Evidence map›Paper›PMID 40562759›Full record

ArticleTranslational psychiatry2025

Elevated plasma GDF15 combined with FGF21 suggests mitochondrial dysfunction in a subgroup of anorexia nervosa patients.

Jingjing Xu, Ruyue Zhang, Vincent Millischer, Miranda Stiernborg, Claire E Tume, Sara Mehdinia, Peter Barker, Zeynep Yilmaz, Vanessa F Gonçalves, Catharina Lavebratt and 4 more

Abstract read
In one paragraph

Article in Translational psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Article
  2. Review
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  8. 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

14 authors.

Jingjing XuDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden. jingjing.xu@ki.se.ORCID http://orcid.org/0000-0002-4019-7181
Ruyue ZhangDepartment of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.ORCID http://orcid.org/0000-0001-5747-9428
Vincent MillischerDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Miranda StiernborgDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Claire E TumeDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.ORCID http://orcid.org/0009-0006-7657-8011
Sara MehdiniaDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Peter BarkerNIHR Cambridge Core Biochemical Assay Laboratory, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Zeynep YilmazDepartment of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Vanessa F GonçalvesMolecular Brain Sciences, Centre for Addiction and Mental Health, Toronto, ON, Canada.ORCID http://orcid.org/0000-0001-5619-8755
Catharina LavebrattDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.ORCID http://orcid.org/0000-0003-4987-2718
Mikael LandénDepartment of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.ORCID http://orcid.org/0000-0002-4496-6451
Stephen O'RahillyMRC Metabolic Diseases Unit, Institute of Metabolic Science, University of Cambridge, Addenbrookes Hospital, Cambridge, UK.
Cynthia M BulikDepartment of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.ORCID http://orcid.org/0000-0001-7772-3264
Ida Ak NilssonDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden. ida.nilsson@ki.se.ORCID http://orcid.org/0000-0002-7676-4299

Funding

Eating Disorders Genetics Initiative (EDGI)R01MH120170 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BULIK, CYNTHIA M · 2019 to 2023
$7.2M
1/3 Eating Disorders Genetics Initiative 2 (EDGI2)R01MH136149 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CYNTHIA M BULIK, Laura Marianne Huckins · 2024 to 2026
$5.1M
Predicting the multi-omic impact of psychiatric GWAS associationsR01MH118278 · NIMH · YALE UNIVERSITY · PI HUCKINS, LAURA MARIANNE · 2019 to 2023
$3.6M
1/7 PGC: Advancing Discovery and ImpactR01MH124871 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BULIK, CYNTHIA M, SULLIVAN, PATRICK F · 2021 to 2025
$3.5M
Predicting Binge and Purge Episodes from Passive and Active Apple Watch Data Using a Dynamical Systems ApproachR01MH119084 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BULIK, CYNTHIA M, BUTNER, JONATHAN · 2019 to 2022
$2.8M
3/3 Eating Disorders Genetics Initiative 2 (EDGI2)R01MH136156 · NIMH · KAROLINSKA INSTITUTE · PI Lisa Dinkler, Lu Yi · 2024 to 2026
$1.5M
Genetic Architecture of Avoidant/Restrictive Food Intake DisorderR56MH129437 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BULIK, CYNTHIA M, MICALI, NADIA · 2022 to 2023
$1.5M
Hjärnfonden (Swedish Brain Foundation) FO2019-0122Hjärnfonden (Swedish Brain Foundation) FO2022-0717NIMH NIH HHS R01 MH118278NIMH NIH HHS R01 MH119084NIMH NIH HHS R01 MH120170NIMH NIH HHS R01 MH124871NIMH NIH HHS R01 MH136149NIMH NIH HHS R01 MH136156NIMH NIH HHS R56 MH129437U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) R01MH136156U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) R56MH129437; R01MH120170; R01MH124871; R01MH119084; R01MH118278; R01 MH124871Vetenskapsrådet (Swedish Research Council) 2022-00242Vetenskapsrådet (Swedish Research Council) 2022-01643Vetenskapsrådet (Swedish Research Council) award: 538-2013-8864
6 · The paper itself

Abstract

Growth and differentiation factor 15 (GDF15) is a significant player in cellular stress and energy homeostasis. GDF15 is elevated in cancer cachexia, chemotherapy-induced anorexia, hyperemesis gravidarum, and mitochondrial disorders. Here we analyze GDF15 in anorexia nervosa (AN), a psychiatric disorder characterized by low weight and persistent restriction of food intake. While no significant difference in plasma GDF15 concentration was seen across the three included groups; active AN, recovered AN, and healthy controls, a subgroup of study participants with high GDF15 plasma was noted to a significantly higher extent in the AN groups. Sparse partial least squares discriminant analysis (sPLS-DA) identified six markers related to inflammatory processes or cellular stress from a set of 74 markers that distinguished AN with high GDF15 from the rest, with fibroblast growth factor 21 (FGF21) being the most important contributor. Moreover, FGF21 plasma concentration was significantly higher in the group with high GDF15, suggesting an involvement of mitochondrial dysfunction. In fact, mitochondrial polygenic risk score (PRS) was significantly associated with AN risk in a large AN case-control cohort. In line with this, we also report elevated liver expression of GDF15 in the anx/anx mouse displaying anorexia associated with mitochondrial dysfunction. We conclude that mitochondrial dysfunction should be further explored in AN. Clinical trials of GDF15 immunoneutralization in patients with AN and high levels of GDF15 are worthy of consideration.

Indexed as

Anorexia NervosaFibroblast Growth FactorsGrowth Differentiation Factor 15MitochondriaMitochondrial DiseasesAdolescentAdultAnimalsBiomarkersCase-Control StudiesFemaleHumansLiverMiceYoung AdultBiomarkersFGF21 protein, humanfibroblast growth factor 21Fibroblast Growth FactorsGDF15 protein, humanGrowth Differentiation Factor 15

Identifiers

PMID40562759
PMCPMC12198413

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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.