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. 2017 Apr 3;9:89. doi: 10.3389/fnagi.2017.00089

Table 3.

Correlations in PD patients between 8-OHdG, 8-ISO, TAC, and MoCA scores with UPDRS scores and clinical disease duration.

Association LRRK2 PD sPD
8-OHdG vs. UPDRS Total score -0.14 (0.56) -0.18 (0.33)
8-OHdG vs. UPDRS Part 3 score -0.11 (0.65) -0.22 (0.22)
8-OHdG vs. clinical duration -0.12 (0.62) -0.39 (0.03)
8-ISO vs. UPDRS Total score 0.10 (0.69) 0.17 (0.35)
8-ISO vs. UPDRS Part 3 score 0.14 (0.56) 0.10 (0.61)
8-ISO vs. clinical duration 0.24 (0.32) -0.24 (0.20)
TAC vs. UPDRS Total score -0.33 (0.17) -0.41 (0.02)
TAC vs. UPDRS Part 3 score -0.30 (0.21) -0.20 (0.29)
TAC vs. clinical duration -0.11 (0.64) -0.37 (0.04)
MoCA score vs. UPDRS Total score -0.30 (0.22) -0.49 (0.005)
MoCA score vs. UPDRS Part 3 score -0.27 (0.27) -0.33 (0.07)
MoCA score vs. clinical duration -0.38 (0.11) -0.18 (0.33)

For the two groups of PD patients, the correlations (Spearman rho values) of 8-OHdG, 8-ISO, TAC, and MoCA scores with UPDRS scores and duration of clinical disease are shown, with p-values in parentheses. TAC was negatively correlated with UPDRS Total scores in both PD groups. 8-OHdG and TAC were negatively correlated with clinical duration in sPD patients, and MoCA scores were negatively associated with UPDRS scores in this group. (8-OHdG, 8-hydroxy-2′-deoxy-guanosine; 8-ISO, 8-isoprostane; TAC, total antioxidant capacity; LRRK2 PD, Parkinson’s disease patients with LRRK2 mutations; sPD, sporadic Parkinson’s disease patients; LRRK2 CTL, healthy control subjects with LRRK2 mutations; CTL, healthy control subjects without known PD-associated mutations; MoCA, Montreal Cognitive Assessment; UPDRS, Unified Parkinson’s Disease Rating Scale).