Your browser doesn't support javascript.
loading
Frequency of CCR5 Gene 32-bp deletion in Pakistani ethnic groups.
Khaliq, S; Hameed, A; Ayub, Q; Mazhar, K; Mohyuddin, A; Mansoor, A; Mehdi, S Qasim.
Afiliación
  • Khaliq S; Biomedical and Genetic Engineering Division, Dr. A.Q. Khan Research Laboratories, Islamabad 44000, Pakistan.
Genet Test ; 6(2): 123-7, 2002.
Article en En | MEDLINE | ID: mdl-12215252
ABSTRACT
CCR5 is a G-protein-coupled chemokine receptor that is used as a co-factor by macrophage-tropic (M-tropic) isolates of human immunodeficiency virus-1 (HIV-1) to gain entry into host cells. A 32-bp deletion in the CCR5 gene (CCR5-Delta32) leads to the production of an altered gene product that prevents HIV-1 from entering the host cell. This study was carried out to determine prevalence of CCR5-Delta32 allele frequency in a large Pakistani population sample (n = 821) representing 10 ethnic groups. No individual was homozygous for the mutant allele and the frequency of the CCR5-Delta32 allele ranged from 0.62% to 3.57%. The CCR5-Delta32 allele frequency was generally lower in populations from southern Pakistan. The overall frequency of the CCR5-Delta32 allele in Pakistan was 2.31%, which is much lower than that found in European populations and similar to that in the Middle East. This is consistent with the historical records and genetic data that indicate a close genetic affinity among these populations. This study demonstrates that the Pakistani population is highly susceptible to M-tropic isolates of HIV-1 and public health measures need to be enforced with urgency if Pakistan is to avoid an HIV epidemic.
Asunto(s)
Buscar en Google
Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Etnicidad / Síndrome de Inmunodeficiencia Adquirida / VIH-1 / Eliminación de Secuencia / Receptores CCR5 / Predisposición Genética a la Enfermedad / Frecuencia de los Genes Tipo de estudio: Risk_factors_studies Límite: Humans País/Región como asunto: Asia / Europa Idioma: En Revista: Genet Test Asunto de la revista: GENETICA Año: 2002 Tipo del documento: Article País de afiliación: Pakistán Pais de publicación: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA
Buscar en Google
Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Etnicidad / Síndrome de Inmunodeficiencia Adquirida / VIH-1 / Eliminación de Secuencia / Receptores CCR5 / Predisposición Genética a la Enfermedad / Frecuencia de los Genes Tipo de estudio: Risk_factors_studies Límite: Humans País/Región como asunto: Asia / Europa Idioma: En Revista: Genet Test Asunto de la revista: GENETICA Año: 2002 Tipo del documento: Article País de afiliación: Pakistán Pais de publicación: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA