Glucose Trnsporter and PEDF in Psoriasis

Sponsor
Assiut University (Other)
Overall Status
Unknown status
CT.gov ID
NCT04242082
Collaborator
(none)
75
7

Study Details

Study Description

Brief Summary

Psoriasis is a chronic relapsing cutaneous immune mediated inflammatory disease(IMID). In which there are skin lesions characterized by erythema, thickness and scale formation with different size from a pinhead to 20 cm in diameter. Prevalence of psoriasis is 2% to 4% worldwide. Psoriasis occurs at any age with two peaks: between 15-20 years and between 55-60 years. Women are presented with psoriasis at younger age than men ,but with less severity. lesions usually present on knee, elbow, scalp and sacral region this may be attributed to higher traumatic incident .

Psoriasis vulgaris is the most common type, and accounts 90% of cases. Patients with psoriasis vulgaris present with pain, itching and bleeding from skin lesions.

There are many theories for psoriasis pathogenesis: angiogenesis, decrease in apoptosis of keratinocyte, hyperproliferation , alteration of cell to cell adhesion and immune-mediated inflammation.

Patients with immune mediated inflammatory disease (IMID) are susceptible to develop diabetes mellitus, metabolic syndrome, hyperlipidemia, and hypertension.A previous study found that psoriatic patients are more susceptible to type 2 diabetes compared to control.

Glucose transporter type 1(GLUT1) is upregulated in psoriatic patient attributed to angiogenesis and execessive cell proliferation in those patients .Also expression of GLUT 1 is found high with hyperglycemia . A study reported that GLUT 1 density in placenta of women with gestational diabetes was found to be two folds higher than control.

Pigment epithelium derived factor (PEDF) has antiangiogenic effect. Topical application of PEDF on mouse model of psoriatic disease helps in reduction of skin proliferation and angiogenesis.

GLUT 1 overexpression was found to be associated with decrease in PEDF expression in diabetic retinopathy.

In view of that we will compare the level of GLUT 1 gene in psoriatic patients and psoriatic patients with diabetes, as well as healthy control, and detect the effect of PEDF on GLUT 1 expression in vitro using human keratinocytes cell line .

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: GLUT 1 gene expression

Study Design

Study Type:
Observational
Anticipated Enrollment :
75 participants
Observational Model:
Case-Control
Time Perspective:
Cross-Sectional
Official Title:
Role of Glucose Transporter (GLUT) Genes Expression in Patients With Psoriasis
Anticipated Study Start Date :
Jul 31, 2020
Anticipated Primary Completion Date :
Jul 31, 2020
Anticipated Study Completion Date :
Mar 1, 2021

Arms and Interventions

Arm Intervention/Treatment
patients with psoriasis vulgaris only

Diagnostic Test: GLUT 1 gene expression
GLUT 1 gene expression will done on blood samples taken from three groups using real time PCR. Pigment epithelium derived factor will used on keratinocytes cell line and compare GLUT 1 gene expression before and after treatment.

patients with psoriasis vulgaris and type 2 diabetes mellitus

Diagnostic Test: GLUT 1 gene expression
GLUT 1 gene expression will done on blood samples taken from three groups using real time PCR. Pigment epithelium derived factor will used on keratinocytes cell line and compare GLUT 1 gene expression before and after treatment.

healthy control

Diagnostic Test: GLUT 1 gene expression
GLUT 1 gene expression will done on blood samples taken from three groups using real time PCR. Pigment epithelium derived factor will used on keratinocytes cell line and compare GLUT 1 gene expression before and after treatment.

Outcome Measures

Primary Outcome Measures

  1. GLUT1 expression in psoriatic patients with or without type 2 diabetes. [through study completion, an average of 2 year]

    assessing fold changes of GLUT1 expression in blood samples using real time PCR.

  2. GLUT1 expression in keratinocyte before and after treatment with pigment epithelium derived factor (PEDF) [through study completion, an average of 2 year]

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Patients with psoriasis vulgaris Patients with psoriasis vulgaris and type 2 diabetes
Exclusion Criteria:
  • Factors affect GLUT 1 expression As: tumors either benign or malignant cause increase GLUT 1 expression

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Assiut University

Investigators

  • Study Director: Naglaa K Idriss, asst. prof, Assiut University
  • Study Director: Ayaat ِA Sayed, asst. prof, Assiut University

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
SSElkady, Demonstrator at Medical Biochemistry department, Assiut University
ClinicalTrials.gov Identifier:
NCT04242082
Other Study ID Numbers:
  • PGLUTPEDF
First Posted:
Jan 27, 2020
Last Update Posted:
May 8, 2020
Last Verified:
May 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by SSElkady, Demonstrator at Medical Biochemistry department, Assiut University
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 8, 2020