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PMID 16213843
Gene Name CYP19A1
Condition Azoospermia, Oligozoospermia
Association The results support a relevant role for the estrogenic pathway, notably the ESR1 gene, in human male reproductive function and advocate a complex trait model for male infertility.

PMID 16213843
Gene Name CYP19A1
Condition Azoospermia, oligospermia
Association The study observed an excess of homozygous infertile men for the ESR1 g.938T>C marker. Multilocus analyses detected genetic interaction between the five candidate gene markers that are influential over male infertility.
PMID 16213843
Gene Name CYP19A1
Condition Male idiopathic infertility
Association The study observed an excess of homozygous infertile men for the ESR1 g.938T>C marker. Multilocus analyses detected genetic interaction between the five candidate gene markers that are influential over male infertility. In addition, we detected a five-loc
Mutation ESR1 g.938T>C, FSHR Ser680Asn, ESR2 *39A>G, CYP19A1*19C>T, and NRIP1 Gly75Gly polymorphism
Population size 199
Population details 199 (104 with azoospermia or severe oligozoospermia, 95 unselected race-matched healthy controls)
Sex Male
Infertility type Male infertility
Associated genes ESR1, FSHR, ESR2, CYP19A1, and NRIP1
Other associated phenotypes Male infertility


Multilocus analyses of estrogen-related genes reveal involvement of the ESR1 gene in male infertility and the polygenic nature of the pathology

Galan JJ, Buch B, Cruz N, Segura A, Moron FJ, Bassas L, Martinez-Pineiro L, Real LM, Ruiz A.

OBJECTIVE: To examine whether polymorphisms within the ESR1, FSHR, ESR2, CYP19A1, and NRIP1 genes are susceptibility factors for human male idiopathic infertility and to test the joint effects of these genes on male reproductive function. DESIGN: Genetic association study of male infertility with polymorphisms, using both single-gene and multilocus approaches. SETTING: Private and public fertility units and a private center for biomedical research. PATIENT(S): One hundred four Spanish men with azoospermia or severe oligozoospermia and 95 unselected race-matched healthy controls from the same geographic region. INTERVENTION(S): Peripheral blood extraction, DNA purification, and ESR1 g.938T>C, FSHR Ser680Asn, ESR2 *39A>G, CYP19A1 *19C>T, and NRIP1 Gly75Gly polymorphism analyses. MAIN OUTCOME MEASURE(S): Single-gene statistical analyses and multilocus statistical analyses with Sumstat, Permutation and Model-free analysis, and Estimating Haplotypes software. RESULT(S): We observed an excess of homozygous infertile men for the ESR1 g.938T>C marker. Multilocus analyses detected genetic interaction between the five candidate gene markers that are influential over male infertility. In addition, we detected a five-loci protector genetic pattern with a frequency of 9.4% in controls but absent in infertile men. CONCLUSION(S): Our results support a relevant role for the estrogenic pathway, notably the ESR1 gene, in human male reproductive function and advocate a complex trait model for male infertility. FAU - Galan, Jose J AU - Galan JJ AD - Department of Structural Genomics, Neocodex, Seville, Spain. FAU - Buch, Belen AU - Buch B FAU - Cruz, Natalio AU - Cruz N FAU - Segura, Ana AU - Segura A FAU - Moron, Francisco J AU - Moron FJ FAU - Bassas, Lluis AU - Bassas L FAU - Martinez-Pineiro, Luis AU - Martinez-Pineiro L FAU - Real, Luis M AU - Real LM