Effect of Sickle Cell Trait on Human Immunodeficiency Virus Type 1 Infection.

Human Immunodeficiency Sickle Cell Trait Virus Type 1

Journal

The open AIDS journal
ISSN: 1874-6136
Titre abrégé: Open AIDS J
Pays: United Arab Emirates
ID NLM: 101480215

Informations de publication

Date de publication:
2022
Historique:
entrez: 23 1 2023
pubmed: 24 1 2023
medline: 24 1 2023
Statut: ppublish

Résumé

Whereas several studies show that homozygous (HbSS) sickle cell disease protects against human immunodeficiency virus infection, it is not clear if human immunodeficiency virus infection is affected by the heterozygous state of the sickle globin gene (HbAS or sickle cell trait). To evaluate the effects of sickle cell trait on the prevalence and severity of human immunodeficiency virus type 1 infection in a large patient population. Hemoglobin genotype was determined by high performance liquid chromatography (HPLC) in 1,226 HIV-1 patients in Nigeria. Their demographic data were documented. Blood CD4+ cell counts and HIV-1 viral load previously determined on the same blood samples to guide clinical care were used as indices of severity of HIV-1 infection. Statistical analysis of the data was done to evaluate the effects of sickle cell trait on the severity and prevalence of HIV-1 infection, relative to the prevalence of 1.4% in the general population of Nigeria. The distribution of hemoglobin genotypes among the HIV-1 patients was comparable to that in the general population of Nigeria (Chi-squared statistic =1.025; p value = 0.31, not significant). Neither viral load (p = 0.32) nor blood CD4+ cell count (p = 0.30) was significantly different between all HbAS versus all HbAA patients. There was a trend towards lower viral load in females and a significant interaction between gender and HbAS for viral load (P = 0.018), suggesting that sickle cell trait might be associated with the severity of HIV-1 infection in females. The findings suggest that sickle cell trait might be associated with severity of HIV-1 infection in female, but not all, patients. Larger, prospective studies are required to further investigate the effect of sickle cell trait on HIV-1 infection.

Identifiants

pubmed: 36685019
doi: 10.2174/18746136-v16-e2208150
pmc: PMC9851184
mid: NIHMS1862681
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL125005
Pays : United States

Déclaration de conflit d'intérêts

CONFLICT OF INTEREST The authors have no conflict of interest to declare.

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Auteurs

Iheanyi Okpala (I)

Department of Hematology, University of Nigeria Teaching Hospital, Enugu, Nigeria.

Chinwe Chukwuka (C)

Department of Medicine, University of Nigeria Teaching Hospital, Enugu, Nigeria.

Seyed Nouraie (S)

Department of Medicine, University of Pittsburgh, USA.

Sergei Nekhai (S)

Department of Medicine and Center for Sickle Cell Disease, Howard University, Washington DC, USA.

Chima Onwuka (C)

Department of Hematology, University of Nigeria Teaching Hospital, Enugu, Nigeria.

Isa Hezekiah (I)

Department of Hematology University of Abuja, Abuja, Nigeria.

Onochie Obodo (O)

Department of Hematology, University of Nigeria Teaching Hospital, Enugu, Nigeria.

Deborah Maisamari (D)

Department of Hematology University of Abuja, Abuja, Nigeria.

Kelechi Okereke (K)

Department of Hematology, University of Nigeria Teaching Hospital, Enugu, Nigeria.

Ajake Oden (A)

Department of Hematology, University of Nigeria Teaching Hospital, Enugu, Nigeria.

Yohanna Tanko (Y)

Department of Hematology University of Abuja, Abuja, Nigeria.

Chinedu Ezekekwu (C)

Department of Hematology, University of Nigeria Teaching Hospital, Enugu, Nigeria.

Vivian Kwaghi (V)

HIV Unit, University of Abuja Teaching Hospital, Abuja, Nigeria.

Cajetan Onyedum (C)

Department of Medicine, University of Nigeria Teaching Hospital, Enugu, Nigeria.

Obiageli Nnodu (O)

Department of Hematology University of Abuja, Abuja, Nigeria.

Classifications MeSH