期刊文献+
共找到8篇文章
< 1 >
每页显示 20 50 100
Differences in brain-derived neurotrophic factor gene polymorphisms between acute ischemic stroke patients and healthy controls in the Han population of southwest China 被引量:6
1
作者 Jie Zhou Meng-Meng Ma +4 位作者 Jing-Huan Fang Lei Zhao Mu-Ke Zhou Jian Guo Li He 《Neural Regeneration Research》 SCIE CAS CSCD 2019年第8期1404-1411,共8页
Single-nucleotide polymorphisms in the brain-derived neurotrophic factor gene may affect the secretion and function of brain-derived neurotrophic factor, thereby affecting the occurrence, severity and prognosis of isc... Single-nucleotide polymorphisms in the brain-derived neurotrophic factor gene may affect the secretion and function of brain-derived neurotrophic factor, thereby affecting the occurrence, severity and prognosis of ischemic stroke. This case-control study included 778 patients (475 males and 303 females, mean age of 64.0 ± 12.6 years) in the acute phase of ischemic stroke and 865 control subjects (438 males and 427 females, mean age of 51.7 ± 14.7 years) from the Department of Neurology, Wes: China Hospital, Sichuan University, China between September 2011 and December 2014. The patients' severities of neurological defici:s in the acute phase were assessed using the National Institutes of Health Stroke Scale immediately after admission to hospital. The ischemic stroke patients were divided into different subtypes according to the Trial of Org 10172 in Acute Stroke Treatment classification. Early prognosis was evaluated using the Modified Rankin Scale when the patients were discharged. Genomic DNA was extracted from peripheral blood of participants. Genotyping of rs7124442 and rs6265 was performed using Kompetitive Allele Specific polymerase chain reaction genotyping technology. Our results demonstrated that patients who carried the C allele of the rs7124442 locus had a lower risk of poor prognosis than the T allele carriers (odds ratio [OR]= 0.67;95% confidence interval [CI]: 0.45-1.00;P = 0.048). The patients with the CC or TC genotype also exhibited lower risk than TT carriers (OR = 0.65;95% CI: 0.42-1.00;P = 0.049). The AA genotype at the rs6265 locus was associated with the occurrence of ischemic stroke in patients with large-artery atherosclerosis (OR = 0.5& 95% CI: 0.37-0.90;P = 0.015). We found that the C allele (CC and TC genotypes) at the rs7124442 locus may be protective for the prognosis of ischemic stroke. The AA genotype at the rs6265 locus is likely a protective factor against the occurrence of ischemic stroke in patients with large-artery atherosclerosis. The study protocol was approved by the Eth 展开更多
关键词 nerve REGENERATION ischemic STROKE BRAIN-DERIVED NEUROTROPHIC factor single-nucleotide polymorphism risk STROKE severity prognosis rs6265 rs7124442 neural REGENERATION
下载PDF
精神分裂症患者脑源性神经营养因子基因多态性与临床症状的关系 被引量:1
2
作者 罗佳丽 章杰 +2 位作者 万静 余金鸣 平军娇 《四川精神卫生》 2023年第5期409-415,共7页
背景神经发育学说是精神分裂症发病机制的研究重点,脑源性神经营养因子(BDNF)在神经元发育过程中起重要作用,可能是精神分裂症的生物标志物之一。BDNF水平及其基因多态性在精神分裂症的发病机制中具有重要作用,但尚存争议。目的分析精... 背景神经发育学说是精神分裂症发病机制的研究重点,脑源性神经营养因子(BDNF)在神经元发育过程中起重要作用,可能是精神分裂症的生物标志物之一。BDNF水平及其基因多态性在精神分裂症的发病机制中具有重要作用,但尚存争议。目的分析精神分裂症患者BDNF水平与健康对照人群的差异,探讨BDNF单核苷酸多态性(SNPs)位点(rs11030101、rs2030324、rs6265)与BDNF水平的关系,并分析其与临床症状的关系,为精神分裂症的治疗提供参考。方法采用病例对照研究,纳入2019年1月-2020年12月在中山市第三人民医院就诊的、符合《精神障碍诊断与统计手册(第5版)》(DSM-5)精神分裂症诊断标准的55例精神分裂症患者为研究对象,同期在中山市第三人民医院工作人员和社会人群中招募健康对照组31名。使用阳性和阴性症状量表(PANSS)评定精神分裂症患者的临床症状。采用酶联免疫吸附法(ELISA法)经酶标仪定标检测精神分裂症患者和对照组血清BDNF水平,采用聚合酶链式反应产物直接测序确定患者组和对照组BDNF的rs11030101、rs2030324、rs6265位点基因型。结果患者组血清BDNF水平低于对照组,差异有统计学意义(t=-3.804,P<0.01)。临床症状方面,BDNF rs11030101位点不同基因型的患者PANSS总评分、兴奋敌对因子评分和抑郁焦虑因子评分差异均有统计学意义(t=2.022、Z=-2.696、-2.467,P<0.05或0.01)。不同位点的各基因型患者血清BDNF水平差异均无统计学意义(Z=1.483、F=2.584、0.417,P均>0.05)。结论精神分裂症患者BDNF水平偏低。BDNF的rs11030101、rs2030324、rs6265位点多态性与血清BDNF水平水平无关,BDNF的rs11030101位点多态性可能会导致精神分裂症患者兴奋敌对、抑郁焦虑等临床症状。血清BDNF水平可能更多地取决于诊断效果而非基因多态性效应。 展开更多
关键词 精神分裂症 脑源性神经营养因子 rs11030101 rs2030324 rs6265
下载PDF
Brain-derived neurotrophic factor rs6265(Val66Met)single nucleotide polymorphism as a master modifier of human pathophysiology 被引量:3
3
作者 Van Thuan Nguyen Braxton Hill +4 位作者 Naiya Sims Aaron Heck Marcus Negron Claire Lusk Cristi LGalindo 《Neural Regeneration Research》 SCIE CAS CSCD 2023年第1期102-106,共5页
Brain-derived neurotrophic factor is the most prevalent member of the nerve growth factor family.Since its discovery in 1978,this enigmatic molecule has spawned more than 27,000 publications,most of which are focused ... Brain-derived neurotrophic factor is the most prevalent member of the nerve growth factor family.Since its discovery in 1978,this enigmatic molecule has spawned more than 27,000 publications,most of which are focused on neurological disorders.Brain-derived neurotrophic factor is indispensable during embryogenesis and postnatally for the normal development and function of both the central and peripheral nervous systems.It is becoming increasingly clear,however,that brain-derived neurotrophic factor likewise plays crucial roles in a variety of other biological functions independently of sympathetic or parasympathetic involvement.Brain-derived neurotrophic factor is also increasingly recognized as a sophisticated environmental sensor and master coordinator of whole organismal physiology.To that point,we recently found that a common nonsynonymous(Val66→Met)single nucleotide polymorphism in the brain-derived neurotrophic factor gene(rs6265)not only substantially alters basal cardiac transcriptomics in mice but subtly influences heart gene expression and function differentially in males and females.In addition to a short description of recent results from associative neuropsychiatric studies,this review provides an eclectic assortment of research reports that support a modulatory role for rs6265 including and beyond the central nervous system. 展开更多
关键词 brain-derived neurotrophic factor neuropsychiatric disorders rs6265 Val66Met
下载PDF
A comprehensive evaluation of brain derived neurotropic growth factor gene on Bharatnatyam dancers
4
作者 Nithyakalyani Mohan Anusha Sunder 《Precision Medicine Research》 2022年第2期1-6,共6页
Research significance:Dance symbolizes rhythmic body movements to music intending expression of an idea or emotion that delights the performer.Bharatanatyam,an imperative form of Indian Classical dance,has therapeutic... Research significance:Dance symbolizes rhythmic body movements to music intending expression of an idea or emotion that delights the performer.Bharatanatyam,an imperative form of Indian Classical dance,has therapeutic implications including enhancement of cognitive function.Neurotrophins belonging to the nerve growth factor family essentially regulate neuronal growth,development and maintenance.The Brain-Derived Neurotrophic Factor(BDNF)is a member of this family.Long-term memory and learning are vitally influenced by BDNF.In Bharatanatyam,new movements are learntand they are practiced until perfection.Every newly learntmovement initially stays in short-term memory and with practice,it reaches the long-term memory.And thus,a favorableincrease in plasma BDNF levels can be associated with Bharatanatyam.In the BDNF gene,rs6265 is a common single nucleotide polymorphism,which results in a valine(Val)being substituted with methionine(Met)in the prodomainat codon 66(Val66Met).This genetic variation affects the BDNF protein’s activity-dependent release.Research methods:With an intention to delve into the link between BDNF gene variants and Bharatanatyam,we conducted an observational research study on 93 participants with their due consent.The study group included 45 dancers and 48 non-dancers.Results anddiscussion:Genotype suggesting optimal BDNF production was proportionately higher in dancers(40%)than non-dancers.Many of the dancers with optimal BDNF genotype expressed a feeling of happiness as their mental status after one hour of dancing and also took up other exercises(like skating/badminton/basketball player etc)as well.While amongst dancers with sub-optimal BDNF genotype,most of them did not take up any other exercise(like skating/badminton/basketball player etc)andalso expressed a blank feeling as their mental status after one hour of dancing.Thus,BDNF has an evident role in the formation of new learning and memory. 展开更多
关键词 BDNF Bharatanatyam gene GENOTYPE SNP rs6265 MEMORY COGNITION
下载PDF
卒中后抑郁影响因素及其与脑源性神经营养因子基因多态性的关系研究 被引量:17
5
作者 何明 马飞月 《实用心脑肺血管病杂志》 2019年第5期29-35,共7页
背景 卒中后抑郁(PSD)是卒中常见并发症之一,严重影响患者治疗配合程度及治疗效果,探讨其影响因素有利于早期识别、筛查PSD并及时干预。目的 探讨PSD的影响因素及其与脑源性神经营养因子(BDNF)基因多态性的关系。方法 选取2015年7月—2... 背景 卒中后抑郁(PSD)是卒中常见并发症之一,严重影响患者治疗配合程度及治疗效果,探讨其影响因素有利于早期识别、筛查PSD并及时干预。目的 探讨PSD的影响因素及其与脑源性神经营养因子(BDNF)基因多态性的关系。方法 选取2015年7月—2018年6月上海交通大学医学院附属瑞金医院卢湾分院及其所属区域医疗联合体的3个卫生医疗机构门诊和住院部收治的缺血性卒中患者480例,随访12个月,根据PSD发生情况分为PSD组192例和非PSD组288例。比较两组患者BDNF不同位点基因型及等位基因分布频率、一般资料(包括性别、年龄、抑郁症家族史、性格、受教育程度、居住地、家庭经济收入)、卒中相关情况〔包括梗死部位、梗死面积、美国国立卫生研究院卒中量表(NIHSS)评分、TOAST分型、OCSP分型〕、社会支持评定量表(SSRS)评分、改良Barthel指数(mBI)评分、改良Rankin量表(mRS)评分、治疗情况、医疗费用支付方式;PSD的影响因素分析采用多因素Logistic回归分析。结果 (1)本组患者PSD发生率为40.00%(192/480)。(2)两组患者BDNF rs6265位点基因型、等位基因分布频率及rs10835210位点基因型分布频率比较,差异有统计学意义(P<0.05);两组患者BDNFrs56164415、rs7124442位点基因型、等位基因分布频率及rs10835210位点等位基因分布频率比较,差异无统计学意义(P>0.05)。(3)两组患者性格、居住地、TOAST分型、OCSP分型及治疗情况比较,差异无统计学意义(P>0.05);两组患者性别、年龄、抑郁症家族史、受教育程度、家庭经济收入、梗死部位、梗死面积、NIHSS评分、SSRS评分、mBI评分、mRS评分及医疗费用支付方式比较,差异有统计学意义(P<0.05)。(4)多因素Logistic回归分析结果显示,性别、年龄、性格、脑干/基底核梗死、SSRS评分<20分、NIHSS评分≥14分、mBI评分,BDNF rs6265位点CT基因型和CC基因型,BDNF rs10835210位点AC基因型 展开更多
关键词 卒中 抑郁 脑源性神经营养因子 基因多态性 rs6265位点 rs56164415位点 rs7124442位点 rs10835210位点 影响因素分析
下载PDF
BDNF基因rs6265多态性与父母教育卷入对小学儿童基本数学能力的交互作用 被引量:6
6
作者 张明亮 司继伟 +3 位作者 杨伟星 邢淑芬 李红霞 张佳佳 《心理学报》 CSSCI CSCD 北大核心 2018年第9期1007-1017,共11页
数学能力发展的遗传机制日益成为研究者关注的前沿课题之一,但既有研究尚处于起步阶段。本研究以602名小学儿童及其父母作为被试,旨在考察BDNF基因rs6265多态性与父母教育卷入对儿童基本数学能力的潜在交互影响。结果显示,(1)rs6265多... 数学能力发展的遗传机制日益成为研究者关注的前沿课题之一,但既有研究尚处于起步阶段。本研究以602名小学儿童及其父母作为被试,旨在考察BDNF基因rs6265多态性与父母教育卷入对儿童基本数学能力的潜在交互影响。结果显示,(1)rs6265多态性可显著预测儿童的逻辑思维与空间-视觉功能领域能力(AA基因型携带者的基本数学能力显著高于G等位基因携带者);(2)rs6265多态性与父母教育卷入交互作用于儿童的逻辑思维与空间-视觉功能领域能力,父母教育卷入能显著正向预测G等位基因儿童的逻辑思维与空间-视觉功能领域能力,但对AA基因型儿童的预测作用不显著,该交互作用可能更加符合强素质-压力模型假说(rs6265位点G等位基因可能是风险基因)。上述发现推进了数学能力遗传机制的研究,并为素质-压力假说提供了新的研究证据。 展开更多
关键词 BDNF基因rs6265多态性 数学能力 父母教育卷入 基因与环境交互作用 小学儿童
下载PDF
血清S100β水平与BDNF⁃rs6265基因多态性的交互作用对神经阻滞治疗缺血性脑卒中后吞咽困难疗效的影响
7
作者 姚玉婷 赵鹏 +3 位作者 郜静 刘敏肖 冀笑男 李燕 《国际神经病学神经外科学杂志》 2024年第2期61-68,共8页
目的探讨血清S100β蛋白与脑源性神经营养因子(BDNF)-rs6265基因多态性的交互作用对神经阻滞治疗缺血性脑卒中后吞咽困难疗效的影响。方法285例缺血性脑卒中后吞咽困难的患者接受神经阻滞治疗后,依据洼田饮水试验评价标准分为治疗有效组... 目的探讨血清S100β蛋白与脑源性神经营养因子(BDNF)-rs6265基因多态性的交互作用对神经阻滞治疗缺血性脑卒中后吞咽困难疗效的影响。方法285例缺血性脑卒中后吞咽困难的患者接受神经阻滞治疗后,依据洼田饮水试验评价标准分为治疗有效组(226例)和治疗无效组(59例)。比较2组血清S100β蛋白、BDNF水平及BDNF-rs6265基因型和等位基因频率。分析BDNF-rs6265基因多态性与治疗无效的关系。比较不同基因型患者的临床特征。采用多因素Logistic回归分析神经阻滞治疗无效的影响因素。采用多因子降维法分析BDNF-rs6265基因多态性分别与血清S100β蛋白、BDNF交互作用对神经阻滞治疗无效的影响。结果2组患者年龄、美国国立卫生研究院卒中量表(NIHSS)评分、改良的巴塞尔指数(BI)评分、血清S100β蛋白、BDNF水平、BDNF-rs6265基因型差异具有统计学意义(P<0.05)。校正混杂变量后,CC型基因携带者治疗无效风险是TT基因型患者的1.762倍;CC型、CT型与TT型基因患者间的饮酒史、高血压、NIHSS评分、血清S100β蛋白、BDNF差异均具有统计学意义(P<0.05)。血清S100β蛋白≥0.44 pg/mL、BDNF<6.21 ng/ml、BDNF-rs6265携带C基因型是神经阻滞治疗无效的危险因素(P<0.05)。血清S100β蛋白及BDNF均与BDNF-rs6265基因多态性存在交互作用。具有血清S100β蛋白及BDNF水平异常和BDNF-rs6265基因多态性交互组合人群的神经阻滞治疗无效风险是非上述组合人群神经阻滞治疗无效风险的2.77倍。结论血清S100β蛋白水平、BDNF-rs6265基因多态性与缺血性脑卒中后吞咽困难患者神经阻滞治疗疗效相关,二者存在交互作用。 展开更多
关键词 缺血性脑卒中 血清S100Β蛋白 脑源性神经营养因子-rs6265基因 吞咽困难
下载PDF
BDNF基因rs6265多态性与父母严厉管教对学前儿童工作记忆的交互影响
8
作者 张悦文 王振宏 《科学通报》 EI CAS CSCD 北大核心 2022年第31期3695-3707,共13页
工作记忆是执行功能的重要组成部分,基因与家庭环境因素如何交互影响学前儿童工作记忆,目前尚缺少研究.本研究以632名学前儿童(平均年龄=5.14岁,SD=0.94)为被试,考察了BDNF基因rs6265多态性与父母严厉管教对学前儿童工作记忆的交互影响... 工作记忆是执行功能的重要组成部分,基因与家庭环境因素如何交互影响学前儿童工作记忆,目前尚缺少研究.本研究以632名学前儿童(平均年龄=5.14岁,SD=0.94)为被试,考察了BDNF基因rs6265多态性与父母严厉管教对学前儿童工作记忆的交互影响.研究结果显示,BDNF基因rs6265多态性与父母严厉管教对学前儿童工作记忆成绩的交互作用显著.具体而言,携带Val/Val基因型学前儿童的工作记忆成绩在高父母严厉管教条件下显著降低;对于携带Met等位基因的学前儿童,其工作记忆成绩在不同父母严厉管教条件下没有显著差异.研究结果支持了素质-压力模型,表明对工作记忆发展关键期的学前儿童而言,Val/Val基因型是消极环境的脆弱性因子,携带Val/Val基因型学前儿童的工作记忆容易受到消极环境的负面影响,这为理解学前儿童工作记忆发展的基因与环境交互作用机制提供了新的证据. 展开更多
关键词 BDNF基因rs6265多态性 父母严厉管教 工作记忆 基因-环境交互作用 学前儿童
原文传递
上一页 1 下一页 到第
使用帮助 返回顶部