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Bone Mineral Density, Disease Duration, and Activity in Ankylosing Spondylitis

B

Bezmialem Vakif University

Status

Completed

Conditions

Osteoporosis
BMD
Ankylosing Spondylitis

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Our clinical study aimed to evaluate the prevalence of osteoporosis (OP) in patients with ankylosing spondylitis (AS) and to investigate the relationship between clinical, disease activity, physical function and disease duration, and bone mineral density (BMD).

Full description

In this cross-sectional study, patients who were admitted to the rheumatology clinic between 18 and 65 years of age and diagnosed as AS according to the modified New York diagnostic criteria were included

Patients group was divided two part as patients with (group 1)and without (group 2) osteoporosis.

The patient's global rating scale is a self-assessed scale of the patient with a grade of 10 (1: very bad, 5: moderate, 10: very good). To assess the disease activity, Bath ankylosing spondylitis disease index (BASDAI) and Bath ankylosing spondylitis functional index (BASFI) were evaluated. BASDAI is a self-assessment scale used to determine disease activity in patients with AS.

Schober measurement was used to evaluate lumbar mobility of the patients. Chest expansions were measured in all patients.

Body mass index (BMI) was calculated as kg/height m2. Erythrocyte sedimentation rate (ESH mm / h), C-reactive protein (CRP mg / l) levels were measured in all patients.

BMD measurements were made by using dual-energy x-ray absorptiometry (DEXA) and lumbar vertebra (L1-4) and left femur (femoral neck and total) regions. DEXA measurements (GE / LUNAR DPX PRO) were performed and the results were recorded using standard T score. Bone mineral densities of patients were based on the World Health Organization (WHO) classification of a T score between -1 and -2.5 for osteopenia; and a score of -2.5 for osteoporosis.

Enrollment

111 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients diagnosed as AS according to the modified New York diagnostic criteria were included

Exclusion criteria

  • Patients previously diagnosed with OP,
  • Patients previously treated with OP,
  • Patients with bone fractures previously associated with OP,
  • Those using drugs that affect bone metabolism, metabolic bone diseases (Paget's -disease, osteomalacia, hyperparathyroidism),
  • Diabetes mellitus,
  • Hypothyroidism, hyperthyroidism,
  • Patients with kidney, liver and intestinal diseases,
  • Those using corticosteroids

Trial design

111 participants in 2 patient groups

patients with osteoporosis
Description:
Osteoporosis has been operationally defined on the basis of bone mineral density (BMD) assessment. According to the WHO criteria, osteoporosis is defined as a BMD that lies 2.5 standard deviations or more below the average value for young healthy women (a T-score of \<-2.5 SD)
patients without osteoporosis
Description:
Bone mineral densities of patients were based on the World Health Organization (WHO) classification of a T score between -1 and -2.5 for osteopenia

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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