Evidence map›Paper›PMID 35138411›Full record

ArticleDiabetologia2022

Understanding the pathogenesis of lean non-autoimmune diabetes in an African population with newly diagnosed diabetes.

Davis Kibirige, Isaac Sekitoleko, William Lumu, Angus G Jones, Andrew T Hattersley, Liam Smeeth, Moffat J Nyirenda

Open access · hybridAbstract read
In one paragraph

Article in Diabetologia, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
8.4field-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

40 citing papers in PubMed, 51 citations in OpenAlex.

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  17. Phenotypic and Genetic Diversity in Diabetes Across Populations.The Journal of clinical endocrinology and metabolism · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 2 countries.

Davis KibirigeNon-Communicable Diseases Program, Medical Research Council/Uganda Virus Research Institute and London School of Hygiene and Tropical Medicine Uganda Research Unit, Entebbe, Uganda. kibirigedavis@gmail.com.ORCID 0000-0001-5127-3031
Isaac SekitolekoNon-Communicable Diseases Program, Medical Research Council/Uganda Virus Research Institute and London School of Hygiene and Tropical Medicine Uganda Research Unit, Entebbe, Uganda.
William LumuDepartment of Medicine, Mengo Hospital, Kampala, Uganda.ORCID 0000-0002-4530-8012
Angus G JonesInstitute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK.ORCID 0000-0002-0883-7599
Andrew T HattersleyInstitute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK.ORCID 0000-0001-5620-473X
Liam SmeethDepartment of Non-Communicable Disease Epidemiology, Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, UK.ORCID 0000-0002-9168-6022
Moffat J NyirendaNon-Communicable Diseases Program, Medical Research Council/Uganda Virus Research Institute and London School of Hygiene and Tropical Medicine Uganda Research Unit, Entebbe, Uganda.ORCID 0000-0003-2120-4806
London School of Hygiene & Tropical Medicine · GBUniversity of Exeter · GBMengo Hospital · UGUganda Virus Research Institute · UG

Funding

Department of Health 17/63/131Department of Health CS-2015-15-018Medical Research Council MC_UP_1204/16Wellcome TrustWellcome Trust 098395/Z/12/Z
6 · The paper itself

Abstract

aims/hypothesisApparent type 2 diabetes is increasingly reported in lean adult individuals in sub-Saharan Africa. However, studies undertaking robust clinical and metabolic characterisation of lean individuals with new-onset type 2 diabetes are limited in this population. This cross-sectional study aimed to perform a detailed clinical and metabolic characterisation of newly diagnosed adult patients with diabetes in Uganda, in order to compare features between lean and non-lean individuals.

methodsSocio-demographic, clinical, biophysical and metabolic (including oral glucose tolerance test) data were collected on 568 adult patients with newly diagnosed diabetes. Participants were screened for islet autoantibodies to exclude those with autoimmune diabetes. The remaining participants (with type 2 diabetes) were then classified as lean (BMI <25 kg/m

resultsThirty-four participants (6.4%) were excluded from analyses because they were positive for pancreatic autoantibodies, and a further 34 participants because they had incomplete data. For the remaining 500 participants, the median (IQR) age, BMI and HbA CONCLUSIONS/

interpretationApproximately one-third of participants with incident adult-onset non-autoimmune diabetes had BMI <25 kg/m

Indexed as

Diabetes Mellitus, Type 1Diabetes Mellitus, Type 2AdultAutoantibodiesBlood GlucoseCross-Sectional StudiesFemaleHumansInsulinMaleMiddle AgedAutoantibodiesBlood GlucoseInsulinBeta cell dysfunctionLean non-autoimmune diabetesNewly diagnosed diabetes sub-Saharan AfricaType 2 diabetesUganda

Identifiers

PMID35138411
PMCPMC8894297
OpenAlexW4210845824

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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 OpenQuestion graph.