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. 2022 Mar 15;4(2):fcac040. doi: 10.1093/braincomms/fcac040

Table 3.

Predictors of dementia in Parkinson’s disease within 10 years

Clinical model Univariate Multivariable
Phenotype, at baseline Observed range HR (95% CI) P-value HR (95% CI) P-value
Age 39.7–90.0 years 1.07 (1.04–1.10) <0.001* 1.05 (1.01–1.09) 0.014
Years of education 6–30 years 0.9 (0.8–1.0) 0.019*
Smoker Ever versus never 0.9 (0.5–1.6) 0.740
MADRS score 0–18 1.0 (1.0–1.1) 0.147
Sex Male versus female 1.1 (0.6–1.7) 0.820
H&Y stage 1.0–5.0 2.0 (1.4–2.8) <0.001*
UPDRS total score 8–81 1.0 (1.0–1.1) <0.001*
UPDRS III subscore 5–62 1.0 (1.0–1.1) <0.001* 1.0 (1.0–1.1) 0.004
PIGD score 0–2.4 3.2 (1.8–5.7) <0.001*
Tremor score 0–1.5 0.6 (0.3–1.3) 0.220
Blink frequency 0–80 per minute 1.0 (1.0–1.0) 0.029*
Slow saccades Yes versus no 1.2 (0.6–2.3) 0.463
Postural instability first year Yes versus no 4.6 (2.2–9.7) <0.001*
Symmetrical onset Yes versus no 2.3 (2.2–3.9) 0.003*
MCI Yes versus no 4.5 (2.7–7.6) <0.001* 4.2 (2.2–7.7) <0.001
Olfactory function 0–12 correct 0.8 (0.7–0.9) <0.001* 0.8 (0.7–0.9) <0.001
Alcohol use Yes versus no 0.5 (0.3–0.9) 0.014*
Orthostatic blood pressure drop −22 to 107 mmHg 1.0 (1.0–1.0) 0.006*
Biomarkers, at baseline Biomarker model
BMI 19.2–36.5 1.1 (1.0–1.2) 0.035
APOE ɛ4 genotype 0–2 ɛ4 alleles 1.0 (0.6–1.6) 0.851
MAPT haplotype H1/H2 1.0 (0.6–1.8) 0.923
CSF NfL (pg/ml) 271–8700 1.0 (1.0–1.0) <0.001*
CSF Aβ42 (pg/ml) 249–1373 1.0 (1.0–1.0) <0.001*
CSF NfL to Aβ42 ratio 0.4–10.7 1.3 (1.2–1.7) <0.001* 1.5 (1.2–1.7) <0.001
CSF α-synuclein (pg/ml) 0.3–2.2 1.1 (0–1.0) 0.762
B-TSH 0.1–10.0 0.9 (0.7–1.2) 0.538
B-leucocytes 4.0–11.2 1.0 (1.0–1.1) 0.076
B-B12 vitamin 147–1475 1.0 (1.0–1.0) 0.157
B-folate 6.1–54.0 1.0 (1.0–1.0) 0.073
DAT uptake, putamen −5.2 to −0.4 SD 0.79 (0.56–1.11) 0.179
DAT uptake, most affected caudate −4.7 to 0.1 SD 0.65 (0.50–0.85) 0.002* 0.59 (0.39–0.90) 0.014

Hazard ratio (HR) for the risk of developing dementia (PDD) among 143 patients with Parkinson disease, within 10 years. In the multivariable model, only factors that were significant when corrected for age and sex and that were not excluded because of intercorrelation were retained. APOE genotype was investigated by the number of ɛ4 alleles. Eye movement saccades were assessed clinically. Olfactory function was measured by the number of correct answers on the 12-item brief smell inventory test (BSIT).

*

The variable was significant after the Benjamini–Hochberg correction for false discovery rate, with α = 0.05. MCI, mild cognitive impairment; B, measured in blood; SDs, standard deviations.