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Cross-sectional Evaluation of Biological Markers of Cardiovascular Disease in Children and Adolescents With Psoriasis

Cross-sectional Evaluation of Biological Markers of Cardiovascular Disease in Children and Adolescents With Psoriasis

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01122095
Enrollment
100
Registered
2010-05-12
Start date
2010-04-30
Completion date
2011-04-30
Last updated
2010-05-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Risk, Inflammation, Obesity, Psoriasis

Keywords

Psoriasis, Cardiovascular risk

Brief summary

Hypothesis 1: Patients with psoriasis will have clinical and laboratory assessments differing from control patients. Hypothesis 2: Patients with psoriasis will have laboratory alterations that correlate with other clinical characteristics of their psoriasis.

Detailed description

Psoriasis was initially considered an inflammatory condition primarily of the skin. However, advances in medical knowledge have allowed insight into the wide-ranging systemic effects of long-term uncontrolled inflammation, thus shifting the concept of psoriasis from an inflammatory disease restricted to the skin to a systemic process. Adults w/ psoriasis have higher rates of obesity, hypertension, diabetes, hyperlipidemia and smoking and the prevalence of each risk factor increases as the extent of psoriasis increases.1 It is uncertain if any of this relates to a behavioral reaction to having psoriasis or as a separate part of the disease process. Inflammation has a role in the pathogenesis of cardiovascular disease most noted by multiple observational studies of psoriasis patients which demonstrate an increased risk of arterial or venous events, notably myocardial infarction, cerebrovascular events, pulmonary emboli, cardiovascular death or mortality overall. Specifically, Gelfand et. al. show an increased relative risk for myocardial infarction and an increased hazard ratio for mortality in patients with severe psoriasis, but most notably, show highest risk in younger adult patients. There is a paucity of data on risks with psoriasis in the pediatric and adolescent age group.

Interventions

None listed

Sponsors

Amgen
CollaboratorINDUSTRY
University of California, San Diego
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
No minimum to 18 Years
Healthy volunteers
Yes

Inclusion criteria

Subjects of any race or ethnicity who meet all of the following criteria are eligible for enrollment into the study: 1. The subject has a diagnosis of typical psoriasis, with or without arthritis, based on the clinical evaluation by an investigator or a prior diagnosis by a pediatric dermatologist 2. Persons residing in the US. 3. Subjects 0 to 18 years of age. 4. Subjects/Guardians willing and able to comply with the requirements of the study. 5. Subjects/Guardians willing and able to give informed consent. 6. The subject is in general good health in the opinion of the investigator.

Exclusion criteria

1. Over 18 years of age. 2. Subject has had a diagnosis of congenital heart disease. 3. Subject has had any cardiac catheterizations or surgeries. 4. Subject has taken any cardiac medications (calcium channel blockers, beta blockers, vasotropic medicines) within the past 2 years. 5. Subjects determined to have atypical psoriasis or isolated palmoplantar psoriasis. 6. Subject diagnosed with any other systemic inflammatory disease including atopic dermatitis, severe acne vulgaris, inflammatory bowel disease, juvenile idiopathic arthritis, connective tissue disease and other similar conditions. 7. Having autoimmune or immunodeficiency disease. 8. Presence of active systemic fungal, bacterial, or viral infections. 9. Presence of active systemic malignancy. 10. Mental illness or history of drug or alcohol abuse that, in the opinion of the investigator, would interfere with the participant's ability to comply with study requirements. 11. Inability or unwillingness of a participant to give written informed consent. Control Inclusion Criteria: 1. Age up to 18 years. 2. Ability and willingness to provide informed consent. Control

Design outcomes

Primary

MeasureTime frameDescription
Obesity risk assessment6 monthsBody Mass Index; C-reactive protein (CRP)

Countries

United States

Contacts

Primary ContactLawrence F. Eichenfield, MD
leichenfield@rchsd.org858-966-1700
Backup ContactDonna Pascual, LVN
dpascual@rchsd.org858-571-4295

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026