Osteoporosis in ankylosing spondylitis - prevalence, risk factors and methods of assessment.
Eva Klingberg, Mattias Lorentzon, Dan Mellström...
https://pubmed.ncbi.nlm.nih.gov/22569245/Actively Recruiting
Led by Ankara University · Updated on 2024-08-29
97
Participants Needed
1
Research Sites
12 weeks
Total Duration
Axial spondyloarthritis AxSpA is a chronic inflammatory disease affecting the spine, sacroiliac joints, entheses, and sometimes peripheral joints, with a close link to the HLA-B27 gene. This condition includes both Ankylosing Spondylitis AS, diagnosed by X-rays, and non-radiographic AxSpA, diagnosed via MRI. Osteoporosis and sarcopenia, a loss of muscle mass and strength, are common in AS patients, and their combination, called osteosarcopenia, may increase illness and mortality in people with AxSpA. This study aims to find out how often osteosarcopenia occurs in AxSpA patients and how it relates to different clinical and demographic factors by comparing them to a healthy control group. Participants will be divided into two groups those with AxSpA diagnosed by established criteria and a healthy control group matched by age and gender. Osteoporosis will be assessed using bone mineral density BMD measurements via Dual-energy X-ray absorptiometry DXA, while sarcopenia will be evaluated based on muscle strength, muscle mass, and physical performance using the EWGSOP2 guidelines. Muscle mass will be measured by DXA and bioelectrical impedance analysis BIA, grip strength will assess muscle strength, and gait speed will assess physical performance. The study will explore the link between osteosarcopenia and factors such as age, gender, physical activity, disease duration, medication type, disease activity, spinal mobility, radiological involvement, and functional status. During the study, participants will undergo tests including DXA scans, bioelectrical impedance analysis, grip strength measurements, and gait speed assessments. Researchers will collect information on disease and treatment history, physical activity, and functional status. The primary outcome measure is the presence of osteosarcopenia over 16 months. Secondary outcomes include the presence of osteoporosis and sarcopenia. The study will help identify patients at higher risk for osteosarcopenia and guide early treatment steps. Total participation time spans 16 months from start to outcome evaluation.
CONDITIONS
Osteosarcopenia in Axial Spondyloarthritis
A
Ayşe A Küçükdeveci, MD
İ
İsmail Aksu, MD
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Ankara University
Lead Sponsor
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 16 months
Participants undergo assessments to determine the presence of osteosarcopenia, osteoporosis, and sarcopenia using bone mineral density measurements, muscle strength tests, muscle mass evaluations, and physical performance tests.
1 visit for measurements and assessments
Duration - Up to 16 months
Participants are observed to investigate the relationship between osteosarcopenia and various demographic and clinical factors over time.
Follow-up assessments may occur depending on clinical parameters
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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