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Serum GPER-1 and Oxidant/Antioxidant Levels on Retinopathy in Diabetic Patients

Comparing the Impact of Serum GPER-1 and Oxidant/Antioxidant Levels on Retinopathy in Diabetic Patients and Healthy Individuals: A Pilot Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04930224
Enrollment
120
Registered
2021-06-18
Start date
2019-07-01
Completion date
2020-04-25
Last updated
2021-06-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes Mellitus, Diabetic Retinopathy, Hormones

Keywords

Diabetic retinopathy, GPER-1, oestradiol, progesterone, TSH, oxidative stress, neuronal damage.

Brief summary

Observational, comparative, cross-sectional study

Detailed description

This study was conducted on G protein-mediated estrogen receptor 1 (GPER-1), which is thought to be effective in preventing the development of diabetic retinopathy (DR). There are studies proving that GPER-1 prevents neuroprotective effects and vascular pathology in many tissues. In the study, serum GPER-1 and oxidative stress biomarker levels were compared in diabetic patients and healthy control groups. GPER-1 was found to be significantly increased in diabetic patients. In addition, a positive correlation was found with oxidant markers. This may lead to new treatment models in the future.

Interventions

DIAGNOSTIC_TESTThe effect of GPER-1 on the formation of diabetic retinopathy

Demonstrating the neuroprotective effect of GPER-1 in the formation of diabetic retinopathy and being a guide for new treatment models

Sponsors

Kahramanmaras Sutcu Imam University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
35 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* 40 individuals were required to have Proliferative Diabetic Retinopathy (PDR); * 40 were required to have Non-PDR; * 40 were required to be healthy, without any systemic disease.

Exclusion criteria

* Glaucoma, * Ocular trauma sequelae, * Pathological myopia, * Non-diabetic retinopathy, * A history of previous ocular surgery, * Endocrine disorders (e.g.,thyroidopathy, adrenal gland disorders, pituitary pathologies), * Opacities interfering with fundus examination (e.g., corneal opacity, lens opacity, vitreous cloudiness other than diabetic haemorrhage).

Design outcomes

Primary

MeasureTime frameDescription
G receptor-mediated protein-1 (GPER-1)BaselineVariation of GPER-1 during the development of diabetic retinopathy
Oxidative/antioxidative stress markers (malondialdehyde [MDA])BaselineVariation of oxidative/antioxidative stress markers during the development of diabetic retinopathy
Oxidative/antioxidative stress markers (catalase [CAT])BaselineVariation of oxidative/antioxidative stress markers during the development of diabetic retinopathy
Oxidative/antioxidative stress markers (superoxide dismutase [SOD]BaselineVariation of oxidative/antioxidative stress markers during the development of diabetic retinopathy
Thyroid stimulating hormone (TSH)BaselineVariation of TSH during the development of diabetic retinopathy
ProgesteroneBaselineVariation of progeterone during the development of diabetic retinopathy
oestradiolBaselineVariation of oestradiol during the development of diabetic retinopathy

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026