Angiotensin-Converting Enzyme Inhibitors
"Angiotensin-Converting Enzyme Inhibitors" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A class of drugs whose main indications are the treatment of hypertension and heart failure. They exert their hemodynamic effect mainly by inhibiting the renin-angiotensin system. They also modulate sympathetic nervous system activity and increase prostaglandin synthesis. They cause mainly vasodilation and mild natriuresis without affecting heart rate and contractility.
Descriptor ID |
D000806
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MeSH Number(s) |
D27.505.519.389.745.085
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Concept/Terms |
Angiotensin-Converting Enzyme Inhibitors- Angiotensin-Converting Enzyme Inhibitors
- Angiotensin Converting Enzyme Inhibitors
- Inhibitors, Kininase II
- Kininase II Antagonists
- Kininase II Inhibitors
- Angiotensin I-Converting Enzyme Inhibitors
- Angiotensin I Converting Enzyme Inhibitors
- Antagonists, Angiotensin-Converting Enzyme
- Antagonists, Angiotensin Converting Enzyme
- Antagonists, Kininase II
- Inhibitors, ACE
- ACE Inhibitors
- Inhibitors, Angiotensin-Converting Enzyme
- Enzyme Inhibitors, Angiotensin-Converting
- Inhibitors, Angiotensin Converting Enzyme
- Angiotensin-Converting Enzyme Antagonists
- Angiotensin Converting Enzyme Antagonists
- Enzyme Antagonists, Angiotensin-Converting
|
Below are MeSH descriptors whose meaning is more general than "Angiotensin-Converting Enzyme Inhibitors".
Below are MeSH descriptors whose meaning is more specific than "Angiotensin-Converting Enzyme Inhibitors".
This graph shows the total number of publications written about "Angiotensin-Converting Enzyme Inhibitors" by people in this website by year, and whether "Angiotensin-Converting Enzyme Inhibitors" was a major or minor topic of these publications.
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click here.
Year | Major Topic | Minor Topic | Total |
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1996 | 1 | 2 | 3 |
1997 | 3 | 4 | 7 |
1998 | 0 | 1 | 1 |
1999 | 0 | 1 | 1 |
2001 | 1 | 0 | 1 |
2003 | 1 | 1 | 2 |
2004 | 0 | 1 | 1 |
2005 | 0 | 3 | 3 |
2006 | 0 | 2 | 2 |
2007 | 2 | 3 | 5 |
2008 | 2 | 2 | 4 |
2009 | 1 | 1 | 2 |
2010 | 3 | 0 | 3 |
2011 | 1 | 2 | 3 |
2012 | 1 | 1 | 2 |
2013 | 2 | 2 | 4 |
2014 | 3 | 1 | 4 |
2015 | 3 | 2 | 5 |
2016 | 0 | 1 | 1 |
2017 | 0 | 2 | 2 |
2018 | 1 | 0 | 1 |
2019 | 2 | 1 | 3 |
2020 | 1 | 3 | 4 |
2021 | 2 | 0 | 2 |
2022 | 0 | 3 | 3 |
2024 | 0 | 1 | 1 |
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Below are the most recent publications written about "Angiotensin-Converting Enzyme Inhibitors" by people in Profiles.
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National Trends in Hospital Performance in Guideline-Recommended Pharmacologic Treatment for Heart Failure at Discharge. JACC Heart Fail. 2024 Jun; 12(6):1059-1070.
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Slowing the Progression of Diabetic Kidney Disease. Cells. 2023 07 31; 12(15).
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The histological spectrum of ARB-induced gastritis. Histopathology. 2022 Nov; 81(5):653-660.
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Outcomes of guideline-based medical therapy in patients with acute heart failure and reduced left ventricular ejection fraction: Observations from the Gulf acute heart failure registry (Gulf CARE). Medicine (Baltimore). 2022 Jun 10; 101(23):e29452.
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Effect of Antihypertensives by Class on Cerebral Small Vessel Disease: A Post Hoc Analysis of SPRINT-MIND. Stroke. 2022 08; 53(8):2435-2440.
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Self-Reported Antihypertensive Medication Class and Temporal Relationship to Treatment Guidelines. Hypertension. 2022 02; 79(2):338-348.
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Mineralocorticoid receptor antagonists in diabetic kidney disease - mechanistic and therapeutic effects. Nat Rev Nephrol. 2022 01; 18(1):56-70.
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Cardiovascular Benefits of Angiotensin-Converting Enzyme Inhibition Plus Calcium Channel Blockade in Patients Achieving Tight Blood Pressure Control and With Resistant Hypertension. Am J Hypertens. 2021 05 22; 34(5):531-539.
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Outcomes of Hospitalized COVID-19 Patients Receiving Renin Angiotensin System Blockers and Calcium Channel Blockers. Am J Nephrol. 2021; 52(3):250-260.
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A network medicine approach to investigation and population-based validation of disease manifestations and drug repurposing for COVID-19. PLoS Biol. 2020 11; 18(11):e3000970.