Academic Rheumatology, Clinical Sciences Building, City Hospital Nottingham, University of Nottingham, Hucknall Road, Nottingham, NG5 1PB, UK.
Nottingham NIHR-BRC, Nottingham, UK.
Rheumatol Int. 2022 Sep;42(9):1617-1622. doi: 10.1007/s00296-022-05148-7. Epub 2022 May 28.
To examine the association between common comorbidities, eGFR and loci involved in the hyperuricaemia-gout transition. This study was conducted in people with gout from the UK Biobank. Logistic regression was used to examine the association between self-reported physician-diagnosed hypertension, diabetes, hypercholesterolemia and ischaemic heart disease (IHD) with the following variants: rs1260326(GCKR), rs16890979(SLC2A9), rs2231142(ABCG2), rs1229984(ADH1B) and rs2078267(SLC22A11) and adjusted for age, sex and 10-principal components. Linear regression was used to examine the association with eGFR. 7,049 participants with gout were included. After adjusting for multiple testing, there was a statistically significant positive association between urate lowering allele at SLC2A9 and hypertension, and negative association between urate raising allele at ABCG2 and hypertension (OR 1.17 and OR 0.86, respectively). Number of urate lowering risk alleles associated with hypertension [OR (95%CI) 1.13 (1.06-1.21)]. High eGFR associated with urate raising allele at rs2231142 (β = 1.38). The SNP in ADH1B that protects from alcohol excess showed a negative association with IHD (OR 0.53). Unlike in general population studies urate lowering genetic variants associate with hypertension in gout patients with dose-response. This may be due to high prevalence of other risk factors of hypertension such as obesity, poor diet etc. and needs validation in independent datasets.
为了研究常见合并症、eGFR 与高尿酸血症-痛风转化相关基因座之间的关联。本研究在英国生物银行中的痛风患者中进行。采用逻辑回归分析方法,检验了经医生诊断的高血压、糖尿病、高脂血症和缺血性心脏病(IHD)与以下变异体之间的关联:rs1260326(GCKR)、rs16890979(SLC2A9)、rs2231142(ABCG2)、rs1229984(ADH1B)和 rs2078267(SLC22A11)。并调整了年龄、性别和 10 个主要成分。采用线性回归分析检验与 eGFR 的相关性。共纳入 7049 名痛风患者。经过多重检验调整后,SLC2A9 上的尿酸降低等位基因与高血压之间存在统计学上显著的正相关,而 ABCG2 上的尿酸升高等位基因与高血压之间存在统计学上显著的负相关(OR 分别为 1.17 和 0.86)。与高血压相关的尿酸降低风险等位基因数量 [OR(95%CI)为 1.13(1.06-1.21)]。rs2231142 的尿酸升高等位基因与较高的 eGFR 相关(β=1.38)。保护个体免受过量饮酒影响的 ADH1B 上的 SNP 与 IHD 呈负相关(OR 为 0.53)。与一般人群研究不同,降低尿酸的遗传变异与痛风患者的高血压呈剂量反应关系。这可能是由于高血压的其他危险因素(如肥胖、不良饮食等)的高患病率所致,需要在独立数据集进行验证。