Table 1 The surveys or experiments about Parkinson’s disease and oral diseases
Reference | Sample content | The type of assessments | The situation of the subjects | The disease or symptom | Conclusion |
---|---|---|---|---|---|
Verhoeff et al.12 | 63 studies | Prevalence of self-reported xerostomia and drooling | 534 participants with Parkinson’s disease were involved in the objective studies, and 11 670 participants were included in the subjective studies. The objective and subjective study participants had a mean age of 67 ± 7 and 62 ± 17 years, respectively. | Xerostomia | Parkinsonians’ probability of suffering by xerostomia higher than healthy people. Patients with Parkinson’s disease have a lower salivary flow rate and higher prevalence of both xerostomia and drooling. |
Yilmaz et al.20 | 60 patients and 20 healthy individuals | Recording and comparing the periodontal status, collecting serum, saliva, and gingival revicular fluid samples to judge the level of PD | 60 patients with Stage III, Grade B periodontitis and 20 healthy individuals as controls. | Periodontitis | There is a high positive correlation between PD and periodontitis. |
Minervini et al.34 | 3 studies | Prevalence of TMDs | All together they comprised a total of 55 828 subjects, out of which 12 629 were affected by PD or Parkinsonism, and the remaining 43 199 were non-PD subjects matched for age and sex. | Temporomandibular disorders | There was a higher TMD prevalence in PD subjects compared to non-PD subjects. |
Weintraub et al.37 | 315 patients | Observational data from Parkinson’s Progression Markers Initiative annual visits was used to evaluate prevalence, correlates, and treatment of 10 neuropsychiatric symptoms and cognitive impairment in Parkinson disease participants and matched healthy controls. | Eight neuropsychiatric symptoms studied increased in absolute prevalence by 6.2–20.9% at year 5 relative to baseline, and cognitive impairment increased by 2.7–6.2%. | Neuropsychiatric disorders/ cognitive impairment | PD patients’ probability of cognitive impairment is higher than healthy people obviously. |
Li et al.62 | Data from the UK Biobank, summary statistics from previous genome-wide association studies. | Objective assessments (Cox proportional hazards regression analysis, extensive genetic analyses); About the relevancy between systemic inflammation with CRP IL-6 as symbols and PD. | NA | NA | There is a negatively correlated between CRP and PD; PD and IL-6 haven’t apparent correlation. |
Muñoz-Delgado et al.64 | 555 patients | Clinical features, the peripheral immune profile, and striatal | The patients with different levels of PD (including 211 people in primary-cohort, 344 people in PPMI-cohort). | Systemic inflammation | There is a relationship between systemic inflammation and dopaminergic degeneration in patients with PD. |
Zhang et al.118 | Male C57BL/6J mice aged 8–10 wk | Blood Zn concentrations; degeneration of dopaminergic neurons; Open field test, rotarod test, immunohistochemistry, and RNA sequencing were performed after 13 wk. | The mice were categorized as four types: Saline-ZnA、Saline-ZnD、MPTP-ZnA and MPTP-ZnD | Circulating Zn concentrations | Zn deficiency aggravates movement disorders in PD mice, appropriate Zn supplementation may be beneficial for PD. |