Visvanathan Kala, Gallicchio Lisa, Schilling Chrissy, Babus Janice K, Lewis Lynn M, Miller Susan R, Zacur Howard, Flaws Jodi A
Department of Epidemiology, Johns Hopkins University Bloomberg School of Public Health, Baltimore, Maryland 21201, USA.
Obstet Gynecol. 2005 Dec;106(6):1372-81. doi: 10.1097/01.AOG.0000187308.67021.98.
The purpose of this study was to evaluate whether genetic polymorphisms in selected cytochrome P450 enzymes (CYPc17alpha, CYP1A1, and CYP1B1), estradiol (E2) levels, and estrone levels were associated with hot flushes.
Women with hot flushes were those aged 45-54 years who reported ever experiencing hot flushes (n = 354). Women without hot flushes were those aged 45-54 years who reported never experiencing hot flushes (n = 258). Each participant completed a questionnaire and provided a blood sample for determination of genotypes, E2 levels, and estrone levels.
Carriers of the CYP1B1 (Val432Leu) polymorphism were more likely to report having any hot flushes (risk ratio [RR] 1.16, 95% confidence interval (CI) 0.98-1.37) and at least weekly hot flushes (RR 1.29, 95% CI 0.98-1.70) than women without the polymorphism, although these associations were of borderline statistical significance. In addition, carriers of the CYP1B1 polymorphism were likely to have a statistically significant 30% increased risk of reporting moderate to severe hot flushes (RR 1.30, 95% CI 1.02-1.67) and a statistically significant 27% increased risk of reporting hot flushes lasting a year or more (RR 1.27, 95% CI 1.00-1.61) compared with women without the polymorphism. There were no associations between CYP1A1 or CYPc17alpha polymorphisms and hot flushes. Low E2 and estrone levels were associated with hot flushes, but they did not alter the association between the CYP1B1 polymorphism and hot flushes.
These data suggest that a CYP1B1 polymorphism may be associated with severe and persistent hot flushes, independent of E2 and estrone levels.
本研究旨在评估特定细胞色素P450酶(CYP17α、CYP1A1和CYP1B1)的基因多态性、雌二醇(E2)水平和雌酮水平是否与潮热相关。
有潮热症状的女性为年龄在45至54岁之间且报告曾经历过潮热的女性(n = 354)。无潮热症状的女性为年龄在45至54岁之间且报告从未经历过潮热的女性(n = 258)。每位参与者完成一份问卷,并提供血样以测定基因型、E2水平和雌酮水平。
与无CYP1B1(Val432Leu)基因多态性的女性相比,该基因多态性的携带者更有可能报告有任何潮热症状(风险比[RR] 1.16,95%置信区间[CI] 0.98 - 1.37)以及至少每周有潮热症状(RR 1.29,95% CI 0.98 - 1.70),尽管这些关联具有边缘统计学意义。此外,与无该基因多态性的女性相比,CYP1B1基因多态性的携带者报告中度至重度潮热的风险有统计学意义地增加30%(RR 1.30,95% CI 1.02 - 1.67),报告潮热持续一年或更长时间的风险有统计学意义地增加27%(RR 1.27,95% CI 1.00 - 1.61)。CYP1A1或CYP17α基因多态性与潮热之间无关联。低E2和雌酮水平与潮热相关,但它们并未改变CYP1B1基因多态性与潮热之间的关联。
这些数据表明,CYP1B1基因多态性可能与严重且持续的潮热相关,独立于E2和雌酮水平。