Serum Adropin as an Indicator of Endothelial Dysfunction and Disease Severity in Obstructive Sleep Apnea in Obese Patients

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age20-75
SponsorAswan University

About this trial

1\. Objectives (Aim): To evaluate the role of serum adropin as a potential biomarker of endothelial dysfunction in OSA

1. Compare serum adropin levels between Obese patients with and without OSA. 2. Correlate serum adropin with OSA severity indices including the Apnea-Hypopnea Index (AHI) and Oxygen Desaturation Index (ODI) and cardiovascular complications. 3. Assess the relationship between serum adropin and endothelial dysfunction markers (endothelin-1). 4. Evaluate adropin's predictive ability for endothelial impairment among OSA patients.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

1- Adults aged 20-75 years. 2-obese Patients diagnosed with obstructive sleep apnea (OSA) confirmed by polysomnography.

Disqualifiers

1-Pregnant females 2-Thyroid disorders 3-Autoimmune diseases 4-chronic liver disease 5-chronic kidney disease 6-drugs as statin,glucocorticoids and antidepressant

Trial population

The study will include adult obese participants who are referred to the Sleep Medicine/Chest outpatient clinic with suspected obstructive sleep apnea. Participants will undergo clinical assessment and overnight polysomnography (PSG) to confirm the diagnosis of OSA and determine its severity according to the apnea-hypopnea index (AHI). Participants will be categorized into appropriate study groups according to the presence and severity of OSA. A suitable comparison group of obese participants without OSA may also be included, according to the study design. The study population will include both males and females who meet the predefined inclusion criteria and provide informed consent to participate in the study

Trial design

Design model

Case-control

Time perspective

Retrospective

Treatments tested in this trial

  • Adropin

    Diagnostic test

    Fasting blood samples of Adropin were obtained by venipuncture in the morning following the sleep study.

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Serum adropin levels (measured by ELISA)

* Serum adropin levels (measured by ELISA) * Association between serum adropin and endothelial function (Endothelin -1).

Time frame
12 months

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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