Increased risk of chronic kidney disease and mortality in a cohort of people diagnosed with metabolic dysfunction associated steatotic liver disease with hepatic fibrosis

被引:4
作者
Gurun, Marc [1 ]
Brennan, Paul [1 ,2 ]
Handjiev, Sava [3 ]
Khatib, Aseil [2 ]
Leith, Damien [4 ]
Dillon, John F. [1 ,2 ]
Byrne, Christopher J. [1 ,5 ]
机构
[1] Univ Dundee, Ninewells Hosp & Med Sch, Sch Med, Mol & Clin Med, Dundee, Scotland
[2] Ninewells Hosp & Med Sch, Dept Gastroenterol, NHS Tayside, Dundee, Scotland
[3] Ninewells Hosp & Med Sch, Dept Biochem Med, NHS Tayside, Dundee, Scotland
[4] Univ Dundee, Ninewells Hosp & Med Sch, Sch Med, Populat Hlth & Genom, Dundee, Scotland
[5] Kings Cross Hosp, Directorate Publ Hlth, NHS Tayside, Dundee, Scotland
来源
PLOS ONE | 2024年 / 19卷 / 04期
关键词
NAFLD; EPIDEMIOLOGY; PREVALENCE; OUTCOMES; BURDEN; IMPACT;
D O I
10.1371/journal.pone.0299507
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background and aims Metabolic dysfunction associated steatotic liver disease (MASLD) increases the risk of incident chronic kidney disease (CKD). However, the relative risk of CKD associated with increasing hepatic fibrosis, and consequent mortality risk, remains underexplored in real-world cohorts. In this study, we sought to establish whether hepatic fibrosis is associated with increased CKD risk and explore differences in mortality risk in a cohort of people living with MASLD, contingent on liver fibrosis and CKD status. Methods This was an observational study of people who underwent routine liver function testing in Tayside, Scotland. MASLD was defined as: elevated ALT (>30 U/L) or GGT (>73 U/L); presence of diabetes, and/or hypertension, and/or obesity; weekly alcohol consumption <14 units (112g (+/-8g) alcohol); and negative screen for other aetiologies. Data was collected from digital health records. We used log-binomial models to quantify the risk of CKD among those with and without fibrosis, and Cox regression models to estimate differences in mortality risk dependent on fibrosis and CKD. Results In our cohort (n = 2,046), 1,448 (70.8%) people had MASLD without fibrosis and 598 (29.2%) with fibrosis; 161 (11.1%) and 117 (19.6%) respectively also had CKD. After excluding individuals with structural, autoimmune, or malignant CKD (n = 22), liver fibrosis (n = 593; 18.9% with CKD) was associated with increased CKD risk (aRR = 1.31, 1.04-1.64, p = 0.021). Increased mortality risk was observed for those with liver fibrosis (aHR = 2.30, 1.49-3.56, p = <0.001) and was higher again among people with both fibrosis and CKD (aHR = 5.07, 3.07-8.39, p = <0.014). Conclusions Liver fibrosis was an independent risk factor for CKD in this cohort of people living with MASLD. Furthermore, those with MASLD with liver fibrosis had higher risk for mortality and this risk was further elevated among those with co-morbid CKD. Given the increased risk of CKD, and consequent mortality risk, among people living with MASLD fibrosis, renal function screening should be considered within liver health surveillance programmes and guidelines.
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页数:17
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