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Clinical Factors Associated with Non-Obese Nonalcoholic Fatty Liver Disease Detected among US Adults in the NHANES 2017–2018

NAFLD can occur in non-obese individuals with BMI < 25 kg/m(2). Our goal was to examine the prevalence and clinical factors associated with non-obese NAFLD using vibration-controlled transient elastography (VCTE) with controlled attenuation parameter which estimates steatosis and fibrosis among U...

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Autores principales: Razouki, Zayd Adnan, Zhang, Xiaotao, Hwang, Jessica P., Heredia, Natalia I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9331553/
https://www.ncbi.nlm.nih.gov/pubmed/35893351
http://dx.doi.org/10.3390/jcm11154260
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author Razouki, Zayd Adnan
Zhang, Xiaotao
Hwang, Jessica P.
Heredia, Natalia I.
author_facet Razouki, Zayd Adnan
Zhang, Xiaotao
Hwang, Jessica P.
Heredia, Natalia I.
author_sort Razouki, Zayd Adnan
collection PubMed
description NAFLD can occur in non-obese individuals with BMI < 25 kg/m(2). Our goal was to examine the prevalence and clinical factors associated with non-obese NAFLD using vibration-controlled transient elastography (VCTE) with controlled attenuation parameter which estimates steatosis and fibrosis among US adults. We aggregated data from the 2017–2018 cycle of NHANES and included adults (age ≥ 20 years) with BMI < 25 kg/m(2) with complete data for the survey, medical examination, and VCTE along with controlled attenuation parameter (CAP). We excluded participants with risks of other liver diseases. We considered patients to have non-obese NAFLD if CAP was >285 dB/m, or non-obese NAFLD fibrosis if this CAP criteria was met and liver stiffness was >8.6 kPa. We calculated the adjusted OR and 95% CI for associations with non-obese NAFLD using multivariable logistic regression. The prevalence of non-obese NAFLD was 6.2% and Asian Americans (12.2%) had the highest non-obese NAFLD prevalence. Clinical factors associated with non-obese NAFLD were advanced age and metabolic syndrome (OR(adjuste)(d) = 6.8, 95% CI 3.0–15.5). In a separate model, we found elevated glucose (OR(adjuste) = 4.1, 95% CI 2.1–7.9), triglycerides (OR(adjuste) = 3.8, 95% CI 1.7–8.5), and truncal fat (100-unit increase ORadjusted = 1.07, 95% CI: 1.04–1.10) were associated with higher odds of non-obese NAFLD. Meanwhile, low physical activity (OR(adjuste) = 2.9, 95% CI 1.2–7.1) was also positively associated with non-obese NAFLD. Non-obese NAFLD is prevalent in the US and is highly associated with metabolic conditions and syndrome. Our results support the importance of considering racial/ethnic differences when investigating NAFLD in a clinical setting.
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spelling pubmed-93315532022-07-29 Clinical Factors Associated with Non-Obese Nonalcoholic Fatty Liver Disease Detected among US Adults in the NHANES 2017–2018 Razouki, Zayd Adnan Zhang, Xiaotao Hwang, Jessica P. Heredia, Natalia I. J Clin Med Article NAFLD can occur in non-obese individuals with BMI < 25 kg/m(2). Our goal was to examine the prevalence and clinical factors associated with non-obese NAFLD using vibration-controlled transient elastography (VCTE) with controlled attenuation parameter which estimates steatosis and fibrosis among US adults. We aggregated data from the 2017–2018 cycle of NHANES and included adults (age ≥ 20 years) with BMI < 25 kg/m(2) with complete data for the survey, medical examination, and VCTE along with controlled attenuation parameter (CAP). We excluded participants with risks of other liver diseases. We considered patients to have non-obese NAFLD if CAP was >285 dB/m, or non-obese NAFLD fibrosis if this CAP criteria was met and liver stiffness was >8.6 kPa. We calculated the adjusted OR and 95% CI for associations with non-obese NAFLD using multivariable logistic regression. The prevalence of non-obese NAFLD was 6.2% and Asian Americans (12.2%) had the highest non-obese NAFLD prevalence. Clinical factors associated with non-obese NAFLD were advanced age and metabolic syndrome (OR(adjuste)(d) = 6.8, 95% CI 3.0–15.5). In a separate model, we found elevated glucose (OR(adjuste) = 4.1, 95% CI 2.1–7.9), triglycerides (OR(adjuste) = 3.8, 95% CI 1.7–8.5), and truncal fat (100-unit increase ORadjusted = 1.07, 95% CI: 1.04–1.10) were associated with higher odds of non-obese NAFLD. Meanwhile, low physical activity (OR(adjuste) = 2.9, 95% CI 1.2–7.1) was also positively associated with non-obese NAFLD. Non-obese NAFLD is prevalent in the US and is highly associated with metabolic conditions and syndrome. Our results support the importance of considering racial/ethnic differences when investigating NAFLD in a clinical setting. MDPI 2022-07-22 /pmc/articles/PMC9331553/ /pubmed/35893351 http://dx.doi.org/10.3390/jcm11154260 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Razouki, Zayd Adnan
Zhang, Xiaotao
Hwang, Jessica P.
Heredia, Natalia I.
Clinical Factors Associated with Non-Obese Nonalcoholic Fatty Liver Disease Detected among US Adults in the NHANES 2017–2018
title Clinical Factors Associated with Non-Obese Nonalcoholic Fatty Liver Disease Detected among US Adults in the NHANES 2017–2018
title_full Clinical Factors Associated with Non-Obese Nonalcoholic Fatty Liver Disease Detected among US Adults in the NHANES 2017–2018
title_fullStr Clinical Factors Associated with Non-Obese Nonalcoholic Fatty Liver Disease Detected among US Adults in the NHANES 2017–2018
title_full_unstemmed Clinical Factors Associated with Non-Obese Nonalcoholic Fatty Liver Disease Detected among US Adults in the NHANES 2017–2018
title_short Clinical Factors Associated with Non-Obese Nonalcoholic Fatty Liver Disease Detected among US Adults in the NHANES 2017–2018
title_sort clinical factors associated with non-obese nonalcoholic fatty liver disease detected among us adults in the nhanes 2017–2018
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9331553/
https://www.ncbi.nlm.nih.gov/pubmed/35893351
http://dx.doi.org/10.3390/jcm11154260
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