دورية أكاديمية

Serum Elabela expression is decreased in hypertensive patients and could be associated with the progression of hypertensive renal damage

التفاصيل البيبلوغرافية
العنوان: Serum Elabela expression is decreased in hypertensive patients and could be associated with the progression of hypertensive renal damage
المؤلفون: Geng Tian, Qian Zheng, Qingru Zhang, Xiaoyu Liu, Xuehong Lu
المصدر: European Journal of Medical Research, Vol 29, Iss 1, Pp 1-7 (2024)
بيانات النشر: BMC, 2024.
سنة النشر: 2024
المجموعة: LCC:Medicine
مصطلحات موضوعية: eGFR, Elabela, Hypertension, Malignant hypertension, Renal damage, Systolic blood pressure, Medicine
الوصف: Abstract Background Elabela, a recently discovered hormonal peptide containing 32 amino acids, is a ligand for the apelin receptor. It can lower blood pressure and attenuate renal fibrosis. However, the clinicopathological relationship between Elabela level and renal damage caused by benign hypertension (BHT) and malignant hypertension (MHT) has not been elucidated. Therefore, we investigated the clinicopathological correlation between serum Elabela level and renal damage caused by BHT and MHT. Methods The participants comprised 50 patients and 25 age-matched healthy adults. The 50 patients were separated into two groups: MHT (n = 25) and BHT groups (n = 25). We analyzed their medical histories, demographics, and clinical examinations, including physical and laboratory tests. Results The results showed that serum Elabela level decreased gradually with a continuous increase in blood pressure from the healthy control group, BHT, to MHT. Moreover, Elabela levels negatively correlated with BMI (R = − 0.27, P = 0.02), SBP (r = − 0.64, P
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2047-783X
Relation: https://doaj.org/toc/2047-783X
DOI: 10.1186/s40001-024-01674-1
URL الوصول: https://doaj.org/article/64701be8e81248ad975e91ae05646711
رقم الأكسشن: edsdoj.64701be8e81248ad975e91ae05646711
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:2047783X
DOI:10.1186/s40001-024-01674-1