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MBL2 gene polymorphisms and its relation to infection in Brazilian systemic lupus erythematosus patients: A 10-years follow-up study.
Saldanha, Carla Forgiarini; Kniphoff da Silva, Gabriela; Glesse, Nadine; Tavares Brenol, João Carlos; Xavier, Ricardo Machado; Bogo Chies, José Artur; Monticielo, Odirlei André.
Affiliation
  • Saldanha CF; Division of Rheumatology, Department of Internal Medicine, Hospital de Clínicas de Porto Alegre, RinggoldID:%2028124Universidade Federal Do Rio Grande Do Sul, Uruguaiana, Brazil.
  • Kniphoff da Silva G; Department of Genetics, Programa de Pós-Graduação Em Genética e Biologia Molecular, RinggoldID:%2028124Universidade Federal Do Rio Grande Do Sul, Porto Alegre, Brazil.
  • Glesse N; Department of Genetics, Programa de Pós-Graduação Em Genética e Biologia Molecular, RinggoldID:%2028124Universidade Federal Do Rio Grande Do Sul, Porto Alegre, Brazil.
  • Tavares Brenol JC; Division of Rheumatology, Department of Internal Medicine, Hospital de Clínicas de Porto Alegre, RinggoldID:%2028124Universidade Federal Do Rio Grande Do Sul, Uruguaiana, Brazil.
  • Xavier RM; Division of Rheumatology, Department of Internal Medicine, Hospital de Clínicas de Porto Alegre, RinggoldID:%2028124Universidade Federal Do Rio Grande Do Sul, Uruguaiana, Brazil.
  • Bogo Chies JA; Department of Genetics, Programa de Pós-Graduação Em Genética e Biologia Molecular, RinggoldID:%2028124Universidade Federal Do Rio Grande Do Sul, Porto Alegre, Brazil.
  • Monticielo OA; Division of Rheumatology, Department of Internal Medicine, Hospital de Clínicas de Porto Alegre, RinggoldID:%2028124Universidade Federal Do Rio Grande Do Sul, Uruguaiana, Brazil.
Lupus ; 31(3): 279-286, 2022 Mar.
Article in En | MEDLINE | ID: mdl-35104178
ABSTRACT

INTRODUCTION:

Systemic lupus erythematosus (SLE) is a multifactorial disease and MBL2 genetic variants, which are associated to differential peripheral MBL levels, potentially affect its etiology and increase infection risk in this population.

OBJECTIVE:

To evaluate the potential association of MBL2 polymorphisms of the coding and promoter gene region and haplotypes on hospitalization, number of admission and days of admission for major infection causes in Brazilian SLE patients.

Methods:

325 SLE patients from a southern Brazilian outpatient SLE clinic were genotyped in 2006 for MBL2 gene polymorphisms from coding and promoter region (rs1800450, rs1800451, rs5030737, rs11003125, and rs7096206) and followed until 2016. Clinical and laboratory data from each patient were obtained and information regarding the need for hospitalization, the number of admissions and number of days admitted for infection treatment were compiled and compared with MBL2 gene polymorphisms and haplotypes. A linear regression analysis was constructed considering the variables of bivariate which demonstrated an association (p<0.05) and variables which had a theoretical basement.

RESULTS:

No difference was found in polymorphism prevalence when comparing the group that was admitted for infection treatment and the group who did not. Allele C, and haplotypes LY and HY correlated with more infection hospitalizations [wild-type homozygosis for C 2 (IQR 1-3), heterozygosis for C 3 (IQR 2-6) p=0.038; LY 2 (IQR 1-3) p=0.049; HY 2 (IQR 1-3) p=0.005] and haplotype HY carriers stayed fewer days in hospital for infection treatment 18 (IQR 10-38) p=0.041. When linear regression was applied HY associated with shorter admission time for infections (-18.11 days, p=0.021) and HY (-1.52 admission, p 0.001) carriers with older age at diagnosis had less admissions for infection (HY regression model -0.42, p=0.006; LY regression model -0.04, p=0.010; -0.04, p=0.013).

CONCLUSION:

The presence of the HY promoter haplotype associated to fewer in hospital care for infection treatment probably due to higher MBL plasma levels. Also, HY haplotype and older age at SLE diagnosis is related to less admissions for infection. This factor should be taken into consideration, since infection is a very import cause of mortality in SLE patients being also related to aggressive immunosuppressive treatment.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mannose-Binding Lectin / Lupus Erythematosus, Systemic Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Country/Region as subject: America do sul / Brasil Language: En Journal: Lupus Journal subject: REUMATOLOGIA Year: 2022 Document type: Article Affiliation country: Brasil

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mannose-Binding Lectin / Lupus Erythematosus, Systemic Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Country/Region as subject: America do sul / Brasil Language: En Journal: Lupus Journal subject: REUMATOLOGIA Year: 2022 Document type: Article Affiliation country: Brasil