Identification of Serum Level of Glutathione Peroxidase 4

NCT ID: NCT06554392

Last Updated: 2024-08-15

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

NOT_YET_RECRUITING

Total Enrollment

85 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-09-01

Study Completion Date

2027-07-01

Brief Summary

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* Analysis of the level of glutathione peroxidase 4 (GPX4) in ankylosing spondylitis and axial psoriatic arthritis patients.
* The association of glutathione peroxidase 4 (GPX4) with disease activity and severity in ankylosing spondylitis and axial psoriatic arthritis patients.

Detailed Description

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Ferroptosis, first reported by Dixon et al. in 2012, is a form of non-apoptotic cell death driven by iron-dependent lipid reactive oxygen species (ROS) and accelerated by the accumulation of lipid peroxides, ultimately leading to oxidative damage to phospholipid membranes and cell death .

Ferroptosis could be induced by iron metabolism disorder, lipid peroxidation accumulation, deficiency of glutathione (GSH) and inactivation of the antioxidant enzyme glutathione peroxidase 4 (GPX4).

The morphological features of ferroptotic cells manifest as an aberrant mitochondrial ultrastructure, including a reduction in mitochondrial volume, an increase in mitochondrial membrane density, and the disappearance of mitochondrial cristae in ferroptotic cells .

Recent studies have increasingly reported on complex associations between ferroptosis and the immune system . The regulatory activity of ferroptosis in immune function and inflammation is multifaceted and involves innate, acquired, and autoimmunity.

Accumulating evidence in recent times has shown an association of ferroptosis with the pathogenesis and development of autoimmune diseases .

Spondyloarthropathy comprises a group of chronic inflammatory rheumatic diseases, including ankylosing spondylitis, reactive arthritis (Reiter syndrome), arthritis or spondylitis associated with inflammatory bowel disease, and psoriatic arthritis, as well as undifferentiated spondyloarthritis. These afflictions predominantly affect the axial skeleton, causing pain and stiffness.

Currently, research on ferroptosis is still in its early stages; therefore, exploring the pathogenesis of ferroptosis and its role in various diseases, and proposing effective and targeted treatment methods have significant theoretical significance and practical value.

Conditions

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Spondyloarthropathy

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Ankylosing Spondylitis patients

Identification of Glutathione Peroxidase 4 in blood.

Blood sample

Intervention Type DIAGNOSTIC_TEST

Blood sample from each subject to detect Glutathione Peroxidase 4.

Axial Psoriatic Arthritis Patients

Identification of Glutathione Peroxidase 4 in blood.

Blood sample

Intervention Type DIAGNOSTIC_TEST

Blood sample from each subject to detect Glutathione Peroxidase 4.

healthy controls

Identification of Glutathione Peroxidase 4 in blood.

Blood sample

Intervention Type DIAGNOSTIC_TEST

Blood sample from each subject to detect Glutathione Peroxidase 4.

Interventions

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Blood sample

Blood sample from each subject to detect Glutathione Peroxidase 4.

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* Patients diagnosed as ankylosing spondylitis according to ASAS criteria . \[13\]
* Patients diagnosed as psoriatic arthritis according to CASPAR criteria. \[14\]
* Age (\>18).

Exclusion Criteria

* Patient with other autoimmune Rheumatic diseases.
* patients with any of the following conditions: I) severe liver and kidney dysfunction; II) hematopoietic diseases; III) infectious diseases; IV) tumors; or V) other wasting diseases. \[15\]
* patients received certain drugs (for example, sulfasalazine, artemisinin, statins), and experimental reagents (such as erastin) .\[16\]
Minimum Eligible Age

18 Years

Maximum Eligible Age

85 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Assiut University

OTHER

Sponsor Role lead

Responsible Party

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Gehad Abdel Hakeem Abdullah Fahem

resident doctor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Marwa Abdelaziz, Prof.

Role: STUDY_DIRECTOR

Rheumatology,Rehabilition,Physical therapy Department ,Assiut university

Marwa Galal, Ass. Prof.

Role: STUDY_DIRECTOR

Rheumatology,Rehabilition,Physical therapy Department ,Assiut university

Nesreen Ibrahim, Dr

Role: STUDY_DIRECTOR

Rheumatology,Rehabilition,Physical therapy Department ,Assiut university

Central Contacts

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Gehad Fahem, Rd

Role: CONTACT

+201116770486

References

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Dixon SJ, Lemberg KM, Lamprecht MR, Skouta R, Zaitsev EM, Gleason CE, Patel DN, Bauer AJ, Cantley AM, Yang WS, Morrison B 3rd, Stockwell BR. Ferroptosis: an iron-dependent form of nonapoptotic cell death. Cell. 2012 May 25;149(5):1060-72. doi: 10.1016/j.cell.2012.03.042.

Reference Type BACKGROUND
PMID: 22632970 (View on PubMed)

Chen R, Zhu S, Zeng L, Wang Q, Sheng Y, Zhou B, Tang D, Kang R. AGER-Mediated Lipid Peroxidation Drives Caspase-11 Inflammasome Activation in Sepsis. Front Immunol. 2019 Aug 8;10:1904. doi: 10.3389/fimmu.2019.01904. eCollection 2019.

Reference Type BACKGROUND
PMID: 31440260 (View on PubMed)

Yuan S, Wei C, Liu G, Zhang L, Li J, Li L, Cai S, Fang L. Sorafenib attenuates liver fibrosis by triggering hepatic stellate cell ferroptosis via HIF-1alpha/SLC7A11 pathway. Cell Prolif. 2022 Jan;55(1):e13158. doi: 10.1111/cpr.13158. Epub 2021 Nov 22.

Reference Type BACKGROUND
PMID: 34811833 (View on PubMed)

Gao M, Yi J, Zhu J, Minikes AM, Monian P, Thompson CB, Jiang X. Role of Mitochondria in Ferroptosis. Mol Cell. 2019 Jan 17;73(2):354-363.e3. doi: 10.1016/j.molcel.2018.10.042. Epub 2018 Dec 20.

Reference Type BACKGROUND
PMID: 30581146 (View on PubMed)

Chen X, Kang R, Kroemer G, Tang D. Ferroptosis in infection, inflammation, and immunity. J Exp Med. 2021 Jun 7;218(6):e20210518. doi: 10.1084/jem.20210518. Epub 2021 May 12.

Reference Type BACKGROUND
PMID: 33978684 (View on PubMed)

Other Identifiers

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Glutathione Peroxidase 4

Identifier Type: -

Identifier Source: org_study_id

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