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Hepatol Int. 2020;14(5):798-807.

Portal inflammation predicts renal dysfunction in patients with nonalcoholic fatty liver disease.

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제1저자 안정남, 주세경 · 교신저자 김원

소속 (6)
  1. Division of Nephrology, Department of Internal Medicine, Hallym University Sacred Heart Hospital, Anyang, Gyeonggi-do, South Korea.
  2. Division of Gastroenterology and Hepatology, Department of Internal Medicine, Seoul Metropolitan Government Seoul National University Boramae Medical Center, Seoul National University College of Medicine, 20, Boramae-ro 5-gil, Dongjak-gu, Seoul, 07061, South Korea.
  3. Division of Endocrinology, Department of Internal Medicine, Seoul Metropolitan Government Boramae Medical Center, Seoul National University College of Medicine, Seoul, South Korea.
  4. Department of Pathology, Seoul National University College of Medicine, Seoul, South Korea.
  5. Department of Biostatistics, Seoul Metropolitan Government Boramae Medical Center, Seoul, South Korea.
  6. Division of Gastroenterology and Hepatology, Department of Internal Medicine, Seoul Metropolitan Government Seoul National University Boramae Medical Center, Seoul National University College of Medicine, 20, Boramae-ro 5-gil, Dongjak-gu, Seoul, 07061, South Korea. drwon1@snu.ac.kr.

Abstract

BACKGROUND The association between nonalcoholic fatty liver disease (NAFLD) and renal function changes remains inconclusive. We explored whether the histological severity of NAFLD is associated with early deterioration of renal function.

METHODS Patients with biopsy-proven NAFLD were prospectively followed for renal function monitoring. A renal outcome was defined as a ≥ 50% increase in serum creatinine, a < 30% decrease in the estimated glomerular filtration rate (eGFR) or an eGFR < 45 mL/min/1.73 m2.

RESULTS Among 455 NAFLD patients, 221 (48.6%) had nonalcoholic steatohepatitis (NASH), and no difference in baseline eGFR was found between NASH and NAFL patients. During a median follow-up of 32 months, a renal outcome occurred in 15 patients; the incidence rate was 12.3 per 1,000 person-years. Compared with NAFL, NASH did not increase the risk of renal outcomes. Among the histological components of NAFLD, lobular inflammation (≥ 2), fibrosis (≥ F3), and portal inflammation (≥ 3) significantly increased the risk of renal outcomes in the crude analysis (HR 3.35, 95% CI 1.10-9.11; HR 3.25, 95% CI 1.12-8.84; and HR 7.73, 95% CI 2.86-22.22). After adjustment for risk factors for renal dysfunction, including sex, age, diabetes, hypertension, and chronic kidney disease, only portal inflammation significantly increased the risk of renal outcomes (HR 5.88, 95% CI 1.87-18.42, p = 0.002).

CONCLUSIONS Portal inflammation predicts early deterioration of renal function in patients with biopsy-proven NAFLD. Individualized monitoring of renal function based on the histological severity of NAFLD may be helpful for early identification of long-term renal outcomes.

Keywords

Early deteriorationFibrosisHistologyLobular inflammationNonalcoholic fatty liver diseaseNonalcoholic steatohepatitisPortal inflammationRenal functionRisk factorsSeverity

그 밖의 정보
출판 형태
Journal Article
저널
Hepatology international · eISSN 1936-0541
전자 출판
2020-06-17
MeSH
Biopsy / methods · Disease Progression · Female · Glomerular Filtration Rate · Humans · Inflammation / diagnosis · Kidney Function Tests / methods · Liver* / blood supply / immunology / pathology · Male · Middle Aged · Non-alcoholic Fatty Liver Disease / complications / diagnosis / immunology / physiopathology · Portal System / immunology / pathology · Prognosis · Renal Insufficiency* / diagnosis / etiology · Republic of Korea / epidemiology
연구비
National Research Foundation of Korea 2016R1D1A1B04934590 · Korea Health Industry Development Institute HI17C0912
참고문헌
30편