Abstract

BackgroundThe ovary is an important site where gene variants modulate pubertal timing. The cannabinoid receptor 2 (CB2) is expressed in the ovary, plays a role in folliculogenesis and ovulation, and can be modulated by estrogens. Obesity is strictly associated with early menarche and is characterized by sex hormone and endocannabinoid derangement.AimIn this study, we investigated the role of the CB2 receptor in determining the age at menarche in obese girls.MethodsWe studied a cohort of 240 obese girls (age 11.9±3 years; BMI z-score 2.8±0.8). The age at menarche (if it had already occurred) was recorded at the time of the visit or via phonecall. The CNR2 rs35761398 polymorphism, which leads to the CB2 Q63R variant, was detected by the TaqMan assay.ResultsIn total, 105 patients were homozygous for the R63-coding allele (RR), 113 were QR and 22 were QQ. Variance analysis revealed a significantly earlier age of menarche in subjects carrying the Q63 allele, which was also found after adjusting for BMI z-score (11±1.2 vs. 11.6±1.2 years, p = 0.0003). Logistic regression analysis demonstrated that patients homozygous for the Q allele had a 2.2-fold higher risk (odds ratio = 2.2; CI1.1–3.4; p = 0.02) of presenting with an early menarche (age at menarche <12 years).ConclusionWe demonstrated for the first time the association between the CB2 Q63R functional variant and the age at menarche in a cohort of Italian obese girls.

Highlights

  • The age at menarche is a marker of pubertal timing in females

  • We studied a cohort of 240 obese girls

  • The CNR2 rs35761398 polymorphism, which leads to the cannabinoid receptor 2 (CB2) Q63R variant, was detected by the TaqMan assay

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Summary

Introduction

The age at menarche is a marker of pubertal timing in females. Pubertal timing is widely variable, a result of the interactions of both environmental and genetic determinants. The age at menarche is associated with obesity, type 2 diabetes, cardiovascular disease, breast cancer and all-cause mortality and is characterized by a complex genetic architecture [1,2,3]. Some gene variants such as the lin-28 homolog B (LIN28B) gene polymorphism have been strongly associated with the age at menarche, modulating pubertal timing [4,5]. Early menarche has been associated with childhood obesity [6]. The ovary is an important site where gene variants modulate pubertal timing. The cannabinoid receptor 2 (CB2) is expressed in the ovary, plays a role in folliculogenesis and ovulation, and can be modulated by estrogens. Obesity is strictly associated with early menarche and is characterized by sex hormone and endocannabinoid derangement

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