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Non-alcoholic fatty liver disease and sarcopenia is associated with the risk of albuminuria independent of insulin resistance, and obesity

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Affiliated Author(s)
한유진김미경임승순장병국김혜순
Alternative Author(s)
Han, Eu GeneKim, Hye SoonIm, Seung SoonJang, Byoung Kuk
Journal Title
J Diabetes Complications
ISSN
1056-8727
Issued Date
2022
Keyword
Nonalcoholic fatty liver diseasesFatty liverSteatosisAlbuminuriaSarcopeniaObesityInsulin resistance
Abstract
Background:
Although non-alcoholic fatty liver disease (NAFLD) is associated with metabolic disorders, its influence on albuminuria has not been determined. The aim of this study was to identify the relationship between NAFLD and albuminuria in the general Korean population.

Methods:
Data from the Korea National Health and Nutrition Examination Surveys (KNHANES) of 2008–2011 were analyzed ( n = 1795). Albuminuria was defined as an albumin-to-creatinine ratio of ≥30 mg/g in random spot urine samples. NAFLD was defined as a fatty liver index (FLI) ≥60 or NAFLD liver fat score (LFS) > −0.64.

Results:
A total of 289 (16.1 %) subjects were classified as having albuminuria. Subjects with NAFLD exhibited a higher rate of albuminuria than subjects without NAFLD (crude odds ratios [ORs] = 2.60–2.95, all P < 0.001). Regardless of hypertension, insulin resistance, or obesity, the risk for albuminuria was higher in the NAFLD group than in the group without NAFLD (measured by either FLI or LFS; all P < 0.001). When subjects with NAFLD had sarcopenia, the risk of albuminuria further increased (OR = 4.33–4.64, all P < 0.001). Multiple logistic regression analyses also demonstrated that NAFLD was independently associated with albuminuria (OR = 2.58, 95 % confidence interval [CI] = 1.66–4.02, P < 0.001 for FLI, OR = 1.87, 95 % CI = 1.28–2.75, P = 0.001 for LFS).

Conclusions:
NAFLD was associated with an increased risk of albuminuria in the general Korean population. This association was independent of hypertension, insulin resistance, chronic kidney disease, diabetes and obesity, and stronger in subjects with sarcopenia.
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