CYP17 and CYP19 gene polymorphisms in women affected with endometriosis
Objective
To investigate whether CYP17 T>C polymorphism and polymorphisms C1558T and Val80 of CYP19 are related to endometriosis.
Design
Clinical study.
Patient(s)
Women affected with endometriosis (n = 104) and control group (n = 86). The diagnosis of endometriosis was confirmed by the histologic examination of the endometriotic lesions.
Result(s)
In patients affected with endometriosis, we observed that AA and CC genotypes were significantly represented in Val80 and C1558T polymorphisms of CYP19.
Conclusion(s)
The molecular mechanisms that underlie the development of endometriosis are unclear. Both environmental and genetic factors are involved in the pathogenesis of the disease. The inheritable susceptibility to endometriosis justifies the growing interest in identifying genes and/or genetic polymorphisms that predispose women to an increased risk of developing endometriosis. The identification of single-nucleotide polymorphism (SNP), probably linked to endometriosis, could help to explain its pathogenesis.
Key Words: Endometriosis, CYP17, CYP19, single-nucleotide polymorphisms (SNPs)
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M.T.V. has nothing to declare. M.C. has nothing to declare. M.S. has nothing to declare. S.S. has nothing to declare. P.B. has nothing to declare. E.T. has nothing to declare. M.A. has nothing to declare. N.C. has nothing to declare. A.M.N. has nothing to declare. L.C. has nothing to declare.
Teresa Vietri and Michele Cioffi contributed equally to this article.
PII: S0015-0282(08)03577-2
doi:10.1016/j.fertnstert.2008.07.1786
Published by Elsevier Inc.
