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. Author manuscript; available in PMC: 2017 Sep 1.
Published in final edited form as: Parkinsonism Relat Disord. 2016 Jun 16;30:40–45. doi: 10.1016/j.parkreldis.2016.06.010

Table 4.

Associations between the H2 haplotype (rs8070723) and MSA subtypes

Series/MSA subtype N MAF
(%)
OR (95% CI) P-value
Controls 1312 23.0 1.00 (reference) N/A
Pathologically confirmed MSA-P patients 51 29.4 1.38 (0.89, 2.13) 0.15
Pathologically confirmed MSA-C patients 20 7.5 0.27 (0.08, 0.88) 0.030
Pathologically confirmed MSA-mixed patients 56 8.9 0.33 (0.17, 0.64) 0.001
Pathologically confirmed MSA-P or MSA-Mixed patients 107 18.7 0.77 (0.54, 1.10) 0.15
Pathologically confirmed MSA-C or MSA-Mixed patients 76 8.6 0.32 (0.18, 0.56) <0.0001
Clinically diagnosed MSA-P patients 52 25.0 1.11 (0.71, 1.73) 0.66
Clinically diagnosed MSA-C patients 24 27.1 1.22 (0.65, 2.28) 0.53
Clinically diagnosed MSA-Mixed patients 10 35.0 N/A1 N/A
Clinically diagnosed MSA-P or MSA-Mixed patients 62 26.6 1.20 (0.80, 1.80) 0.38
Clinically diagnosed MSA-C or MSA-Mixed patients 34 29.4 1.37 (0.81, 2.30) 0.24
All MSA-P patients 103 27.2 1.23 (0.90, 1.70) 0.19
All MSA-C patients 44 18.2 0.74 (0.43, 1.27) 0.28
All MSA-Mixed patients 66 12.9 0.50 (0.30, 0.84) 0.008
All MSA-P or MSA-Mixed patients 169 21.6 0.92 (0.70, 1.21) 0.55
All MSA-C or MSA-Mixed patients 110 15.0 0.60 (0.41, 0.87) 0.007

ORs, 95% CIs, and p-values result from logistic regression models adjusted for age (age at death in pathologically confirmed MSA patients and age at blood collection in clinically diagnosed MSA patients and controls) and gender. ORs correspond to each additional H2 allele.

1

Logistic regression analysis was not performed owing to the small number of clinically diagnosed MSA-mixed patients.

MSA=multiple system atrophy; MAF=minor allele frequency; OR=odds ratio; CI=confidence interval