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Data · dataset · 2026

Association of Sequence Similarity 13 Member A Gene Variants with the Risk of Chronic Obstructive Pulmonary Disease

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Prior evidence has linked DNA sequence variations in the FAM13A locus to the onset of respiratory pathologies.

Description

Conducted as a hospital-based case-control investigation, this study sought to clarify whether selected single nucleotide polymorphisms in FAM13A influence the likelihood of developing COPD in older adults belonging to the Chinese Han population. The cohort comprised 541 participants, among whom 270 were diagnosed COPD patients and 271 served as healthy comparators.

DNA was isolated from peripheral blood leukocytes and subjected to microarray-based genotyping. Five SNPs---namely rs2602119, rs1801915, rs11944668, rs3756050, and rs2869950---were evaluated through multivariable logistic regression modeling, while potential epistatic interactions were probed via multifactor dimensionality reduction (MDR). Carriage of the rs2869950 C allele conferred greater odds of COPD occurrence.

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Likewise, individuals harboring the heterozygous TC genotype at this locus displayed a markedly elevated disease risk. Stratified analyses further demonstrated that the risk effect of rs2869950 was particularly pronounced among women, cigarette smokers, alcohol consumers, subjects older than 71 years, and those whose body mass index fell below 24 kg/m^2. MDR assessment uncovered synergistic interplay among the examined variants, and the four-locus combination achieved maximal testing balanced accuracy together with optimal cross-validation consistency.

Taken together, these data indicate that both the C allele and the TC genotype at rs2869950 constitute susceptibility factors for COPD in the population under investigation.

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Catalogue records · 1

Topics

Inferred from text
Disease 75% · Genetics 71%
Provenance · 1 source records, 12 field assertions
SourceKeyLast seenRaw
ScienceDB10.57760/sciencedb.393249 d agoJSON v1
FieldAssertionExtractorEvidence
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concepts[field].anzsrc:group:3105enrichment · scidb cntaxonomy-embedding@1.0.0title+keywords+description (71%)
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