Evidence map›Paper›PMID 30283460›Full record

ArticleFrontiers in immunology2018

Autoantibodies Against Perilipin 1 as a Cause of Acquired Generalized Lipodystrophy.

Fernando Corvillo, Verónica Aparicio, Alberto López-Lera, Sofía Garrido, David Araújo-Vilar, María P de Miguel, Margarita López-Trascasa

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 16% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Pooled it
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  7. 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
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  19. Severe insulin resistance syndromes.The Journal of clinical investigation · 2021
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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 3 institutions in 1 country.

Fernando CorvilloLa Paz University Hospital Research Institute, Madrid, Spain.
Verónica AparicioCell Engineering Laboratory, La Paz University Hospital Research Institute, Madrid, Spain.
Alberto López-LeraLa Paz University Hospital Research Institute, Madrid, Spain.
Sofía GarridoLa Paz University Hospital Research Institute, Madrid, Spain.
David Araújo-VilarThyroid and Metabolic Diseases Unit (U.E.T.eM.), Department of Medicine, Universidad de Santiago de Compostela, Santiago de Compostela, Spain.
María P de MiguelCell Engineering Laboratory, La Paz University Hospital Research Institute, Madrid, Spain.
Margarita López-TrascasaLa Paz University Hospital Research Institute, Madrid, Spain.
Centre for Biomedical Network Research on Rare Diseases · ESHospital Universitario La Paz · ESUniversidade de Santiago de Compostela · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acquired generalized lipodystrophy (AGL) is a rare condition characterized by an altered distribution of adipose tissue and predisposition to develop hepatic steatosis and fibrosis, diabetes, and hypertriglyceridemia. Diagnosis of AGL is based on the observation of generalized fat loss, autoimmunity and lack of family history of lipodystrophy. The pathogenic mechanism of fat destruction remains unknown but evidences suggest an autoimmune origin. Anti-adipocyte antibodies have been previously reported in patients with AGL, although their involvement in the pathogenesis has been poorly studied and the autoantibody target/s remain/s to be identified. Using a combination of immunochemical and cellular studies, we investigated the presence of anti-adipocyte autoantibodies in patients with AGL, acquired partial lipodystrophy, localized lipoatrophy due to intradermic insulin injections or systemic lupus erythematosus. Moreover, the impact of anti-adipocyte autoantibodies from AGL patients was assessed in cultured mouse preadipocytes. Following this approach, we identified anti-perilipin 1 IgG autoantibodies in the serum of patients with autoimmune variety-AGL, but in no other lipodystrophies tested. These autoantibodies altered the ability of perilipin 1 to regulate lipolysis in cultured preadipocytes causing abnormal, significantly elevated basal lipolysis. Our data provide strong support for the conclusion that perilipin 1 autoantibodies are a cause of generalized lipodystrophy in these patients.

Indexed as

3T3-L1 CellsAdipocytesAdolescentAdultAnimalsAutoantibodiesBiomarkersCells, CulturedChildFemaleHumansLipid DropletsLipodystrophy, Congenital GeneralizedLipolysisMaleMiceAutoantibodiesBiomarkersPerilipin-1autoimmunitygeneralized lipodystrophyLawrence syndromelipolysisperilipin

Identifiers

PMID30283460
PMCPMC6156147
OpenAlexW2891013123

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.