Evidence mapPaperPMID 35522035Full record

ArticleDiabetes care2022

An Atypical Form of Diabetes Among Individuals With Low BMI.

Eric Lontchi-Yimagou, Riddhi Dasgupta, Shajith Anoop, Sylvia Kehlenbrink, Sudha Koppaka, Akankasha Goyal, Padmanaban Venkatesan, Roshan Livingstone, Kenny Ye, Aaron Chapla and 13 more

Open access · bronzeAbstract read
In one paragraph

Article in Diabetes care, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
7.0field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 64 citations in OpenAlex.

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  7. Undernutrition-related diabetes in mice is linked to early undernutrition.American journal of physiology. Endocrinology and metabolism · 2026
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  17. Phenotypic and Genetic Diversity in Diabetes Across Populations.The Journal of clinical endocrinology and metabolism · 2025
    Review
  18. Heterogeneity of type 2 diabetes in rural India.Frontiers in endocrinology · 2025
    Article
  19. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors at 5 institutions in 2 countries.

Eric Lontchi-YimagouAlbert Einstein College of Medicine, Bronx, NY.
Riddhi DasguptaDepartment of Endocrinology, Diabetes and Metabolism, Christian Medical College, Vellore, Vellore, India.ORCID 0000-0003-0838-1015
Shajith AnoopDepartment of Endocrinology, Diabetes and Metabolism, Christian Medical College, Vellore, Vellore, India.
Sylvia KehlenbrinkBrigham and Women's Hospital, Harvard Medical School, Boston, MA.
Sudha KoppakaAlbert Einstein College of Medicine, Bronx, NY.
Akankasha GoyalNew York University Langone Health, New York, NY.
Padmanaban VenkatesanDepartment of Endocrinology, Diabetes and Metabolism, Christian Medical College, Vellore, Vellore, India.
Roshan LivingstoneDepartment of Endocrinology, Diabetes and Metabolism, Christian Medical College, Vellore, Vellore, India.
Kenny YeAlbert Einstein College of Medicine, Bronx, NY.
Aaron ChaplaDepartment of Endocrinology, Diabetes and Metabolism, Christian Medical College, Vellore, Vellore, India.ORCID 0000-0003-4157-6041
Michelle CareyCenter for Drug Evaluation and Research, U.S. Food and Drug Administration, Silver Spring, MD.
Arun JoseDepartment of Biochemistry, Christian Medical College, Vellore, Vellore, India.
Grace RebekahDepartment of Biostatistics, Christian Medical College Vellore, Vellore, India.
Anneka WickramanayakeLaterite, Kigali, Rwanda.
Mini JosephDepartment of Endocrinology, Diabetes and Metabolism, Christian Medical College, Vellore, Vellore, India.
Priyanka MathiasAlbert Einstein College of Medicine, Bronx, NY.ORCID 0000-0002-9495-677X
Anjali ManavalanAlbert Einstein College of Medicine, Bronx, NY.
Mathews Edatharayil KurianDepartment of Endocrinology, Diabetes and Metabolism, Christian Medical College, Vellore, Vellore, India.
Mercy InbakumariDepartment of Endocrinology, Diabetes and Metabolism, Christian Medical College, Vellore, Vellore, India.
Flory ChristinaDepartment of Endocrinology, Diabetes and Metabolism, Christian Medical College, Vellore, Vellore, India.
Daniel SteinAlbert Einstein College of Medicine, Bronx, NY.
Nihal ThomasDepartment of Endocrinology, Diabetes and Metabolism, Christian Medical College, Vellore, Vellore, India.
Meredith HawkinsAlbert Einstein College of Medicine, Bronx, NY.ORCID 0000-0003-3121-010X
Christian Medical College, Vellore · INAlbert Einstein College of Medicine · USBrigham and Women's Hospital · USNYU Langone Health · USUnited States Food and Drug Administration · US

Funding

PROMOTING OPHTHALMIC SCREENING IN MANAGED CAREP60DK020541 · YESHIVA UNIVERSITY · 1986 to 2005
$12.6M
NYR-Diabetes Research Center (NYR-DRC)P30DK020541 · ALBERT EINSTEIN COLLEGE OF MEDICINE · 2025 to 2025
$2.4M
NIDDK NIH HHS P30 DK020541NIDDK NIH HHS P60 DK020541
6 · The paper itself

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.

Indexed as

Diabetes Mellitus, Type 2Insulin ResistanceBlood GlucoseBody Mass IndexGlucose Clamp TechniqueHumansInsulinBlood GlucoseInsulin

Identifiers

PMID35522035
PMCPMC9184261
OpenAlexW4229037939

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.