Evidence map›Paper›PMID 32651428›Full record

ArticleScientific reports2020

Molecular neuroanatomy of anorexia nervosa.

Derek Howard, Priscilla Negraes, Aristotle N Voineskos, Allan S Kaplan, Alysson R Muotri, Vikas Duvvuri, Leon French

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. 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
1.1field-weighted citation impact, top 14% 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

8 citing papers in PubMed, 19 citations in OpenAlex.

  1. A lifespan staging model of basal forebrain cholinergic vulnerability.Alzheimer's & dementia : the journal of the Alzheimer's Association · 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

7 authors at 3 institutions in 2 countries.

Derek HowardCampbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Canada.
Priscilla NegraesDepartment of Pediatrics, School of Medicine, University of California San Diego, La Jolla, CA, USA.
Aristotle N VoineskosCampbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Canada.
Allan S KaplanCampbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Canada.
Alysson R MuotriDepartment of Pediatrics/Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA, USA.
Vikas DuvvuriDepartment of Pediatrics and Psychiatry, School of Medicine, University of California San Diego, La Jolla, CA, USA.
Leon FrenchCampbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Canada. leonfrench@gmail.com.
University of California, San Diego · USCentre for Addiction and Mental Health · CAUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anorexia nervosa is a complex eating disorder with genetic, metabolic, and psychosocial underpinnings. Using genome-wide methods, recent studies have associated many genes with the disorder. We characterized these genes by projecting them into reference transcriptomic atlases of the prenatal and adult human brain to determine where these genes are expressed in fine detail. We found that genes from an induced stem cell study of anorexia nervosa cases are expressed at higher levels in the lateral parabrachial nucleus. Although weaker, expression enrichment of the adult lateral parabrachial is also found with genes from independent genetic studies. Candidate causal genes from the largest genetic study of anorexia nervosa to date were enriched for expression in the arcuate nucleus of the hypothalamus. We also found an enrichment of anorexia nervosa associated genes in the adult and fetal raphe and ventral tegmental areas. Motivated by enrichment of these feeding circuits, we tested if these genes respond to fasting in mice hypothalami, which highlighted the differential expression of Rps26 and Dalrd3. This work improves our understanding of the neurobiology of anorexia nervosa by suggesting disturbances in subcortical appetitive circuits.

Indexed as

Gene Expression ProfilingTranscriptomeAdultAnimalsAnorexia NervosaBrainExomeFemaleGenetic MarkersGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansHypothalamusInduced Pluripotent Stem CellsMaleMiceDALRD3 protein, humanGenetic MarkersRibosomal ProteinsRPS26 protein, humantRNA Methyltransferases

Identifiers

PMID32651428
PMCPMC7351758
OpenAlexW3041172123

What OpenQuestion holds

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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.