Evidence map›Paper›PMID 34799866›Full record

ArticleJournal of clinical laboratory analysis2022

Association of a common genetic variant (insertion/deletion) in ACE gene with prostate cancer susceptibility in a Tunisian population.

Rahma Said, Rim Jenni, Sami Boussetta, Feryel Ammous, Skander Zouari, Selim Zaghbib, Marouene Chakroun, Amine Derouiche, Mohamed Chebil, Slah Ouerhani

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 20% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Alu Deletions inInternational journal of molecular sciences · 2022
    Article
  5. Article
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

10 authors at 2 institutions in 1 country.

Rahma SaidLaboratory of Protein Engineering and Bio-active Molecules, National Institute of Applied Science and Technology - University of Carthage, Tunis, Tunisia.
Rim JenniLaboratory of Protein Engineering and Bio-active Molecules, National Institute of Applied Science and Technology - University of Carthage, Tunis, Tunisia.
Sami BoussettaLaboratory of Genetics, Immunology, and Human Pathology, Faculty of Sciences of Tunis.
Feryel AmmousLaboratory of Genetics, Immunology, and Human Pathology, Faculty of Sciences of Tunis.
Skander ZouariUrology Department, Charles Nicolle Hospital, Tunis, Tunisia.ORCID https://orcid.org/0000-0003-4644-489X
Selim ZaghbibUrology Department, Charles Nicolle Hospital, Tunis, Tunisia.
Marouene ChakrounUrology Department, Charles Nicolle Hospital, Tunis, Tunisia.
Amine DerouicheUrology Department, Charles Nicolle Hospital, Tunis, Tunisia.
Mohamed ChebilUrology Department, Charles Nicolle Hospital, Tunis, Tunisia.
Slah OuerhaniLaboratory of Protein Engineering and Bio-active Molecules, National Institute of Applied Science and Technology - University of Carthage, Tunis, Tunisia.ORCID https://orcid.org/0000-0002-3651-4690
Hôpital Charles-Nicolle · TNUniversity of Carthage · TN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAngiotensin-converting enzyme (ACE) plays a pivotal role in several pathologies including cancers. The association of insertion/deletion (I/D) polymorphism of the ACE gene with prostate cancer (PC) risk remains controversial. We aimed to investigate for the first time, to our Knowledge, in North Africa the potential relationship between ACE I/D polymorphism with PC susceptibility and clinical outcomes of PC patients.

methodsThis case-control study included 143 healthy individuals and 124 patients diagnosed with PC. Using genomic DNA, the samples were genotyped for ACE I/D polymorphism by polymerase chain reaction (PCR).

resultsWe found that The D allele is significantly associated with an increased risk of PC and D/D + D/I genotypes were at 3 times increased risk of PC ([p = 0.005], OR = 2.95, IC 95% = 1.26-7.09) compared with I/I genotype (p = 0.003, OR = 0.3, IC 95% = 0.12-0.74). We observed an association between D/D and D/I genotypes with advanced age (≥70 years) (p = 0.014; r

conclusionThe ACE I/D polymorphism is likely to predispose to PC and could play a role in PC progression and aggressiveness.

Indexed as

Genetic Predisposition to DiseaseProstatic NeoplasmsAgedAged, 80 and overAlu ElementsCase-Control StudiesHumansINDEL MutationMaleMiddle AgedPeptidyl-Dipeptidase APolymorphism, GeneticTunisiaACE protein, humanPeptidyl-Dipeptidase AAlu repeat sequenceangiotensin conversion enzymesNorth Africapolymorphismprostate cancerTunisia

Identifiers

PMID34799866
PMCPMC8761439
OpenAlexW3213648696

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.