Multiple Sclerosis
|
0.500 |
Biomarker
|
disease |
BEFREE |
This meta-analysis provides strong evidence that EBV alone, HLA-DRB1*1501 alone or their interaction is associated with an elevated risks of MS.
|
26656273 |
2015 |
Multiple Sclerosis
|
0.500 |
Biomarker
|
disease |
BEFREE |
This approach, much simpler than previously available methods, should facilitate research on MS by making accurate identification of DRB1*1501 accessible to neuroscience laboratories.
|
20493561 |
2010 |
Multiple Sclerosis
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
We investigated the influence of KIR genes on MS susceptibility in 447 MS Portuguese patients, and also whether genetic interactions between specific KIR genes and their HLA class I ligands could contribute to the pathogenesis of MS. We observed a negative association between the activating KIR2DS1 gene and MS (adjusted OR=0.450, p=0.030) independently from the presence of HLA-DRB1*15 allele.
|
24529855 |
2014 |
Multiple Sclerosis
|
0.500 |
Biomarker
|
disease |
BEFREE |
KIR2DL3-dependent risk reduction remained significant after elimination of patients carrying MS-associated DRB1*15, DRB1*03, DRB1*01 alleles.
|
22185807 |
2012 |
Multiple Sclerosis
|
0.500 |
Biomarker
|
disease |
BEFREE |
Antibody response levels toward Epstein Barr virus (EBV), cytomegalovirus (CMV), and herpes simplex virus (HSV)-1, and HLA-DRB1*1501 status were determined in pediatric MS patients (n=189) and controls (n=38).
|
23232601 |
2013 |
Multiple Sclerosis
|
0.500 |
Biomarker
|
disease |
BEFREE |
Logistic analysis revealed independent associations of [P] allele in the profiles for PvuII (p=0.0005, adjusted odds ratio (aOR)=3.17) and DRB1*1501 (p=0.0089, aOR=2.61) with conventional MS. Synergistic elevated risk of MS due to interaction between the [P] allele and HLA-DRB1*1501 allele was found among female patients (odds ratio=16.0; 95% CI=3.99-63.8, p<0.0001).
|
12098513 |
2002 |
Multiple Sclerosis
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
DRB1*1501, DQB1*0602 and DQB1*0608 alleles were the only positive HLA association with MS.
|
18312478 |
2008 |
Multiple Sclerosis
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
The HLA-DR2 haplotype (DRB1*1501, DQB1*0602) on chromosome 6p21 has consistently demonstrated both association and linkage with multiple sclerosis (MS) in case-control and family studies, particularly in Caucasians of Northern European descent.
|
12225902 |
2002 |
Multiple Sclerosis
|
0.500 |
GeneticVariation
|
disease |
LHGDN |
However, we show for the first time that HLA-DRB1*15 allele modulates the course of MS for relapsing-remitting (RR) onset patients likely by precipitating the secondary progressive (SP) phase.
|
18615093 |
2008 |
Multiple Sclerosis
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
The putative haplotype, DRB1*1501.DQA1*0102.DQB1*0602, was weakly positively associated with MS in both races.
|
7761978 |
1995 |
Multiple Sclerosis
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
The HLA-DR15 extended haplotype HLA-DRB1*15:01-DQA1*01:02-DQB1*06:02 comprises the strongest genetic risk factor for multiple sclerosis (MS).
|
30836273 |
2019 |
Multiple Sclerosis
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Cross-ethnic comparison between the two HLA haplotypes associated with MS in Sardinians and the DRB1*1501 (DR2)-DQA1*0102-DQB1* 0602 haplotype, associated with MS in other Caucasian populations, failed to identify any shared epitopes in the DR and DQ molecules that segregated with disease susceptibility.
|
9668164 |
1998 |
Multiple Sclerosis
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Moreover, the risky genotypes TT and TC were showed to be associated with an increased MS risk, and this was aggravated by the homozygous carriage of the HLA-DRB1*15:01 allele (OR = 2.82 vs. 4.86, p < .0001).
|
30875612 |
2019 |
Multiple Sclerosis
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Multiple sclerosis (MS) is a complex trait in which alleles at or near the class II loci HLA-DRB1 and HLA-DQB1 contribute significantly to genetic risk.
|
18606010 |
2008 |
Multiple Sclerosis
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
While in these 397 families, 8 markers showed significant association with MS, through conditional tests we determined that these MOG variants were not associated with MS independently of the main DRB1-DQB1 disease associations.
|
17509152 |
2007 |
Multiple Sclerosis
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
CNS-specific ANA were more frequent in MS than in NMOSD patients or HCs (13.5% vs 0% for both comparisons, both p < .05) and were associated with HLA-DRB1*15:01 (p = .0174).
|
31835211 |
2020 |
Multiple Sclerosis
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
The expected MS associated HLA-pattern of Caucasoid patients, however, was found in the MS-only patients (42% carried DRB1*1501-DQB1*0602, 58% carried DQA1*0102), while the prevalence of T1DM susceptibility and 'resistance' alleles was not different from the general population.
|
12149602 |
2002 |
Multiple Sclerosis
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Although the interaction was not statistically significant, there appeared to be a trend of increasing risk of MS in participants who were homozygous for the HLA-DRB1*1501 allele in association with the more active form of the VDR (Fok1).
|
21816760 |
2012 |
Multiple Sclerosis
|
0.500 |
Biomarker
|
disease |
BEFREE |
Integrating risk factors: HLA-DRB1*1501 and Epstein-Barr virus in multiple sclerosis.
|
18272866 |
2008 |
Multiple Sclerosis
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
We confirmed the association of DRB1*1501-DQB1*0602 haplotype carriage with MS in both Wexford [odds ratio (OR) = 2.95, P= 0.0020, P(cor)= 0.0220] and Donegal (OR = 2.29, P= 0.0030, P(cor)= 0.0420).
|
16948649 |
2006 |
Multiple Sclerosis
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Furthermore, the DR2-associated DRB1*1501 allele and DRB5*0101 allele were associated with Western-type MS (41.2%), but not with either Asian-type MS (0%) or healthy control subjects (14.2%).
|
8871575 |
1996 |
Multiple Sclerosis
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
To closer model presentation of human MOG by astrocytes in MS patients, we generated astrocytes from transgenic mice expressing the MS-associated MHC class II alleles HLA-DR2 (DRB1*1501) and HLA-DR4 (DRB1*0401).
|
16386804 |
2006 |
Multiple Sclerosis
|
0.500 |
Biomarker
|
disease |
BEFREE |
We demonstrate an independent effect by HLA-DRB1*1501, adolescent summer sun habits, and body mass index at the age of 20 on age at onset of MS.
|
26446064 |
2016 |
Multiple Sclerosis
|
0.500 |
Biomarker
|
disease |
LHGDN |
Multiple sclerosis immunopathic trait and HLA-DR(2)15 as independent risk factors in multiple sclerosis.
|
17463066 |
2007 |
Multiple Sclerosis
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Conventional MS in Japanese people is, like MS in white people, associated with HLA-DRB1*1501, whereas opticospinal MS is associated with HLA-DPB1*0501.
|
12849268 |
2003 |