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      Why should we be concerned about early menarche?

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      , MD, PhD
      Clinical and Experimental Pediatrics
      Korean Pediatric Society

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          Abstract

          Puberty is a transitional period between childhood and adulthood during which sexual maturation occurs. Menarche, the first menstruation, is a milestone event of pubertal development in girls since it represents the onset of the female reproductive capacity. Menarche, a late event during puberty, usually occurs 2-2.5 years after pubertal onset and is characterized by breast enlargement and pubic hair development. Several studies have reported that the mean age at menarche decreased from 17 years in 1840 to approximately 12 years in 2000 in most developed countries. According to a recent review, the age at menarche has remained stable over the past few decades [1]. Age at menarche varies among countries, generations, and races. According to the Korean National Health and Nutrition Survey, in Korea, mean age at menarche decreased from 16.90 years for women born between 1920 and 1925 to 13.79 years for those born between 1980 and 1985 [2]. Menarche is a complex phenomenon that is influenced by genetic and environmental factors. Approximately half of the variations in menarcheal age among developing countries may be due to genetic and heritable factors. The age at menarche is similar between mother and daughter, which supports the genetic influence on menarcheal age. Genome-wide association studies reported that several genes or loci, including LIN28B, TAC3R, ESR1, and 9q31.2, were associated with age at menarche [3]. Environmental factors including nutrition, psychosocial variables, and endocrine-disruptor chemicals also influence the timing of menarche. The decrease in menarcheal age can be explained by environmental factors such as nutritional status and the increased prevalence of obesity, although genetic factors also play a crucial role in pubertal progression. Early menarche is usually defined as menarche before the age of 12 years, although some researchers set it at ≤10 or 11 years. In Korea, 21.4% of subjects experienced menarche before the age of 12 years in 2001 versus 34.6% in 2010/2011 [4]. Nutritional habits such as formula feeding during early infancy, increased subcutaneous fat, a high body mass index, early exposure to endocrine-disruptor chemicals, and the consumption of sugar-sweetened beverages (SSB) as well as the increased prevalence of precocious puberty are possible factors responsible for early menarche. Early menarche is associated with physical and psychosocial problems such as anxiety/depression, substance use, and suicidal behavior in adolescents. It can also cause early fusion of the epiphyseal growth plates; therefore, the young woman’s final adult height may be shorter than her potential genetic height. In the Korean population, menarche before 12 years of age is associated with an increased risk of metabolic syndrome and type 2 diabetes mellitus in young and middle-aged women [5]. It has also been linked to an increased prevalence of obesity, insulin resistance, and hypercholesterolemia in adulthood, culminating in higher risks of cardiovascular diseases such as hypertension, coronary heart disease, stroke, and diabetes in women. Furthermore, women who experience menarche before 12 years of age have a 23% higher risk of developing breast cancer than those who first menstruate at 15 years of age or later [6]. Recent public concern about early menarche or precocious puberty has increased due to its adverse consequences in later life. Kim and Lim [7] suggested that such consequences can be prevented through health education targeting a reduction in the consumption of fructose, concentrations of which are high in SSB. Carwile et al. [8] reported that girls consuming more than 1.5 SSB per day experienced menarche 2.7 months earlier than those consuming less than 2 SSB per week. In Korea, the consumption of SSB rapidly increased from 32 kcal/day to 82 kcal/day over an 11-year period [9]. The removal of SSB from vending machines in schools and education to encourage the consumption of a balanced diet could be effective ways to reduce fructose consumption. Menarche is not just a moment during pubertal progression. Its timing, especially when early, may be associated with several health problems in adolescence and adulthood. This finding highlights the need for increased awareness of and efforts to prevent early menarche.

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          Most cited references9

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          Epidemiology of breast cancer.

          Breast cancer is the commonest cause of cancer death in women worldwide. Rates vary about five-fold around the world, but they are increasing in regions that until recently had low rates of the disease. Many of the established risk factors are linked to oestrogens. Risk is increased by early menarche, late menopause, and obesity in postmenopausal women, and prospective studies have shown that high concentrations of endogenous oestradiol are associated with an increase in risk. Childbearing reduces risk, with greater protection for early first birth and a larger number of births; breastfeeding probably has a protective effect. Both oral contraceptives and hormonal therapy for menopause cause a small increase in breast-cancer risk, which appears to diminish once use stops. Alcohol increases risk, whereas physical activity is probably protective. Mutations in certain genes greatly increase breast-cancer risk, but these account for a minority of cases.
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            Age at menarche in a Korean population: secular trends and influencing factors.

            This study was designed to identify the secular trend in the age at menarche and to investigate the possible factors that influence the age at menarche using representative Korean data from the 2005 Korean National Health and Nutrition Survey. Three thousand five hundred sixty-two women born between 1920 and 1985 were enrolled to identify secular trends in the age at menarche and 620 girls born between 1986 and 1995 were recruited to evaluate the factors influencing the age at onset of menarche. Mean age at menarche decreased from 16.90 +/- 1.25 years for women born between 1920 and 1925 to 13.79 +/- 1.37 years for those born between 1980 and 1985, indicating a downward trend of 0.68 years per decade (95% CI, 0.64-0.71) in age at menarche. Mean age at menarche of girls born between 1986 and 1995 was 13.10 +/- 0.06 years as estimated by the Kaplan-Meier method. Among girls born between 1986 and 1995, menarcheal girls had a larger waist circumference, a higher body mass index (BMI), and lower maternal menarcheal age and maternal age at birth than premenarcheal girls. The energy and nutrient intake of protein, sugar, fiber, ash, phosphate, natrium, thiamine, riboflavin, and niacin were greater for menarcheal girls than for premenarcheal girls. These data indicate a decreasing secular trend of age at menarche in a Korean population born between 1920 and 1995. Furthermore, maternal menarcheal age, BMI, maternal age at birth, and nutrition are important variables that appear to influence age at menarche in Korean girls.
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              Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.

              To identify loci for age at menarche, we performed a meta-analysis of 32 genome-wide association studies in 87,802 women of European descent, with replication in up to 14,731 women. In addition to the known loci at LIN28B (P = 5.4 × 10⁻⁶⁰) and 9q31.2 (P = 2.2 × 10⁻³³), we identified 30 new menarche loci (all P < 5 × 10⁻⁸) and found suggestive evidence for a further 10 loci (P < 1.9 × 10⁻⁶). The new loci included four previously associated with body mass index (in or near FTO, SEC16B, TRA2B and TMEM18), three in or near other genes implicated in energy homeostasis (BSX, CRTC1 and MCHR2) and three in or near genes implicated in hormonal regulation (INHBA, PCSK2 and RXRG). Ingenuity and gene-set enrichment pathway analyses identified coenzyme A and fatty acid biosynthesis as biological processes related to menarche timing.
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                Author and article information

                Journal
                Clin Exp Pediatr
                Clin Exp Pediatr
                CEP
                Clinical and Experimental Pediatrics
                Korean Pediatric Society
                2713-4148
                January 2021
                13 July 2020
                : 64
                : 1
                : 26-27
                Affiliations
                Department of Pediatrics, Ajou University Hospital, Ajou University School of Medicine, Suwon, Korea
                Author notes
                Corresponding author: Hae Sang Lee MD, PhD. Department of Pediatrics, Ajou University Hospital, Ajou University School of Medicine, 164 World cup-ro, Yeongtong-gu, Suwon 16499, Korea E-mail: seaon77@ 123456gmail.com
                Author information
                http://orcid.org/0000-0002-9684-4042
                Article
                cep-2020-00521
                10.3345/cep.2020.00521
                7806408
                32683812
                b1655fd9-b9d6-4e83-b15e-24182ad7b19c
                Copyright © 2021 by The Korean Pediatric Society

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 1 April 2020
                : 21 May 2020
                Categories
                Editorial
                General Pediatrics

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