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2型脱碘酶Thr92Ala多态性与日本儿童肥胖症的关联:一项病例对照研究

Association of Type 2 Deiodinase Thr92Ala Polymorphism with Pediatric Obesity in Japanese Children: A Case-Control Study.

作者信息

Ota Takeshi, Mori Jun, Kawabe Yasuhiro, Morimoto Hidechika, Fukuhara Shota, Kodo Kazuki, Sugimoto Satoru, Kosaka Kitaro, Nakajima Hisakazu, Hosoi Hajime

机构信息

Department of Pediatrics, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto 602-8566, Japan.

出版信息

Children (Basel). 2022 Sep 20;9(10):1421. doi: 10.3390/children9101421.

DOI:10.3390/children9101421
PMID:36291357
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9600981/
Abstract

Genetic factors play critical roles in the onset and progression of obesity. Brown adipose tissue (BAT) activity is also critical for adiposity. The objective of this study was to evaluate the prevalence and effects of BAT gene polymorphisms in pediatric obesity. This case-control study included 270 non-obese and 86 obese children. All participants underwent genotyping for type 2 deiodinase (DIO2) Thr92Ala (rs225014). The prevalence of the homozygous Ala/Ala allele of the DIO2 gene in the obese group was 15.1% versus 6.3% in the non-obese group, resulting in an odds ratio (OR) of 3.393 ( = 0.003). The results of this study indicate that the homozygous Ala/Ala allele of the DIO2 gene is associated with an increased risk of pediatric obesity and suggest that pediatric obesity might be suitable for assessing the association with gene polymorphisms related to BAT, especially DIO2 Thr92Ala.

摘要

遗传因素在肥胖症的发生和发展中起着关键作用。棕色脂肪组织(BAT)的活性对肥胖也至关重要。本研究的目的是评估儿童肥胖中BAT基因多态性的患病率及其影响。这项病例对照研究纳入了270名非肥胖儿童和86名肥胖儿童。所有参与者均接受了2型脱碘酶(DIO2)Thr92Ala(rs225014)的基因分型。肥胖组中DIO2基因纯合Ala/Ala等位基因的患病率为15.1%,而非肥胖组为6.3%,比值比(OR)为3.393(P = 0.003)。本研究结果表明,DIO2基因的纯合Ala/Ala等位基因与儿童肥胖风险增加相关,并提示儿童肥胖可能适合用于评估与BAT相关的基因多态性的关联,尤其是DIO2 Thr92Ala。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bac4/9600981/26b2a45e3095/children-09-01421-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bac4/9600981/26b2a45e3095/children-09-01421-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bac4/9600981/26b2a45e3095/children-09-01421-g001.jpg

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本文引用的文献

1
Changes in the Incidence of Childhood Obesity.儿童肥胖症发病率的变化。
Pediatrics. 2022 Aug 1;150(2). doi: 10.1542/peds.2021-053708.
2
Childhood obesity on the rise during COVID-19: A request for global leaders to change the trajectory.新冠疫情期间儿童肥胖率上升:呼吁全球领导人改变这一趋势。
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ACE2 exerts anti-obesity effect via stimulating brown adipose tissue and induction of browning in white adipose tissue.ACE2 通过刺激棕色脂肪组织和诱导白色脂肪组织褐变发挥抗肥胖作用。
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Association Between Trp64arg Polymorphism of the β3 adrenoreceptor Gene and Female Sex in Obese Turkish Children and Adolescents.β3肾上腺素能受体基因Trp64arg多态性与肥胖土耳其儿童及青少年女性性别的关联
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The value of anthropometric indices for childhood obesity in Japan.日本儿童肥胖人体测量指标的价值。
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Variants in MCT10 protein do not affect FT3 levels in athyreotic patients.MCT10 蛋白变异不会影响甲状腺功能减退患者的 FT3 水平。
Endocrine. 2019 Dec;66(3):551-556. doi: 10.1007/s12020-019-02001-z. Epub 2019 Jul 6.
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Deiodinases and their intricate role in thyroid hormone homeostasis.脱碘酶及其在甲状腺激素动态平衡中的复杂作用。
Nat Rev Endocrinol. 2019 Aug;15(8):479-488. doi: 10.1038/s41574-019-0218-2.
8
Effect of Iodothyronines on Thermogenesis: Focus on Brown Adipose Tissue.甲状腺素对产热的影响:聚焦于棕色脂肪组织。
Front Endocrinol (Lausanne). 2018 May 23;9:254. doi: 10.3389/fendo.2018.00254. eCollection 2018.
9
Angiotensin 1-7 stimulates brown adipose tissue and reduces diet-induced obesity.血管紧张素 1-7 可刺激棕色脂肪组织并减少饮食诱导的肥胖。
Am J Physiol Endocrinol Metab. 2018 Feb 1;314(2):E131-E138. doi: 10.1152/ajpendo.00192.2017. Epub 2017 Oct 24.
10
Hypothyroid Patients Encoding Combined MCT10 and DIO2 Gene Polymorphisms May Prefer L-T3 + L-T4 Combination Treatment - Data Using a Blind, Randomized, Clinical Study.编码MCT10和DIO2基因多态性的甲状腺功能减退患者可能更适合左甲状腺素钠(L-T3)+左旋甲状腺素(L-T4)联合治疗——一项采用盲法、随机化的临床研究数据
Eur Thyroid J. 2017 Jul;6(3):143-151. doi: 10.1159/000469709. Epub 2017 Apr 24.