Evidence map›Paper›PMID 42222091›Full record

ArticleFrontiers in endocrinology2026

Gestational exposure to the artificial sweetener erythritol reprograms ovarian function through AMH suppression and oxidative stress-mediated disruption of autophagy and PI3K signaling.

Amina Fallata, Saber Nahdi, Hassan S Alamri, Tlili Barhoumi, Mohamed Alanazi, Md Ataur Rahman, Saleh Alwasel, Abdel Halim Harrath

Abstract read
In one paragraph

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

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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

8 authors.

Amina FallataDepartment of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia.
Saber NahdiDepartment of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia.
Hassan S AlamriDepartment of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Abdullah International Medical Research Center, King Saud bin Abdulaziz University for Health Sciences, Ministry of the National Guard-Health Affairs, Riyadh, Saudi Arabia.
Tlili BarhoumiCore Lab Facility, King Abdullah International Medical Research Center, King Saud bin Abdulaziz University for Health Sciences, Ministry of the National Guard-Health Affairs, Riyadh, Saudi Arabia.
Mohamed AlanaziDepartment of Biochemistry, College of Science, King Saud University, Riyadh, Saudi Arabia.
Md Ataur RahmanDepartment of Neurology, University of Michigan, Ann Arbor, MI, United States.
Saleh AlwaselDepartment of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia.
Abdel Halim HarrathDepartment of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Erythritol is a widely used non-nutritive sweetener generally regarded as safe. However, recent emerging evidence has begun to reveal potential adverse effects, including possible associations with cancer and cardiovascular disease. Nevertheless, its potential impact on female reproductive health remains largely unexplored. Methods: The present study investigated the transgenerational effects of gestational erythritol exposure on ovarian morphology and molecular signaling in Wistar rats. Pregnant females were administered 0.4 or 4 g/kg/day of erythritol from gestational day 6 until parturition. Ovarian histopathological architecture along with oxidative stress and molecular signaling markers were evaluated in F1 and F2 female offspring at the prepubertal stage. Results: We found that Discussion: Collectively, these findings demonstrate that gestational erythritol exposure promotes oxidative stress, disrupts autophagy, impairs steroidogenesis, and inhibits PI3K signaling, culminating in transgenerational ovarian dysfunction.

Indexed as

Anti-Mullerian HormoneAutophagyErythritolOvaryOxidative StressPhosphatidylinositol 3-KinasesPrenatal Exposure Delayed EffectsSweetening AgentsAnimalsFemalePregnancyRatsRats, WistarSignal TransductionAnti-Mullerian HormoneErythritolPhosphatidylinositol 3-KinasesSweetening Agentsagingautophagyerythritolovaryoxidative stressPI3K signalingsweeteners

Identifiers

PMID42222091
PMCPMC13218215

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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.