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. 2017 Sep 4;137(1):91–98. doi: 10.1111/ane.12812

Table 4.

Longitudinal cognitive function and cerebrospinal fluid data in 134 Parkinson's disease patients, in relation to COMT Val158Met‐ and DRD2 C957T genotype

Cognitive domain Mean difference, measured in SDs (95% CI) P‐value
COMT 158Val/Val genotype vs. any Met allele
Episodic memory −0.05 (−0.25‐0.15) .598
Working memory −0.14 (−0.53‐0.25) .482
Attention −0.18 (−0.20‐0.56) .350
Executive function −0.19 (−0.51‐0.13) .245
Visuospatial function −0.20 (−0.62‐0.22) .343
DRD2 957T/T genotype vs. any C allele
Episodic memory −0.25 (−0.43 to −0.07) .007a
Free recall −0.42 (−0.78 to −0.07) .021a
Cued recall 0.36 (0.04‐0.67) .026a
Working memory −0.33 (−0.69‐0.01) .060
Attention −0.58 (−0.91 to −0.26) <.001a
Executive function −0.31 (−0.61 to −0.02) .034
Visuospatial function −0.38 (−0.75 to −0.01) .044
Cerebrospinal fluid NFL concentration Difference, ng/L (95% CI) P‐value
COMT 158Val/Val genotype vs. any Met allele 3.8 (−433.0‐440.7) .986
DRD2 957T/T genotype vs. any C allele 265.2 (−125.7‐656.1) .181

Fixed effects estimates for differences at 0, 1, 3, 5, and 8 years (for NFL concentration at 0, 1, and 3 years), after correction for age, sex, disease duration, time of testing, and years of education.

a

Significant (P < 0.05) after Holm‐Bonferroni correction.

COMT, catechol‐O‐methyltransferase; DRD2, dopamine receptor D2; SD, standard deviation; NFL, neurofilament light chain protein.