Heritability of dehydroepiandrosterone sulfate in women with polycystic ovary syndrome and their sisters

被引:33
作者
Yildiz, Bulent O.
Goodarzi, Mark O.
Guo, Xiuqing
Rotter, Jerome I.
Azziz, Ricardo
机构
[1] Cedars Sinai Med Ctr, Dept Obstet & Gynecol, Los Angeles, CA 90048 USA
[2] Cedars Sinai Med Ctr, Dept Med, Los Angeles, CA 90048 USA
[3] Cedars Sinai Med Ctr, Inst Med Genet, Los Angeles, CA 90048 USA
[4] Hacettepe Univ, Fac Med, Dept Internal Med, Endocrinol & Metab Unit, TR-06100 Ankara, Turkey
[5] Univ Alabama Birmingham, Dept Obstet & Gynecol, Birmingham, AL USA
[6] Univ Alabama Birmingham, Dept Med, Birmingham, AL USA
关键词
polycystic ovary; adrenal; genetics; androgen excess; phenotype; sibling; ADRENAL ANDROGEN EXCESS; INSULIN-RESISTANCE; DEGREE RELATIVES; HEALTHY WOMEN; GENETIC-BASIS; PREVALENCE; HYPERANDROGENEMIA; SECRETION; DEHYDROISOANDROSTERONE; REPLACEMENT;
D O I
10.1016/j.fertnstert.2006.05.045
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To test the hypothesis that adrenal androgen (AA) secretion is an inherited trait in PCOS and that serum DHEAS concentrations, as a marker of AA secretion, will be correlated between women with PCOS and their sisters. Design: Prospective case-control. Setting: Tertiary care center. Patient(s): Sixty-two PCOS probands and 69 sisters. Intervention(s): None. Main Outcome Measure(s): The DHEAS concentrations and clinical phenotypes were obtained. Familial correlation between sisters was estimated. A variance components model was used to estimate the heritability (h(2)) of the DHEAS levels. Body mass index (BMI)-adjusted DHEAS levels were used in all of the analyses. Result(s): There was no difference in age between the proband and sister groups (28.7 +/- 8.1 years vs. 28.0 +/- 8.8 years, P = .65), and probands had higher BMI values (33.4 +/- 7.6 kg/m(2) vs. 27.9 +/- 7.0 kg/m(2), P < .001). Sixteen of the 69 (23.2%) sisters were affected by PCOS. The sister-sister correlation of DHEAS level was 0.28 +/- 0.12 for the whole group (P < .05), and this correlation was higher, at 0.38 +/- 0.14 (P <= .05), after excluding 31% of the affected sisters and 34% of the unaffected sisters who received hormonal therapy at or within 3 months of the time of the study. The h(2) estimates of DHEAS were 0.43 (P = .037) and 0.44 (P = .062) when all sisters and only untreated sisters, respectively, were included in the analysis. Conclusion(s): The correlation of serum DHEAS levels between PCOS probands and their sisters suggests a familial component in the regulation of DHEAS levels and possibly AA production in PCOS. The h(2) estimates of 0.43-0.44 for BMI-adjusted DHEAS suggest that genetic factors account for between 40% and 50% of the overall variation in DHEAS levels in these women. Our results support the hypothesis that circulating AA levels represent an inherited trait in PCOS.
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收藏
页码:1688 / 1693
页数:6
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