Fetal genetically determined birth weight plays a causal role in earlier puberty timing: evidence from human genetic studies

Peng, Qinghui1,2; Qiu, Wenjuan3; Li, Zengjun1,2; Zhao, Jian4,5,8; Zhu, Cairong1,2,6,7

2024-04-03

10.1093/humrep/deae019

HUMAN REPRODUCTION   影响因子和分区

0268-1161

1460-2350

["STUDY QUESTION Does fetal genetically determined birth weight associate with the timing of puberty?SUMMARY ANSWER Lower fetal genetically determined birth weight was causally associated with an earlier onset of puberty, independent of the indirect effects of the maternal intrauterine environment.WHAT IS KNOWN ALREADY Previous Mendelian randomization (MR) studies have indicated a potential causal link between birth weight, childhood BMI, and the onset of puberty. However, they did not distinguish between genetic variants that have a direct impact on birth weight through the fetal genome (referred to as fetal genetic effects) and those that influence birth weight indirectly by affecting the intrauterine environment (known as maternal genetic effects). It is crucial to emphasize that previous studies were limited because they did not account for the potential bias caused by unaddressed correlations between maternal and fetal genetic effects. Additionally, the proportion of birth weight variation explained by the fetal genome is considerably larger than that of the maternal genome.STUDY DESIGN, SIZE, DURATION We performed two-sample MR analyses to investigate the causal effect of fetal genetically determined birth weight on puberty timing using summary data from large-scale genome-wide association studies (GWASs) in individuals of European ancestry.PARTICIPANTS/MATERIALS, SETTING, METHODS From the two most recent GWASs specifically centered on birth weight, which included 406 063 individuals and 423 683 individuals (63 365 trios) respectively, we identified genetic variants associated with fetal genetically determined birth weight, while adjusting for maternal genetic effects. We identified genetic variants associated with childhood BMI from an independent GWAS involving 21 309 European participants. On this basis, we employed two-sample MR techniques to examine the possible causal effects of fetal genetically determined birth weight on puberty timing using a large-scale GWAS of puberty timing (including 179 117 females of European ancestry). Furthermore, we employed advanced analytical methods, specifically MR mediation and MR-Cluster, to enhance our comprehension of the causal relationship between birth weight determined by fetal genetics and the timing of puberty. We also explored the pathways through which childhood BMI might act as a mediator in this relationship.MAIN RESULTS AND THE ROLE OF CHANCE In the univariable MR analysis, a one SD decrease in fetal genetically determined birth weight (similar to 418 g) was associated with a 0.16 (95% CI [0.07-0.26]) years earlier onset of puberty. The multivariable MR analysis including fetal genetically determined birth weight and childhood BMI in relation to puberty timing provided compelling evidence that birth weight had a direct influence on the timing of puberty. Lower birth weight (one SD) was associated with an earlier onset of puberty, with a difference of 0.23 (95% CI [0.05-0.42]) years. We found little evidence to support a mediating role of childhood BMI between birth weight and puberty timing (-0.07 years, 95% CI [-0.20 to 0.06]).LIMITATIONS, REASONS FOR CAUTION Our data came from European ancestry populations, which may restrict the generalizability of our results to other populations. Moreover, our analysis could not investigate potential non-linear relationships between birth weight and puberty timing due to limitations in genetic summary data.","WIDER IMPLICATIONS OF THE FINDINGS Findings from this study suggested that low birth weight, determined by the fetal genome, contributes to early puberty, and offered supporting evidence to enhance comprehension of the fetal origins of disease hypothesis.STUDY FUNDING/COMPETING INTEREST(S) C.Z. was funded by the Sichuan Province Science and Technology Program [grant number 2021JDR0189]. J.Z. was supported by grants from the National Natural Science Foundation of China [grant number 82373588]. No other authors declare any sources of funding. The authors have no conflicts of interest.TRIAL REGISTRATION NUMBER N/A."]

puberty timing birth weight Mendelian randomization fetal genetic effects early-life growth

SCI

英语

通讯

Sichuan Province Science and Technology Program[2021JDR0189] ; National Natural Science Foundation of China[82373588]

Obstetrics & Gynecology ; Reproductive Biology

Obstetrics & Gynecology ; Reproductive Biology

WOS:001183378000001

OXFORD UNIV PRESS

CLINICAL MEDICINE

Web of Science

1.Sichuan Univ, West China Sch Publ Hlth, Dept Epidemiol & Hlth Stat, Chengdu, Peoples R China
2.Sichuan Univ, West China Hosp 4, Chengdu, Peoples R China
3.Shanghai Jiao Tong Univ, Xinhua Hosp, Shanghai Inst Paediat Res, Dept Paediat Endocrinol & Genet Metab,Sch Med, Shanghai, Peoples R China
4.Southern Univ Sci & Technol, Sch Publ Hlth & Emergency Management, Shenzhen, Guangdong, Peoples R China
5.Univ Bristol, MRC Integrat Epidemiol Unit, Bristol, England
6.Sichuan Univ, West China Sch Publ Hlth, Dept Epidemiol & Hlth Stat, 18,Sect 3,South Renmin Rd, Chengdu 610041, Peoples R China
7.Sichuan Univ, West China Hosp 4, 18,Sect 3,South Renmin Rd, Chengdu 610041, Peoples R China
8.Southern Univ Sci & Technol, Sch Publ Hlth & Emergency Management, 1088 Xueyuan Ave, Shenzhen 518055, Guangdong, Peoples R China

Peng, Qinghui,Qiu, Wenjuan,Li, Zengjun,et al. Fetal genetically determined birth weight plays a causal role in earlier puberty timing: evidence from human genetic studies[J]. HUMAN REPRODUCTION,2024,39(4).

Peng, Qinghui,Qiu, Wenjuan,Li, Zengjun,Zhao, Jian,&Zhu, Cairong.(2024).Fetal genetically determined birth weight plays a causal role in earlier puberty timing: evidence from human genetic studies.HUMAN REPRODUCTION,39(4).

Peng, Qinghui,et al."Fetal genetically determined birth weight plays a causal role in earlier puberty timing: evidence from human genetic studies".HUMAN REPRODUCTION 39.4(2024).