Cited by 81Nutrition, Genetics, and DiseaseDiabetes Management and ResearchDiabetes Treatment and Management

Digital twin-enabled personalized nutrition improves metabolic dysfunction-associated fatty liver disease in type 2 diabetes: results of a 1-year randomized controlled study

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Joshi, Shashank, Shamanna, Paramesh, Dharmalingam, Mala, Vadavi, Arun, Keshavamurthy, Ashok, Shah, Lisa, Mechanick, Jeffrey I.·2023·Endocrine Practice

Abstract

OBJECTIVE: Postprandial hyperglycemia drives insulin resistance and inflammation, leading to metabolic dysfunction-associated fatty liver disease (MAFLD). Prediction of postprandial glycemic responses by digital twin (DT) technology can fashion a personalized nutrition, activity, and sleep to treat type 2 diabetes (T2D) and MAFLD. This study examines the effects of DT-enabled personalized nutrition, activity, and sleep on glycemic status, surrogate markers of MAFLD, and magnetic resonance imaging-derived proton density fat fraction (MRI-PDFF) in patients with T2D. METHODS: In an open-label randomized trial (2:1), 319 people with T2D were eligible to intervention (DT) or standard care (SC). DT patients followed personalized meal plans with foods suggested by artificial intelligence with least predicted postprandial glycemic response. The primary end point was to compare change in hemoglobin A1c (HbA1c) and medicine reduction between the DT and SC groups. Key secondary end points included remission to compare liver function test scores and visceral adiposity using MRI. RESULTS: was significantly better for DT than for SC (-2.9 [1.8] vs -0.3 [1.2]; P < .001) at 1 year with 72.7% remission of T2D. In patients with abnormal baseline values, significant improvements were seen in DT vs SC patients from baseline to 1 year in nonalcoholic fatty liver disease liver fat score (mean [SD]; -2.5 [2.0] vs -0.1 [1.5]; P < .001) and nonalcoholic fatty liver disease fibrosis score (-1.20 [0.9] vs -0.1 [1.0]; P < .001), respectively. Improvements are seen with DT compared with SC in other liver fat, fibrosis score, and %liver fat by MRI-PDFF. CONCLUSION: At 1 year, DT-enabled personalized treatment significantly improved hyperglycemia and surrogate markers of MAFLD and MRI-PDFF.

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Authors
Joshi, S., Shamanna, P., Dharmalingam, M., Vadavi, A., Keshavamurthy, A., Shah, L., & Mechanick, J. I.
Affiliations
  • Lilavati Hospital & Research Centre (IN)
  • Bangalore Diabetes Centre (IN)
  • M.S. Ramaiah Medical College (IN)
  • Icahn School of Medicine at Mount Sinai (US)
Corresponding author
  • Shamanna, Paramesh
  • Vadavi, Arun
  • Keshavamurthy, Ashok
  • Shah, Lisa
  • Mechanick, Jeffrey I.
Venue
Endocrine Practice
Publisher
Elsevier BV
Published
2023-12
Volume
29
Issue
12
Pages
960-970
ISSN
1530-891X (ISSN-L)
OpenAlex
W4387165744
Cited by
81
References
27
Citations by year
2026: 35 · 2025: 27 · 2024: 19
FWCI
13.30
Type
journal article
Language
en
Open access
Locations
  • Endocrine Practice (publishedVersion, cc-by)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Nutrition, Genetics, and Disease
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Management and Research
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
Keywords
digital twin, personalized nutrition, non-alcoholic fatty liver disease, type 2 diabetes, postprandial hyperglycemia, insulin resistance, HbA1c, diabetes remission, liver fat fraction, liver fibrosis, visceral fat
MeSH terms
Artificial Intelligence, Diabetes Mellitus, Type 2, Fibrosis, Glycated Hemoglobin, Humans, Liver, Magnetic Resonance Imaging, Biomarkers, Non-alcoholic Fatty Liver Disease

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