), BMI SDS (p=0.9; Table 1, Figure 1C) and MUAC (p=0.2; Table 1), but lower height SDS (p=0.04; Table 1, Figure 1B) and greater skin fold thickness (p<0.001; Table 1) than boys.

Gender differences in body composition were more marked at age 18 years: girls gained more weight for height than boys during puberty and up to age 18 years (Table 1, Figure 1A-C). Girls age 18 years had higher weight SDS (p<0.001; Table 1, Figure 1A), height SDS (p<0.001; Table 1, Figure 1B), BMI SDS (p<0.001; Table 1, Figure 1C), whole-body fat mass (p<0.001; Table 1), percentage fat mass (p<0.001; Table 1), whole-body fat mass corrected for height (p<0.001; Table 1) and whole-body fat mass to fat-free mass ratio (p<0.001; Table 1).

Relation of infancy weight gain to body size and composition from birth to age 18 years

290 (46% male) out of the total of 2352 children showed catch-up weight gain between birth and age 1 year. They were born an average of 1.1 weeks earlier (p<0.001; Table 2) and had lower birth weight SDS (p<0.001; Table 2; Figure 2A) than children who did not show rapid change in weight or those with catch-down weight gain during infancy. The difference in birth weight persisted after adjustment for smoking during pregnancy, birth order, gestational age, formula-milk feeding and household socio-economic status (p<0.001; Table 2).

Table 2.

Body size and composition from birth to age 18 years for subjects who showed catch-up weight gain, no significant change in weight or catch-down weight gain from birth to age 1 year. Data are unadjusted means (SD) adjusted for smoking during pregnancy, birth order, gestational age, formula-milk feeding and household socio-economic status where indicated.

Catch-down n=511 No change n=938 Catch-up n=903 Unadjusted p-value Adjusted p-value
Birth
Gestational age (weeks) 38.7 (1.3) 38.5 (1.4) 37.5 (2.6) <0.001a,b <0.001a,b
Weight (kg) 3.53 (0.38) 3.15 (0.34) 2.71 (0.50) <0.001a,b <0.001a,b
Weight SDS 0.48 (0.76) −0.33 (0.74) −1.35 (1.23) <0.001a,b <0.001a,b
Age 1 year
Weight (kg) 8.4 (0.8) 9.0 (0.8) 9.9 (1.4) <0.001a,b <0.001a,b
Weight SDS −0.99 (0.79) −0.30 (0.72) 0.53 (1.12) <0.001a,b <0.001a,b
Height (cm) 72.1 (2.6) 73.4 (2.6) 74.5 (3.1) <0.001a,b <0.001a,b
Height SDS −1.17 (1.02) −0.59 (1.02) −0.14 (1.20) <0.001a,b <0.001a,b
BMI (kg/m2) 16.0 (1.3) 16.8 (1.3) 18.1 (2.0) <0.001a,b <0.001a,b
BMI SDS −0.49 (1.03) 0.11 (0.92) 0.96 (1.21) <0.001a,b <0.001a,b
Age 8 years
Weight (kg) 25.0 (4.5) 24.4 (3.8) 24.5 (4.7) 0.2 0.2
Weight SDS −0.42 (1.12) −0.54 (1.00) −0.55 (1.13) 0.3 0.2
Height (cm) 124.5 (6.2) 124.1 (5.7) 124.1 (6.1) 0.8 0.01 b
Height SDS −0.71 (1.03) −0.73 (0.97) −0.74 (1.00) 0.9 0.02 b
BMI (kg/m2) 16.1 (2.1) 15.8 (1.6) 15.8 (2.1) 0.1 0.2
BMI SDS 0.00 (1.05) −0.14 (0.90) −0.17 (1.07) 0.1b 0.2
MUAC (cm) 18.1 (1.9) 17.8 (1.7) 17.8 (2.0) 0.2 0.1a
Sum of skin folds (mm) 15.0 (6.0) 14.7 (4.8) 15.2 (5.8) 0.4 0.1a
Age 18 years
Weight (kg) 56.6 (10.5) 57.9 (10.0) 62.3 (13.7) <0.001a,b <0.001a,b
Weight SDS −0.88 (1.31) −0.68 (1.34) −0.15 (1.47) <0.001a,b <0.001a,b
Height (cm) 164.8 (9.1) 164.6 (9.0) 165.7 (8.8) 0.1a 0.6
Height SDS −0.63 (1.40) −0.63 (1.38) −0.42 (1.32) 0.01 a,b 0.6
BMI (kg/m2) 20.9 (3.9) 21.4 (3.8) 22.7 (4.9) <0.001a,b <0.001a,b
BMI SDS −0.43 (1.17) −0.21 (1.15) 0.12 (1.24) <0.001a,b 0.001 a,b
Fat mass (kg) 14.0 (8.7) 13.4 (8.0) 14.4 (8.6) 0.2 0.3
Percentage fat mass (%) 23.3 (11.2) 22.7 (10.8) 24.2 (11.3) 0.1a 0.3
Fat mass/height (kg/m) 8.6 (5.1) 8.3 (4.9) 8.9 (5.5) 0.2 0.3
Fat-free mass (kg) 44.4 (8.3) 44.0 (8.3) 43.0 (7.7) 0.04 b 0.7
Fat mass/fat-free mass 0.86 (0.25) 0.85 (0.25) 0.87 (0.26) 0.3 0.4

Additional adjustment for sex.

Additional adjustment for age and sex.

Additional adjustment for age, sex and height.

a

p<0.05 for ‘catch-up’ versus ‘no change’.

b

p<0.05 for ‘catch-up’ versus ‘catch-down’.

Figure 2.

Figure 2

Relation of change in weight SDS from birth to age 1 year to weight SDS (A), height SDS (B) and BMI SDS (C) from birth to age 18 years. Data are means ± standard error. ▲ = catch-down weight gain. ■ = no rapid change in weight. ● = catch-up weight gain.

By age 4 years, children with infancy catch-up weight gain had similar weight SDS, height SDS and BMI SDS to children without rapid change in weight or catch-down weight gain during infancy (Figure 2A-C). This similarity in body size persisted (Figure 2A-C) albeit lower height SDS at age 8 years in children with infancy catch-up weight gain versus other children after adjustment for smoking during pregnancy, birth order, gestational age, formula-milk feeding and household socio-economic status (p=0.02; Table 2). Children age 8 years with infancy catch-up weight gain also had greater MUAC (p=0.04; Table 2) and skin fold thickness (p=0.048; Table 2) than children without rapid change in weight during infancy after adjustment for smoking during pregnancy, birth order, gestational age, formula-milk feeding and household socio-economic status, sex, current age and height.

By at age 18 years, subjects with infancy catch-up weight gain had higher weight SDS (p<0.001; Table 2, Figure 2A), BMI SDS (p=0.001; Table 2, Figure 2C) and similar height SDS (p=0.6; Table 2, Figure 2B) than other subjects after adjustment for smoking during pregnancy, birth order, gestational age, formula-milk feeding and household socio-economic status. Subjects age 18 years with infancy catch-up weight gain had higher percentage fat mass than subjects without rapid change in weight during infancy (p=0.04; Table 2) and lower fat-free mass than other subjects (p=0.04; Table 2). These differences did not persist after adjustment for smoking during pregnancy, birth order, gestational age, formula-milk feeding, household socio-economic status, sex, current age and height (Table 2). If women are singled out and age at menarche is added as a covariate, the association between infancy catch-up weight gain and higher weight SDS and BMI SDS at age 18 years persists (p=0.005 and p=0.008 respectively). Infancy catch-up weight gain then also shows a trend towards an association with higher DEXA-derived measures of fat mass (p=0.08) and fat to fat-free mass ratio (p=0.08).

Infancy weight gain and age at menarche

Catch-up weight gain from birth to age 1 year was associated with earlier menarche (12.5±0.1 vs. 12.6±0.1 vs. 13.1±0.1 years for catch-up weight gain, no rapid change in weight and catch-down weight gain; p<0.001; Figure 3). This association persisted after adjustment for smoking during pregnancy, birth order, gestational age, formula-milk feeding and household socio-economic status (p=0.005). Accordingly, girls who were youngest at menarche had higher weight SDS (p=0.001; Figure 4A) and BMI SDS (p=0.008; Figure 4C) during childhood and adolescence. These associations persisted after adjustment for smoking during pregnancy, birth order, gestational age, formula-milk feeding, household socio-economic status (p=0.03 and p=0.02 respectively). Girls who were youngest at menarche also had higher height SDS before age 4 years (p<0.001; Figure 4B). This association persisted for girls youngest versus oldest at menarche after adjustment for smoking during pregnancy, birth order, gestational age, formula-milk feeding, household socio-economic status (p=0.046).

Figure 3.

Figure 3

Relationship between change in weight SDS from birth to age 1 year and age at menarche. Data are means ± standard error.

Figure 4.

Figure 4

Relation of age at menarche to weight SDS (A), height SDS (B) and BMI SDS (C) from birth to age 18 years. Data are means ± standard error. ● = menarche at age <12 years. ■ = menarche at age 12 or 13 years. ▲ = menarche at age >13 years.

Discussion

We explored the relationship between infancy weight gain, subsequent body size and body composition in boys and girls at ages 8 and 18 years as well as timing of pubertal development in girls in a prospective birth cohort of black children born in a low-income metropolitan area of Johannesburg-Soweto, South Africa. The main findings were the associations between transient catch-up weight gain from birth to age 1 year and higher BMI at age 18 years and earlier menarche.

A debate continues about the timing and tempo of rapid postnatal weight gain that conveys the greatest risk of later obesity. Most studies to date have focussed on growth patterns in the first two postnatal years 5-9, but there are data to suggest that growth trajectories in the first 3-6 months may be more important for determining the risk of later cardio-metabolic disease 28-30. There are even observational and trial data linking weight gain and nutrition during the first 8-14 days of life to later risks of obesity and insulin resistance 31, 32. An improved characterisation of the most detrimental features of weight gain in childhood would allow interventions to be directed towards potentially modifiable critical windows that contribute to metabolic functional capacity 33. In the majority of low- and middle-income countries, catch-up weight gain is transient; it tends to cease by age 1 year and is followed by growth faltering due to the combined effect of poverty, infection, poor hygiene and under-nutrition 19-21. We observed a similar growth pattern in children of the Bt20 study with catch-up weight gain during infancy but relative loss in weight and height in the following year. Nonetheless, children who showed catch-up weight gain from birth to age 1 year became relatively adipose during adolescence with distinctly higher weight and BMI at age 18 years, even after adjustment for sex, age, height, smoking during pregnancy, birth order, gestational age, formula-milk feeding and household socio-economic status.

The relationship between weight and onset of puberty, usually assessed by age at menarche in girls, is more complex. Earlier menarche is a robust marker of increased childhood and adult risk of obesity as well as being predictive of adult-onset diabetes 10-12, 15, 34, 35. However, girls who are younger at menarche are more likely to be overweight before the onset of puberty 36, 37 so that adult disease associations with earlier menarche may simply reflect the effect of rapid weight gain during earlier parts of childhood. The current study confirms these findings in children born into the low-income area of Johannesburg-Soweto amongst whom catch-up weight gain from birth to age 1 year was associated with younger age at menarche, even after adjustment for smoking during pregnancy, birth order, gestational age, formula-milk feeding and household socio-economic status. Earlier menarche could therefore represent a marker of higher risk of obesity in adult life in low-income countries. It is also unclear whether our finding can be extended to timing of puberty in boys, a more challenging undertaking because self-reported markers of puberty onset are less reliable among boys than girls. Nonetheless, we recently reported that the trajectory to earlier sexual maturation in males (time of voice breaking) of the 1946 British Birth Cohort Study was associated with faster weight gain from birth to age 2 years and led to higher adult BMI 17.

A study population of only black children born in one specific area may limit the generalisability of our findings; however, our data are consistent with those in other settings and ethnic groups. We only had access to weight, height, MUAC and skin fold thickness during childhood, which are relatively inaccurate estimates of body composition. We also did not have the means of adjusting the analyses for parental adiposity. At age 18 years, DEXA-derived measures of fat and fat-free mass were available for 1208 out of the original 2352 subjects, which may not have provided enough statistical power to determine differences in body composition despite greater weight and BMI gains in those who showed infancy catch-up weight gain. Our analyses of associations with infancy catch-up weight gain were further limited by not being able to adjust for age at maternal menarche, nutritional factors during childhood and adolescence, stressful psychological and physiological circumstances, objective markers of first- and second-hand smoking, and we did not screen for genetic conditions such as Turner syndrome.

In conclusion, transient catch-up weight gain between birth and age 1 year was common in black children who live in a low-income area of South Africa. Despite being followed by growth faltering between ages 1 and 2 years, this was associated with greater adiposity in early adulthood and with earlier menarche in girls, an observation that may be important for public health policy. Directly modifiable determinants of infancy weight gain such as feeding practices, mother’s age at pregnancy and smoking could be targeted in order to prevent later obesity and earlier puberty in the offspring 38. Given that younger age at menarche in mothers predicts faster weight gain of their offspring during infancy, but not during childhood, in male and female offspring 34, we speculate that mechanisms linking infancy catch-up and subsequent weight gains to earlier menarche may reflect transgenerational factors that include metabolic programming and epigenetic modification.

Acknowledgements

We are grateful to all study participants, their families and research assistants. Bt20 has been supported by The Wellcome Trust, Human Sciences Research Council, Medical Research Council, University of the Witwatersrand, the South African-Netherlands Programme on Alternative Development and the Anglo American Chairman’s Fund.

Footnotes

Conflict of interest

The authors have no conflict of interest.

References

  • 1.Law CM, Shiell AW, Newsome CA, Syddall HE, Shinebourne EA, Fayers PM, et al. Fetal, infant, and childhood growth and adult blood pressure: a longitudinal study from birth to 22 years of age. Circulation. 2002;105(9):1088–92. doi: 10.1161/hc0902.104677. [DOI] [PubMed] [Google Scholar]
  • 2.Reilly JJ, Methven E, McDowell ZC, Hacking B, Alexander D, Stewart L, et al. Health consequences of obesity. Arch Dis Child. 2003;88(9):748–52. doi: 10.1136/adc.88.9.748. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Wardle J, Brodersen NH, Cole TJ, Jarvis MJ, Boniface DR. Development of adiposity in adolescence: five year longitudinal study of an ethnically and socioeconomically diverse sample of young people in Britain. Bmj. 2006;332(7550):1130–5. doi: 10.1136/bmj.38807.594792.AE. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Baker JL, Olsen LW, Sorensen TI. Childhood body-mass index and the risk of coronary heart disease in adulthood. N Engl J Med. 2007;357(23):2329–37. doi: 10.1056/NEJMoa072515. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Baird J, Fisher D, Lucas P, Kleijnen J, Roberts H, Law C. Being big or growing fast: systematic review of size and growth in infancy and later obesity. Bmj. 2005;331(7522):929. doi: 10.1136/bmj.38586.411273.E0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Euser AM, Finken MJ, Keijzer-Veen MG, Hille ET, Wit JM, Dekker FW. Associations between prenatal and infancy weight gain and BMI, fat mass, and fat distribution in young adulthood: a prospective cohort study in males and females born very preterm. Am J Clin Nutr. 2005;81(2):480–7. doi: 10.1093/ajcn.81.2.480. [DOI] [PubMed] [Google Scholar]
  • 7.Monteiro PO, Victora CG. Rapid growth in infancy and childhood and obesity in later life--a systematic review. Obesity reviews: an official journal of the International Association for the Study of Obesity. 2005;6(2):143–54. doi: 10.1111/j.1467-789X.2005.00183.x. [DOI] [PubMed] [Google Scholar]
  • 8.Ong KK, Loos RJ. Rapid infancy weight gain and subsequent obesity: systematic reviews and hopeful suggestions. Acta Paediatr. 2006;95(8):904–8. doi: 10.1080/08035250600719754. [DOI] [PubMed] [Google Scholar]
  • 9.Bouhours-Nouet N, Dufresne S, de Casson FB, Mathieu E, Douay O, Gatelais F, et al. High birth weight and early postnatal weight gain protect obese children and adolescents from truncal adiposity and insulin resistance: metabolically healthy but obese subjects? Diabetes Care. 2008;31(5):1031–6. doi: 10.2337/dc07-1647. [DOI] [PubMed] [Google Scholar]
  • 10.Garn SM, LaVelle M, Rosenberg KR, Hawthorne VM. Maturational timing as a factor in female fatness and obesity. Am J Clin Nutr. 1986;43(6):879–83. doi: 10.1093/ajcn/43.6.879. [DOI] [PubMed] [Google Scholar]
  • 11.Helm P, Munster K, Schmidt L. Recalled menarche in relation to infertility and adult weight and height. Acta Obstet Gynecol Scand. 1995;74(9):718–22. doi: 10.3109/00016349509021181. [DOI] [PubMed] [Google Scholar]
  • 12.van Lenthe FJ, Kemper CG, van Mechelen W. Rapid maturation in adolescence results in greater obesity in adulthood: the Amsterdam Growth and Health Study. Am J Clin Nutr. 1996;64(1):18–24. doi: 10.1093/ajcn/64.1.18. [DOI] [PubMed] [Google Scholar]
  • 13.Ong KK, Petry CJ, Emmett PM, Sandhu MS, Kiess W, Hales CN, et al. Insulin sensitivity and secretion in normal children related to size at birth, postnatal growth, and plasma insulin-like growth factor-I levels. Diabetologia. 2004;47(6):1064–70. doi: 10.1007/s00125-004-1405-8. [DOI] [PubMed] [Google Scholar]
  • 14.Ahmed ML, Ong KK, Dunger DB. Childhood obesity and the timing of puberty. Trends Endocrinol Metab. 2009;20(5):237–42. doi: 10.1016/j.tem.2009.02.004. [DOI] [PubMed] [Google Scholar]
  • 15.Ong KK, Emmett P, Northstone K, Golding J, Rogers I, Ness AR, et al. Infancy weight gain predicts childhood body fat and age at menarche in girls. J Clin Endocrinol Metab. 2009;94(5):1527–32. doi: 10.1210/jc.2008-2489. [DOI] [PubMed] [Google Scholar]
  • 16.Maisonet M, Christensen KY, Rubin C, Holmes A, Flanders WD, Heron J, et al. Role of prenatal characteristics and early growth on pubertal attainment of British girls. Pediatrics. 2010;126(3):e591–600. doi: 10.1542/peds.2009-2636. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Ong KK, Bann D, Wills AK, Ward K, Adams JE, Hardy R, et al. Timing of voice breaking in males associated with growth and weight gain across the life course. J Clin Endocrinol Metab. 2012;97(8):2844–52. doi: 10.1210/jc.2011-3445. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Wang Y, Dinse GE, Rogan WJ. Birth weight, early weight gain and pubertal maturation: a longitudinal study. Pediatric obesity. 2012;7(2):101–9. doi: 10.1111/j.2047-6310.2011.00022.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Black RE, Allen LH, Bhutta ZA, Caulfield LE, de Onis M, Ezzati M, et al. Maternal and child undernutrition: global and regional exposures and health consequences. Lancet. 2008;371(9608):243–60. doi: 10.1016/S0140-6736(07)61690-0. [DOI] [PubMed] [Google Scholar]
  • 20.Victora CG, de Onis M, Hallal PC, Blossner M, Shrimpton R. Worldwide timing of growth faltering: revisiting implications for interventions. Pediatrics. 2010;125(3):e473–80. doi: 10.1542/peds.2009-1519. [DOI] [PubMed] [Google Scholar]
  • 21.Prentice AM, Moore SE, Fulford AJ. Growth faltering in low-income countries. World review of nutrition and dietetics. 2013;106:90–9. doi: 10.1159/000342563. [DOI] [PubMed] [Google Scholar]
  • 22.Richter LM, Norris SA, De Wet T. Transition from Birth to Ten to Birth to Twenty: the South African cohort reaches 13 years of age. Paediatr Perinat Epidemiol. 2004;18(4):290–301. doi: 10.1111/j.1365-3016.2004.00572.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Richter L, Norris S, Pettifor J, Yach D, Cameron N. Cohort Profile: Mandela’s children: the 1990 Birth to Twenty study in South Africa. Int J Epidemiol. 2007;36(3):504–11. doi: 10.1093/ije/dym016. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Tanner JM. Growth at Adolescence. Blackwell Scientific Publications; Oxford: 1962. [Google Scholar]
  • 25.Tanner JM. Standards of normal growth. In: Tanner JM, editor. Foetus into Man: Physical Growth from Conception to Maturity. Open Books; London: 1978. pp. 196–201. [Google Scholar]
  • 26.Norris SA, Richter LM. Application and validation of tanner pubertal self-rating to urban Black adolescents in South Africa. J Adolesc Res. 2005;(15):609–624. [Google Scholar]
  • 27.Ong KK, Ahmed ML, Emmett PM, Preece MA, Dunger DB. Association between postnatal catch-up growth and obesity in childhood: prospective cohort study. Bmj. 2000;320(7240):967–71. doi: 10.1136/bmj.320.7240.967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Ekelund U, Ong KK, Linne Y, Neovius M, Brage S, Dunger DB, et al. Association of weight gain in infancy and early childhood with metabolic risk in young adults. J Clin Endocrinol Metab. 2007;92(1):98–103. doi: 10.1210/jc.2006-1071. [DOI] [PubMed] [Google Scholar]
  • 29.Leunissen RW, Kerkhof GF, Stijnen T, Hokken-Koelega A. Timing and tempo of first-year rapid growth in relation to cardiovascular and metabolic risk profile in early adulthood. JAMA. 2009;301(21):2234–42. doi: 10.1001/jama.2009.761. [DOI] [PubMed] [Google Scholar]
  • 30.Chomtho S, Wells JC, Williams JE, Davies PS, Lucas A, Fewtrell MS. Infant growth and later body composition: evidence from the 4-component model. Am J Clin Nutr. 2008;87(6):1776–84. doi: 10.1093/ajcn/87.6.1776. [DOI] [PubMed] [Google Scholar]
  • 31.Singhal A, Fewtrell M, Cole TJ, Lucas A. Low nutrient intake and early growth for later insulin resistance in adolescents born preterm. Lancet. 2003;361(9363):1089–97. doi: 10.1016/S0140-6736(03)12895-4. [DOI] [PubMed] [Google Scholar]
  • 32.Stettler N, Stallings VA, Troxel AB, Zhao J, Schinnar R, Nelson SE, et al. Weight gain in the first week of life and overweight in adulthood: a cohort study of European American subjects fed infant formula. Circulation. 2005;111(15):1897–903. doi: 10.1161/01.CIR.0000161797.67671.A7. [DOI] [PubMed] [Google Scholar]
  • 33.McCance RA, Widdowson EM. The effects of chronic undernutrition and of total starvation on growing and adult rats. The British journal of nutrition. 1956;10(4):363–73. doi: 10.1079/bjn19560054. [DOI] [PubMed] [Google Scholar]
  • 34.Ong KK, Northstone K, Wells JC, Rubin C, Ness AR, Golding J, et al. Earlier mother’s age at menarche predicts rapid infancy growth and childhood obesity. PLoS medicine. 2007;4(4):e132. doi: 10.1371/journal.pmed.0040132. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Lakshman R, Forouhi N, Luben R, Bingham S, Khaw K, Wareham N, et al. Association between age at menarche and risk of diabetes in adults: results from the EPIC-Norfolk cohort study. Diabetologia. 2008;51(5):781–6. doi: 10.1007/s00125-008-0948-5. [DOI] [PubMed] [Google Scholar]
  • 36.Freedman DS, Khan LK, Serdula MK, Dietz WH, Srinivasan SR, Berenson GS. The relation of menarcheal age to obesity in childhood and adulthood: the Bogalusa heart study. BMC pediatrics. 2003;3:3. doi: 10.1186/1471-2431-3-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Must A, Naumova EN, Phillips SM, Blum M, Dawson-Hughes B, Rand WM. Childhood overweight and maturational timing in the development of adult overweight and fatness: the Newton Girls Study and its follow-up. Pediatrics. 2005;116(3):620–7. doi: 10.1542/peds.2004-1604. [DOI] [PubMed] [Google Scholar]
  • 38.Ong KK, Preece MA, Emmett PM, Ahmed ML, Dunger DB. Size at birth and early childhood growth in relation to maternal smoking, parity and infant breast-feeding: longitudinal birth cohort study and analysis. Pediatr Res. 2002;52(6):863–7. doi: 10.1203/00006450-200212000-00009. [DOI] [PubMed] [Google Scholar]

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