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Genetic Risk Factors for Systemic Lupus Erythematosus : From Candidate Genes to Functional Variants
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- Abelson, Anna-Karin, 1978- (författare)
- Uppsala universitet,Institutionen för genetik och patologi
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- Alarcón-Riquelme, Marta, Docent (preses)
- Uppsala universitet,Institutionen för genetik och patologi
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- Luthman, Holger, Professor (opponent)
- Institutionen för kliniska vetenskaper (Malmö), Lunds universitet
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(creator_code:org_t)
- ISBN 9789155473365
- Uppsala : Universitetsbiblioteket, 2008
- Engelska 61 s.
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Serie: Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Medicine, 1651-6206 ; 395
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Abstract
Ämnesord
Stäng
- The aim of this thesis has been to identify genetic variants that increase the susceptibility for Systemic Lupus Erythematosus (SLE), an autoimmune disease caused by a complex interplay between various genetic and environmental factors. Five different candidate genes were selected through different strategies, and were analysed for association with SLE in an attempt to distinguish some of the underlying mechanisms of this disease. Two of these genes, PD-L1 and PD-L2, appeared not to contain any major risk factors for SLE in the analysed European and Latin American populations. In two other genes, CD24 and STAT4, there appeared to be population-specific effects. The A57V amino acid substitution in the CD24 gene, previously implicated with multiple sclerosis, was associated in a Spanish cohort, with a weak trend in German samples, and no association in Swedish. The previously reported and highly convincing association of the STAT4 transcription factor gene was confirmed in all our cohorts. Interestingly, the results indicate the presence of at least two independent risk variants: the first, represented by a previously reported SNP, was the strongest in individuals of Northern European ancestry, and the second was more pronounced in individuals from Southern Europe and Latin America. We also report the identification of a novel susceptibility gene. The BANK1 gene, encoding a scaffold protein involved in B-cell activation, contains functional variants affecting important domains, which are associated in all investigated cohorts from Europe and Latin America. These results confirm the existence of replicable associations between genetic variants and SLE, which are common and present in many populations. The results also illustrate a certain degree of heterogeneity, where some risk factors could have variable effect in different populations.
Ämnesord
- MEDICIN OCH HÄLSOVETENSKAP -- Medicinska och farmaceutiska grundvetenskaper -- Medicinsk genetik (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Basic Medicine -- Medical Genetics (hsv//eng)
Nyckelord
- Systemic Lupus Erythematosus
- SLE
- association study
- complex disease
- genetic
- Medical genetics
- Medicinsk genetik
Publikations- och innehållstyp
- vet (ämneskategori)
- dok (ämneskategori)
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