Research Article Details
Article ID: | A49248 |
PMID: | 35811043 |
Source: | Clin Gastroenterol Hepatol |
Title: | The prevalence and determinants of NAFLD and MAFLD and their severity in the VA primary care setting. |
Abstract: | BACKGROUND AIMS: A recent panel of international experts proposed the disease acronym metabolic (dysfunction) associated fatty liver disease (MAFLD) in lieu of non-alcoholic fatty liver disease (NAFLD). We aimed to estimate the burden of and risk factors for NAFLD and MAFLD, and to examine the concordance between definitions in a Veterans population. METHODS: We conducted a cross-sectional study among randomly selected patients within primary care at the Houston VA. Participants completed a survey, provided blood, and underwent Fibroscan. In the absence of heavy alcohol, HCV and HBV, a CAP median ≥290 dB/m was used to define NAFLD, while MAFLD was defined as CAP median ≥290 dB/m and either BMI ≥25 kg/m2 or diabetes, or 2 or more of the following: hypertension, high triglycerides, low HDL cholesterol, and high LDL cholesterol. RESULTS: The mean age of participants was 50.9 years, 55.4% were women, 42.8% white, and 43.8% Black. The prevalence of NAFLD was 40.6% (82/202). All 82 NAFLD patients had a BMI ≥25 and therefore met our criteria for MAFLD (i.e., 100% concordance). Compared with patients with no metabolic trait, patients with ≥3 traits 48-fold (adjusted OR, 47.6; 95% CI, 11.3-200) higher risk of NAFLD/MAFLD. Overall, 19 participants (9.4% of the total, 15.9% of NAFLD) had at least moderate fibrosis. CONCLUSIONS: NAFLD was present in 40% of veterans registered in primary care; 9.4% of Veterans had at least moderate hepatic fibrosis, with most having concurrent NAFLD. There was perfect concordance between NAFLD and the alternative MAFLD definition. |
DOI: | 10.1016/j.cgh.2022.05.046 |

Strategy ID | Therapy Strategy | Synonyms | Therapy Targets | Therapy Drugs | |
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S03 | Anti-fibrosis | fibrosis | Angiotensin Receptor Blocker (ARB); CCR2/CCR5 antagonist; Thyroid receptor β agonist; PEGylated human FGF21 analogue; Monoclonal antibody to lysyl oxidase-like 2 (LOXL2); Galectin-3 inhibitor; FGF19 variant | Losartan; Cenicriviroc; VK-2809; MGL-3196; Pegbelfermin; Simtuzumab; GR-MD-02; NGM282 | Details |
Target ID | Target Name | GENE | Action | Class | UniProtKB ID | Entry Name |
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Diseases ID | DO ID | Disease Name | Definition | Class | |
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I12 | 10763 | Hypertension | An artery disease characterized by chronic elevated blood pressure in the arteries. https://en.wikipedia.org/wiki/Hypertension, https://www.ncbi.nlm.nih.gov/pubmed/24352797 | disease of anatomical entity/ cardiovascular system disease/vascular disease/ artery disease | Details |
I14 | 9970 | Obesity | An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness. https://en.wikipedia.org/wiki/Obesity | disease of metabolism/acquired metabolic disease/ nutrition disease/overnutrition | Details |