Assessing Biomarker in Giant Cell Arteritis and Polymyalgia Rheumatic

NCT ID: NCT06460142

Last Updated: 2025-04-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-09-01

Study Completion Date

2027-09-30

Brief Summary

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The GCAIO study is an innovative, multimodal research initiative designed to enhance the understanding, diagnosis, and management of giant cell arteritis (GCA) and frequently associated polymyalgia rheumatica (PMR). This longitudinal study aims to dissect the complex immunological landscape and systemic manifestations of these conditions through a combination of diagnostic imaging and detailed immunological profiling.

The study focuses on three primary objectives: (1) Identifying and analyzing cytokine profiles and immune cell phenotypes, employing techniques like flow cytometry, enzyme-linked immunosorbent assays (ELISA), and next-generation sequencing to predict disease activity and therapeutic responses. (2) Advancing diagnostic and monitoring capabilities through the application of novel and established imaging technologies, including MRI, optical coherence tomography angiography (OCTA), and ultrasound. These modalities aim to improve the detection of neuro-ophthalmological, cardiac, and aortic complications in GCA, potentially offering more precise monitoring and earlier diagnosis. (3) Enhancing the understanding of PMR within the context of GCA by exploring specific biomarkers and advanced imaging to refine diagnostic accuracy and treatment strategies, thus improving patient outcomes.

Detailed Description

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GCA is an immune-mediated vasculitis that affects medium and large-sized vessels, leading to vascular changes and occlusion due to severe vascular inflammation, neoangiogenesis, and remodeling. GCA has the potential to impact almost any organ. Despite advancements in understanding the pathophysiology and clinical manifestations of GCA, many aspects of the disease remain unexplored. The GCAIO study aims to fill these gaps using an integrative research approach to enhance the diagnosis, understanding, and management of GCA.

The GCAIO study cohort includes patients at their first diagnosis, throughout the disease, and during recurrent activity, facilitating a thorough longitudinal analysis of GCA. The research focuses on the complex immunological processes of the disease. Techniques such as flow cytometry (FACS), enzyme-linked immunosorbent assays (ELISA), and 3'-mRNA transcriptome analysis are employed to identify biomarkers that can assess GCA activity, track disease progression, and predict therapeutic responses, particularly for those unresponsive to interleukin (IL)-6 receptor (R) inhibitors. Additionally, the project is pioneering personalized treatment protocols tailored to individual immune profiles by developing a cell-based ex-vivo assay designed to forecast how patients will respond to different disease-modifying anti-rheumatic drugs (DMARDs).

Alongside the immunological research, the project emphasizes improving diagnostic and monitoring techniques through imaging technologies. Recent advancements have demonstrated that optimized diagnostics significantly enhance treatment outcomes for GCA patients. The planned prospective multimodal imaging aims to investigate potential neuro-ophthalmological, cardiac, and aortic manifestations during the course of GCA, enabling a detailed assessment of the involvement of various structures. Established imaging methods such as magnetic resonance imaging (MRI), optical coherence tomography angiography (OCTA), and vascular ultrasound are being extended into new areas to evaluate their diagnostic and prognostic merits. Furthermore, the investigators are exploring innovative diagnostic tools like transorbital ultrasound (TOS) and contrast-enhanced ultrasound (CEUS) for their potential as predictive biomarkers, facilitating earlier diagnosis and more precise disease monitoring. By correlating imaging findings with immunological data, our goal is to alter the way GCA is detected and monitored.

The inclusion of patients with PMR enhances our understanding of its pathophysiology, clinical manifestations, and its connection to often-associated GCA. The investigators are dedicated to developing new diagnostic criteria and exploring alternative therapeutic approaches for PMR maintenance therapy. By identifying alternative clinical, laboratory, or instrumental diagnostic methods to predict PMR, the investigators aim to set new diagnostic standards and deepen our understanding of its pathophysiology and immunological processes.

In summary, the goal of the GCAIO study is to make substantial contributions to the fields of GCA and PMR by developing innovative diagnostic and therapeutic strategies that improve treatment and quality of life for affected patients. The identification of specific biomarkers and the establishment of new diagnostic standards could lead to more precise diagnoses and optimized management of therapy, thereby enhancing patient care and reducing the risk of complications and therapy failures.

Conditions

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Giant Cell Arteritis Polymyalgia Rheumatica

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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PMR/ GCA

Patients diagnosed with GCA and/or PMR will be enrolled in this cohort. They will undergo a series of interventions including immunological profiling (cytokine profiling and immune cell phenotyping using flow cytometry, ELISA, 3'mRNA sequencing, high content analysis via a cell-based ex-vivo assay), and diagnostic imaging (MRI, OCTA including further ophthalmological assessment, vascular and transorbital ultrasound. Samples will be collected from patients at various stages of the disease (t=0, t=6, t=12, t=18 months, during flare-ups). Furthermore, TAB will be stained with a VAP-1 antibody to assess the expression and localization of VAP-1 in the arterial tissue.

Aortic/ cardiac magnetic resonance imaging

Intervention Type DIAGNOSTIC_TEST

MRI scans will be performed to detect systemic vascular involvement in GCA patients, aiming to provide detailed images of affected tissues.

Vascular ultrasound

Intervention Type DIAGNOSTIC_TEST

Vascular ultrasound will be employed to examine the temporal and axillary arteries in GCA patients, searching for signs indicative of active inflammation.

Transorbital Ultrasound

Intervention Type DIAGNOSTIC_TEST

Transorbital ultrasound will be employed to assess the ophthalmic artery and its branches in GCA patients to detect intracranial inflammatory processes that could lead to severe neuro-ophthalmological complications.

Contrast-Enhanced Ultrasound

Intervention Type DIAGNOSTIC_TEST

Contrast-Enhanced Ultrasound (CEUS) is utilized to evaluate aortic involvement in GCA patients as an alternative, bed-side, realtime, radiation-free diagnostic tool.

Optical coherence tomography angiography

Intervention Type DIAGNOSTIC_TEST

OCTA will be used to assess vascular changes in the retina of GCA patients, providing detailed imaging that can help detect early signs of ocular involvement and identify risk factors of anterior ischemic optic neuropathy.

Fluorescein angiography

Intervention Type DIAGNOSTIC_TEST

Fluorescein angiography will be performed to evaluate blood circulation and highlight any blockages in the blood vessels of the retina in patients with GCA to detect vascular abnormalities that may lead to severe vision complications.

Fundus autofluorescence

Intervention Type DIAGNOSTIC_TEST

This imaging technique will be used to observe the health of the retina and detect any changes in GCA patients that could suggest disease activity, particularly useful for assessing the integrity of the retinal pigment epithelium.

Color Fundus Photography

Intervention Type DIAGNOSTIC_TEST

Color fundus photography will be used to document the appearance of the optic disc and retinal vasculature in GCA patients, aiding in the long-term monitoring of ocular changes and the effects of therapeutic interventions.

Cell-based ex-vivo assay with high-content analysis

Intervention Type DIAGNOSTIC_TEST

This assay predicts individual patient responses to different DMARDs by analyzing patient-derived PBMCs for specific immune responses to therapeutic agents.

3'mRNA sequencing

Intervention Type DIAGNOSTIC_TEST

3'mRNA sequencing analyzes gene expression profiles related to the immune response in PMR/GCA patients, aiding in understanding the genetic underpinnings of inflammation and vascular remodeling.

Enzyme-linked immunosorbent assay

Intervention Type DIAGNOSTIC_TEST

Used to measure cytokine levels in the serum and plasma of PMR/GCA patients, ELISA aids in profiling inflammatory markers that are indicative of disease activity and response to treatment.

Flow cytometry

Intervention Type DIAGNOSTIC_TEST

Employed to analyze immune cell phenotypes in patients with PMR and/or GCA, this test helps identify various immune cell subsets and their activation states, which are critical for understanding disease mechanisms and guiding therapy.

Laboratory assessment:

Intervention Type DIAGNOSTIC_TEST

Serum Chemistry (nt-proBNP, troponin T, CRP, ESR, blood count)

Immunohistochemistry of Temporal Artery Biopsies

Intervention Type DIAGNOSTIC_TEST

Immunohistochemistry staining of TAB to assess local expression of endothelial adhesion molecules in acute inflammation.

Functional assessment questionnaires

Intervention Type DIAGNOSTIC_TEST

The following questionnaires will be applied: FACIT-Fatigue, SF-36, BAS, Birmingham Vasculitis Activity Score, Montreal Cognitive Assessment, Mini-Mental Status Examination. These questionnaires collectively provide a comprehensive evaluation of the functional status, quality of life, and mental health of patients with GCA and PMR.

Control Group

Age- and gender-matched healthy subjects will serve as the control group to provide baseline data for comparative purposes. This group will not receive any treatment related to GCA or PMR but undergoes similar diagnostic procedures for baseline measurements, including imaging and immunological assessments.

Aortic/ cardiac magnetic resonance imaging

Intervention Type DIAGNOSTIC_TEST

MRI scans will be performed to detect systemic vascular involvement in GCA patients, aiming to provide detailed images of affected tissues.

Vascular ultrasound

Intervention Type DIAGNOSTIC_TEST

Vascular ultrasound will be employed to examine the temporal and axillary arteries in GCA patients, searching for signs indicative of active inflammation.

Transorbital Ultrasound

Intervention Type DIAGNOSTIC_TEST

Transorbital ultrasound will be employed to assess the ophthalmic artery and its branches in GCA patients to detect intracranial inflammatory processes that could lead to severe neuro-ophthalmological complications.

Contrast-Enhanced Ultrasound

Intervention Type DIAGNOSTIC_TEST

Contrast-Enhanced Ultrasound (CEUS) is utilized to evaluate aortic involvement in GCA patients as an alternative, bed-side, realtime, radiation-free diagnostic tool.

Optical coherence tomography angiography

Intervention Type DIAGNOSTIC_TEST

OCTA will be used to assess vascular changes in the retina of GCA patients, providing detailed imaging that can help detect early signs of ocular involvement and identify risk factors of anterior ischemic optic neuropathy.

Fluorescein angiography

Intervention Type DIAGNOSTIC_TEST

Fluorescein angiography will be performed to evaluate blood circulation and highlight any blockages in the blood vessels of the retina in patients with GCA to detect vascular abnormalities that may lead to severe vision complications.

Fundus autofluorescence

Intervention Type DIAGNOSTIC_TEST

This imaging technique will be used to observe the health of the retina and detect any changes in GCA patients that could suggest disease activity, particularly useful for assessing the integrity of the retinal pigment epithelium.

Color Fundus Photography

Intervention Type DIAGNOSTIC_TEST

Color fundus photography will be used to document the appearance of the optic disc and retinal vasculature in GCA patients, aiding in the long-term monitoring of ocular changes and the effects of therapeutic interventions.

Cell-based ex-vivo assay with high-content analysis

Intervention Type DIAGNOSTIC_TEST

This assay predicts individual patient responses to different DMARDs by analyzing patient-derived PBMCs for specific immune responses to therapeutic agents.

3'mRNA sequencing

Intervention Type DIAGNOSTIC_TEST

3'mRNA sequencing analyzes gene expression profiles related to the immune response in PMR/GCA patients, aiding in understanding the genetic underpinnings of inflammation and vascular remodeling.

Enzyme-linked immunosorbent assay

Intervention Type DIAGNOSTIC_TEST

Used to measure cytokine levels in the serum and plasma of PMR/GCA patients, ELISA aids in profiling inflammatory markers that are indicative of disease activity and response to treatment.

Flow cytometry

Intervention Type DIAGNOSTIC_TEST

Employed to analyze immune cell phenotypes in patients with PMR and/or GCA, this test helps identify various immune cell subsets and their activation states, which are critical for understanding disease mechanisms and guiding therapy.

Laboratory assessment:

Intervention Type DIAGNOSTIC_TEST

Serum Chemistry (nt-proBNP, troponin T, CRP, ESR, blood count)

Functional assessment questionnaires

Intervention Type DIAGNOSTIC_TEST

The following questionnaires will be applied: FACIT-Fatigue, SF-36, BAS, Birmingham Vasculitis Activity Score, Montreal Cognitive Assessment, Mini-Mental Status Examination. These questionnaires collectively provide a comprehensive evaluation of the functional status, quality of life, and mental health of patients with GCA and PMR.

Interventions

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Aortic/ cardiac magnetic resonance imaging

MRI scans will be performed to detect systemic vascular involvement in GCA patients, aiming to provide detailed images of affected tissues.

Intervention Type DIAGNOSTIC_TEST

Vascular ultrasound

Vascular ultrasound will be employed to examine the temporal and axillary arteries in GCA patients, searching for signs indicative of active inflammation.

Intervention Type DIAGNOSTIC_TEST

Transorbital Ultrasound

Transorbital ultrasound will be employed to assess the ophthalmic artery and its branches in GCA patients to detect intracranial inflammatory processes that could lead to severe neuro-ophthalmological complications.

Intervention Type DIAGNOSTIC_TEST

Contrast-Enhanced Ultrasound

Contrast-Enhanced Ultrasound (CEUS) is utilized to evaluate aortic involvement in GCA patients as an alternative, bed-side, realtime, radiation-free diagnostic tool.

Intervention Type DIAGNOSTIC_TEST

Optical coherence tomography angiography

OCTA will be used to assess vascular changes in the retina of GCA patients, providing detailed imaging that can help detect early signs of ocular involvement and identify risk factors of anterior ischemic optic neuropathy.

Intervention Type DIAGNOSTIC_TEST

Fluorescein angiography

Fluorescein angiography will be performed to evaluate blood circulation and highlight any blockages in the blood vessels of the retina in patients with GCA to detect vascular abnormalities that may lead to severe vision complications.

Intervention Type DIAGNOSTIC_TEST

Fundus autofluorescence

This imaging technique will be used to observe the health of the retina and detect any changes in GCA patients that could suggest disease activity, particularly useful for assessing the integrity of the retinal pigment epithelium.

Intervention Type DIAGNOSTIC_TEST

Color Fundus Photography

Color fundus photography will be used to document the appearance of the optic disc and retinal vasculature in GCA patients, aiding in the long-term monitoring of ocular changes and the effects of therapeutic interventions.

Intervention Type DIAGNOSTIC_TEST

Cell-based ex-vivo assay with high-content analysis

This assay predicts individual patient responses to different DMARDs by analyzing patient-derived PBMCs for specific immune responses to therapeutic agents.

Intervention Type DIAGNOSTIC_TEST

3'mRNA sequencing

3'mRNA sequencing analyzes gene expression profiles related to the immune response in PMR/GCA patients, aiding in understanding the genetic underpinnings of inflammation and vascular remodeling.

Intervention Type DIAGNOSTIC_TEST

Enzyme-linked immunosorbent assay

Used to measure cytokine levels in the serum and plasma of PMR/GCA patients, ELISA aids in profiling inflammatory markers that are indicative of disease activity and response to treatment.

Intervention Type DIAGNOSTIC_TEST

Flow cytometry

Employed to analyze immune cell phenotypes in patients with PMR and/or GCA, this test helps identify various immune cell subsets and their activation states, which are critical for understanding disease mechanisms and guiding therapy.

Intervention Type DIAGNOSTIC_TEST

Laboratory assessment:

Serum Chemistry (nt-proBNP, troponin T, CRP, ESR, blood count)

Intervention Type DIAGNOSTIC_TEST

Immunohistochemistry of Temporal Artery Biopsies

Immunohistochemistry staining of TAB to assess local expression of endothelial adhesion molecules in acute inflammation.

Intervention Type DIAGNOSTIC_TEST

Functional assessment questionnaires

The following questionnaires will be applied: FACIT-Fatigue, SF-36, BAS, Birmingham Vasculitis Activity Score, Montreal Cognitive Assessment, Mini-Mental Status Examination. These questionnaires collectively provide a comprehensive evaluation of the functional status, quality of life, and mental health of patients with GCA and PMR.

Intervention Type DIAGNOSTIC_TEST

Other Intervention Names

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Aortic/ cardiac MRI TOS CEUS OCTA GCAIO-essay ELISA FACS IHC TAB

Eligibility Criteria

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Inclusion Criteria

* Informed Consent: Participants (\>18 years) must provide written informed consent to voluntarily participate in the study.
* Confirmed Diagnosis: Diagnosis of GCA or PMR confirmed by the treating physician and fulfilling expanded ACR-EULAR classification criteria. Patients must have been either newly diagnosed within the last three days or have experienced a disease flare within the same timeframe.

Exclusion Criteria

* Severe Renal Insufficiency: Chronic glomerular filtration rate (GFR) less than 30 mL/min.
* Other Medical Conditions Requiring Glucocorticoids: Presence of medical conditions other than GCA or PMR that necessitate continuous or intermittent treatment with oral or parenteral glucocorticoids.
* Other Inflammatory Rheumatic Diseases: Patients with other inflammatory rheumatic diseases.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Bonn

OTHER

Sponsor Role lead

Responsible Party

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Valentin Schäfer

Univ. Prof. Dr. med. Valentin Sebastian Schäfer

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Valentin S. Schäfer, Univ. Prof.

Role: PRINCIPAL_INVESTIGATOR

Department of Rheumatology and Clinical Immunology, University Hospital Bonn

Locations

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University Hospital Bonn

Bonn, North Rhine-Westphalia, Germany

Site Status RECRUITING

Countries

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Germany

Central Contacts

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Simon M. Petzinna, Dr. med.

Role: CONTACT

0049 151 582 337 07

Valentin S. Schäfer, Univ. Prof.

Role: CONTACT

0049 228 287 17016

Facility Contacts

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Simon M. Petzinna, Dr. med.

Role: primary

0049 151 582 337 07

Valentin S. Schäfer, Univ. Prof.

Role: backup

0049 228 287 17016

Related Links

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Other Identifiers

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321/22

Identifier Type: -

Identifier Source: org_study_id

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