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Effects of Weight-loss Treatment in Obese Patients With Psoriatic Arthritis (VIPsA)

Primary Purpose

Obesity, Psoriatic Arthritis, Metabolic Syndrome

Status
Completed
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Very Low Energy Diet (VLED)
Sponsored by
Vastra Gotaland Region
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity focused on measuring Obesity, Psoriatic arthritis, Psoriasis, Metabolic syndrome, Cardiovascular disease

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • PsA fulfilling the Classification for Psoriatic Arthritis (CASPAR) criteria
  • BMI≥33 kg/m2
  • Age 18-75 years

Exclusion Criteria:

  • Pregnancy
  • Porphyria
  • Epilepsy
  • Diabetes type 1
  • Severe heart or kidney disease
  • Eating disorder
  • Severe catabolic disease

Sites / Locations

  • Department of Rheumatology at the Hospital of Alingsås
  • Department of Rheumatology at the Hospital of Borås
  • Department of Obesity and Internal Medicine at Sahlgrenska University Hospital
  • Department of Rheumatology at Sahlgrenska University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Other

Arm Label

Patients with PsA and obesity

Patients with obesity

Arm Description

Very Low Energy Diet (VLED)

Very Low Energy Diet (VLED)

Outcomes

Primary Outcome Measures

Minimal Disease Activity (MDA) which is a composite outcome measure
5 of 7 of the following criteria: Tender joint count ≤ 1 Swollen joint count ≤ 1 PASI ≤ 1or BSA ≤ 3 Patient pain VAS ≤ 15 Patient global activity VAS ≤ 20 HAQ ≤ 0.5 Tender entheseal points ≤ 1 BSA: body surface area; HAQ: Health Assessment Questionnaire; PASI

Secondary Outcome Measures

Full Information

First Posted
September 21, 2016
Last Updated
October 11, 2021
Sponsor
Vastra Gotaland Region
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1. Study Identification

Unique Protocol Identification Number
NCT02917434
Brief Title
Effects of Weight-loss Treatment in Obese Patients With Psoriatic Arthritis
Acronym
VIPsA
Official Title
Effects of Weight-loss Treatment in Obese Patients With Psoriatic Arthritis
Study Type
Interventional

2. Study Status

Record Verification Date
May 2020
Overall Recruitment Status
Completed
Study Start Date
April 2016 (undefined)
Primary Completion Date
December 12, 2019 (Actual)
Study Completion Date
October 6, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Vastra Gotaland Region

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The study is an open intervention study with the aim to determine the effects of weight-loss treatment with Low-Energy liquid Diet (LED) on disease activity, quality of life and markers of the metabolic syndrome in patients with psoriatic arthritis and obesity.
Detailed Description
BACKGROUND Psoriasis is a common skin disease affecting around 2-3% of the population in Sweden. Approximately 20-30% of the individuals with psoriasis develop psoriatic arthritis (PsA). PsA mainly engage the musculoskeletal apparatus and causes inflammation of joints, tendons and ligaments, but the disease also increases the risk of developing anterior uveitis and inflammatory bowel disease, especially Crohn's disease. Both psoriasis and PsA are strongly associated with obesity and the metabolic syndrome (Mets). Observational studies have reported a frequency of obesity (body mass index; BMI≥30 kg/m2) in 45% and of MetS in 30-45% of PsA patients. Earlier studies have shown that obesity increases the risk of developing both psoriasis and PsA and that obesity is associated with increased disease activity, poorer treatment response and lower chance of achieving minimal disease activity. Although the association between PsA and obesity is well known, there are only a small number of interventional studies which have assessed the effects of weight loss on disease activity in PsA. Patients with PsA also have an increased risk of cardiovascular disease. [12, 13] Chronic inflammation, which accelerates the atherosclerotic process, in combination with a higher prevalence of cardiovascular risk factors among PsA patients is believed to contribute to this increased risk. Obesity causes a low grade systemic inflammation via the production of pro-inflammatory mediators in the white adipose tissue, such as adipokines and cytokines (e.g. tumour necrosis factor-α and interleukin-6), which are also involved in the pathogenic process if PsA. Obesity-related inflammation could thus act synergistically with autoimmune inflammation in the development and the maintenance of disease in psoriasis and PsA. Weight-loss treatment with Very Low Energy Diet (VLED) is an effective and approved method in clinical use in Sweden. In severe obesity, BMI 35 kg/m2 or more, a strict energy restriction is needed for optimal weight-loss. The LED gives a daily intake of 640 calories together with the recommended doses of vitamins and minerals. During an initial period of 12 weeks the patients only consume LED. The weight-loss with this intake is 1-2 kilograms per weeks. After the strict period food is successively reintroduced during a period of 18 weeks. The treatment is given within the framework of a structured program including support and medical follow-up from a team of doctors, nurses and dieticians. AIMS The aims of this study are To determine the effects of weight loss treatment on disease activity, function, quality of life and markers for the metabolic syndrome in patients with psoriatic arthritis To study the specific effects on the immune system of the negative energy balance during the strict energy restriction period and prospectively, during a two year follow-up To investigate if there are differences in body-composition, markers for Mets and adipokines between patients with PsA and obesity and controls with obesity before during and after weight loss treatment. PATIENTS AND METHODS Patients with PsA and obesity registered at the Rheumatology clinics of Sahlgrenska University hospital and the hospitals of Alingsås and Borås are invited to participate. The results of the PsA patients will be compared with control patients with obesity (PsA or psoriasis) matched for age, sex and BMI who undergo the same weight loss treatment with VLED. Disease activity, physical function and quality of life will be assessed by physical examination (including anthropometric measures, joints, tendons, back mobility and skin) and by validated questionnaires at baseline (start of weight-loss treatment), 3 months, 6 months, 12 months and 24 months. Blood samples will be collected at the same appointments. Body-composition will be measured at baseline and 12 months. Muscle strengths and physical function will be measured at baseline, 6 months and 12 months and physical activity will be assessed with questionnaires and accelerometers. Informed written consent will be obtained from all patients and controls. The study was approved by the local regional ethics committee in Gothenburg and will be carried out in accordance with the Helsinki Declaration.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Psoriatic Arthritis, Metabolic Syndrome, Psoriasis, Cardiovascular Disease
Keywords
Obesity, Psoriatic arthritis, Psoriasis, Metabolic syndrome, Cardiovascular disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
90 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Patients with PsA and obesity
Arm Type
Active Comparator
Arm Description
Very Low Energy Diet (VLED)
Arm Title
Patients with obesity
Arm Type
Other
Arm Description
Very Low Energy Diet (VLED)
Intervention Type
Dietary Supplement
Intervention Name(s)
Very Low Energy Diet (VLED)
Intervention Description
Very Low Energy Diet (VLED), divided into 4 daily doses, gives any intake of 640 calories per day together with the recommended doses of vitamins and minerals. During an initial period of 12 weeks the patients only consume VLED. After the strict period food is successively reintroduced during a period of 18 weeks.
Primary Outcome Measure Information:
Title
Minimal Disease Activity (MDA) which is a composite outcome measure
Description
5 of 7 of the following criteria: Tender joint count ≤ 1 Swollen joint count ≤ 1 PASI ≤ 1or BSA ≤ 3 Patient pain VAS ≤ 15 Patient global activity VAS ≤ 20 HAQ ≤ 0.5 Tender entheseal points ≤ 1 BSA: body surface area; HAQ: Health Assessment Questionnaire; PASI
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: PsA fulfilling the Classification for Psoriatic Arthritis (CASPAR) criteria BMI≥33 kg/m2 Age 18-75 years Exclusion Criteria: Pregnancy Porphyria Epilepsy Diabetes type 1 Severe heart or kidney disease Eating disorder Severe catabolic disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eva Klingberg, M.D., Ph.D.
Organizational Affiliation
Department of Rheumatology and Inflammation Research, Sahlgrenska Academy at the University of Gothenburg, Sweden
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Rheumatology at the Hospital of Alingsås
City
Alingsås
ZIP/Postal Code
441 33
Country
Sweden
Facility Name
Department of Rheumatology at the Hospital of Borås
City
Borås
ZIP/Postal Code
501 82
Country
Sweden
Facility Name
Department of Obesity and Internal Medicine at Sahlgrenska University Hospital
City
Gothenburg
ZIP/Postal Code
SE-41345
Country
Sweden
Facility Name
Department of Rheumatology at Sahlgrenska University Hospital
City
Gothenburg
ZIP/Postal Code
SE-41345
Country
Sweden

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
35648298
Citation
Bilberg A, Larsson I, Bjorkman S, Eliasson B, Klingberg E. The impact of a structured weight-loss treatment on physical fitness in patients with psoriatic arthritis and obesity compared to matched controls: a prospective interventional study. Clin Rheumatol. 2022 Sep;41(9):2745-2754. doi: 10.1007/s10067-022-06164-5. Epub 2022 Jun 1.
Results Reference
derived
PubMed Identifier
33092646
Citation
Klingberg E, Bjorkman S, Eliasson B, Larsson I, Bilberg A. Weight loss is associated with sustained improvement of disease activity and cardiovascular risk factors in patients with psoriatic arthritis and obesity: a prospective intervention study with two years of follow-up. Arthritis Res Ther. 2020 Oct 22;22(1):254. doi: 10.1186/s13075-020-02350-5.
Results Reference
derived
PubMed Identifier
30635024
Citation
Klingberg E, Bilberg A, Bjorkman S, Hedberg M, Jacobsson L, Forsblad-d'Elia H, Carlsten H, Eliasson B, Larsson I. Weight loss improves disease activity in patients with psoriatic arthritis and obesity: an interventional study. Arthritis Res Ther. 2019 Jan 11;21(1):17. doi: 10.1186/s13075-019-1810-5.
Results Reference
derived

Learn more about this trial

Effects of Weight-loss Treatment in Obese Patients With Psoriatic Arthritis

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