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Evaluation of Adipokines and Fat Tissue in Psoriasis and Psoriatic Arthritis

Evaluation of Adipokines and Fat Tissue in Psoriasis and Psoriatic Arthritis and Assessment of Their Relations With the Risk of Cardiovascular Disease

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02849795
Acronym
ADIPSO
Enrollment
199
Registered
2016-07-29
Start date
2014-04-30
Completion date
2017-10-17
Last updated
2018-02-12

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

Conditions

Psoriasis, Arthritic Psoriasis

Keywords

Obesity, Abdominal, Adipokines, Risk of cardiovascular diseases

Brief summary

Body composition analysis and especially body fat distribution in regions of interest (android and in particular intra-abdominal region) provides some information on the risk of cardiovascular disease. There is little data available on the body composition analysis in psoriasis and psoriatic arthritis (diseases with higher risk of cardiovascular disease), in particular data on fat distribution in regions of interest regarding the risk of cardiovascular disease. Adipokines, secreted by the adipose tissue, have pro or anti-inflammatory and metabolic properties that are interesting to explore in pathologies with a higher risk of cardiovascular disease like psoriasis or psoriatic arthritis. Adipokines have been investigated in psoriasis but fat tissue and in particular its distribution (android/visceral or intra-abdominal) has not been studied in parallel. Moreover, relation between adipokines and psoriasis area or severity has been studied but the relation between adipokines and cardiovascular risk factors has not yet been investigated. The aim of this study is to investigate relations between the body fat distribution, adipokines rates and the risk of cardiovascular disease of these patients.

Interventions

OTHERquestionnaires

Sponsors

Centre Hospitalier Universitaire de Besancon
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* diagnosis of psoriasis vulgaris or psoriasis pustulosa confirmed by a dermatologist or a diagnosis of psoriatic arthritis (CASPAR criteria) confirmed by a rheumatologist * Age ≥ 18 and ≤ 80 years old * Control group: patients matching with sex, age ± 5 years, BMI (4 groups), coming to the same hospital for a consultation. (BMI groups : BMI \< 18,5 kg/m²; 18,5 ≤ BMI ≤ 24,99 kg/m²; 25≤ BMI ≤ 29,99 kg/m²; BMI ≥ 30 kg/m²) Control group patients for psoriatic arthritis will be included during a rheumatologist consultation. They may have a non-inflammatory common disco-vertebral pathology (lumbago, lumbosciatic, spinal stenosis, neck pain, cervical arthritis and cervicobrachial neuralgia). Control group patients for psoriasis will be included during a dermatologist consultation. They may have a non-inflammatory skin disease (acne, acne rosacea, idiopathic Raynaud's phenomenon, basal cell carcinoma, acanthosis nigricans). In case of recruitment difficulties, healthy volunteers can be included. * Postmenopausal women (for at least 24 months), surgically sterilized, or for women of childbearing age, efficacy use of contraceptive methods (contraceptive pills, injections or patches, intra-uterine device, double-barrier contraception), * Signature of informed consent form * French social security Affiliation

Exclusion criteria

* Pregnant woman * Corticosteroid therapy \>10 mg of prednisone or equivalent /day * Patients taking biological therapy (anti-TNFalpha therapy: infliximab, etanercept, adalimumab, golimumab, certolizumab ; anti-Interleukin-12/Interleukin-23: ustekinumab). * Legal incapacity or limited legal capacity * Presence of any condition hampering compliance with the study protocol, at the discretion of the investigator * No french social security affiliation

Design outcomes

Primary

MeasureTime frame
Android fat distribution measured by bone densitometry (DEXA) (LUNAR GE iDXA device)day 1

Secondary

MeasureTime frame
body massesday 1
Intra-abdominal body fat mass (measured by CoreScan)day 1
Gynoid distribution of body fatday 1
SCORE (Systematic COronary Risk Evaluation).day 1
Body fatday 1
Homeostasis model assessment of insulin resistanceday 1
Bone mineral density of rachis, femoral neck, whole bodyday 1
levels of ghrelinday 1
levels of adipokinesday 1

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 17, 2026