PRODDIAG¶
Table Description: Prodromal, Genetic Unaffected and Registry Unaffected Cohorts - Diagnostic Questionnaire
Detailed notes for this table are included below.
View Source CRFs¶
1.0 CRFs: Click on any PAG_NAME link below to be taken to the CRF used in the PPMI 1.0 Study.
1.0 Data Dictionary¶
ITM_NAME |
DSCR_1.0 |
|---|---|
OTHNEURO |
Other neurological disorder(s) (specify) |
PRIMDIAG |
Most likely primary diagnosis |
PSLVL2 |
Confidence level-motor signs of PS |
1.0 Code Book¶
ITM_NAME |
CODE |
DECODE_1.0 |
|---|---|---|
PRIMDIAG |
1 |
Idiopathic PD |
PRIMDIAG |
2 |
Alzheimer’s disease |
PRIMDIAG |
3 |
Chromosome-17 frontotemporal dementia |
PRIMDIAG |
4 |
Corticobasal degeneration |
PRIMDIAG |
5 |
Dementia with Lewy bodies |
PRIMDIAG |
6 |
Dopa-responsive dystonia |
PRIMDIAG |
7 |
Essential tremor |
PRIMDIAG |
8 |
Hemiparkinson/hemiatrophy syndrome |
PRIMDIAG |
9 |
Juv. autosomal recessive parkinsonism |
PRIMDIAG |
10 |
Motor neuron disease with parkinsonism |
PRIMDIAG |
11 |
Multiple system atrophy |
PRIMDIAG |
12 |
Neuroleptic-induced parkinsonism |
PRIMDIAG |
13 |
Normal pressure hydrocephalus |
PRIMDIAG |
14 |
Progressive supranuclear palsy |
PRIMDIAG |
15 |
Psychogenic illness |
PRIMDIAG |
16 |
Vascular parkinsonism |
PRIMDIAG |
17 |
No PD nor other neurological disorder |
PRIMDIAG |
18 |
Spinocerebellar Ataxia (SCA) |
PRIMDIAG |
23 |
Prodromal non-motor PD |
PRIMDIAG |
24 |
Prodromal motor PD |
PRIMDIAG |
97 |
Other neurological disorder(s) (specify) |
PSLVL2 |
1 |
Motor abnormalities are PS (90-100%) |
PSLVL2 |
2 |
Motor abnormalities likely PS (70-89%) |
PSLVL2 |
3 |
Motor abnormalities may be PS (50-69%) |
PSLVL2 |
4 |
Non-specific motor abnormalities(25-49%) |
PSLVL2 |
5 |
No evidence of park. motor signs (0-24%) |
Details¶
As of the transition to the PPMI Extended schema, this table is inactive. However, two variables that were captured in this table are now being captured in the PRIMDXPD table. These include OTHNEURO and PRIMDIAG.