整合基因和社会经济数据,预测非酒精性脂肪肝的进展。

IF 1.7 2区 生物学 Q1 ANTHROPOLOGY American Journal of Biological Anthropology Pub Date : 2024-05-22 DOI:10.1002/ajpa.24979
Maria C. Rieman-Klingler, Jinho Jung, Kaleb Tesfai, Rohit Loomba, Amy L. Non
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摘要

目的:非酒精性脂肪肝(NAFLD)是全球慢性肝病的主要病因,估计发病率超过 25%。PNPLA3和HSD17B13基因的变异一直是围绕非酒精性脂肪肝的病因和进展进行调查的重点,并且被认为是造成西班牙裔美国人疾病负担加重的原因之一。然而,人们对影响非酒精性脂肪肝进展的社会经济因素或非酒精性脂肪肝在西班牙裔美国人中发病率增加的情况知之甚少:我们对264名患者进行了横截面分析,以评估遗传和社会经济变量在非酒精性脂肪肝高危人群晚期肝纤维化发展中的作用:对年龄、性别、体重指数和PNPLA3基因型进行调整后,没有大学学历与晚期肝纤维化几率高出3.3倍(95%置信区间[CI]:1.21-8.76,p = 0.019)有关,这一效应与拥有主要PNPLA3风险变体的效应相当。值得注意的是,在对教育程度和其他社会经济指标进行调整后,PNPLA3 基因型对晚期纤维化的影响减弱至无显著性。此外,经教育程度调整后,保护性HSD17B13变异的影响减弱(比值比[OR]:0.39[95% CI:0.13-1.16,p = 0.092]),而经多变量调整后,教育程度较低仍可预测晚期纤维化,OR为8.0(95% CI:1.91-33.86,p = 0.005):讨论:调整教育程度可减轻基因型和西班牙裔对肝纤维化的影响,这表明在某些人群中,社会因素而非基因或种族可能是疾病严重程度的驱动因素。研究结果揭示了在考虑遗传或种族在复杂疾病中的作用时纳入社会环境控制的重要性。
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Integrating genetic and socioeconomic data to predict the progression of nonalcoholic fatty liver disease

Objectives

Nonalcoholic fatty liver disease (NAFLD) is the leading cause of chronic liver disease globally, with an estimated prevalence exceeding 25%. Variants in the PNPLA3 and HSD17B13 genes have been a focus of investigations surrounding the etiology and progression of NAFLD and are believed to contribute to a greater burden of disease experienced by Hispanic Americans. However, little is known about socioeconomic factors influencing NAFLD progression or its increased prevalence among Hispanics.

Materials and Methods

We cross-sectionally analyzed 264 patients to assess the role of genetic and socioeconomic variables in the development of advanced liver fibrosis in individuals at risk for NAFLD.

Results

Adjusting for age, sex, body mass index, and PNPLA3 genotype, lacking a college degree was associated with 3.3 times higher odds of advanced fibrosis (95% confidence interval [CI]: 1.21–8.76, p = 0.019), an effect comparable to that of possessing the major PNPLA3 risk variant. Notably, the effect of PNPLA3 genotype on advanced fibrosis was attenuated to nonsignificance following adjustment for education and other socioeconomic markers. The effect of the protective HSD17B13 variant, moreover, diminished after adjustment for education (odds ratio [OR]: 0.39 [95% CI: 0.13–1.16, p = 0.092]), while lower education continued to predict advanced fibrosis following multivariable adjustment with an OR of 8.0 (95% CI: 1.91–33.86, p = 0.005).

Discussion

Adjusting for education attenuated the effects of genotype and Hispanic ethnicity on liver fibrosis, suggesting that social factors—rather than genes or ethnicity—may be driving disease severity within some populations. Findings reveal the importance of including socioenvironmental controls when considering the role of genetics or ethnicity in complex disease.

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