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The rapid CD4 + T-lymphocyte decline and human immunodeficiency virus progression in females compared to males

CD4 + T-lymphocyte counts are used to assess CD4 + decline and the stage of human immunodeficiency virus (HIV) progression in HIV-infected patients. Clinical observation suggests that HIV progress more rapid in females than males. Of the original 5000 HIV-infected population of Western New York HIV/...

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Autores principales: Parsa, Nader, Zaheri, Pari Mahlagha, Hewitt, Ross G., Karimi Akhormeh, Ali, Taravatmanesh, Samira, Wallin, Lisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7544823/
https://www.ncbi.nlm.nih.gov/pubmed/33033335
http://dx.doi.org/10.1038/s41598-020-73852-0
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author Parsa, Nader
Zaheri, Pari Mahlagha
Hewitt, Ross G.
Karimi Akhormeh, Ali
Taravatmanesh, Samira
Wallin, Lisa
author_facet Parsa, Nader
Zaheri, Pari Mahlagha
Hewitt, Ross G.
Karimi Akhormeh, Ali
Taravatmanesh, Samira
Wallin, Lisa
author_sort Parsa, Nader
collection PubMed
description CD4 + T-lymphocyte counts are used to assess CD4 + decline and the stage of human immunodeficiency virus (HIV) progression in HIV-infected patients. Clinical observation suggests that HIV progress more rapid in females than males. Of the original 5000 HIV-infected population of Western New York HIV/AIDS, Referral Center at Erie County Medical Center (ECMC), 1422 participated in the cohort study. We identified 333 HIV-infected patients with CD4 + T-cell-counts ≥ 500/µƖ, among them 178 met the inclusion criteria for the 10-year study. Females had higher mode (600 vs. 540) and mean (741.9 vs. 712.2) CD4 + counts than males at baseline. However, CD4 + declined faster among females in a shorter time than males (234.5 vs. 158.6, P < 0.004), with rapid HIV progression. Univariate analyses determined that females had a 40% higher risk for CD4 + decline than males. The bivariate analyses specified CD4 + decline remained greater in females than males. Multivariate analyses which employed Cox’s proportional Hazard-Model to adjust for numerous variables simultaneously identified women had almost twice the risk for CD4 + decline and rapid HIV progression than males (RR = 1.93; 95%CI 1.24, 2.99). Although the biological mechanism remains unknown, findings suggest gender differences in CD4 + decline, with a higher risk of rapid HIV progression and shorter longevity in females.
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spelling pubmed-75448232020-10-14 The rapid CD4 + T-lymphocyte decline and human immunodeficiency virus progression in females compared to males Parsa, Nader Zaheri, Pari Mahlagha Hewitt, Ross G. Karimi Akhormeh, Ali Taravatmanesh, Samira Wallin, Lisa Sci Rep Article CD4 + T-lymphocyte counts are used to assess CD4 + decline and the stage of human immunodeficiency virus (HIV) progression in HIV-infected patients. Clinical observation suggests that HIV progress more rapid in females than males. Of the original 5000 HIV-infected population of Western New York HIV/AIDS, Referral Center at Erie County Medical Center (ECMC), 1422 participated in the cohort study. We identified 333 HIV-infected patients with CD4 + T-cell-counts ≥ 500/µƖ, among them 178 met the inclusion criteria for the 10-year study. Females had higher mode (600 vs. 540) and mean (741.9 vs. 712.2) CD4 + counts than males at baseline. However, CD4 + declined faster among females in a shorter time than males (234.5 vs. 158.6, P < 0.004), with rapid HIV progression. Univariate analyses determined that females had a 40% higher risk for CD4 + decline than males. The bivariate analyses specified CD4 + decline remained greater in females than males. Multivariate analyses which employed Cox’s proportional Hazard-Model to adjust for numerous variables simultaneously identified women had almost twice the risk for CD4 + decline and rapid HIV progression than males (RR = 1.93; 95%CI 1.24, 2.99). Although the biological mechanism remains unknown, findings suggest gender differences in CD4 + decline, with a higher risk of rapid HIV progression and shorter longevity in females. Nature Publishing Group UK 2020-10-08 /pmc/articles/PMC7544823/ /pubmed/33033335 http://dx.doi.org/10.1038/s41598-020-73852-0 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Parsa, Nader
Zaheri, Pari Mahlagha
Hewitt, Ross G.
Karimi Akhormeh, Ali
Taravatmanesh, Samira
Wallin, Lisa
The rapid CD4 + T-lymphocyte decline and human immunodeficiency virus progression in females compared to males
title The rapid CD4 + T-lymphocyte decline and human immunodeficiency virus progression in females compared to males
title_full The rapid CD4 + T-lymphocyte decline and human immunodeficiency virus progression in females compared to males
title_fullStr The rapid CD4 + T-lymphocyte decline and human immunodeficiency virus progression in females compared to males
title_full_unstemmed The rapid CD4 + T-lymphocyte decline and human immunodeficiency virus progression in females compared to males
title_short The rapid CD4 + T-lymphocyte decline and human immunodeficiency virus progression in females compared to males
title_sort rapid cd4 + t-lymphocyte decline and human immunodeficiency virus progression in females compared to males
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7544823/
https://www.ncbi.nlm.nih.gov/pubmed/33033335
http://dx.doi.org/10.1038/s41598-020-73852-0
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