Oxidative stress is associated with suspected non-alcoholic fatty liver disease and all-cause mortality in the general population

被引:32
作者
Damba, Turtushikh [1 ,2 ]
Bourgonje, Arno R. [1 ]
Abdulle, Amaal E. [3 ]
Pasch, Andreas [4 ]
Sydor, Svenja [5 ]
van den Berg, Eline H. [1 ]
Gansevoort, Ron T. [6 ]
Bakker, Stephan J. L. [6 ]
Blokzijl, Hans [1 ]
Dullaart, Robin P. F. [7 ]
van Goor, Harry [8 ]
Moshage, Han [1 ,9 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Gastroenterol & Hepatol, Hanzepl 1, NL-9713 GZ Groningen, Netherlands
[2] Univ Groningen, Mongolian Natl Univ Med Sci, Sch Pharm, Ulaanbaatar, Mongolia
[3] Univ Groningen, Univ Med Ctr Groningen, Div Vasc Med, Dept Internal Med, Groningen, Netherlands
[4] Johannes Kepler Univ Linz, Inst Physiol & Pathophysiol, Linz, Austria
[5] Otto Von Guericke Univ Hosp Magdeburg, Dept Gastroenterol Hepatol & Infect Dis, Magdeburg, Germany
[6] Univ Groningen, Univ Med Ctr Groningen, Div Nephrol, Dept Internal Med, Groningen, Netherlands
[7] Univ Groningen, Univ Med Ctr Groningen, Dept Endocrinol, Groningen, Netherlands
[8] Univ Groningen, Univ Med Ctr Groningen, Dept Pathol & Med Biol, Groningen, Netherlands
[9] Univ Groningen, Univ Med Ctr Groningen, Dept Lab Med, Groningen, Netherlands
关键词
fatty liver index FLI; free thiols; NAFLD; oxidative stress; DENSITY-LIPOPROTEIN CHOLESTEROL; HYDROGEN-SULFIDE; RISK-FACTORS; HOMEOSTASIS; NAFLD; ALBUMIN; MARKERS; PLASMA; THIOLS;
D O I
10.1111/liv.14562
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims Non-alcoholic fatty liver disease (NAFLD) is characterized by excessive lipid accumulation, inflammation and an imbalanced redox homeostasis. We hypothesized that systemic free thiol levels, as a proxy of systemic oxidative stress, are associated with NAFLD. Methods Protein-adjusted serum free thiol concentrations were determined in participants from the Prevention of Renal and Vascular End-Stage Disease (PREVEND) cohort study (n = 5562). Suspected NAFLD was defined by the Fatty Liver Index (FLI >= 60) and Hepatic Steatosis Index (HSI > 36). Results Protein-adjusted serum free thiols were significantly reduced in subjects with FLI >= 60 (n = 1651). In multivariable logistic regression analyses, protein-adjusted serum free thiols were associated with NAFLD (FLI >= 60) (OR per doubling of concentration: 0.78 [95% CI 0.64-0.96],P = .016) even when adjusted for potential confounding factors, including systolic blood pressure, diabetes, current smoking, use of alcohol and total cholesterol (OR 0.80 [95% CI 0.65-0.99],P = .04). This association lost its significance (OR 0.94 [95% CI 0.73-1.21],P = .65) after additional adjustment for high-sensitive C-reactive protein. Stratified analyses showed significantly differential associations of protein-adjusted serum free thiol concentrations with suspected NAFLD for gender (P < .02), hypertension (P < .001) and hypercholesterolemia (P < .003). Longitudinally, protein-adjusted serum free thiols were significantly associated with the risk of all-cause mortality in subjects with NAFLD (FLI >= 60) (HR 0.27 [95% CI 0.17-0.45],P < .001). Conclusion Protein-adjusted serum free thiol levels are reduced and significantly associated with all-cause mortality in subjects with suspected NAFLD. Quantification of free thiols may be a promising, minimally invasive strategy to improve detection of NAFLD and associated risk of all-cause mortality in the general population.
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收藏
页码:2148 / 2159
页数:12
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