Evidence map›Paper›PMID 37301794›Full record

ArticleDiabetologia2023

Interaction between plasma phospholipid odd-chain fatty acids and GAD65 autoantibodies on the incidence of adult-onset diabetes: the EPIC-InterAct case-cohort study.

Anna-Maria Lampousi, Sofia Carlsson, Josefin E Löfvenborg, Natalia Cabrera-Castro, María-Dolores Chirlaque, Guy Fagherazzi, Paul W Franks, Christiane S Hampe, Paula Jakszyn, Albert Koulman and 13 more

Open access · hybridAbstract read
In one paragraph

Article in Diabetologia, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

7 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Molecular and cellular mechanisms of pentadecanoic acid.World journal of biological chemistry · 2025
    Review
  5. Article
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  7. Article
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

23 authors at 16 institutions in 10 countries.

Anna-Maria LampousiInstitute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden. annamaria.lampousi@ki.se.ORCID http://orcid.org/0000-0002-3640-3827
Sofia CarlssonInstitute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.ORCID http://orcid.org/0000-0002-9497-2331
Josefin E LöfvenborgInstitute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.ORCID http://orcid.org/0000-0002-0099-969X
Natalia Cabrera-CastroDepartment of Epidemiology, Regional Health Council, IMIB-Arrixaca, Murcia, Spain.
María-Dolores ChirlaqueDepartment of Epidemiology, Regional Health Council, IMIB-Arrixaca, Murcia, Spain.ORCID http://orcid.org/0000-0001-9242-3040
Guy FagherazziDeep Digital Phenotyping Research Unit, Department of Precision Health, Luxembourg Institute of Health, Strassen, Luxembourg.ORCID http://orcid.org/0000-0001-5033-5966
Paul W FranksDepartment of Clinical Sciences, Clinical Research Center, Skåne University Hospital, Lund University, Malmö, Sweden.ORCID http://orcid.org/0000-0002-0520-7604
Christiane S HampeDepartment of Medicine, University of Washington School of Medicine, Seattle, WA, USA.ORCID http://orcid.org/0000-0001-9111-6671
Paula JakszynUnit of Nutrition and Cancer, Cancer Epidemiology Research Program, Catalan Institute of Oncology (ICO-IDIBELL), Barcelona, Spain.ORCID http://orcid.org/0000-0003-0672-8847
Albert KoulmanMedical Research Council Epidemiology Unit, Institute of Metabolic Science, University of Cambridge School of Clinical Medicine, Cambridge, UK.ORCID http://orcid.org/0000-0001-9998-051X
Cecilie KyrøDanish Cancer Society Research Center, Copenhagen, Denmark.ORCID http://orcid.org/0000-0002-9083-8960
Conchi Moreno-IribasConsortium for Biomedical Research in Epidemiology and Public Health (CIBERESP), Madrid, Spain.ORCID http://orcid.org/0000-0001-6537-0131
Peter M NilssonDepartment of Clinical Sciences, Clinical Research Center, Skåne University Hospital, Lund University, Malmö, Sweden.ORCID http://orcid.org/0000-0002-5652-8459
Salvatore PanicoDipartimento di Medicina Clinica e Chirurgia, Federico II University, Naples, Italy.ORCID http://orcid.org/0000-0002-5498-8312
Keren PapierCancer Epidemiology Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0002-4102-6835
Yvonne T van der SchouwJulius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0002-4605-435X
Matthias B SchulzeDepartment of Molecular Epidemiology, German Institute of Human Nutrition Potsdam-Rehbruecke, Nuthetal, Germany.ORCID http://orcid.org/0000-0002-0830-5277
Elisabete WeiderpassInternational Agency for Research on Cancer, World Health Organization, Lyon, France.ORCID http://orcid.org/0000-0003-2237-0128
Raul Zamora-RosUnit of Nutrition and Cancer, Cancer Epidemiology Research Program, Catalan Institute of Oncology (ICO-IDIBELL), Barcelona, Spain.ORCID http://orcid.org/0000-0002-6236-6804
Nita G ForouhiMedical Research Council Epidemiology Unit, Institute of Metabolic Science, University of Cambridge School of Clinical Medicine, Cambridge, UK.ORCID http://orcid.org/0000-0002-5041-248X
Stephen J SharpMedical Research Council Epidemiology Unit, Institute of Metabolic Science, University of Cambridge School of Clinical Medicine, Cambridge, UK.ORCID http://orcid.org/0000-0003-2375-1440
Olov RolandssonDepartment of Public Health and Clinical Medicine, Family Medicine, Umeå University, Umeå, Sweden.ORCID http://orcid.org/0000-0002-1341-6828
Nicholas J WarehamMedical Research Council Epidemiology Unit, Institute of Metabolic Science, University of Cambridge School of Clinical Medicine, Cambridge, UK.ORCID http://orcid.org/0000-0003-1422-2993
University of Cambridge · GBInstitut Català d'Oncologia · ESInstituto Murciano de Investigación Biosanitaria · ESKarolinska Institutet · SELund University · SECentre international de recherche sur le cancer · FRDanish Cancer Society · DKFederico II University Hospital · ITInstituto de Salud Pública de Navarra · ESLuxembourg Institute of Health · LUNational Food Administration · SEUmeå University · SEUniversity of Oxford · GBUniversity of Potsdam · DEUniversity of Washington · USUtrecht University · NL

Funding

ISLET CELL MEMBRANE ANTIBODIES IN DIABTESR01DK026190 · NIDDK · UNIVERSITY OF WASHINGTON · PI HAMPE, CHRISTIANE S · 1986 to 2016
$4.9M
Medical Research Council MC_UU_00006/1Medical Research Council MC_UU_00006/3NIDDK NIH HHS R01 DK026190World Health Organization 001
6 · The paper itself

Abstract

aims/hypothesisIslet autoimmunity may progress to adult-onset diabetes. We investigated whether circulating odd-chain fatty acids (OCFA) 15:0 and 17:0, which are inversely associated with type 2 diabetes, interact with autoantibodies against GAD65 (GAD65Ab) on the incidence of adult-onset diabetes.

methodsWe used the European EPIC-InterAct case-cohort study including 11,124 incident adult-onset diabetes cases and a subcohort of 14,866 randomly selected individuals. Adjusted Prentice-weighted Cox regression estimated HRs and 95% CIs of diabetes in relation to 1 SD lower plasma phospholipid 15:0 and/or 17:0 concentrations or their main contributor, dairy intake, among GAD65Ab-negative and -positive individuals. Interactions between tertiles of OCFA and GAD65Ab status were estimated by proportion attributable to interaction (AP).

resultsLow concentrations of OCFA, particularly 17:0, were associated with a higher incidence of adult-onset diabetes in both GAD65Ab-negative (HR 1.55 [95% CI 1.48, 1.64]) and GAD65Ab-positive (HR 1.69 [95% CI 1.34, 2.13]) individuals. The combination of low 17:0 and high GAD65Ab positivity vs high 17:0 and GAD65Ab negativity conferred an HR of 7.51 (95% CI 4.83, 11.69), with evidence of additive interaction (AP 0.25 [95% CI 0.05, 0.45]). Low dairy intake was not associated with diabetes incidence in either GAD65Ab-negative (HR 0.98 [95% CI 0.94, 1.02]) or GAD65Ab-positive individuals (HR 0.97 [95% CI 0.79, 1.18]). CONCLUSIONS/

interpretationLow plasma phospholipid 17:0 concentrations may promote the progression from GAD65Ab positivity to adult-onset diabetes.

Indexed as

Diabetes Mellitus, Type 2AdultAutoantibodiesCohort StudiesFatty AcidsGlutamate DecarboxylaseHumansIncidencePhospholipidsAutoantibodiesFatty AcidsGlutamate DecarboxylasePhospholipidsDiabetesGAD65AbHeptadecanoicIslet autoimmunityOCFAPentadecanoic

Identifiers

PMID37301794
PMCPMC10317878
OpenAlexW4380203301

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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.