Evidence map›Paper›PMID 41459362›Full record

ArticleThe Pan African medical journal2025

Association of angiotensin-converting enzyme gene insertion/deletion polymorphism (rs4646994) with schizophrenia in an eastern Algerian population: a case-control study.

Yasmina Boukhenaf, Ouarda Sariyah Ayachi, Amina Iness Bernou, Rayene Achou, Mohamed Lebsir, Fatima Zohra Madoui, Karima Sifi, Mohamed Larbi Rezgoun

Abstract read
In one paragraph

Article in The Pan African medical journal, 2025. 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

8 authors.

Yasmina BoukhenafLaboratory of Molecular and Cellular Biology, Department of Animal Biology, University of Constantine 1, Constantine, Algeria.
Ouarda Sariyah AyachiPathology, Diagnosis and Therapy, Health and Biotechnology Division, National Research Center of Biotechnology, Constantine, Algeria.
Amina Iness BernouLaboratory of Molecular and Cellular Biology, Department of Animal Biology, University of Constantine 1, Constantine, Algeria.
Rayene AchouLaboratory of Molecular and Cellular Biology, Department of Animal Biology, University of Constantine 1, Constantine, Algeria.
Mohamed LebsirLaboratory of Molecular and Cellular Biology, Department of Animal Biology, University of Constantine 1, Constantine, Algeria.
Fatima Zohra MadouiPsychiatric Hospital Mahmoud Belamri, Constantine, Algeria.
Karima SifiLaboratory of Biology and Molecular Genetics, University Hospital Center Benbadis, University of Constantine 3, Constantine, Algeria.
Mohamed Larbi RezgounLaboratory of Molecular and Cellular Biology, Department of Animal Biology, University of Constantine 1, Constantine, Algeria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: the Angiotensin-Converting Enzyme (ACE) is a critical enzyme in the renin-angiotensin system and influences neurotransmitter regulation, including dopamine. Previous studies have suggested a potential association between ACE gene polymorphisms and psychiatric disorders, including schizophrenia. This study aimed to investigate the association between the insertion/deletion (I/D) polymorphism in the ACE gene and schizophrenia in an Eastern Algerian population. Methods: a case-control study was conducted involving 157 schizophrenia patients and 222 healthy controls. Deoxyribonucleic acid (DNA) was extracted from peripheral blood using the salting-out method, and the ACE I/D polymorphism was genotyped using the polymerase chain reaction (PCR) technique. Statistical analyses were performed using SPSS version 26.0. Results: no significant association was observed between the ACE I/D polymorphism and schizophrenia. Compared to the DD genotype, the ID genotype showed OR = 0.84 (95% CI: 0.47-1.50, P = 0.66), and the II genotype OR = 0.47 (95% CI: 0.05-4.54, P = 0.66). The I allele was also not significantly associated (OR = 0.80, 95% CI: 0.47-1.33, P = 0.38). Dominant, over-dominant, and recessive models showed no significant results. Conclusion: these findings suggest that the ACE I/D polymorphism does not contribute to the genetic susceptibility to schizophrenia in this population. Further research with larger sample sizes and consideration of gene-environment interactions is needed to provide deeper insights into the role of ACE in schizophrenia.

Indexed as

Peptidyl-Dipeptidase ASchizophreniaAdultAlgeriaAllelesCase-Control StudiesFemaleGenetic Predisposition to DiseaseGenotypeHumansINDEL MutationMaleMiddle AgedPolymerase Chain ReactionPolymorphism, GeneticYoung AdultACE protein, humanPeptidyl-Dipeptidase AAngiotensin-converting enzymecase-control studiesgeneticspolymorphismschizophrenia

Identifiers

PMID41459362
PMCPMC12741978

What OpenQuestion holds

Textmetadata
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.