The Parkinson's progression markers initiative (PPMI) - establishing a PD biomarker cohort

被引:331
作者
Marek, Kenneth [1 ]
Chowdhury, Sohini [2 ]
Siderowf, Andrew [3 ]
Lasch, Shirley [1 ]
Coffey, Christopher S. [4 ]
Caspell-Garcia, Chelsea [4 ]
Simuni, Tanya [5 ]
Jennings, Danna [6 ]
Tanner, Caroline M. [7 ]
Trojanowski, John Q. [3 ]
Shaw, Leslie M. [3 ]
Seibyl, John [1 ]
Schuff, Norbert [7 ]
Singleton, Andrew [8 ]
Kieburtz, Karl [9 ]
Toga, Arthur W. [8 ]
Mollenhauer, Brit [10 ]
Galasko, Doug
Chahine, Lana M. [3 ]
Weintraub, Daniel [3 ]
Foroud, Tatiana [11 ,12 ]
Tosun-Turgut, Duygu [7 ]
Poston, Kathleen [13 ]
Arnedo, Vanessa [2 ]
Frasier, Mark [2 ]
Sherer, Todd [2 ]
机构
[1] Inst Neurodegenerat Disorders, 60 Temple St,Suite 8A, New Haven, CT 06510 USA
[2] Michael J Fox Fdn Parkinsons Res, New York, NY USA
[3] Univ Penn, Philadelphia, PA 19104 USA
[4] Univ Iowa, Iowa City, IA USA
[5] Northwestern Univ, Chicago, IL 60611 USA
[6] Eli Lilly & Co, New York, NY USA
[7] Univ Calif San Francisco, San Francisco, CA 94143 USA
[8] NIA, NIH, Bethesda, MD 20892 USA
[9] Univ Rochester, Clin Trials Coordinat Ctr, Rochester, NY USA
[10] Paracelsus Elena Klin, Kassel, Germany
[11] Univ Calif San Diego, San Diego, CA 92103 USA
[12] Indiana Univ, Indianapolis, IN 46204 USA
[13] Stanford Univ, Med Ctr, Stanford, CA 94305 USA
来源
ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY | 2018年 / 5卷 / 12期
关键词
CEREBROSPINAL-FLUID; ALPHA-SYNUCLEIN; DE-NOVO; AMYLOID-BETA; DISEASE; TAU; DISORDERS; I-123-IOFLUPANE; QUESTIONNAIRE; PERFORMANCE;
D O I
10.1002/acn3.644
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective The Parkinson's Progression Markers Initiative (PPMI) is an observational, international study designed to establish biomarker-defined cohorts and identify clinical, imaging, genetic, and biospecimen Parkinson's disease (PD) progression markers to accelerate disease-modifying therapeutic trials. Methods A total of 423 untreated PD, 196 Healthy Control (HC) and 64 SWEDD (scans without evidence of dopaminergic deficit) subjects were enrolled at 24 sites. To enroll PD subjects as early as possible following diagnosis, subjects were eligible with only asymmetric bradykinesia or tremor plus a dopamine transporter (DAT) binding deficit on SPECT imaging. Acquisition of data was standardized as detailed at . Results Approximately 9% of enrolled subjects had a single PD sign at baseline. DAT imaging excluded 16% of potential PD subjects with SWEDD. The total MDS-UPDRS for PD was 32.4 compared to 4.6 for HC and 28.2 for SWEDD. On average, PD subjects demonstrated 45% and 68% reduction in mean striatal and contralateral putamen Specific Binding Ratios (SBR), respectively. Cerebrospinal fluid (CSF) was acquired from >97% of all subjects. CSF (PD/HC/SWEDD pg/mL) alpha-synuclein (1845/2204/2141) was reduced in PD vs HC or SWEDD (P < 0.03). Similarly, t-tau (45/53) and p-tau (16/18) were reduced in PD versus HC (P < 0.01), Interpretation PPMI has detailed the biomarker signature for an early PD cohort defined by clinical features and imaging biomarkers. This strategy provides the framework to establish biomarker cohorts and to define longitudinal progression biomarkers to support future PD treatment trials.
引用
收藏
页码:1460 / 1477
页数:18
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