Low-variance RNAs identify Parkinson's disease molecular signature in blood.

TitleLow-variance RNAs identify Parkinson's disease molecular signature in blood.
Publication TypeJournal Article
Year of Publication2015
AuthorsChikina, MD, Gerald, CP, Li, X, Ge, Y, Pincas, H, Nair, VD, Wong, AK, Krishnan, A, Troyanskaya, OG, Raymond, D, Saunders-Pullman, R, Bressman, SB, Yue, Z, Sealfon, SC
JournalMov Disord
Volume30
Issue6
Pagination813-21
Date Published2015 30 05
ISSN1531-8257
KeywordsAged, Aged, 80 and over, Animals, Biomarkers, Case-Control Studies, Early Diagnosis, Female, Gene Expression, Genetic Predisposition to Disease, Heterozygote, Humans, Jews, Leucine-Rich Repeat Serine-Threonine Protein Kinase-2, Male, Mice, Mice, Transgenic, Middle Aged, Mutation, Parkinson Disease, Protein-Serine-Threonine Kinases, RNA, Messenger
Abstract

The diagnosis of Parkinson's disease (PD) is usually not established until advanced neurodegeneration leads to clinically detectable symptoms. Previous blood PD transcriptome studies show low concordance, possibly resulting from the use of microarray technology, which has high measurement variation. The Leucine-rich repeat kinase 2 (LRRK2) G2019S mutation predisposes to PD. Using preclinical and clinical studies, we sought to develop a novel statistically motivated transcriptomic-based approach to identify a molecular signature in the blood of Ashkenazi Jewish PD patients, including LRRK2 mutation carriers. Using a digital gene expression platform to quantify 175 messenger RNA (mRNA) markers with low coefficients of variation (CV), we first compared whole-blood transcript levels in mouse models (1) overexpressing wild-type (WT) LRRK2, (2) overexpressing G2019S LRRK2, (3) lacking LRRK2 (knockout), and (4) and in WT controls. We then studied an Ashkenazi Jewish cohort of 34 symptomatic PD patients (both WT LRRK2 and G2019S LRRK2) and 32 asymptomatic controls. The expression profiles distinguished the four mouse groups with different genetic background. In patients, we detected significant differences in blood transcript levels both between individuals differing in LRRK2 genotype and between PD patients and controls. Discriminatory PD markers included genes associated with innate and adaptive immunity and inflammatory disease. Notably, gene expression patterns in levodopa-treated PD patients were significantly closer to those of healthy controls in a dose-dependent manner. We identify whole-blood mRNA signatures correlating with LRRK2 genotype and with PD disease state. This approach may provide insight into pathogenesis and a route to early disease detection.

DOI10.1002/mds.26205
Alternate JournalMov. Disord.
PubMed ID25786808
PubMed Central IDPMC4439364
Grant ListR01 NS060809 / NS / NINDS NIH HHS / United States
R01 NS072359 / NS / NINDS NIH HHS / United States
R01NS060809 / NS / NINDS NIH HHS / United States
R01NS072359 / NS / NINDS NIH HHS / United States