Parkinson disease (PD) is the second most common neurodegenerative disorder. Its diagnosis relies solely on a clinical examination and is not straightforward because no diagnostic test exists. Large, population-based, prospective cohort studies designed to examine other outcomes that are more common than PD might provide cost-efficient alternatives for studying the disease. However, most cohort studies have not implemented rigorous systematic screening for PD. A majority of epidemiologic studies that utilize population-based prospective designs rely on secondary data sources to identify PD cases. Direct validation of these secondary sources against clinical diagnostic criteria is lacking. The Framingham Heart Study has prospectively screened and evaluated participants for PD based on clinical diagnostic criteria. We assessed the predictive value of secondary sources for PD identification relative to clinical diagnostic criteria in the Framingham Heart Study (2001)(2002)(2003)(2004)(2005)(2006)(2007)(2008)(2009)(2010)(2011)(2012). We found positive predictive values of 1.0 (95% confidence interval: 0.868, 1.0), 1.0 (95% confidence interval: 0.839, 1.0), and 0.50 (95% confidence interval: 0.307, 0.694) for PD identified from self-report, use of antiparkinsonian medications, and Medicare claims, respectively. The negative predictive values were all higher than 0.99. Our results highlight the limitations of using only Medicare claims data and suggest that population-based cohorts may be utilized for the study of PD determined via self-report or medication inventories while preserving a high degree of confidence in the validity of PD case identification. Parkinson disease (PD) is the second most common neurodegenerative disorder after Alzheimer disease. PD afflicts more than 4 million people worldwide and is projected to affect 9 million people by 2030 (1). The etiology for most sporadic cases remains unknown, as genetic variants account for only approximately 10% of cases (2). PD has a low incidence (8-18 per 100,000 person-years), and it is impractical to conduct a prospective, longitudinal epidemiologic study on a condition that relies on a clinical examination for a diagnosis because there is no biomarker or simple laboratory test that can confirm a PD diagnosis except autopsy. Registries for PD that cover large populations do not exist. Case-control studies are often limited by retrospective recall or ascertainment of exposures.Large, population-based, prospective cohort studies designed to examine more common diseases might provide cost-effective ways to study PD within a longitudinal framework. Such studies have accumulated sufficient numbers of patients with incident PD to allow examinations of the associations with multiple potential risk factors and associations that develop over long periods of time. Indeed, the use of existing cohorts to study PD has resulted in numerous significant findings (2). However, most cohort studies have not implemented rigorous systematic screening for PD and have necessarily re...