TABLE 4.
Longitudinal correlation of clinical assessments with demographic factors and UPSIT: Rmcorr analysis.
| MoCA | Part III | COG | ADL | |||||
| r rm | p | r rm | p | r rm | p | r rm | p | |
| Anosmia | ||||||||
| Age | −0.464 | 0.004* | 0.156 | 0.364 | −0.082 | 0.634 | −0.039 | 0.822 |
| Duration | −0.457 | 0.005* | 0.071 | 0.681 | −0.099 | 0.565 | −0.104 | 0.546 |
| LEDD | −0.213 | 0.213 | −0.192 | 0.262 | −0.238 | 0.162 | −0.438 | 0.007* |
| UPSIT | 0.139 | 0.420 | 0.239 | 0.160 | 0.193 | 0.259 | 0.324 | 0.054 |
| Non-anosmia | ||||||||
| Age | −0.166 | 0.373 | 0.418 | 0.019* | 0.074 | 0.694 | −0.081 | 0.665 |
| Duration | −0.118 | 0.528 | 0.360 | 0.047* | 0.081 | 0.665 | −0.147 | 0.432 |
| LEDD | −0.030 | 0.872 | 0.120 | 0.520 | −0.011 | 0.951 | −0.242 | 0.190 |
| UPSIT | −0.073 | 0.696 | −0.479 | 0.006* | −0.345 | 0.058 | −0.078 | 0.676 |
The above table shows a negative correlation between UPSIT scores and part III scores in the non-anosmia group (rrm = −0.479, p = 0.006), related to Figure 3. Anosmia: baseline UPSIT < 19; Non-anosmia: baseline UPSIT ≥ 19. ADL, activities of daily living of PDQ-39; COG, cognitions of PDQ-39; LEDD, levodopa equivalent daily dose; MoCA, Montreal cognitive assessment; Part III, part III of movement disorder society-sponsored revision of the Unified Parkinson’s Disease Rating Scale; PDQ-39, Chinese-translated version of 39-item Parkinson’s Disease Questionnaire; Rmcorr, repeated measures correlation; rrm, coefficient or repeat measurement correlation; UPSIT, traditional Chinese version of the University of Pennsylvania Smell Identification Test.
*p < 0.05.