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临床试验/NCT07117344
NCT07117344进行中(未招募)不适用

"Progranulin in Ankylosing Spondylitis Patients: A Potential Biomarker?"

Kirsehir Ahi Evran Universitesi1 个研究点 分布在 1 个国家目标入组 160 人开始时间: 2026年1月15日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
160
试验地点
1
主要终点
In this study, we aimed to compare serum PGRN and TNF-α levels in AS patients with healthy controls and to determine the relationship between TNF-α inhibitor use and PGRN levels in AS patients.

研究概览

简要总结

In this study, we aimed to compare serum PGRN(progranulin) and TNF-α levels in AS patients with healthy controls and to determine the relationship between TNF-α inhibitor use and PGRN levels in AS patients.

详细描述

Axial Spondyloarthritis is a heterogeneous group of diseases characterised by inflammatory low back pain, sacroiliitis, asymmetric oligoarthritis, dactylitis, enthesitis and uveitis.

The fact that PGRN acts by binding to TNF-α receptors, the use of TNF-α inhibitors in current treatment in patients with AS and the importance of this pathway in disease pathogenesis suggested that PGRN may be a marker associated with disease activity in these patients. In this study, we aimed to compare serum PGRN and TNF-α levels in patients with AS with healthy control group and to determine the relationship between TNF-α inhibitor use and PGRN levels in patients with AS.

In our study, 80 patients aged 20-65 years who were diagnosed with AS according to ASAS 2009 criteria and followed up in our clinic will be included. Patients with pregnancy or lactation status, acute or chronic infection findings, malignancy, and the presence of concurrent secondary rheumatic diseases other than AS will be excluded. As a healthy control group, 80 people aged 20-65 years without pregnancy or lactation, acute or chronic infection, malignancy and rheumatic disease will be recruited. Age, gender, comorbidities, duration of the disease, and medications used by all patients will be recorded. In addition, BASDAI, BASFI, BASMI, ASQoL, ASDAS-CRP, ESR, CRP levels will be recorded to determine the severity of AS clinically in the patient group. Participants in the patient and control groups will be seen at one time and serum PGRN and TNF levels will be measured by ELISA method.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Cross Sectional

入排标准

年龄范围
20 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Between the ages of 20-65
  • •Signing the informed consent form
  • •Axial spondyloarthropathy diagnosis according to ASAS 2009 criteria

排除标准

  • •Pregnancy or lactation
  • •Having signs of acute or chronic infection
  • •Presence of malignancy
  • •Having concurrent secondary rheumatic disease other than Axial Spondyloarthropathy

研究组 & 干预措施

Control

Participants will be seen at one time and serum PGRN and TNF levels will be measured from each of them by ELISA method.

Patients with ankylosing spondylitis on TNF inhibitors

Participants will be seen at one time and serum PGRN and TNF levels will be measured from each of them by ELISA method.

patients with ankylosing spondylitis taking non-steroidal anti-inflammatory drugs

Participants will be seen at one time and serum PGRN and TNF levels will be measured from each of them by ELISA method.

结局指标

主要结局

In this study, we aimed to compare serum PGRN and TNF-α levels in AS patients with healthy controls and to determine the relationship between TNF-α inhibitor use and PGRN levels in AS patients.

时间窗: Patient will be seen only once

In this study, we aimed to compare serum PGRN and TNF-α levels in AS patients with healthy controls and to determine the relationship between TNF-α inhibitor use and PGRN levels in AS patients.

次要结局

  • Bath Ankylosing Spondylitis Disease Activity Index (BASDAI)(Patient will be seen only once)
  • Bath Ankylosing Spondylitis Functional Index (BASFI)(Patient will be seen only once)
  • Ankylosing Spondylitis Quality of Life Scale (ASQoL)(Patient will be seen only once)
  • Ankylosing Spondylitis Disease Activity Scoring-CRP (ASDAS-CRP)(Patient will be seen only once)
  • Bath Ankylosing Spondylitis Metrology Index (BASMI)(Patient will be seen only once)

研究者

发起方
Kirsehir Ahi Evran Universitesi
申办方类型
Other
责任方
Principal Investigator
主要研究者

Seyda Sultan Eraslan

MD

Kirsehir Ahi Evran Universitesi

研究点 (1)

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