nominally significantp = 0.021
Results We observed a nominally significant association of the IL1β rs1143623 C allele with the risk for Parkinson’s disease ( OR = 0.59; 95%CI = 0.38–0.92, p = 0.021).
Results We observed a nominally significant association of the IL1β rs1143623 C allele with the risk for Parkinson’s disease ( OR = 0.59; 95%CI = 0.38–0.92, p = 0.021).
The IL1β rs1143623 T allele showed a nonsignificant trend towards association with lower odds for developing OH (OR = 0.57; 95%CI = 0.32–1.00, p = 0.050), while heterozygotes had nominally significant lower odds for developing OH (OR = 0.51; 95%CI = 0.28–0.93, p = 0.028).