Macrophage migration inhibitory factor - 794 CATT 5-8 microsatellite polymorphism and susceptibility of tuberculosis

The establishment of candidate genetic determinants associated with tuberculosis (TB) is a challenge, considering the divergent frequencies among populations. The objective of this study was to evaluate the association between MIF - 794 CATT   polymorphism and susceptibility to TB. Case-control stud...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Infection 2021-06, Vol.49 (3), p.457
Hauptverfasser: Machado, Felipe Dominguez, Gehlen, Mirela, Caron, Vitória Schmidt, Mousquer, Gabriel Tassi, Bello, Graziele Lima, Anton, Camila, Bernardi, Rafaela Manzoni, Freitas, Alana Ambos, Unis, Gisela, Costa, Elis Regina Dalla, Rossetti, Maria Lucia Rosa, Silva, Denise Rossato
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The establishment of candidate genetic determinants associated with tuberculosis (TB) is a challenge, considering the divergent frequencies among populations. The objective of this study was to evaluate the association between MIF - 794 CATT   polymorphism and susceptibility to TB. Case-control study. Patients > 18 years, with pulmonary TB were included. The control group consisted of blood donors and household contacts, not relatives, healthy and > 18 years. MIF - 794 CATT   were genotyped using sequencing of PCR and capillary electrophoresis. 126 patients and 119 controls were included. The genotype 5/5 was more frequent among cases (15.1%) than in controls (5.9%) (p = 0.019). Cases had more frequently the allele 5 (29.4%) as compared with controls (19.3%) (p = 0.010). Prevalence of 7/X + 8/X genotypes was not different between cases and controls (p = 0.821). There was no difference between patients with alleles 7 and 8 and those with alleles 5 and 6 (p = 0.608). The genotype 5/5 and the allele 5 of MIF - 794 CATT   were more frequent among TB patients than in controls.
ISSN:1439-0973
DOI:10.1007/s15010-020-01562-w