Diabetes mellitus and Parkinson disease
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Abstract
Objective To investigate whether diabetes mellitus is associated with Parkinson-like pathology in people without Parkinson disease and to evaluate the effect of diabetes mellitus on markers of Parkinson pathology and clinical progression in drug-naive patients with early-stage Parkinson disease.
Methods We compared 25 patients with Parkinson disease and diabetes mellitus to 25 without diabetes mellitus, and 14 patients with diabetes mellitus and no Parkinson disease to 14 healthy controls (people with no diabetes mellitus or Parkinson disease). The clinical diagnosis of diabetes mellitus was confirmed by 2 consecutive fasting measurements of serum glucose levels >126 mL/dL. Over a 36-month follow-up period, we then investigated in the population with Parkinson disease whether the presence of diabetes mellitus was associated with faster motor progression or cognitive decline.
Results The presence of diabetes mellitus was associated with higher motor scores (p < 0.01), lower striatal dopamine transporter binding (p < 0.05), and higher tau CSF levels (p < 0.05) in patients with Parkinson disease. In patients with diabetes but without Parkinson disease, the presence of diabetes mellitus was associated with lower striatal dopamine transporter binding (p < 0.05) and higher tau (p < 0.05) and α-synuclein (p < 0.05) CSF levels compared to healthy controls. At the Cox survival analysis in the population of patients with Parkinson disease, the presence of diabetes mellitus was associated with faster motor progression (hazard ratio = 4.521, 95% confidence interval = 1.468–13.926; p < 0.01) and cognitive decline (hazard ratio = 9.314, 95% confidence interval = 1.164–74.519; p < 0.05).
Conclusions Diabetes mellitus may predispose toward a Parkinson-like pathology, and when present in patients with Parkinson disease, can induce a more aggressive phenotype.
Glossary
- C-DM=
- controls with diabetes mellitus;
- CI=
- confidence interval;
- DM=
- diabetes mellitus;
- DMT=
- disease-modifying therapy;
- DPP-4=
- dipeptidyl peptidase-4;
- [123I]FP-CIT=
- [123I]-2β-carbomethoxy-3β-(4-iodophenyl)-N-(3-fluoropropyl)nortropane;
- GIP=
- glucose-dependent insulinotropic peptide;
- GLP-1=
- glucagon-like peptide 1;
- H&Y=
- Hoehn and Yahr;
- HC=
- controls without diabetes mellitus;
- HR=
- hazard ratio;
- MDS-UPDRS=
- Movement Disorder Society–Unified Parkinson’s Disease Rating Scale;
- MoCA=
- Montreal Cognitive Assessment;
- PD=
- Parkinson disease;
- PPMI=
- Parkinson's Progression Markers Initiative;
- ROI=
- region of interest;
- SBR=
- specific binding ratio
Footnotes
Go to Neurology.org/N for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.
CME Course: NPub.org/cme
Editorial, page 869
- Received September 11, 2017.
- Accepted in final form February 8, 2018.
- © 2018 American Academy of Neurology
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