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Inappropriately elevated endothelin-1 plays a role in the pathogenesis of intradialytic hypertension
Jie Teng1, Jie Tian, Wen-Lv Lv
1Department of Nephrology, Zhongshan Hospital, Shanghai Medical College, Fudan University, No 180 Fenglin Road, Shanghai, 200032, China; Kidney and Dialysis Institute of Shanghai, No 180 Fenglin Road, Shanghai, 200032, China; Kidney and Blood Purification Laboratory of Shanghai, No 180 Fenglin Road, Shanghai, 200032, China.
Insights
Elevated endothelin-1 (ET-1) plasma levels are linked to intradialytic hypertension (IDH) in hemodialysis patients. This finding suggests ET-1 plays a key role in the development of IDH during dialysis.
Area of Science:
- Nephrology
- Cardiovascular Physiology
- Biochemistry
Background:
- Intradialytic hypertension (IDH) is a complication during maintenance hemodialysis.
- The role of endogenous vasoactive substances in IDH pathogenesis requires further investigation.
Purpose of the Study:
- To investigate the effects of endogenous vasoactive substances on the occurrence of intradialytic hypertension (IDH) in patients undergoing maintenance hemodialysis.
Main Methods:
- Retrospective comparison of 34 maintenance hemodialysis patients (17 with IDH, 17 controls).
- Measurement of plasma levels of vasoactive substances (e.g., endothelin-1, nitric oxide, aldosterone) pre- and post-dialysis.
- Analysis of blood pressure changes during hemodialysis sessions.
Main Results:
- Post-dialysis endothelin-1 (ET-1) concentrations were significantly higher in IDH patients compared to controls.
- The ratio of nitric oxide (NO) to ET-1 was significantly lower in IDH patients post-dialysis.
- Aldosterone and norepinephrine levels showed different pre- to post-dialysis changes in controls versus IDH patients.
Conclusions:
- Inappropriately elevated ET-1 plasma concentrations appear to play a predominant role in the pathogenesis of IDH.
- The balance between vasoconstrictors like ET-1 and vasodilators like NO is crucial in IDH development.
- Further research into ET-1 modulation could offer therapeutic strategies for IDH.
Abstract:
The aim of this study is to investigate the effects of endogenous vasoactive substances on the occurrence of intradialytic hypertension (IDH) in patients during maintenance hemodialysis. Thirty-four maintenance hemodialysis patients were enrolled in this trial, and 17 of them were diagnosed with IDH (defined as an increase in blood pressure of at least 10 mmHg during or immediately after a hemodialysis session), while 17 age-matched and sex-matched controls without IDH were selected for a retrospective comparison. We collected patients' blood samples before and after a dialysis session and measured the plasma levels of N-terminal fragment brain natriuretic peptide, renin, angiotensin-II, aldosterone (ALD), angiotensin-converting enzyme (ACE), endothelin-1 (ET-1), nitric oxide (NO), norepinephrine (NOR), and adrenomedullin. The post-dialysis serum ET-1 concentrations were significantly higher (4.09 ± 2.06 vs. 2.75 ± 1.34 pg/mL, P < 0.05), while the post-dialysis ratio of NO to ET-1 was lower (17.79 ± 5.65 vs. 24.78 ± 12.04, P < 0.05) in IDH patients compared with the control group. Post-dialysis ALD and NOR values were significantly lower (P < 0.01) and ACE levels were significantly higher (P < 0.01) than the pre-dialysis concentrations only in the control and not in the IDH group. All other measured factors did not differ significantly between the groups and between pre-dialysis and post-dialysis determinations. Compared with blood angiotensin-II, ALD, ACE, NOR, adrenomedullin, N-terminal fragment brain natriuretic peptide, and NO status, inappropriately elevated ET-1 plasma concentrations may play a predominant role in the pathogenesis of IDH.
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