Evidence map›Paper›PMID 35709010›Full record

ArticleDiabetes2023

Autoantibodies to Perilipin-1 Define a Subset of Acquired Generalized Lipodystrophy.

Caleigh Mandel-Brehm, Sara E Vazquez, Christopher Liverman, Mickie Cheng, Zoe Quandt, Andrew F Kung, Audrey Parent, Brenda Miao, Emmanuel Disse, Christine Cugnet-Anceau and 17 more

Open access · greenAbstract read
In one paragraph

Article in Diabetes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

24 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
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  8. Review
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  10. Perilipin-1 autoantibodies are a robust marker of acquired lipodystrophy and may precede clinical detection.Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology · 2025
    Article
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  15. Aire in Autoimmunity.Annual review of immunology · 2024
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

27 authors at 9 institutions in 4 countries.

Caleigh Mandel-BrehmDepartment of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, CA.ORCID 0000-0001-7764-6529
Sara E VazquezDepartment of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, CA.
Christopher LivermanDepartment of Pathology, University of California, San Francisco, San Francisco, CA.
Mickie ChengDiabetes Center, University of California, San Francisco, San Francisco, CA.
Zoe QuandtDiabetes Center, University of California, San Francisco, San Francisco, CA.
Andrew F KungDepartment of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, CA.
Audrey ParentDiabetes Center, University of California, San Francisco, San Francisco, CA.
Brenda MiaoDepartment of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, CA.
Emmanuel DisseEndocrinology Diabetology and Nutrition Department, Lyon Sud Hospital, Hospices Civils de Lyon, Pierre-Bénite, France.ORCID 0000-0002-4045-0503
Christine Cugnet-AnceauEndocrinology Diabetology and Nutrition Department, Lyon Sud Hospital, Hospices Civils de Lyon, Pierre-Bénite, France.
Stéphane DalleImmuCare, Cancer Institute of Hospices Civils de Lyon (IC-HCL), Lyon, France.
Elizaveta OrlovaEndocrinology Research Centre, Institute of Paediatric Endocrinology, Moscow, Russia.
Elena FrolovaNational Medical Research Center of Children's Health, Moscow, Russia.
Diana AlbaDiabetes Center, University of California, San Francisco, San Francisco, CA.ORCID 0000-0002-1398-9861
Aaron MichelsBarbara Davis Center for Childhood Diabetes, University of Colorado School of Medicine, Aurora, CO.ORCID 0000-0003-3766-5244
Bergithe E OftedalUniversity of Bergen, Bergen, Norway.
Michail S LionakisFungal Pathogenesis Section, Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD.
Eystein S HusebyeDepartment of Medicine, Haukeland University Hospital, Bergen, Norway.
Anil K AgarwalDivision of Nutrition and Metabolic Diseases, Department of Internal Medicine, UT Southwestern Medical Center, Dallas, TX.
Xilong LiDepartment of Population and Data Sciences, UT Southwestern Medical Center, Dallas, TX.
Chengsong ZhuDepartment of Immunology, UT Southwestern Medical Center, Dallas, TX.
Quan LiDepartment of Immunology, UT Southwestern Medical Center, Dallas, TX.
Elif OralDivision of Metabolism, Endocrinology & Diabetes and Caswell Diabetes Institute, University of Michigan, Ann Arbor, MI.
Rebecca BrownEunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD.ORCID 0000-0002-2589-7382
Mark S AndersonDiabetes Center, University of California, San Francisco, San Francisco, CA.ORCID 0000-0002-3093-4758
Abhimanyu GargDivision of Nutrition and Metabolic Diseases, Department of Internal Medicine, UT Southwestern Medical Center, Dallas, TX.ORCID 0000-0001-7209-6986
Joseph L DeRisiDepartment of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, CA.
University of California, San Francisco · USSouthwestern Medical Center · USHospices Civils de Lyon · FRHaukeland University Hospital · NONational Institutes of Health · USEndocrinology Research Center · RUScientific Center of Children's Health · RUUniversity of Colorado Denver · USUniversity of Michigan · US

Funding

Immunopathogenesis of Fungal InfectionsZIAAI001175 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI LIONAKIS, MICHAIL · 2012 to 2025
$23.9M
Project 3: Epitope Selection in Type 1 DiabetesP01AI118688 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KAPPLER, JOHN W · 2016 to 2020
$8.4M
BMI Bioinformatics Training GrantsT32GM067547 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HERNANDEZ, RYAN D. · 2003 to 2022
$6.6M
Genetic and Metabolic Basis of Familial LipodystrophiesR01DK105448 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI Abhimanyu Garg · 2015 to 2026
$6.5M
Molecular and Clinical Studies of Insulin ResistanceZIADK047050 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI BROWN, REBECCA · 2009 to 2025
$6.1M
Autoimmune Encephalitis - Ataxia and Psychiatric Disease: Identifying and Characterizing Novel Antibody TargetsR01MH122471 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI JOSEPH L. DERISI, SAMUEL JEREMY PLEASURE · 2020 to 2026
$4.7M
Modeling autoimmune pathogenesis and beta cell destruction by T1D immune systemsU01DK123559 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI ANDERSON, MARK S, PARENT, AUDREY · 2019 to 2023
$4.3M
Thymic medullary epithelial cell turnover and control of immune toleranceR37AI097457 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Mark S Anderson · 2017 to 2026
$4.0M
Molecular understanding of self immunity in the brainK99NS117800 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MANDEL-BREHM, CALEIGH · 2020 to 2021
$211k
The Role of RFX6 in Type 1 DiabetesF30DK123915 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI VAZQUEZ, SARA · 2019 to 2022
$183k
Intramural NIH HHS ZIA AI001175NIAID NIH HHS P01 AI118688NIAID NIH HHS R37 AI097457NIDDK NIH HHS F30 DK123915NIDDK NIH HHS R01 DK105448NIDDK NIH HHS U01 DK123559NIGMS NIH HHS T32 GM067547NIMH NIH HHS R01 MH122471NINDS NIH HHS K99 NS117800
6 · The paper itself

Abstract

Acquired lipodystrophy is often characterized as an idiopathic subtype of lipodystrophy. Despite suspicion of an immune-mediated pathology, biomarkers such as autoantibodies are generally lacking. Here, we used an unbiased proteome-wide screening approach to identify autoantibodies to the adipocyte-specific lipid droplet protein perilipin 1 (PLIN1) in a murine model of autoimmune polyendocrine syndrome type 1 (APS1). We then tested for PLIN1 autoantibodies in human subjects with acquired lipodystrophy with two independent severe breaks in immune tolerance (including APS1) along with control subjects using a specific radioligand binding assay and indirect immunofluorescence on fat tissue. We identified autoantibodies to PLIN1 in these two cases, including the first reported case of APS1 with acquired lipodystrophy and a second patient who acquired lipodystrophy as an immune-related adverse event following cancer immunotherapy. Lastly, we also found PLIN1 autoantibodies to be specifically enriched in a subset of patients with acquired generalized lipodystrophy (17 of 46 [37%]), particularly those with panniculitis and other features of autoimmunity. These data lend additional support to new literature that suggests that PLIN1 autoantibodies represent a marker of acquired autoimmune lipodystrophies and further link them to a break in immune tolerance.

Indexed as

LipodystrophyLipodystrophy, Congenital GeneralizedAdipose TissueAnimalsAutoantibodiesHumansMicePerilipin-1AutoantibodiesPerilipin-1

Identifiers

PMID35709010
PMCPMC9797316
OpenAlexW4282975426

What OpenQuestion holds

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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.