Study of HLA as a predisposing factor and its possible influence on the outcome of multiple sclerosis in the sanitary district of Calatayud, NorthernSpain

Citation
Ma. Pina et al., Study of HLA as a predisposing factor and its possible influence on the outcome of multiple sclerosis in the sanitary district of Calatayud, NorthernSpain, NEUROEPIDEM, 18(4), 1999, pp. 203-209
Citations number
34
Categorie Soggetti
Neurosciences & Behavoir
Journal title
NEUROEPIDEMIOLOGY
ISSN journal
02515350 → ACNP
Volume
18
Issue
4
Year of publication
1999
Pages
203 - 209
Database
ISI
SICI code
0251-5350(199907/08)18:4<203:SOHAAP>2.0.ZU;2-X
Abstract
The relationship between multiple sclerosis (MS) and the HLA antigens DR2 a nd DQ1 is well recognised, but, in Spain, it has not been clearly defined. The aim of our study was to investigate the relationship between MS and HLA antigens in the sanitary district of Calatayud, northern Spain, and to cor relate these antigens with the progression of the disease. Thirty-four pati ents were selected from a long-term (October 1990 to July 1996) prospective survey in the region where there was a prevalence rate of 58 per 100,000 p opulation. The HLA antigens were determined in 31 patients. A control group of 895 people of Caucasian race was recruited from the same population. We performed serologic tests on all participants. Nucleotide typing was carri ed out in DR2-positive patients. The most frequent antigens in excess in MS were: A19 (odds ratio, OR: 2.29, p = 0.04), 85 (OR: 2.85, p = 0.02), B41 ( OR: 7.65, p = 0.04), CW7 (OR: 3.4, p = 0.004), DR6 (OR: 6.18, p = 0.0001) a nd DR10 (OR: 3.4, p = 0.004). The DR2 antigen was also more frequent in MS patients (39%) than in controls (19%; OR: 2.69, p = 0.01). All positive DR2 patients showed the DR15(2) split but not the DR16(2) split. The frequency of antigens CW4 and DR1 was lower in MS patients than in controls. The CW4 antigen was detected in 12% of the patients and in 33% of the controls (OR : 0.28, p = 0.04). The DR1 antigen was found in 20% of the controls and in none of the MS patients (OR: undefined, p = 0.01). The DQ1 antigen was obse rved in 68% of the patients and in 50% of the controls (OR: 2.1, p = 0.07). We did not find any relationship between HLA antigens and progression of t he disease. Although we found that DR2 antigen is linked to MS, we also fou nd other antigens related to the disease. This suggests a genetic heterogen eity in our geographic area. We also concluded that the DR1 antigen may pla y a protective role, as it was detected in 20% of the controls and in none of the MS cases.