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Selenoprotein and Renalase Blood Levels in Patients With Hypertensive Heart Disease and Obstructive Sleep Apnea

The Role of Selenoprotein Activity and Blood Renalase Level in the Pathogenesis of Hypertension and Obstructive Sleep Apnea

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05040516
Enrollment
150
Registered
2021-09-10
Start date
2020-01-27
Completion date
2021-10-01
Last updated
2021-09-10

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

Conditions

Hypertension, Obstructive Sleep Apnea

Keywords

hypertension, renalase, selenoprotein

Brief summary

The aim of the study is to determine whether selenoprotein activity and blood renalase level correlate with subclinical hypertensive heart disease and obstructive sleep apnea. The correlation will be assessed using selected electrocardiographic, ultrasound and laboratory indicators.

Detailed description

The study will be conducted in the Department and Clinic of Internal Medicine, Occupational Diseases, Hypertension and Clinical Oncology at Borowska 213 street in Wroclaw. This decision follows the high percentage of people with obstructive sleep apnea and hypertension among those hospitalized in the Clinic and also the wide availability of research tools in the hospital. 150 more patients with hypertension and obstructive sleep apnea will be included in the planned observational study. The study is observational, research procedures are non-invasive and no additional medical experiment is planned. The study was approved by the Bioethics Committee of the Wroclaw Medical University. Patients enrolled in the study will be asked to share the results of their previously performed examinations or, in case they do not have any, new examinations will be performed to complement the diagnostic process of hypertension and obstructive sleep apnea. The planned procedures include: medical interview, physical examination with basic anthropometric measurements (age, height, body weight); biochemical tests including blood selenium, selenoproteins, renalase and creatinine levels; total antioxidant status (TAS), 24-hour Holter electrocardiography, polysomnography, ultrasound assessment of peripheral vascular endothelial function and echocardiography. Laboratory tests will be performed using commercially available standardized tests. The levels of selenoproteins, renalase and creatinine in the blood, as well as TAS will be determined by ELISA (Enzyme-linked immunosorbent assay) in accordance with the instructions. Blood selenium level will be measured by means of atomic absorption spectrometry (AAS). 24-hour Holter ECG monitoring will be performed using a Lifecard CF recorder, followed by an analysis of the record by the Impresario Solo system (Delmar Reynolds, Hertford, UK). Ultrasound examination will be performed using the ProSound Alpha 6 (Aloka Inc, Tokyo, Japan).

Interventions

None listed

Sponsors

Wroclaw Medical University
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* arterial hypertension

Exclusion criteria

* age \<18 * pregnancy * refusal to participate in the study

Design outcomes

Primary

MeasureTime frameDescription
Assesment of blood renalase levelOne dayThe Enzyme-linked immunosorbent assay (ELISA) to know blood renalase level
Assesment of blood selenoprotein P levelOne dayThe Enzyme-linked immunosorbent assay (ELISA) to know blood selenoprotein P level
Assesment of the severity of obstructive sleep apneaOne dayFull polysomnography
Assessment of arrhythmiasOne day24-hour Holter ECG monitoring
Assessment of arrhythmias and cardiac morphologyOne dayEchocardiography

Secondary

MeasureTime frameDescription
Assesment of Blood Total Antioxidant Status (TAS)One dayThe Enzyme-linked immunosorbent assay (ELISA) to know Blood Total Antioxidant Status (TAS)

Countries

Poland

Contacts

Primary ContactKarolina Czerwińska, MD
karolina.czerwinska@student.umed.wroc.pl+48 790 404 619
Backup ContactPaweł Gać, ASSOC PROF
pawel.gac@umed.wroc.pl+48 71 784 15 01

Outcome results

None listed

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