Evidence map›Paper›PMID 39586906›Full record

ArticleActa neuropathologica2024

Lipid storage myopathy associated with sertraline treatment is an acquired mitochondrial disorder with respiratory chain deficiency.

Carola Hedberg-Oldfors, Ulrika Lindgren, Kittichate Visuttijai, Yan Shen, Andreea Ilinca, Sara Nordström, Christopher Lindberg, Anders Oldfors

Abstract read
In one paragraph

Article in Acta neuropathologica, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

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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

9 citing papers in PubMed.

  1. Article
  2. Sertraline use in mitochondrial cytopathy-associated depression: A case report.Dusunen adam : Bakirkoy Ruh ve Sinir Hastaliklari Hastanesi yayin organi · 2026
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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

8 authors.

Carola Hedberg-OldforsDepartment of Laboratory Medicine, University of Gothenburg, Gothenburg, Sweden.
Ulrika LindgrenDepartment of Laboratory Medicine, University of Gothenburg, Gothenburg, Sweden.
Kittichate VisuttijaiDepartment of Laboratory Medicine, University of Gothenburg, Gothenburg, Sweden.
Yan ShenDepartment of Laboratory Medicine, University of Gothenburg, Gothenburg, Sweden.
Andreea IlincaDepartment of Neurology, Division of Neurology, Skåne University Hospital, Lund, Sweden.
Sara NordströmNeuromuscular Centre, Department of Neurology, Sahlgrenska University Hospital, Gothenburg, Sweden.
Christopher LindbergNeuromuscular Centre, Department of Neurology, Sahlgrenska University Hospital, Gothenburg, Sweden.
Anders OldforsDepartment of Laboratory Medicine, University of Gothenburg, Gothenburg, Sweden. anders.oldfors@gu.se.

Funding

The Gothenburg Society of Medicine GLS-999464The Swedish Research Council 2018-02821The Swedish state under the agreement between the Swedish government and the county councils, the ALF-agreement ALFGBG-716821The Swedish state under the agreement between the Swedish government and the county councils, the ALF-agreement ALFGBG-965898
6 · The paper itself

Abstract

Lipid storage myopathies are considered inborn errors of metabolism affecting the fatty acid metabolism and leading to accumulation of lipid droplets in the cytoplasm of muscle fibers. Specific diagnosis is based on investigation of organic aids in urine, acylcarnitines in blood and genetic testing. An acquired lipid storage myopathy in patients treated with the antidepressant drug sertraline, a serotonin reuptake inhibitor, has recently emerged as a new tentative differential diagnosis. We analyzed the muscle biopsy tissue in a group of 11 adult patients with muscle weakness and lipid storage myopathy which developed at a time when they were on sertraline treatment. This group comprise most patients with lipid storage myopathies in western Sweden during the recent nine-year period. By enzyme histochemistry, electron microscopy, quantitative proteomics, immunofluorescence of the respiratory chain subunits, western blot and genetic analyses we demonstrate that muscle tissue in this group of patients exhibit a characteristic morphological and proteomic profile. The patients also showed an acylcarnitine profile in blood suggestive of multiple acyl-coenzyme A dehydrogenase deficiency, but no genetic explanation was found by whole genome or exome sequencing. By proteomic analysis the muscle tissue revealed a profound loss of Complex I subunits from the respiratory chain and to some extent also deficiency of Complex II and IV. Most other components of the respiratory chain as well as the fatty acid oxidation and citric acid cycle were upregulated in accordance with the massive mitochondrial proliferation. The respiratory chain deficiency was verified by immunofluorescence analysis, western blot analysis and enzyme histochemistry. The typical ultrastructural changes of the mitochondria included pleomorphism, dark matrix and frequent round osmiophilic inclusions. Our results show that lipid storage myopathy associated with sertraline treatment is a mitochondrial disorder with respiratory chain deficiency and is an important differential diagnosis with characteristic features.

Indexed as

Lipid Metabolism, Inborn ErrorsSertralineAdultAgedCarnitineElectron TransportFemaleHumansMaleMiddle AgedMitochondrial DiseasesMuscle, SkeletalMuscular DiseasesMuscular DystrophiesProteomicsacylcarnitineCarnitineSertralineLipid storage myopathyMetabolic crisisMultiple acyl-CoA dehydrogenase deficiencyMuscle weaknessSertralineSSRI

Identifiers

PMID39586906
PMCPMC11588938

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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.