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生活方式干预对儿童/青少年体脂变化的影响及 NYD-SP18 和 TMEM18 变异体。

Body Adiposity Changes After Lifestyle Interventions in Children/Adolescents and the NYD-SP18 and TMEM18 Variants.

机构信息

3rd Department of Medicine, 1st Faculty of Medicine of Charles University and General University Hospital in Prague, Prague, Czech Republic.

Center for Experimental Medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.

出版信息

Med Sci Monit. 2018 Oct 20;24:7493-7498. doi: 10.12659/MSM.907180.

DOI:10.12659/MSM.907180
PMID:30341978
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6204654/
Abstract

BACKGROUND This study was carried out to determine the relationship between the common TMEM-18 (rs4854344, G>T) and NYD-SP18 (rs6971091, G>A) gene variants and weight loss after lifestyle interventions (increased physical activity in conjunction with optimal dietary intake) in overweight/obese children/adolescents. MATERIAL AND METHODS We genotyped 684 unrelated, white, non-diabetic children (age 12.7±2.1 years, average BMI at baseline 30.66±4.80 kg/m²). Anthropometric and biochemical examinations were performed before and after 4 weeks of an intensive lifestyle intervention. RESULTS The mean weight loss achieved was 5.20±2.02 kg (P<0.001). NYDSP-18 AA homozygotes had significantly higher abdominal skinfold value before and after the intervention (both, P=0.001). No significant associations between BMI decrease and the NYD-SP18 and TMEM18 variants were found. Associations between all anthropometrical and biochemical changes and genes remained non-significant after data were adjusted for sex, age, and baseline values. CONCLUSIONS Decreased body weight in overweight/obese children is not significantly influenced by the NYD-SP18 rs6971091 or TMEM18 rs4854344 polymorphisms.

摘要

背景 本研究旨在确定 TMEM-18(rs4854344,G>T)和 NYD-SP18(rs6971091,G>A)基因变异与超重/肥胖儿童/青少年生活方式干预(增加体力活动与最佳饮食摄入相结合)后体重减轻之间的关系。 材料与方法 我们对 684 名无关的白种、非糖尿病儿童(年龄 12.7±2.1 岁,基线平均 BMI 为 30.66±4.80 kg/m²)进行了基因分型。在强化生活方式干预 4 周前后进行了人体测量和生化检查。 结果 平均体重减轻 5.20±2.02 kg(P<0.001)。NYDSP-18 AA 纯合子在干预前后的腹部皮褶厚度值显著更高(均 P=0.001)。BMI 下降与 NYD-SP18 和 TMEM18 变异体之间无显著相关性。在调整性别、年龄和基线值后,所有人体测量和生化变化与基因之间的关联仍然不显著。 结论 超重/肥胖儿童的体重减轻与 NYD-SP18 rs6971091 或 TMEM18 rs4854344 多态性无显著相关性。

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本文引用的文献

1
Obesity-associated gene has a role in the central control of appetite and body weight regulation.肥胖相关基因在食欲的中枢控制和体重调节中起作用。
Proc Natl Acad Sci U S A. 2017 Aug 29;114(35):9421-9426. doi: 10.1073/pnas.1707310114. Epub 2017 Aug 15.
2
Lack of Association between NYD-SP18 Variant and Obesity. The Health Alcohol and Psychosocial Factors in Eastern Europe Study.NYD-SP18变异与肥胖之间不存在关联。东欧健康、酒精及社会心理因素研究。
Ann Nutr Metab. 2016;68(4):244-8. doi: 10.1159/000445982. Epub 2016 May 31.
3
The Impact of Physical Activity and Dietary Measures on the Biochemical and Anthropometric Parameters in Obese Children. Is There Any Genetic Predisposition?体育活动和饮食措施对肥胖儿童生化及人体测量学参数的影响。是否存在遗传易感性?
Cent Eur J Public Health. 2015 Nov;23 Suppl:S62-6. doi: 10.21101/cejph.a4191.
4
Body Composition Changes in Adult Females after Lifestyle Intervention Are Influenced by the NYD-SP18 Variant.生活方式干预后成年女性身体成分的变化受NYD-SP18变体的影响。
Cent Eur J Public Health. 2015 Nov;23 Suppl:S19-22. doi: 10.21101/cejph.a4105.
5
Genetic and biochemical characteristics in the Roma minority in the South Bohemia Region.南波希米亚地区罗姆少数民族的遗传和生化特征。
Neuro Endocrinol Lett. 2015;36 Suppl 2:29-34.
6
Strong gender-specific additive effects of the NYD-SP18 and FTO variants on BMI values.NYD-SP18和FTO变异对BMI值有强烈的性别特异性加性效应。
Physiol Res. 2015;64(Suppl 3):S419-26. doi: 10.33549/physiolres.933149.
7
SIRT1 gene variants are related to risk of childhood obesity.SIRT1基因变异与儿童肥胖风险相关。
Eur J Pediatr. 2015 Apr;174(4):473-9. doi: 10.1007/s00431-014-2424-1. Epub 2014 Sep 20.
8
The role of IL-6 572 C/G, 190 C/T, and 174 G/C gene polymorphisms in children's obesity.白细胞介素-6基因572 C/G、190 C/T和174 G/C多态性在儿童肥胖中的作用
Eur J Pediatr. 2014 Oct;173(10):1285-96. doi: 10.1007/s00431-014-2315-5. Epub 2014 Apr 17.
9
No impact of obesity susceptibility loci on weight regain after a lifestyle intervention in overweight children.肥胖易感性基因座对超重儿童生活方式干预后体重反弹无影响。
J Pediatr Endocrinol Metab. 2013;26(11-12):1209-13. doi: 10.1515/jpem-2013-0179.
10
Replication of established common genetic variants for adult BMI and childhood obesity in Greek adolescents: the TEENAGE study.希腊青少年中成人BMI和儿童肥胖常见遗传变异的复制:青少年研究
Ann Hum Genet. 2013 May;77(3):268-74. doi: 10.1111/ahg.12012. Epub 2013 Jan 24.