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GWAS Study

Pathway-Wide Genetic Risks in Chlamydial Infections Overlap between Tissue Tropisms: A Genome-Wide Association Scan.

Roberts CH, Ouburg S, Preston MD et al.

29967566 PubMed ID
GWAS Study Type
240 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

RC
Roberts CH
OS
Ouburg S
PM
Preston MD
DV
de Vries HJC
HM
Holland MJ
MS
Morré SA
Chapter II

Abstract

Summary of the research findings

Chlamydia trachomatis is the most commonly diagnosed bacterial sexually transmitted infection and can lead to tubal factor infertility, a disease characterised by fibrosis of the fallopian tubes. Genetic polymorphisms in molecular pathways involving G protein-coupled receptor signalling, the Akt/PI3K cascade, the mitotic cell cycle, and immune response have been identified in association with the development of trachomatous scarring, an ocular form of chlamydia-related fibrotic pathology. In this case-control study, we performed genome-wide association and pathways-based analysis in a sample of 71 Dutch women who attended an STI clinic who were seropositive for Chlamydia trachomatis antibodies and 169 high-risk Dutch women who sought similar health services but who were seronegative. We identified two regions of within-gene SNP association with Chlamydia trachomatis serological response and found that GPCR signalling and cell cycle pathways were also associated with the trait. These pathway-level associations appear to be common to immunological sequelae of chlamydial infections in both ocular and urogenital tropisms. These pathways may be central mediators of human refractoriness to chlamydial diseases.

71 Dutch ancestry cases, 169 Dutch ancestry controls

Chapter III

Study Statistics

Key metrics and study information

240
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Netherlands
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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