An Atypical Form of Diabetes Among Individuals With Low BMI

Author:

Lontchi-Yimagou Eric1,Dasgupta Riddhi2ORCID,Anoop Shajith2,Kehlenbrink Sylvia3,Koppaka Sudha1,Goyal Akankasha4,Venkatesan Padmanaban2,Livingstone Roshan2,Ye Kenny1,Chapla Aaron2ORCID,Carey Michelle5,Jose Arun6,Rebekah Grace7,Wickramanayake Anneka8,Joseph Mini2,Mathias Priyanka1ORCID,Manavalan Anjali1,Kurian Mathews Edatharayil2,Inbakumari Mercy2,Christina Flory2,Stein Daniel1,Thomas Nihal2,Hawkins Meredith1ORCID

Affiliation:

1. 1Albert Einstein College of Medicine, Bronx, NY

2. 2Department of Endocrinology, Diabetes and Metabolism, Christian Medical College, Vellore, Vellore, India

3. 3Brigham and Women’s Hospital, Harvard Medical School, Boston, MA

4. 4New York University Langone Health, New York, NY

5. 5Center for Drug Evaluation and Research, U.S. Food and Drug Administration, Silver Spring, MD

6. 6Department of Biochemistry, Christian Medical College, Vellore, Vellore, India

7. 7Department of Biostatistics, Christian Medical College Vellore, Vellore, India

8. 8Laterite, Kigali, Rwanda

Abstract

OBJECTIVEDiabetes among individuals with low BMI (<19 kg/m2) has been recognized for >60 years as a prevalent entity in low- and middle-income countries (LMICs) and was formally classified as “malnutrition-related diabetes mellitus” by the World Health Organization (WHO) in 1985. Since the WHO withdrew this category in 1999, our objective was to define the metabolic characteristics of these individuals to establish that this is a distinct form of diabetes.RESEARCH DESIGN AND METHODSState-of-the-art metabolic studies were used to characterize Indian individuals with “low BMI diabetes” (LD) in whom all known forms of diabetes were excluded by immunogenetic analysis. They were compared with demographically matched groups: a group with type 1 diabetes (T1D), a group with type 2 diabetes (T2D), and a group without diabetes. Insulin secretion was assessed by C-peptide deconvolution. Hepatic and peripheral insulin sensitivity were analyzed with stepped hyperinsulinemic-euglycemic pancreatic clamp studies. Hepatic and myocellular lipid contents were assessed with 1H-nuclear magnetic resonance spectroscopy.RESULTSThe total insulin secretory response was lower in the LD group in comparison with the lean group without diabetes and the T2D group. Endogenous glucose production was significantly lower in the LD group than the T2D group (mean ± SEM 0.50 ± 0.1 vs. 0.84 ± 0.1 mg/kg · min, respectively; P < 0.05). Glucose uptake was significantly higher in the LD group in comparison with the T2D group (10.1 ± 0.7 vs. 4.2 ± 0.5 mg/kg · min; P < 0.001). Visceral adipose tissue and hepatocellular lipids were significantly lower in LD than in T2D.CONCLUSIONSThese studies are the first to demonstrate that LD individuals in LMICs have a unique metabolic profile, suggesting that this is a distinct entity that warrants further investigation.

Publisher

American Diabetes Association

Subject

Advanced and Specialized Nursing,Endocrinology, Diabetes and Metabolism,Internal Medicine

Reference54 articles.

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2. HLA-DR and -DQ antigens in malnutrition-related diabetes mellitus in Ethiopians: a clue to its etiology?;Abdulkadir;Tissue Antigens,1989

3. Protein deficient diabetes mellitus (PDDM) in India;Tripathy;Int J Diabetes Dev Ctries,1993

4. Malnutrition-related diabetes mellitus in young adult diabetic patients attending a Nigerian diabetic clinic;Akanji;J Trop Med Hyg,1990

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