中华医学遗传学杂志
中華醫學遺傳學雜誌
중화의학유전학잡지
CHINESE JOURNAL OF MEDICAL GENETICS
2001年
1期
47-50
,共4页
吴涤%刘学%倪佳桐%金永堂%陈大方%徐希平
吳滌%劉學%倪佳桐%金永堂%陳大方%徐希平
오조%류학%예가동%금영당%진대방%서희평
痛经%遗传易感性%细胞色素P4501A1%谷胱甘肽S转移酶%遗传多态性
痛經%遺傳易感性%細胞色素P4501A1%穀胱甘肽S轉移酶%遺傳多態性
통경%유전역감성%세포색소P4501A1%곡광감태S전이매%유전다태성
目的 研究原发性痛经的遗传易感性。方法 收集某纺织厂499名新婚女工的资料,采用Logistic回归分析,评价CYP1A1-HincⅡ和GSTT1多态性与重度原发性痛经的关系。结果 在未调整环境因素时CYP1A1-HincⅡ变异基因型虽对痛经有缓解趋势,但差异无显著性(CYP1A1-HincⅡ:OR=0.64 95% CI:0.35~1.17)。而GSTT1变异基因型可增加重度原发性痛经危险性(GSTT1:OR=1.83,95% CI:1.04~3.21)。调整潜在环境影响因素后,CY1A1-HincⅡ变异基因型显示对原发性痛经有缓解趋势(CYP1A1-HincⅡ:OR=0.58,95% CI:0.31~1.08),但差异仍无显著性。而GSTT1变异基因型仍显示可增加重度原发性痛经的危险性(GSTT1:OR=2.01,95% CI:1.12~3.62)。结论 重度原发性痛经与GSTT1遗传多态性相关。
目的 研究原髮性痛經的遺傳易感性。方法 收集某紡織廠499名新婚女工的資料,採用Logistic迴歸分析,評價CYP1A1-HincⅡ和GSTT1多態性與重度原髮性痛經的關繫。結果 在未調整環境因素時CYP1A1-HincⅡ變異基因型雖對痛經有緩解趨勢,但差異無顯著性(CYP1A1-HincⅡ:OR=0.64 95% CI:0.35~1.17)。而GSTT1變異基因型可增加重度原髮性痛經危險性(GSTT1:OR=1.83,95% CI:1.04~3.21)。調整潛在環境影響因素後,CY1A1-HincⅡ變異基因型顯示對原髮性痛經有緩解趨勢(CYP1A1-HincⅡ:OR=0.58,95% CI:0.31~1.08),但差異仍無顯著性。而GSTT1變異基因型仍顯示可增加重度原髮性痛經的危險性(GSTT1:OR=2.01,95% CI:1.12~3.62)。結論 重度原髮性痛經與GSTT1遺傳多態性相關。
목적 연구원발성통경적유전역감성。방법 수집모방직엄499명신혼녀공적자료,채용Logistic회귀분석,평개CYP1A1-HincⅡ화GSTT1다태성여중도원발성통경적관계。결과 재미조정배경인소시CYP1A1-HincⅡ변이기인형수대통경유완해추세,단차이무현저성(CYP1A1-HincⅡ:OR=0.64 95% CI:0.35~1.17)。이GSTT1변이기인형가증가중도원발성통경위험성(GSTT1:OR=1.83,95% CI:1.04~3.21)。조정잠재배경영향인소후,CY1A1-HincⅡ변이기인형현시대원발성통경유완해추세(CYP1A1-HincⅡ:OR=0.58,95% CI:0.31~1.08),단차이잉무현저성。이GSTT1변이기인형잉현시가증가중도원발성통경적위험성(GSTT1:OR=2.01,95% CI:1.12~3.62)。결론 중도원발성통경여GSTT1유전다태성상관。
Objective To investigate the genetic susceptibility to primary dysmenorrhea.Methods Data of 499 female workers in a textile mill were collected. The associations of cytochrome P450 1A1-HincⅡ(CYP1A1-HincⅡ) and glutathion S-transferase-theta(GSTT1) polymorphisms with heavy primary dysmenorrhea were evaluated by Logistic regression, with adjustment for potential confounders.Results The result showed variant of CYP1A1-HincⅡ genotypes slightly reduced the risk of primary dysmenorrhea, but its OR value was not statistically significant (CYP1A1-HincⅡ:OR=0.64,95% CI 0.35-1.17).The GSTT1 genotype variant increased the risk of primary dysmenorrhea (GSTT1:OR=1.83,95% CI 1.04-3.21). After potential confounders were adjusted, the data showed that CYP1A1-HincⅡ variant had the trend of decreasing the risk of dysmenorrhea (CYP1A1-HincⅡ:OR=0.58,95% CI 0.31-1.08), but its decreasing scope was still not statistically significant. The GSTT1 variant genotypes showed a significantly increased risk of dysmenorrhea (GSTT1:OR=2.01, 95% CI 1.12-3.62).Conclusion The results suggested that GSTT1 polymorphism be associated with heavy primary dysmenorrhea.