No evidence of mutations in the P450 aromatase gene in patients with polycystic ovary syndrome.

[aromatase deficiency]

Etiology and inheritance pattern in polycystic ovary syndrome (PCOS ) remain uncertain . Granulosa cells from follicles of women with PCOS have little , if any , aromatase (encoded by the CYP 19 gene ) activity ; follicles contain low levels of estradiol , P 450 arom mRNA and aromatase stimulating bioactivity . Mice with targeted disruption of the CYP 19 gene present cystic follicles . It has been proposed that chronic exposure to high levels of LH , because of aromatase deficiency , determines the development of ovarian cysts . Herein , we investigated if mutations in the CYP 19 gene and /or its ovary promoter are causal in patients with PCOS .Twenty -five patients with PCOS and 50 control women were studied . PCR analysis of genomic DNA and complete sequence of all exons of the aromatase gene and its ovary promoter were performed .No heterozygous or homozygous mutant alleles were present in any of the patients studied .In the population studied , mutations of the P 450 arom gene or its promoter are not the cause of PCOS . However , these findings do not preclude the possible importance of an aromatase disorder in PCOS etiology . Variations in aromatase complex function could play a role in PCOS etiology , but the determinants of such variations might be located in other genes .

Diseases
Validation

Diseases presenting "polycystic ovary syndrome" symptom

aromatase deficiency

congenital adrenal hyperplasia

cushing syndrome

kallmann syndrome

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