Evidence map›Paper›PMID 38424564›Full record

ArticleBMC medical genomics2024

Contribution of HLA class I (A, B, C) and HLA class II (DRB1, DQA1, DQB1) alleles and haplotypes in exploring ethnic origin of central Tunisians.

Amène Ben Bnina, Amri Yessine, Yasmine El Bahri, Saoussen Chouchene, Nada Ben Lazrek, Mariem Mimouna, Zeineb Mlika, Aziza Messoudi, Dorsaf Zellama, Wissal Sahtout and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMC medical genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

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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

11 authors at 4 institutions in 1 country.

Amène Ben BninaHematology Laboratory, Sahloul University Hospital, Sousse, Tunisia.
Amri YessineBiochemistry Laboratory, Béchir Hamza Children's Hospital, Bab Saadoun Square, 1007, Tunis, Tunisia. amri.yessine@yahoo.com.
Yasmine El BahriHematology Laboratory, Sahloul University Hospital, Sousse, Tunisia.
Saoussen ChoucheneHematology Laboratory, Fatouma Bourguiba Teaching Hospital, Sousse, Tunisia.
Nada Ben LazrekHematology Laboratory, Sahloul University Hospital, Sousse, Tunisia.
Mariem MimounaHematology Laboratory, Sahloul University Hospital, Sousse, Tunisia.
Zeineb MlikaHematology Laboratory, Sahloul University Hospital, Sousse, Tunisia.
Aziza MessoudiHematology Laboratory, Sahloul University Hospital, Sousse, Tunisia.
Dorsaf ZellamaNephrology Department, Sahloul University Hospital, Sousse, Tunisia.
Wissal SahtoutNephrology Department, Sahloul University Hospital, Sousse, Tunisia.
Amina BouatayHematology Laboratory, Sahloul University Hospital, Sousse, Tunisia.
Hôpital Sahloul · TNUniversity of Monastir · TNUniversity of Sousse · TNChildren's Hospital · TN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEstimation of HLA (Human leukocyte Antigen) alleles' frequencies in populations is essential to explore their ethnic origin. Anthropologic studies of central Tunisian population were rarely reported. Then, in this work, we aimed to explore the origin of central Tunisian population using HLA alleles and haplotypes frequencies.

methodsHLA class I (A, B, C) and HLA class II (DRB1, DQA1, DQB1) loci genotyping of 272 healthy unrelated organ donors was performed by Polymerase Chain Reaction-Sequence Specific Oligonucleotide (PCR-SSO). We compared central Tunisians with other populations (Arabs, Berbers, Mediterraneans, Europeans, Africans, etc.) using alleles and haplotypes frequencies, genetic distances, Neighbour-Joining dendrogram and correspondence analysis.

resultsAmong the 19 HLA A alleles, the 26 HLA B alleles, the 13 HLA C alleles, the 15 HLA DRB1 alleles, the 6 HLA DQA1 alleles and the 5 HLA DQB1 alleles identified in the studied population, HLA A*02 (22.8%), HLA B*50 (13.1%), HLA C*06 (21.8%), HLA DRB1*07 (17.8%), HLA DQA1*01 (32.1%) and HLA DQB1*03 (31.6%) were the most frequent alleles. The extended haplotypes HLA A*02-B*50-C*06-DRB1*07-DQA1*02-DQB1*02 (1.97%) was the most frequent HLA six-loci haplotype.

conclusionCentral Tunisians were very close to other Tunisian populations, to Iberians and North Africans. They were rather distant from sub-Saharan populations and eastern Mediterraneans especially Arabs although the strong cultural and religious impact of Arabs in this population.

Indexed as

HLA-C AntigensNorth African PeoplePolymorphism, GeneticAllelesGene FrequencyHaplotypesHLA-A AntigensHLA-B AntigensHLA-DRB1 ChainsHumansHLA-A AntigensHLA-B AntigensHLA-C AntigensHLA-DRB1 ChainsAnthropologyGenetic polymorphismHaplotypesHuman leukocyte Antigen (HLA)

Identifiers

PMID38424564
PMCPMC10903062
OpenAlexW4392284040

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LicenceCC BY
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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.