Metabolic abnormalities play a crucial role in non-obese people suffering from non-alcoholic fatty liver disease (NAFLD)
Letter to the Editor

Metabolic abnormalities play a crucial role in non-obese people suffering from non-alcoholic fatty liver disease (NAFLD)

Qing Ye1, Takanori Ito2, Linda Henry3, Mindie H. Nguyen3

1Department of Hepatology of The Third Central Hospital of Tianjin, Tianjin, China; 2Department of Gastroenterology and Hepatology, Nagoya University Graduate School of Medicine, Nagoya, Japan; 3Division of Gastroenterology and Hepatology, Stanford University Medical Center, Palo Alto, CA, USA

Correspondence to: Mindie H. Nguyen, MD, MAS. Professor of Medicine, Division of Gastroenterology and Hepatology, Stanford University Medical Center, Palo Alto, CA 94304, USA. Email: mindiehn@stanford.edu.

Submitted Jan 19, 2022. Accepted for publication Mar 14, 2022.

doi: 10.21037/hbsn-22-26


We read the article entitled “The presence of NAFLD in nonobese subjects increased the risk of metabolic abnormalities than obese subjects without NAFLD: A population-based cross-sectional study” by Hu et al. (1), which was published in the latest issue of Hepatobiliary Surgery Nutrition, with great pleasure. As the authors described, due to rapid urbanization and sedentary lifestyles, the prevalence of non-alcoholic fatty liver disease (NAFLD) has increased. In this population-based, cross-sectional health survey study, in which the data were obtained from community health centers, the investigators reported that the prevalence of NAFLD in Shanghai, China grew from 15% in 2005 to 32.7% in 2017 (1). To gain a better understanding of the prevalence of metabolic features in relation to NAFLD status, gender, and age, the authors quantified the risks of having different metabolic conditions between the following 4 groups: (I) the non-obese NAFLD group; (II) the non-obese non-NAFLD group; (III) the obese non-NAFLD group; and (IV) the obese NAFLD group (1).

We applaud the authors for their work in confirming the findings of previous studies (2-5) for their cohort in China. Additionally, their results that identified gender differences based on age and obesity are important in understanding how to better risk stratify persons for follow-up care and interventions. As most persons with NAFLD are treated in a community setting, guidelines have been developed to help identify both patients who are at risk of having NAFLD and those who should be referred to a specialist due to the potential presence of a more advanced disease (2,3). To this point, it would have been helpful to know how many persons were at risk for advanced disease and how the completion of the risk stratification would inform future practices, especially for the group with the highest risk of mortality (4). This is especially important given that better non-invasive tests for diagnosing advanced disease and fibrosis are coming to market (5,6).

However, we disagree with the authors’ conclusions that the presence of NAFLD in non-obese subjects significantly increases the risk for metabolic diseases. The exact pathophysiologic mechanisms of NAFLD disease development are still under study, but most researchers agree that NAFLD is not the cause of metabolic comorbidities and that those with certain metabolic comorbidities are at a higher risk for developing or finding NAFLD on examination (7). We know that non-obese NAFLD is not uncommon, and that the prognosis of such individuals may be worse (8). In general, as the prevalence of non-obese NAFLD increases with age (9), it is clear that the increase in metabolic complications with age is strongly related to the development of NAFLD.

Again, we would like to thank the authors for their thoughtful study. As NAFLD continues to increase, the characterization of those with NAFLD has gained much attention, which is important if appropriate interventions are to be to developed; however, to reverse the course of the disease, a better understanding of how to increase awareness of this disease is also needed (10,11) as are interventions that are both successful and accessible.


Acknowledgments

Funding: None.


Footnote

Provenance and Peer Review: This article was a standard submission to the editorial office, Hepatobiliary Surgery and Nutrition. The article did not undergo external peer review.

Conflicts of Interest: All the authors have completed the ICMJE uniform disclosure form (available at https://hbsn.amegroups.com/article/view/10.21037/hbsn-22-26/coif). MHN reports receiving grants or contracts from Glycotest, Gilead, Pfizer, Enanta, B.K. Kee Foundation, National Cancer Institute, Vir Biotech; and consulting fees from Spring Bank, Novartis, Janssen, Gilead, Eisai, Bayer, Intercept, Exact Science, Laboratory of Advanced Medicine, Helio, Eli Lilly. The other authors have no conflicts of interest to declare.

Ethical Statement: The authors are accountable for all aspects of the work, including ensuring that any questions related to the accuracy or integrity of any part of the work have been appropriately investigated and resolved.

Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.


References

  1. Hu PF, Zeng X, Zou ZY, et al. The presence of NAFLD in nonobese subjects increased the risk of metabolic abnormalities than obese subjects without NAFLD: a population-based cross-sectional study. Hepatobiliary Surg Nutr 2021;10:811-24. [Crossref] [PubMed]
  2. Younossi ZM, Corey KE, Alkhouri N, et al. Clinical assessment for high-risk patients with non-alcoholic fatty liver disease in primary care and diabetology practices. Aliment Pharmacol Ther 2020;52:513-26. [Crossref] [PubMed]
  3. Lazarus JV, Anstee QM, Hagström H, et al. Defining comprehensive models of care for NAFLD. Nat Rev Gastroenterol Hepatol 2021;18:717-29. [Crossref] [PubMed]
  4. Dulai PS, Singh S, Patel J, et al. Increased risk of mortality by fibrosis stage in nonalcoholic fatty liver disease: Systematic review and meta-analysis. Hepatology 2017;65:1557-65. [Crossref] [PubMed]
  5. Younossi ZM, Noureddin M, Bernstein D, et al. Role of Noninvasive Tests in Clinical Gastroenterology Practices to Identify Patients With Nonalcoholic Steatohepatitis at High Risk of Adverse Outcomes: Expert Panel Recommendations. Am J Gastroenterol 2021;116:254-62. [Crossref] [PubMed]
  6. Brunt EM, Kleiner DE, Carpenter DH, et al. NAFLD: Reporting Histologic Findings in Clinical Practice. Hepatology 2021;73:2028-38. [Crossref] [PubMed]
  7. Li J, Zou B, Yeo YH, et al. Prevalence, incidence, and outcome of non-alcoholic fatty liver disease in Asia, 1999-2019: a systematic review and meta-analysis. Lancet Gastroenterol Hepatol 2019;4:389-98. [Crossref] [PubMed]
  8. Ye Q, Zou B, Yeo YH, et al. Global prevalence, incidence, and outcomes of non-obese or lean non-alcoholic fatty liver disease: a systematic review and meta-analysis. Lancet Gastroenterol Hepatol 2020;5:739-52. [Crossref] [PubMed]
  9. Ito T, Ishigami M, Zou B, et al. The epidemiology of NAFLD and lean NAFLD in Japan: a meta-analysis with individual and forecasting analysis, 1995-2040. Hepatol Int 2021;15:366-79. [Crossref] [PubMed]
  10. Alqahtani SA, Paik JM, Biswas R, et al. Poor Awareness of Liver Disease Among Adults With NAFLD in the United States. Hepatol Commun 2021;5:1833-47. [Crossref] [PubMed]
  11. Le MH, Yeo YH, Cheung R, et al. Ethnic influence on nonalcoholic fatty liver disease prevalence and lack of disease awareness in the United States, 2011-2016. J Intern Med 2020;287:711-22. [Crossref] [PubMed]
Cite this article as: Ye Q, Ito T, Henry L, Nguyen MH. Metabolic abnormalities play a crucial role in non-obese people suffering from non-alcoholic fatty liver disease (NAFLD). HepatoBiliary Surg Nutr 2022;11(2):333-334. doi: 10.21037/hbsn-22-26

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