Rheumatoid Arthritis and Osteosarcopenia: Associated Factors

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age50+
SponsorKonya Beyhekim Training and Research Hospital

About this trial

Our study is a cross-sectional study, and its aim is to compare and analyze the prevalence of sarcopenia and osteoporosis in patients with rheumatoid arthritis (RA) with a control group and to reveal the impact of sarcopenia on osteoporosis, fall risk, and fracture risk. This prospective cross-sectional study will include 100 rheumatoid arthritis patients and 100 healthy controls, matched for age and sex. Patients will be consecutively and meticulously enrolled based on inclusion and exclusion criteria.

A detailed medical history and examination will be performed on the patients, and their clinical and sociodemographic characteristics will be recorded. Blood tests for RA (RF, Anti-Cyclic Citrullinated Peptide (anti-CCP), CRP, ESR) and disease activity levels (DAS28) will be recorded. The prevalence of osteosarcopenia will be assessed in both the RA and healthy control groups.These groups will be evaluated using various scales and tests (including power, performance tests) including musculoskeletal ultrasonographic measurements and clinical functional assessment tests. he sarcopenic group will be categorized based on the level of sarcopenia, according to the new ISarcoPRM criteria (non-sarcopenic, dynapenic, sarcopenic, and severe sarcopenic). Osteosarcopenia will be evaluated for both groups, and the collected data will be analyzed with primary and secondary outcomes. The analysis will explore the potential relationships between rheumatoid inflammation, sarcopenia, and osteoporosis.

Eligibility criteria

Qualifiers

Being diagnosed with RA according to the ACR/EULAR 2010 criteria

Being a female or male over the age of 50

Having the mental and physical capacity to complete the study questionnaires and tests

Providing voluntary consent to participate in the study by signing the Informed Consent Form

Disqualifiers

Having an acute illness/disability or significant cognitive impairment that prevents understanding and performing the required tests

Having thyroid or parathyroid disease, uncontrolled diabetes, Cushing's syndrome, anemia.

History of malignancy

Severe cardiovascular disease, enal failure, advanced-stage COPD, decompensated liver disease

Trial design

Treatments tested in this trial

  • Osteosarcopenia in Patients with Rheumatoid Arthritis
  • Osteosarcopenia in Healthy Control Group

Treatment groups

200 Participants
are divided into 2 treatment groups