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Rationale and Design of the Brigham Cohort for psoriasis and psoriatic arthritis registry (COPPAR)

Overview of attention for article published in BMC Dermatology, August 2017
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Title
Rationale and Design of the Brigham Cohort for psoriasis and psoriatic arthritis registry (COPPAR)
Published in
BMC Dermatology, August 2017
DOI 10.1186/s12895-017-0063-8
Pubmed ID
Authors

Maria Schneeweiss, Joseph F. Merola, Elizabeth W. Karlson, Daniel H. Solomon

Abstract

Psoriasis (PsO) and psoriatic arthritis (PsA) are related conditions with poorly defined transition among them, risk factors for progression, complex treatment algorithms, and biomarkers for treatment response and long-term outcomes. We describe the development of a PsO/PsA registry at an academic medical center. We developed a single-center PsO/PsA longitudinal disease registry including biorepository that captures relevant disease markers and treatment choices in a circumscribed population with a defined catchment area. We searched the electronic medical record for patients with visits in the last year for PsO or PsA. They formed the potentially eligible registry population. Baseline patient and provider questionnaires were developed using standardized measures, including demographics, comorbidities, medications, specific disease characteristics, functional status, quality of life, mental health, and resource use. An abbreviated set of items was collected every six month and at visits with treatment changes or disease flares. Biospecimens included blood (serum, plasma, DNA, RNA) and skin biopsy samples, with repeat collections of serum and plasma. Data from the EMR to augment the registry questionnaires are available on all patients. Searching the Brigham EMR system from 2013 through 2014, we found 1694 patients with PsO and 1028 with PsA. Their mean age was 55 years and 53% were female. Of these 17% had diabetes, 38% hyperlipidemia, and 45% hypertension. The median BMI was 29.6. PsA patients used more systemic prednisone, MTX, and TNF alpha inhibitors (47%, 60%, and 66%) compared to PsO patients (28%, 20% and 21%). We have collected plasma in 410 patients, DNA/RNA in 453 patients. In conclusion, we have developed a PsO/PsA registry to better define longitudinal disease characteristics, perform biomarker studies, and examine treatment trends.

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Mendeley readers

The data shown below were compiled from readership statistics for 73 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 73 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 13 18%
Student > Master 9 12%
Researcher 7 10%
Student > Bachelor 6 8%
Student > Doctoral Student 5 7%
Other 13 18%
Unknown 20 27%
Readers by discipline Count As %
Medicine and Dentistry 21 29%
Psychology 5 7%
Social Sciences 5 7%
Pharmacology, Toxicology and Pharmaceutical Science 4 5%
Computer Science 2 3%
Other 11 15%
Unknown 25 34%