Literature DB >> 31516266

Magnitude of Nonalcoholic Fatty Liver Disease: Western Perspective.

Naga S Samji1, Rajanshu Verma1,2, Sanjaya K Satapathy3.   

Abstract

The incidence of nonalcoholic fatty liver disease (NAFLD) is continuing to rise worldwide, and it is estimated that this disquieting trend will continue for another 10-15 years before prevalence begins to decrease. NAFLD is the hepatic manifestation of metabolic syndrome. As obesity, diabetes, and other lifestyle-related diseases continue to rise, the spectrum of NAFLD, e.g., nonalcoholic steatohepatitis, liver fibrosis, liver cirrhosis, liver-related morbidity, and mortality, will increase in parallel. Its widespread prevalence and associated economic burden have drawn significant attention, and a multitude of pharmaceutical companies are participating in active research trying to find a "cure". Unfortunately, as of now, no targeted treatment exists to treat this condition, and therefore, emphasis has been on its prevention. The current review focuses on the epidemiology, clinical characteristics, risk factors, and clinical outcomes of NAFLD in Western countries. It is important to understand the magnitude of NAFLD and its risk factors in Western countries where the prevalence of NAFLD has now reached epidemic proportions to identify the best strategy to prevent and possibly control this epidemic.

Entities:  

Keywords:  BMI, body mass index; CKD, chronic kidney disease; NAFLD, nonalcoholic fatty liver disease; NASH, nonalcoholic steatohepatitis; OSA, obstructive sleep apnea; PNPLA3, patatin-like phospholipase domain–containing protein 3; TM6SF2, transmembrane 6 superfamily 2; Western world; liver transplantation; metabolic syndrome; non‐alcoholic fatty liver disease; non‐alcoholic steatohepatitis

Year:  2019        PMID: 31516266      PMCID: PMC6728535          DOI: 10.1016/j.jceh.2019.05.001

Source DB:  PubMed          Journal:  J Clin Exp Hepatol        ISSN: 0973-6883


  115 in total

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2.  The major lipid peroxidation product, trans-4-hydroxy-2-nonenal, preferentially forms DNA adducts at codon 249 of human p53 gene, a unique mutational hotspot in hepatocellular carcinoma.

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Authors:  S Bellentani; G Saccoccio; F Masutti; L S Crocè; G Brandi; F Sasso; G Cristanini; C Tiribelli
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Authors:  P Angulo; J C Keach; K P Batts; K D Lindor
Journal:  Hepatology       Date:  1999-12       Impact factor: 17.425

6.  Association of nonalcoholic fatty liver disease with insulin resistance.

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7.  Nonalcoholic fatty liver disease: a spectrum of clinical and pathological severity.

Authors:  C A Matteoni; Z M Younossi; T Gramlich; N Boparai; Y C Liu; A J McCullough
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8.  Mitochondrial adaptations to obesity-related oxidant stress.

Authors:  S Yang; H Zhu; Y Li; H Lin; K Gabrielson; M A Trush; A M Diehl
Journal:  Arch Biochem Biophys       Date:  2000-06-15       Impact factor: 4.013

9.  Reactive oxygen metabolites (ROMs) as an index of oxidative stress in obstructive sleep apnea patients.

Authors:  Kostas Christou; Nikolaos Markoulis; Anargyros N Moulas; Chaido Pastaka; Kostantinos I Gourgoulianis
Journal:  Sleep Breath       Date:  2003-09       Impact factor: 2.816

10.  Diabetes increases the risk of chronic liver disease and hepatocellular carcinoma.

Authors:  Hashem B El-Serag; Thomas Tran; James E Everhart
Journal:  Gastroenterology       Date:  2004-02       Impact factor: 22.682

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  7 in total

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Review 2.  Dietary Patterns and Components in Nonalcoholic Fatty Liver Disease (NAFLD): What Key Messages Can Health Care Providers Offer?

Authors:  Kiarash Riazi; Maitreyi Raman; Lorian Taylor; Mark G Swain; Abdel Aziz Shaheen
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4.  Pericardial fat, thoracic peri-aortic adipose tissue, and systemic inflammatory marker in nonalcoholic fatty liver and abdominal obesity phenotype.

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5.  The association of pericardial fat and peri-aortic fat with severity of nonalcoholic fatty liver disease.

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6.  Living Donor Liver Transplant in Patients Aged 60 Years or Older: Experience from a Large Volume Centre in India.

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7.  Liver fat storage is controlled by HNF4α through induction of lipophagy and is reversed by a potent HNF4α agonist.

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  7 in total

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