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Updated: May 13, 2026

Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry
Published on: June 21, 2018
IL-8 -251T/A and IL-12B 1188A/C polymorphisms are associated with gout in a Chinese male population
1Shandong Provincial Key Laboratory of Metabolic Disease, Qingdao University, Qingdao, PR China.
Objectives:
Gout is caused by monosodium urate (MSU) crystal-induced inflammation of the joints and periarticular tissues. MSU crystals activate NALP3 and mediate interleukin (IL)-1β generation from its inactive pro-form, resulting in cellular activation and an IL-8-mediated neutrophil influx into the joint. IL-8 and IL-12 are important chemokines related to the initiation and amplification of acute and chronic inflammatory processes. In this study, we investigated whether the IL-8 -251T/A and IL-12 1188A/C polymorphisms are associated with susceptibility to gout in a Chinese Han male population.
Methods:
Overall, 387 patients with gout and 576 controls were included in this study. Genotyping was performed by polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP). An association analysis was carried out using the χ2 test. A genotype-phenotype analysis was also conducted.
Results:
The T allele of IL-8 -251 was associated with risk of gout [p = 0.031 (odds ratio (OR) 1.229, 95% confidence interval (CI) 1.019-1.483]. There was a clear link between the IL-12 1188 AA and AC genotypic and A allelic frequencies between gout cases and controls (p < 0.001, df = 2 by genotype; p < 0.001, OR 1.404, 95% CI 1.165-1.691 by allele).
Conclusions:
Our results suggest that the IL-8 -251T/A and IL-12B 1188A/C polymorphisms may be relevant host susceptibility factors for the development of gout.
Insights
Genetic variations in interleukin-8 (IL-8) and interleukin-12 (IL-12) are linked to gout susceptibility in Chinese men. These findings highlight specific gene polymorphisms as potential risk factors for developing gout.
Area of Science:
- Immunogenetics
- Rheumatology
- Molecular Biology
Background:
- Gout is an inflammatory joint disease caused by monosodium urate (MSU) crystals.
- MSU crystals trigger inflammation via NALP3 inflammasome activation, leading to interleukin-1 beta (IL-1β) generation.
- Interleukin-8 (IL-8) and IL-12 are key chemokines in initiating and amplifying inflammatory responses, particularly neutrophil influx into joints.
Purpose of the Study:
- To investigate the association between IL-8 -251T/A and IL-12B 1188A/C gene polymorphisms and gout susceptibility.
- To determine if these polymorphisms are relevant host factors for gout development in a Chinese Han male population.
Main Methods:
- Genotyping of 387 gout patients and 576 controls using polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP).
- Association analysis conducted using the chi-squared (χ2) test.
- Genotype-phenotype analysis performed to correlate genetic variations with gout status.
Main Results:
- The T allele of IL-8 -251 was significantly associated with an increased risk of gout (p = 0.031, OR = 1.229).
- Significant associations were found between IL-12B 1188 gene polymorphisms (AA and AC genotypes, A allele) and gout cases compared to controls (p < 0.001 for both genotype and allele frequencies).
- The IL-12B 1188 A allele showed a higher frequency in gout patients (OR = 1.404).
Conclusions:
- The IL-8 -251T/A and IL-12B 1188A/C polymorphisms are suggested as potential host susceptibility factors for gout.
- These genetic variations may play a role in the development of gout in the studied Chinese Han male population.
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