Genetic Risk for Earlier Menarche also Influences Peripubertal Body Mass Index

被引:17
作者
Johnson, William [1 ]
Choh, Audrey C. [2 ]
Curran, Joanne E. [3 ]
Czerwinski, Stefan A. [2 ]
Bellis, Claire [3 ]
Dyer, Thomas D. [3 ]
Blangero, John [3 ]
Towne, Bradford [2 ,4 ]
Demerath, Ellen W. [1 ]
机构
[1] Univ Minnesota, Div Epidemiol & Community Hlth, Sch Publ Hlth, Minneapolis, MN 55454 USA
[2] Wright State Univ, Boonshoft Sch Med, Dept Community Hlth, Dayton, OH 45435 USA
[3] Texas Biomed Res Inst, Dept Genet, San Antonio, TX USA
[4] Wright State Univ, Boonshoft Sch Med, Dept Pediat, Dayton, OH 45435 USA
基金
美国国家卫生研究院;
关键词
genetic variants; menarche; developmental timing; pleiotropy; body mass index; GENOME-WIDE ASSOCIATION; BRITISH BIRTH COHORT; ENERGY-BALANCE; EATING-DISORDERS; TEENAGE GIRLS; UNITED-STATES; ADULT OBESITY; WEIGHT-LOSS; US GIRLS; AGE;
D O I
10.1002/ajpa.22121
中图分类号
Q98 [人类学];
学科分类号
030303 ;
摘要
It is unclear whether earlier age at menarche is associated with higher body mass index (BMI) because they share a common genetic underpinning. We investigated the impact of single nucleotide polymorphisms (SNPs) influencing menarche timing on peripubertal BMI. For 556 Fels Longitudinal Study children (277 boys/279 girls) born 1928-1992, a genetic risk score (GRS(42)) was computed as the sum of the number of risk alleles in 42 putative menarche SNPs. Serial BMI Z-scores within +/- 66.99 years from each individual's age at peak height velocity (Age@PHV) were grouped into seven time points (-6 years, -4 years, -2 years, Age@PHV, +2 years, +4years, and +6 years). Heritability of BMI ranged from 0.53 to 0.85 across the time points. The effect of GRS(42) on BMI Z-scores at each time point was modeled using variance components-based procedures. GRS(42) had a significant (P < 0.05) effect at every time point; an increase of one risk allele was associated with an increase of 0.03-0.08 BMI Z-scores. A separate score (GRS(29)) was computed that excluded 13 of the menarche SNPs previously documented to also influence adiposity; significant main effects were observed at Age@PHV+4 and 16 years. This finding supports a causal effect of advanced sexual development on post-Age@PHV BMI. Significant positive GRS(42) (or GRS(29))-by-birth year interactions indicate that some genetic influences on BMI have amplified over the 20th century. This gene-by-environment interaction also suggests that children with a genetic predisposition to earlier sexual development might avoid elevated BMI through alteration of their nutritional environment. Am J Phys Anthropol 150:10-20, 2013. (C)2012 Wiley Periodicals, Inc.
引用
收藏
页码:10 / 20
页数:11
相关论文
共 75 条
  • [51] Prentice A. M., 1996, European Journal of Clinical Nutrition, V50, pS82
  • [52] Roche A.F., 1992, GROWTH MATURATION BO
  • [53] Increasing Genetic Variance of Body Mass Index during the Swedish Obesity Epidemic
    Rokholm, Benjamin
    Silventoinen, Karri
    Tynelius, Per
    Gamborg, Michael
    Sorensen, Thorkild I. A.
    Rasmussen, Finn
    [J]. PLOS ONE, 2011, 6 (11):
  • [54] Thelarche, Pubarche, and Menarche Attainment in Children With Normal and Elevated Body Mass Index
    Rosenfield, Robert L.
    Lipton, Rebecca B.
    Drum, Melinda L.
    [J]. PEDIATRICS, 2009, 123 (01) : 84 - 88
  • [55] A role for brain-specific homeobox factor Bsx in the control of hyperphgia and locomotory behavior
    Sakkou, Maria
    Wiedmer, Petra
    Anlag, Katrin
    Hamm, Anne
    Seuntjens, Eve
    Ettwiller, Laurence
    Tschoep, Matthias H.
    Treier, Mathias
    [J]. CELL METABOLISM, 2007, 5 (06) : 450 - 463
  • [56] Growth Differences by Age of Menarche in African American and White Girls
    Salsberry, Pamela J.
    Reagan, Patricia B.
    Pajer, Kathleen
    [J]. NURSING RESEARCH, 2009, 58 (06) : 382 - 390
  • [57] Schousboe K, 2003, TWIN RES, V6, P409, DOI 10.1375/136905203770326411
  • [58] CRITICAL FAT, MENARCHE, AND THE MAINTENANCE OF MENSTRUAL CYCLES - A CRITICAL-REVIEW
    SCOTT, EC
    JOHNSTON, FE
    [J]. JOURNAL OF ADOLESCENT HEALTH, 1982, 2 (04) : 249 - 260
  • [59] 'Mendelian randomization': can genetic epidemiology contribute to understanding environmental determinants of disease?
    Smith, GD
    Ebrahim, S
    [J]. INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2003, 32 (01) : 1 - 22
  • [60] Multipoint estimation of identity-by-descent probabilities at arbitrary positions among marker loci on general pedigrees
    Sobel, E
    Sengul, H
    Weeks, DE
    [J]. HUMAN HEREDITY, 2001, 52 (03) : 121 - 131