中华神经医学杂志
中華神經醫學雜誌
중화신경의학잡지
CHINESE JOURNAL OF NEUROMEDICINE
2010年
8期
768-771
,共4页
陈江瑛%闫振文%张素平%邓婉青%王慕真%梁瑞华%何锐
陳江瑛%閆振文%張素平%鄧婉青%王慕真%樑瑞華%何銳
진강영%염진문%장소평%산완청%왕모진%량서화%하예
卒中%瘦素%瘦素受体%基因多态性
卒中%瘦素%瘦素受體%基因多態性
졸중%수소%수소수체%기인다태성
Stroke%Leptin%Leptin receptor%Gene polymorphism
目的 探讨血清瘦素水平及瘦素受体基因多态性与卒中发病的关系. 方法 选择广州红十字会医院神经内科自2007年1月至2008年12月99例住院卒中患者[脑血管病(CVD)组]及97例同期住院的非卒中患者(对照组)做为研究对象,采用聚合酶链反应结合限制性片段长度多态性对2组患者进行瘦素受体基因Gln223Arg多态性进行检测,ELISA分析法检测血清瘦素水平. 结果 CVD组患者瘦素受体Gln223Arg的GG、GA、AA基因型分布频率分别为66.67%、20.20%、13.13%,与对照组的78.35%、15.46%、6.19%分布频率差异无统计学意义(P>0.05);CVD组G和A等位基因频率分别为76.77%和25.23%,与对照组的86.08%和13.92%基因分布频率差异有统计学意义(P<0.05).CVD组的血清瘦素水平明显高于对照组,差异有统计学意义(P<0.05).非条件Logistic回归多因素分析表明高血压史、空腹血糖升高、TC升高、血清瘦素水平升高与卒中的发病相关. 结论 瘦素受体基因Gln223Arg的A等位基因、瘦素水平升高、高血压、空腹血糖升高、TC升高会增加卒中的发病风险.
目的 探討血清瘦素水平及瘦素受體基因多態性與卒中髮病的關繫. 方法 選擇廣州紅十字會醫院神經內科自2007年1月至2008年12月99例住院卒中患者[腦血管病(CVD)組]及97例同期住院的非卒中患者(對照組)做為研究對象,採用聚閤酶鏈反應結閤限製性片段長度多態性對2組患者進行瘦素受體基因Gln223Arg多態性進行檢測,ELISA分析法檢測血清瘦素水平. 結果 CVD組患者瘦素受體Gln223Arg的GG、GA、AA基因型分佈頻率分彆為66.67%、20.20%、13.13%,與對照組的78.35%、15.46%、6.19%分佈頻率差異無統計學意義(P>0.05);CVD組G和A等位基因頻率分彆為76.77%和25.23%,與對照組的86.08%和13.92%基因分佈頻率差異有統計學意義(P<0.05).CVD組的血清瘦素水平明顯高于對照組,差異有統計學意義(P<0.05).非條件Logistic迴歸多因素分析錶明高血壓史、空腹血糖升高、TC升高、血清瘦素水平升高與卒中的髮病相關. 結論 瘦素受體基因Gln223Arg的A等位基因、瘦素水平升高、高血壓、空腹血糖升高、TC升高會增加卒中的髮病風險.
목적 탐토혈청수소수평급수소수체기인다태성여졸중발병적관계. 방법 선택엄주홍십자회의원신경내과자2007년1월지2008년12월99례주원졸중환자[뇌혈관병(CVD)조]급97례동기주원적비졸중환자(대조조)주위연구대상,채용취합매련반응결합한제성편단장도다태성대2조환자진행수소수체기인Gln223Arg다태성진행검측,ELISA분석법검측혈청수소수평. 결과 CVD조환자수소수체Gln223Arg적GG、GA、AA기인형분포빈솔분별위66.67%、20.20%、13.13%,여대조조적78.35%、15.46%、6.19%분포빈솔차이무통계학의의(P>0.05);CVD조G화A등위기인빈솔분별위76.77%화25.23%,여대조조적86.08%화13.92%기인분포빈솔차이유통계학의의(P<0.05).CVD조적혈청수소수평명현고우대조조,차이유통계학의의(P<0.05).비조건Logistic회귀다인소분석표명고혈압사、공복혈당승고、TC승고、혈청수소수평승고여졸중적발병상관. 결론 수소수체기인Gln223Arg적A등위기인、수소수평승고、고혈압、공복혈당승고、TC승고회증가졸중적발병풍험.
Objective To study the relation between stroke and both plasma leptin level and polymorphism of leptin receptor gene. Methods Ninty-nine patients with stroke and 97 patients with other diseases (controls), admitted to our hospital from January 2007 to December 2008, were chosen in the experiment. Polymerase chain reaction-restriction fragment length polymorphism (LEPR) examination was performed to detect the leptin receptor gene (Gln223A rg gene) polymorphism in these patients. The level of serum leptin was analyzed by enzyme linked immunosorbent assay. Results The genotype frequencies of GG, GA and AA in Gln223Arg gene in patients with stroke were 66.67%, 20.20% and 13.13%, respectively, while those in controls were 78.35%, 15.46% and 6.19%, respectively; those in these 2 groups were not significantly different (P>0.05). The allele frequencies of A and G in patients with stroke were 76.77% and 25.23%, while those in controls were 86.08% and 13.92%; those in the 2 groups were significantly different (P<0.05). The level ofleptin in patients with stroke was markedly higher that that in controls (P<0.05). Binary regression analyses showed that history of hypertension, elevated fasting blood glucose and cholesterol, increased plasma leptin level were associated with stroke. Conclusion The allele frequencies of A in Gln223A rg gene, hypertension, elevated fasting blood glucose and cholesterol and increased plasma leptin level might be correlated with the increased risk of stroke.