Genetic contribution of the interleukin-10 promoter polymorphism in endometriosis susceptibility

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AI-generated summary by claude@2026-06, 2026-06-10

This study investigated IL-10 promoter polymorphisms in endometriosis and found no association with susceptibility, but did link the -592*CC genotype and -592*C allele to anti-CA II antibodies in patients.

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Abstract

PROBLEM: Interleukin-10 (IL-10) is an important immunomodulatory cytokine. The aim of this study was to investigate whether polymorphisms of the IL-10 gene promoter polymorphisms may be responsible in part for genetic susceptibility to endometriosis. METHODS OF STUDY: Polymorphisms at position -1082 and -592 in the IL-10 promoter region were determined in 196 patients with endometriosis and 160 fertile healthy women by polymerase chain reaction (PCR)-restriction fragment length polymorphism (RFLP). RESULTS: There were no statistically significant differences in the genotype and allele frequencies of IL-10 promoter polymorphism between the endometriosis and control groups. However, when subgrouped according to clinical features, the frequencies of the -592*CC genotype and -592*C allele were significantly increased in patients with autoantibodies to carbonic anhydrase II (anti-CA II ab) compared with controls. CONCLUSION: IL-10 promoter polymorphisms were associated with the production of anti-CA II ab in patients with endometriosis, suggesting a role in the genetic susceptibility for endometriosis.

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Condition tags

endometriosis

MeSH descriptors

Endometriosis Endometriosis Interleukin-10 Polymorphism, Genetic Promoter Regions, Genetic Adult Alleles Autoantibodies Autoantibodies Carbonic Anhydrase II Carbonic Anhydrase II Case-Control Studies Endometriosis Female Gene Frequency Genotype Humans Interleukin-10 Middle Aged Polymerase Chain Reaction

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Source provenance

europepmc
last seen: 2026-06-23T06:15:44.889181+00:00
pubmed
last seen: 2026-05-13T22:13:13.417725+00:00
unpaywall
last seen: 2026-05-14T19:30:52.867331+00:00
License: public-domain-us · commercial use OK · attribution required
Courtesy of the U.S. National Library of Medicine