Evidence map›Paper›PMID 42890939›Full record

ArticleFrontiers in psychiatry2026

Vulnerability and resilience to activity-based anorexia are not sex-dependent.

Julie Zhao, Jeff A Beeler, Nesha S Burghardt

Abstract read
In one paragraph

Article in Frontiers in psychiatry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Julie ZhaoBiology Program, The Graduate Center, City University of New York, New York, NY, United States.
Jeff A BeelerBiology Program, The Graduate Center, City University of New York, New York, NY, United States.
Nesha S BurghardtDepartment of Psychology, Hunter College, City University of New York, New York, NY, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Anorexia nervosa (AN) is more prevalent in women than men, although rates in men are rising. Animal models can provide insight into whether this differential prevalence is rooted in biological mechanisms, but prior studies have yielded conflicting findings. Using the activity-based anorexia (ABA) model, we previously demonstrated that female mice exhibit distinct vulnerable and resilient phenotypes. Here, we use this phenotypic framework to investigate sex differences in ABA susceptibility. Methods: We tested young adult male C57BL/6N mice using the same ABA protocol used to test age-matched C57BL/6N females. Individual differences in daily bodyweight, food intake, water intake, and wheel running were analyzed and compared across sexes. Results: Males exhibit the same vulnerable and resilient phenotypes as females, with no sex difference in the proportion of mice exhibiting each phenotype or the repertoire of behaviors characterizing them. In both sexes, vulnerable mice exhibit catastrophic weight loss that is associated with excessive light cycle running, while resilient mice exhibit weight stabilization that is associated with adaptive changes in consumption. When food is available, vulnerable mice do not run more than resilient mice, indicating that vulnerability is not characterized by a decision to run instead of eat in either sex. Conclusions: Our findings indicate that there are no sex differences in ABA in C57BL/6N mice. The shared behavioral responses to starvation observed across sexes demonstrate that ABA can be used to model adaptive and maladaptive responses to food restriction in men and women.

Indexed as

activity-based anorexiaanorexia nervosaexercisefood restrictionmouse modelsphenotypesresiliencesex differences

Identifiers

PMID42890939
PMCPMC13672643

What OpenQuestion holds

Textmetadata
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.