Increased risk for microvascular outcomes in NAFLD—A nationwide, population‐based cohort study

Author:

Ebert Thomas12ORCID,Widman Linnea3,Stenvinkel Peter1ORCID,Hagström Hannes34ORCID

Affiliation:

1. Department of Clinical Science, Intervention and Technology, Division of Renal Medicine Karolinska Institutet Stockholm Sweden

2. Medical Department III ‐ Endocrinology, Nephrology, Rheumatology University of Leipzig Medical Center Leipzig Germany

3. Department of Medicine, Huddinge Karolinska Institutet Stockholm Sweden

4. Department of Upper GI Diseases Karolinska University Hospital Stockholm Sweden

Abstract

AbstractIntroductionNonalcoholic fatty liver disease (NAFLD) is considered a multisystem disease, as it is bidirectionally linked to other cardiometabolic disorders, such as type 2 diabetes (T2D). However, the long‐term risk for microvascular outcomes in NAFLD is unclear.MethodsUsing the outpatient part of the nationwide Swedish Patient Register in the time period between 01/01/2002 and 12/31/2019, we identified all individuals with a first NAFLD diagnosis (N = 6785) and matched these (age, sex, and municipality) with up to 10 reference individuals from the general population (N = 61,136). Using population‐based registers, we ascertained the development of microvascular diseases. The primary outcome was defined as a composite outcome of any diagnosis representative of microvascular disease (chronic kidney disease, retinopathy, or neuropathy). As secondary outcomes, we separately examined the risk of each specific microvascular outcome. Hazard ratios (aHR, adjusted for cirrhosis and time‐varying T2D, hypertension, and hyperlipidemia) for the outcomes were calculated by Cox proportional‐hazards models.ResultsMedian follow‐up was 5.7 years. The incidence rate of microvascular diseases was >twofold higher in patients with NAFLD (10.8 per 1000 person‐years [95% confidence interval (CI) = 9.9–11.8]) versus reference individuals (4.7 per 1000 person‐years [95%CI = 4.5–4.9]). NAFLD was independently and positively associated with the development of microvascular diseases compared to non‐NAFLD subjects (aHR = 1.45 [95%CI = 1.28–1.63]). When stratifying the analysis by follow‐up time, sex, or age categories, results remain virtually unchanged.ConclusionsNAFLD is positively and independently associated with the development of microvascular diseases. The risk for development of microvascular diseases should be taken into account in the personalized risk assessment of individuals with NAFLD.

Publisher

Wiley

Subject

Internal Medicine

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