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ORIGINAL RESEARCH article

Front. Endocrinol.

Sec. Bone Research

This article is part of the Research TopicThe MASLD Spectrum: An emerging epidemic of Cardiometabolic and Extra-Hepatic DimensionsView all 4 articles

Metabolic Dysfunction-Associated Steatotic Liver Disease and Bone Mineral Density in Type 2 Diabetes Mellitus: Insights from a Single-Centre Cross-Sectional Study in North India

Provisionally accepted
Dogga  SudhakarDogga Sudhakar1,2Sumit  RajotiyaSumit Rajotiya2,3*Sourav  DebnathSourav Debnath2,3Nishant  JainNishant Jain1,2Monal  SherekarMonal Sherekar4Shivang  MishraShivang Mishra2,3Anurag  Kumar SinghAnurag Kumar Singh2,3MAHAVEER  SINGHMAHAVEER SINGH1,2*Avinash  MunshiAvinash Munshi1,2Deepak  NathiyaDeepak Nathiya2,3Balvir  Singh TomarBalvir Singh Tomar1,2
  • 1National Institute of Medical Sciences & Research, Jaipur, India
  • 2NIMS University, Jaipur, India
  • 3NIMS Institute of Pharmacy, Jaipur, India
  • 4Family Medicine consultant, Connect and Heal Primary Care Pvt Ltd., , Karnataka;, Bengaluru, India

The final, formatted version of the article will be published soon.

Introduction: Metabolic dysfunction-associated steatotic liver disease (MASLD), recently redefined from non-alcoholic fatty liver disease, commonly coexists with type 2 diabetes mellitus and may adversely affect skeletal health through inflammation and insulin resistance. However, research on site-specific bone mineral density (BMD) effects in South Asian populations, particularly Indians, remains limited. This study aimed to evaluate the association between MASLD and BMD at different skeletal sites among adults with type 2 diabetes mellitus in North India. Methods: This cross-sectional study included 100 adults (50 with T2DM and 50 controls) at a tertiary care center in Jaipur, India. MASLD was evaluated using the fibrosis-4 (FIB-4) index, hepato-renal index, and two-dimensional shear wave elastography. BMD at lumbar spine (L1-L4), left total hip (proximal femur), and left forearm was assessed by dual-energy X-ray absorptiometry. Associations between MASLD parameters and BMD were analyzed using multivariable linear regression, adjusting for age, sex, and smoking status. Results: T2DM patients showed significantly lower lumbar spine (L1-L4) BMD (0.93 vs. 0.98 g/cm²; P=0.026) and T-scores (-1.33 vs. -0.72; P=0.004), especially in males ≥50 years. No statistically significant differences were observed in proximal femur and forearm BMD between groups. FIB-4 scores were higher (P=0.004), with 60% at intermediate-to-high fibrosis risk versus 28% of controls; advanced fibrosis occurred in 10% vs. 2%. Hepatic steatosis positively associated with hip BMD (β=0.738; P=0.022). Conclusion: This study establishes significant, site-specific associations between MASLD and reduced bone mineral density in type 2 diabetes mellitus patients, particularly affecting trabecular-rich, weight-bearing skeletal sites. The complex relationship between hepatic steatosis and skeletal health highlights the multisystemic nature of metabolic dysfunction. These findings support integrating bone health assessments and non-invasive hepatic fibrosis screening into routine diabetes care to improve early risk stratification.

Keywords: bone mineral density, fibrosis-4 index, India, Metabolic dysfunction-associated steatotic liver disease, type 2 diabetes mellitus

Received: 02 Dec 2025; Accepted: 12 Feb 2026.

Copyright: © 2026 Sudhakar, Rajotiya, Debnath, Jain, Sherekar, Mishra, Singh, SINGH, Munshi, Nathiya and Tomar. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence:
Sumit Rajotiya
MAHAVEER SINGH

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