Monocyte Chemoattractant Protein-1 in Psoriatic Arthritis Patients

NCT ID: NCT05637905

Last Updated: 2022-12-06

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Total Enrollment

44 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-01-31

Study Completion Date

2025-06-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

1. Evaluate serum levels of (MCP-1) in PsA with or without cardiovascular affaction .
2. Detect subclinical cardiovascular affaction in patients with PsA for early diagnosis and management .

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Psoriatic arthritis (PSA) is an autoimmune disease arising from the interply between proinflamatory cytokines

\[1\]and external stimuli in genetically predisposed individuals.\[2\]

* The disease is chronic and affects the peripheral joints and may include axial skeleton with or without extrarticular manifestations.\[3\]
* Abnormal activation of the innate and adaptive immune systems contributes to chronic disease processes in both psoriasis and PSA .\[4\] The skin and the joints exhibit a prominent lymphocytic infiltrate consisting of activated CD4+ and CD8+ T cells as well as an increase in neutrophil infiltration\[5\].

Patients with PsA have a higher risk of developing a cardiovascular(CV) events than the general population. This could be attributed to the higher prevalence of traditional cardiovascular risk factors and to the disease characteristics such as systemic inflammation. \[6\] These patients may show asymptomatic cardiomyopathy even in the absence of traditional risk factors \[7\].Cardiac dysfunction is associated with a poor prognosis, increased mortality, and affact socioecenomic function of patients therefore, the diagnosis of the cardiac dysfunction in the asymptomatic phase of the disease \[8\] is important for the timely introduction of therapy \[9\].Monocyte chemotactic protien1(MCP-1) is a member of chemotactic chemokines(CC) which are secreted by immune effector cells and dysfunctional endothelium \[10\].

* The pivotal function of MCP-1 is to attract monocyte in the arterial wall through increased expression of adhesion molecules on their surface that interacts with endothelium\[11\].
* MCP-1 induce maturation of monocyte in the arterial wall ,which then become specialized macrophage in early atheroma and produce tissue factors supporting coagulation and proinflammatory cytokines such as IL-1 and IL-6. It affects the functions of the surrounding immune effector cells in locally thickened intima.\[12\]
* During active disease in psoriatic skin lesions and synovial tissue, activated monocytes represent the major source of proinflammatory mediators, including the chemokine MCP-1 \[13\]. MCP-1 is thought to be involved in the pathogenesis of oedema and bone erosion in patients with PsA \[14\].

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Psoriatic Arthritis

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_CONTROL

Study Time Perspective

OTHER

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

psoriatic arthritis patients group

No interventions assigned to this group

health control group

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* PsA patients (age ≥ 18years) who fulfilled the CASPAR classification criteria\[15\]for psoriatic arthritis

Exclusion Criteria

* PsA patients with

1. infection.
2. bone marrow disorders.
3. other autoimmune diseases.
4. diabetes.
5. hypertention .
6. hyperlipidemia.
7. liver diseases.
8. renal diseases.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Assiut University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Amira Anas Mostafa Mohamed

doctor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Eman Abass, doctor

Role: STUDY_DIRECTOR

Assiut University

Mohamed Raouf, doctor

Role: STUDY_DIRECTOR

Assiut University

Esraa Ahmed, doctor

Role: STUDY_DIRECTOR

Assiut University

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Amira Anas, Master

Role: CONTACT

01066633924

Related Links

Access external resources that provide additional context or updates about the study.

http://pubmed.ncbi.nlm.nih.gov/30910989/

1.V.Chandran,F.Abji,A.V. Perruccio et al.,"Serum-basedsoluble markers difffferentiate psoriatic arthritis from osteoarthritis," Annals of the Rheumatic Diseases,vol.78, no.6, pp.796-801,2019.

http://pubmed.ncbi.nlm.nih.gov/30910989/

A. L. Carvalho and C. M. Hedrich, "The molecular pathophysiology of psoriatic arthritis-the complex interplay between genetic predisposition, epigenetics factors, and the microbiome," Frontiers in Molecular Biosciences, vol. 8, p. 662047, 2021.

http://pubmed.ncbi.nlm.nih.gov/30910989/

A. B. Gottlieb and J. F. Merola, "Axial psoriatic arthritis: an update for dermatologists," Journal of the American Academy of Dermatology, vol. 84, no. 1, pp. 92-101, 2021

http://pubmed.ncbi.nlm.nih.gov/30910989/

Lories RJ, de Vlam K. Is psoriatic arthritis a result of abnormalities in acquired or innate immunity? Curr Rheumatol Rep 2012; 14: 375-382.

http://pubmed.ncbi.nlm.nih.gov/30910989/

.Lowes MA, Kikuchi T, Fuentes-Duculan J, Cardinale I, Zaba LC, Haider AS, et al. Psoriasis vulgaris lesions contain discrete populations of Th1 and Th17 T cells. J Invest Dermatol 2008; 128: 1207-12

http://pubmed.ncbi.nlm.nih.gov/30910989/

Risk Reclassification According to Cardiovascular Six Traditional Cardiovascular Risk Algorithms and a Carotid Ultrasound in Psoriatic Arthritis Patients

http://pubmed.ncbi.nlm.nih.gov/30910989/

A. Rana, V. K. Mahajan, K. S. Mehta et al., "Cardiomyopathy and echocardiographic abnormalities in Indian patients with psoriasis: results of a pilot study," International Journal of Clinical Practice, vol. 75, no. 3, p. e13756, 2021.

http://pubmed.ncbi.nlm.nih.gov/30910989/

P. S. Pagel, J. N. Tawil, B. T. Boettcher et al., "Heart failure with preserved ejection fraction: a comprehensive review and update of diagnosis,pathophysiology, treatment, and perioperative implications," Journal of Cardiothoracic and Vascular Anesthes

http://pubmed.ncbi.nlm.nih.gov/30910989/

.E. L. Potter, S. Ramkumar, H. Kawakami et al., "Association of asymptomatic diastolic dysfunction assessed by left atrial strain with incident heart failure,"JACC: Cardiovascular Imaging, vol. 13, no. 11, pp. 2316-2326, 2020.

http://pubmed.ncbi.nlm.nih.gov/30910989/

Lin, V. Kakkar, and X. Lu, "Impact of MCP -1 in atherosclerosis," Current Pharmaceutical Design, vol. 20, no. 28, pp. 4580-4588, 2014.

http://pubmed.ncbi.nlm.nih.gov/30910989/

C. Papadopoulou, V. Corrigall, P. R. Taylor, and R. N. Poston, "The role of the chemokines MCP-1, GRO-α, IL-8 and their receptors in the adhesion of monocytic cells to human atherosclerotic plaques," Cytokine, vol. 43, no. 2, pp. 181-186, 2008.

http://pubmed.ncbi.nlm.nih.gov/30910989/

P. Aukrust, B. Halvorsen, A. Yndestad et al., "Chemokines and cardiovascular risk," Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 28, no. 11, pp. 1909-1919

http://pubmed.ncbi.nlm.nih.gov/30910989/

D. E. Furst and J. S. Louie, "Targeting inflammatory pathways in axial spondyloarthritis," Arthritis Research \& Therapy, vol. 21, no. 1, p. 135, 2019.

http://pubmed.ncbi.nlm.nih.gov/30910989/

Y. R. Woo, C. J. Park, H. Kang, and J. E. Kim, "The risk of systemic diseases in those with psoriasis and psoriatic arthritis:from mechanisms to clinic," International Journal of Molecular Sciences, vol. 21, no. 19, p. 7041, 2020.

http://pubmed.ncbi.nlm.nih.gov/30910989/

.Moll JM, Wright V Psoriatic arthritis. Semin Arthritis Rheum 1973;3:55-78.CrossRefPubMedGoogle Scholar.

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

MCP-1

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.