APOE, MAPT, and COMT and Parkinson's Disease Susceptibility and Cognitive Symptom Progression

Gene variants that predict cognitive decline in PD. It is said that much of the heterogeneity that underlies PD is genetically determined. We are finding out more about this all the time. It may be useful in due course to test for certain variants to allow better prognostication, and hopefully one day, tailored treatment...

J Parkinsons Dis. 2016 Apr 2. [Epub ahead of print]

Paul KC, Rausch R, Creek MM, Sinsheimer JS, Bronstein JM, Bordelon Y, Ritz B.

http://content.iospress.com/articles/journal-of-parkinsons-disease/jpd150762

BACKGROUND:

Cognitive decline is well recognized in Parkinson's disease (PD) and a major concern for patients and caregivers. Apolipoprotein E (APOE), catechol-O-methyl transferase (COMT), and microtubule-associated protein tau (MAPT) are of interest related to their contributions to cognitive decline or dementia in PD.

OBJECTIVE:

Here, we investigate whether APOE, COMT, or MAPT influence the rate of cognitive decline in PD patients.

METHODS:

We relied on 634 PD patients and 879 controls to examine gene-PD susceptibility associations, and nested longitudinal cohort of 246 patients from the case-control study, which followed patients on average 5 years and 7.5 years into disease. We repeatedly assessed cognitive symptom progression with the MMSE and conducted a full neuropsychological battery on a subset of 183 cognitively normal patients. We used repeated-measures regression analyses to assess longitudinal associations between genotypes and cognitive progression scores.

RESULTS:

The MAPT H1 haplotype was associated with PD susceptibility. APOE 4 carriers (ɛ4+) (p = 0.03) and possibly COMT Met/Met (p = 0.06) carriers exhibited faster annual decline on the MMSE. Additionally, APOEɛ4+ carriers showed faster decline in many of the neuropsychological test scores. No such differences in neuropsychological outcomes were seen for the COMT genotypes.

CONCLUSION:

This work supports a growing set of research identifying overlapping etiology and pathology between synucleinopathies, such as PD, Alzheimer's disease, and tauopathies, especially in the context of cognitive dysfunction in PD. We provide support for the argument that APOE ɛ4+ and COMT Met/Met genotypes can be used as predictors of faster cognitive decline in PD.

KEYWORDS:

APOE; COMT; MAPT; Parkinson’s disease; cognition; cognitive decline