Factors influencing subclinical atherosclerosis in patients with biopsy-proven nonalcoholic fatty liver disease.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2019
Historique:
received: 17 06 2019
accepted: 06 10 2019
entrez: 14 11 2019
pubmed: 14 11 2019
medline: 17 3 2020
Statut: epublish

Résumé

Although the presence of nonalcoholic fatty liver disease (NAFLD) is known to be related to subclinical atherosclerosis, the relationship between the severity of NAFLD and subclinical atherosclerosis is not clear. This study aimed to clarify the factors related to subclinical arteriosclerosis, including the histopathological severity of the disease and PNPLA3 gene polymorphisms, in NAFLD patients. We measured brachial-ankle pulse wave velocity (baPWV) as an index of arterial stiffness in 153 biopsy-proven NAFLD patients. The baPWV values were significantly higher in the advanced fibrosis group than in the less advanced group (median, 1679 cm/s vs 1489 cm/s; p = 5.49×10-4). Multiple logistic regression analysis revealed that older age (≥55 years) (p = 8.57×10-3; OR = 3.03), hypertension (p = 1.05×10-3; OR = 3.46), and advanced fibrosis (p = 9.22×10-3; OR = 2.94) were independently linked to baPWV ≥1600 cm/s. NAFLD patients were categorized into low-risk group (number of risk factors = 0), intermediate-risk group (= 1), and high-risk group (≥2) based on their risk factors, including older age, hypertension, and biopsy-confirmed advanced fibrosis. The prevalence of baPWV ≥1600 cm/s was 7.1% (3/42) in the low-risk group, 30.8% (12/39) in the intermediate-risk group, and 63.9% (46/72) in the high-risk group. Non-invasive liver fibrosis markers and scores, including the FIB-4 index, NAFLD fibrosis score, hyaluronic acid, Wisteria floribunda agglutinin positive Mac-2-binding protein, and type IV collagen 7s, were feasible substitutes for invasive liver biopsy. Older age, hypertension, and advanced fibrosis are independently related to arterial stiffness, and a combination of these three factors may predict risk of arteriosclerosis in NAFLD patients.

Identifiants

pubmed: 31721770
doi: 10.1371/journal.pone.0224184
pii: PONE-D-19-17091
pmc: PMC6853607
doi:

Substances chimiques

Membrane Proteins 0
Lipase EC 3.1.1.3
adiponutrin, human EC 3.1.1.3

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0224184

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Taeang Arai (T)

Division of Gastroenterology and Hepatology, Nippon Medical School, Tokyo, Japan.

Masanori Atsukawa (M)

Division of Gastroenterology and Hepatology, Nippon Medical School, Tokyo, Japan.

Akihito Tsubota (A)

Core Research Facilities for Basic Science, Research Center for Medical Sciences, The Jikei University School of Medicine, Tokyo, Japan.

Tadamichi Kawano (T)

Division of Gastroenterology and Hepatology, Nippon Medical School, Tokyo, Japan.

Mai Koeda (M)

Division of Gastroenterology, Nippon Medical School Chiba Hokusoh Hospital, Inzai, Japan.

Yuji Yoshida (Y)

Division of Gastroenterology, Nippon Medical School Chiba Hokusoh Hospital, Inzai, Japan.

Tomohide Tanabe (T)

Division of Gastroenterology and Hepatology, Nippon Medical School, Tokyo, Japan.

Tomomi Okubo (T)

Division of Gastroenterology, Nippon Medical School Chiba Hokusoh Hospital, Inzai, Japan.

Korenobu Hayama (K)

Division of Gastroenterology and Hepatology, Nippon Medical School, Tokyo, Japan.

Ai Iwashita (A)

Division of Gastroenterology and Hepatology, Nippon Medical School, Tokyo, Japan.

Norio Itokawa (N)

Division of Gastroenterology, Nippon Medical School Chiba Hokusoh Hospital, Inzai, Japan.

Chisa Kondo (C)

Division of Gastroenterology and Hepatology, Nippon Medical School, Tokyo, Japan.

Keiko Kaneko (K)

Division of Gastroenterology and Hepatology, Nippon Medical School, Tokyo, Japan.

Chiaki Kawamoto (C)

Division of Gastroenterology and Hepatology, Nippon Medical School, Tokyo, Japan.

Tsutomu Hatori (T)

Division of Pathology, Nippon Medical School Chiba Hokusoh Hospital, Inzai, Japan.

Naoya Emoto (N)

Division of Endocrinology, Nippon Medical School Chiba Hokusoh Hospital, Inzai, Japan.

Etsuko Iio (E)

Department of Virology and Liver Unit, Nagoya City University Graduate School of Medicinal Sciences, Nagoya, Japan.

Yasuhito Tanaka (Y)

Department of Virology and Liver Unit, Nagoya City University Graduate School of Medicinal Sciences, Nagoya, Japan.

Katsuhiko Iwakiri (K)

Division of Gastroenterology and Hepatology, Nippon Medical School, Tokyo, Japan.

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