Can Serum Lumican Level Identify a Hidden Fragility Phenotype Beyond Bone Mineral Density in Postmenopausal Women?

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age45+
SponsorKanuni Sultan Suleyman Training and Research Hospital

About this trial

Osteoporosis is a major cause of morbidity and fragility fractures in postmenopausal women. Bone mineral density (BMD) alone may not fully reflect fracture risk and skeletal fragility. Lumican, an extracellular matrix proteoglycan involved in collagen organization and musculoskeletal tissue homeostasis, has emerged as a potential biomarker for bone health. This prospective observational study aims to investigate the relationship between serum lumican levels, bone mineral density, muscle strength, and clinical fragility indicators in postmenopausal women. Approximately 100 participants will undergo routine osteoporosis assessment including DEXA, laboratory testing, FRAX evaluation, and handgrip strength measurement. The study will evaluate whether serum lumican levels can identify a hidden fragility phenotype beyond conventional bone mineral density measurements.

Eligibility criteria

Qualifiers

Female sex

Age 45 years or older

Postmenopausal status

Attendance at the Physical Medicine and Rehabilitation outpatient clinic

Disqualifiers

Premenopausal women

Secondary causes of osteoporosis (e.g., malignancy, advanced renal failure, severe liver disease, significant endocrine disorders)

Active infection or acute inflammatory disease

Major surgery within the previous 6 months

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

98 Participants
are grouped into 1 trial group