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2
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本文引用的文献

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The Association Between Weight-Based Teasing from Peers and Family in Childhood and Depressive Symptoms in Childhood and Adulthood: A Systematic Review.同伴和家庭的体重相关嘲笑与儿童期和成年期抑郁症状的关系:系统评价。
Curr Obes Rep. 2020 Mar;9(1):15-29. doi: 10.1007/s13679-020-00367-0.
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BDNF Polymorphism: A Review of Its Diagnostic and Clinical Relevance in Neurodegenerative Disorders.脑源性神经营养因子多态性:关于其在神经退行性疾病中的诊断及临床相关性的综述
Aging Dis. 2018 Jun 1;9(3):523-536. doi: 10.14336/AD.2017.0717. eCollection 2018 Jun.
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The effect of exercise intensity on brain derived neurotrophic factor and memory in adolescents.运动强度对青少年脑源性神经营养因子和记忆力的影响。
Environ Health Prev Med. 2017 Apr 4;22(1):27. doi: 10.1186/s12199-017-0643-6.
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BDNF Val66Met polymorphism, life stress and depression: A meta-analysis of gene-environment interaction.脑源性神经营养因子 Val66Met 多态性、生活应激与抑郁:基因-环境交互作用的荟萃分析。
J Affect Disord. 2018 Feb;227:226-235. doi: 10.1016/j.jad.2017.10.024. Epub 2017 Oct 16.
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The effect of acute exercise on blood concentrations of brain-derived neurotrophic factor in healthy adults: a meta-analysis.急性运动对健康成年人血液中脑源性神经营养因子浓度的影响:一项荟萃分析。
Eur J Neurosci. 2017 Jul;46(1):1635-1646. doi: 10.1111/ejn.13603. Epub 2017 Jun 19.
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The Effect of Exercise Training on Resting Concentrations of Peripheral Brain-Derived Neurotrophic Factor (BDNF): A Meta-Analysis.运动训练对周围脑源性神经营养因子(BDNF)静息浓度的影响:一项荟萃分析。
PLoS One. 2016 Sep 22;11(9):e0163037. doi: 10.1371/journal.pone.0163037. eCollection 2016.
7
Signaling pathways controlling activity-dependent local translation of BDNF and their localization in dendritic arbors.控制脑源性神经营养因子(BDNF)活性依赖性局部翻译的信号通路及其在树突分支中的定位。
J Cell Sci. 2016 Jul 15;129(14):2852-64. doi: 10.1242/jcs.177626. Epub 2016 Jun 6.
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The Involvement of Genes in Adolescent Depression: A Systematic Review.基因与青少年抑郁症的关联:一项系统综述。
Front Behav Neurosci. 2015 Dec 21;9:329. doi: 10.3389/fnbeh.2015.00329. eCollection 2015.
9
BDNF as a biomarker for successful treatment of mood disorders: a systematic & quantitative meta-analysis.脑源性神经营养因子作为情绪障碍成功治疗的生物标志物:一项系统定量的荟萃分析。
J Affect Disord. 2015 Mar 15;174:432-40. doi: 10.1016/j.jad.2014.11.044. Epub 2014 Nov 29.
10
The Effects of 12 Weeks Regular Aerobic Exercise on Brain-derived Neurotrophic Factor and Inflammatory Factors in Juvenile Obesity and Type 2 Diabetes Mellitus.12周规律有氧运动对青少年肥胖及2型糖尿病患者脑源性神经营养因子和炎症因子的影响
J Phys Ther Sci. 2014 Aug;26(8):1199-204. doi: 10.1589/jpts.26.1199. Epub 2014 Aug 30.

脑源性神经营养因子 Val66Met 多态性与肥胖青少年的健康相关生活质量。

The BDNF Val66Met polymorphism and health-related quality of life in youth with obesity.

机构信息

Healthy Active Living and Obesity Research Group, Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada.

Department of Pediatrics, University of Ottawa, Ottawa, Ontario, Canada.

出版信息

Physiol Rep. 2024 Jul;12(13):e16140. doi: 10.14814/phy2.16140.

DOI:10.14814/phy2.16140
PMID:38997217
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11245332/
Abstract

The brain derived-neurotrophic factor (BDNF) Val66Met polymorphism causes functional changes in BDNF, and is associated with obesity and some psychiatric disorders, but its relationship to health-related quality of life (HRQoL) remains unknown. This study examined, in youth with obesity, whether carriers of the BDNF Val66met polymorphism Met-alleles (A/A or G/A) differed from noncarriers (G/G) on HRQoL. The participants were 187 adolescents with obesity. Ninety-nine youth were carriers of the homozygous Val/Val (G/G) alleles, and 88 were carriers of the Val/Met (G/A) or Met/Met (A/A) alleles. Blood samples were drawn in the morning after an overnight fast for genotyping. HRQoL was measured using the Pediatric-Quality of Life core version. Compared to carriers of the Val66Met Val (G/G) alleles, carriers of the Met-Alleles reported significantly higher physical -HRQoL (p = 0.02), school-related HRQoL, (p = 0.05), social-related HRQoL (p = 0.05), and total HRQoL (p = 0.03), and a trend for Psychosocial-HRQoL. Research is needed to confirm our findings and determine whether carriers of the BDNF Val66Met homozygous Val (G/G) alleles may be at risk of diminished HRQoL, information that can influence interventions in a high-risk population of inactive youth with obesity.

摘要

脑源性神经营养因子(BDNF)Val66Met 多态性导致 BDNF 的功能改变,与肥胖和一些精神疾病有关,但它与健康相关生活质量(HRQoL)的关系尚不清楚。本研究在肥胖的年轻人中,研究了 BDNF Val66met 多态性 Met 等位基因(A/A 或 G/A)携带者与非携带者(G/G)在 HRQoL 上是否存在差异。参与者为 187 名肥胖青少年。99 名青年为纯合 Val/Val(G/G)等位基因携带者,88 名青年为 Val/Met(G/A)或 Met/Met(A/A)等位基因携带者。采血时间为禁食一夜后的清晨,用于基因分型。使用儿科生活质量核心版本测量 HRQoL。与 Val66Met Val(G/G)等位基因携带者相比,Met 等位基因携带者报告的身体 HRQoL 明显更高(p=0.02)、与学校相关的 HRQoL(p=0.05)、与社会相关的 HRQoL(p=0.05)和总 HRQoL(p=0.03),以及心理社会 HRQoL 呈趋势。需要进一步的研究来证实我们的发现,并确定 BDNF Val66Met 纯合 Val(G/G)等位基因携带者是否可能面临 HRQoL 降低的风险,这些信息可能会影响肥胖不活跃青少年这一高危人群的干预措施。