Evidence map›Paper›PMID 40474948›Full record

ReviewReproductive medicine and biology

Potential Role of CREM in Diabetes-Associated Testicular Dysfunction: Current Evidence and Future Perspectives.

Olabimpe Caroline Badejogbin, Oyedayo Phillips Akano, Oluwafisayo Elizabeth Boluwatife Julius, Mary Olaoluwa Agunloye, Makinde Vincent Olubiyi, Ojichukwuka Ebere Chijioke-Agu, Matthew Agene Obekpa, Adesina Paul Arikawe, Kehinde Samuel Olaniyi

Abstract readReview
In one paragraph

Review in Reproductive medicine and biology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
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

9 authors.

Olabimpe Caroline BadejogbinDepartment of Physiology College of Basic Medical Sciences, Babcock University Ilishan-Remo Ogun State Nigeria.
Oyedayo Phillips AkanoDepartment of Physiology College of Basic Medical Sciences, Babcock University Ilishan-Remo Ogun State Nigeria.
Oluwafisayo Elizabeth Boluwatife JuliusDepartment of Physiology College of Basic Medical Sciences, Babcock University Ilishan-Remo Ogun State Nigeria.
Mary Olaoluwa AgunloyeDepartment of Physiology Kampala International University, Western Campus Ishaka Uganda.ORCID https://orcid.org/0009-0000-3825-491X
Makinde Vincent OlubiyiDepartment of Medical Physiology University of Rwanda Huye Rwanda.
Ojichukwuka Ebere Chijioke-AguDepartment of Physiology Alex-Ekwueme Federal University Abakaliki Ebonyi State Nigeria.
Matthew Agene ObekpaDepartment of Physiology University of Ilorin Ilorin Kwara State Nigeria.
Adesina Paul ArikaweDepartment of Physiology College of Medicine, University of Lagos State Idi-Araba Lagos State Nigeria.
Kehinde Samuel OlaniyiDepartment of Physiology College of Medicine and Health Sciences, Afe Babalola University Ado-Ekiti Ekiti State Nigeria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Type 2 diabetes mellitus (T2D) is a growing metabolic disorder affecting all age groups and is linked to testiculopathy, a key contributor to male infertility. Testiculopathy disrupts spermatogenesis and the sperm microenvironment, with the cyclic adenosine monophosphate (cAMP) response element modulator (CREM) playing a pivotal role in testicular function. Understanding the interplay between T2D and CREM dysregulation is essential for developing targeted therapies for diabetic testicular dysfunction. Methods: A systematic review of PubMed, Web of Science, Scopus, and Google Scholar was conducted to identify peer-reviewed studies, both preclinical and clinical, that explored CREM's role in diabetes-induced testicular dysfunction. Extracted data focused on CREM expression, oxidative stress, apoptosis, and spermatogenic impairment in diabetic models. Main Findings: Research from studies on diabetic patients and animal models highlights the detrimental effects of diabetes on the reproductive system, including hypothalamic-pituitary-testicular (HPT) axis dysregulation. CREM regulates spermatogenic gene expression, influenced by luteinizing hormone (LH), follicle-stimulating hormone (FSH), and cAMP signaling. Conclusion: CREM has a therapeutic role in maintaining testicular function, and its disruption may contribute to testiculopathy in T2D, highlighting its potential therapeutic target for preserving male fertility in diabetic patients. Further research is needed to explore its molecular mechanisms and therapeutic implications.

Indexed as

CREMmale infertilityreproductionspermatogenesistesticulopathytype 2 diabetes mellitus

Identifiers

PMID40474948
PMCPMC12138204

What OpenQuestion holds

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Registered trials

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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.