Evidence map›Paper›PMID 23157689›Full record

ArticleDiabetic medicine : a journal of the British Diabetic Association2013

Apolipoprotein M can discriminate HNF1A-MODY from Type 1 diabetes.

S A Mughal, R Park, N Nowak, A L Gloyn, F Karpe, H Matile, M T Malecki, M I McCarthy, M Stoffel, K R Owen

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In one paragraph

Article in Diabetic medicine : a journal of the British Diabetic Association, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
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  8. Apolipoprotein M gene polymorphisms in childhood-onset type 1 diabetes in southern Brazil.International journal of biochemistry and molecular biology · 2023
    Article
  9. Article
  10. Review
  11. Update on Monogenic Diabetes in Korea.Diabetes & metabolism journal · 2020
    Review
  12. Article
  13. Using Clinical Indices to Distinguish MODY2 (GCK Mutation) and MODY3 (HNF1A Mutation) from Type 1 Diabetes in a Young Chinese Population.Diabetes therapy : research, treatment and education of diabetes and related disorders · 2019
    Article
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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

10 authors at 4 institutions in 3 countries.

S A MughalOxford Centre for Diabetes, Endocrinology and Metabolism, University of Oxford, Oxford, UK.
R Park
N Nowak
A L Gloyn
F Karpe
H Matile
M T Malecki
M I McCarthy
M Stoffel
K R Owen
University of Oxford · GBJagiellonian University · PLCentre for Human Genetics · GBRoche (Switzerland) · CH

Funding

Department of Health DHCS/07/07/008Wellcome Trust 090532Wellcome Trust 095101Wellcome Trust 095101/Z/10/Z
6 · The paper itself

Abstract

aimsMissed diagnosis of maturity-onset diabetes of the young (MODY) has led to an interest in biomarkers that enable efficient prioritization of patients for definitive molecular testing. Apolipoprotein M (apoM) was suggested as a biomarker for hepatocyte nuclear factor 1 alpha (HNF1A)-MODY because of its reduced expression in Hnf1a(-/-) mice. However, subsequent human studies examining apoM as a biomarker have yielded conflicting results. We aimed to evaluate apoM as a biomarker for HNF1A-MODY using a highly specific and sensitive ELISA.

methodsApoM concentration was measured in subjects with HNF1A-MODY (n = 69), Type 1 diabetes (n = 50), Type 2 diabetes (n = 120) and healthy control subjects (n = 100). The discriminative accuracy of apoM and of the apoM/HDL ratio for diabetes aetiology was evaluated.

resultsMean (standard deviation) serum apoM concentration (μmol/l) was significantly lower for subjects with HNF1A-MODY [0.86 (0.29)], than for those with Type 1 diabetes [1.37 (0.26), P = 3.1 × 10(-18) ) and control subjects [1.34 (0.22), P = 7.2 × 10(-19) ). There was no significant difference in apoM concentration between subjects with HNF1A-MODY and Type 2 diabetes [0.89 (0.28), P = 0.13]. The C-statistic measure of discriminative accuracy for apoM was 0.91 for HNF1A-MODY vs. Type 1 diabetes, indicating high discriminative accuracy. The apoM/HDL ratio was significantly lower in HNF1A-MODY than other study groups. However, this ratio did not perform well in discriminating HNF1A-MODY from either Type 1 diabetes (C-statistic = 0.79) or Type 2 diabetes (C-statistic = 0.68).

conclusionsWe confirm an earlier report that serum apoM levels are lower in HNF1A-MODY than in controls. Serum apoM provides good discrimination between HNF1A-MODY and Type 1 diabetes and warrants further investigation for clinical utility in diabetes diagnostics.

Indexed as

AdultAge of OnsetAnimalsApolipoproteinsApolipoproteins MBiomarkersBody Mass IndexDiabetes Mellitus, Type 1Diabetes Mellitus, Type 2Diagnosis, DifferentialEnzyme-Linked Immunosorbent AssayFemaleGene Expression RegulationHepatocyte Nuclear Factor 1-alphaHumansLipocalinsApolipoproteinsApolipoproteins MAPOM protein, humanBiomarkersHepatocyte Nuclear Factor 1-alphaHNF1A protein, humanLipocalins

Identifiers

PMID23157689
PMCPMC4193536
OpenAlexW2083433288

What OpenQuestion holds

Textmetadata
LicenceTDM
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 OpenQuestion graph.