Angiotensin II receptor blocker: Difference between revisions

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{{Short description|Group of pharmaceuticals that modulate the renin–angiotensin system}}

[[Image:Losartan structure.svg|thumb|Losartan, the first ARB|250px|right]]

'''Angiotensin II receptor blockers''' ('''ARBs'''), formally '''angiotensin II receptor type 1 (AT₁) antagonists''', also known as '''angiotensin receptor blockers''', '''angiotensin II receptor antagonists''', or '''AT₁ receptor antagonists''', are a group of pharmaceuticals that bind to and inhibit the [[angiotensin II receptor type 1]] (AT₁) and thereby block the [[Vasoconstriction|arteriolar contraction]] and [[sodium retention]] effects of [[renin–angiotensin system]].

Their main uses are in the treatment of [[hypertension]] (high blood pressure), [[diabetic nephropathy]] ([[kidney damage]] due to [[diabetes mellitus|diabetes]]) and [[congestive heart failure]]. They ''selectively'' [[receptor antagonist|block]] the activation of the [[Angiotensin II receptor type 1|AT₁ receptor]], preventing the [[Ligand (biochemistry)|binding]] of [[angiotensin#Angiotensin II|angiotensin II]] compared to [[ACE inhibitors]].

ARBs and the similar-attributed ACE inhibitors are both indicated as the first-line [[antihypertensive]]s in patients developing [[hypertension]] along with [[left ventricular|left-sided]] [[heart failure]]. However, ARBs appear to produce less adverse effects compared to ACE inhibitors.

Angiotensin II receptor blockers are used primarily for the treatment of [[hypertension]] where the patient is intolerant of [[ACE inhibitor]] therapy primarily because of persistent and/or dry [[cough]].  They do not inhibit the breakdown of [[bradykinin]] or other [[kinin]]s, and are thus only rarely associated with the persistent dry cough and/or [[angioedema]] that limit ACE inhibitor therapy.  More recently, they have been used for the treatment of [[heart failure]] in patients intolerant of ACE inhibitor therapy, in particular [[candesartan]]. [[Irbesartan]] and [[losartan]] have trial data showing benefit in hypertensive patients with [[type 2 diabetes]], and may delay the progression of [[diabetic nephropathy]]. A 1998 double-blind study found "that [[lisinopril]] improved [[insulin sensitivity]] whereas losartan did not affect it." [[Candesartan]] is used experimentally in preventive treatment of [[migraine]]. Lisinopril has been found less often effective than candesartan at preventing migraine.

The angiotensin II receptor blockers have differing potencies in relation to blood pressure control, with statistically differing effects at the maximal doses.  When used in clinical practice, the particular agent used may vary based on the degree of response required.

Some of these drugs have a [[uricosuric]] effect.

Angiotensin II, through [[AT1 receptor|AT₁ receptor]] stimulation, is a major [[stress hormone]] and, because (ARBs) block these receptors, in addition to their eliciting anti-hypertensive effects, may be considered for the treatment of [[stress-related disorders]].

In 2008, they were reported to have a remarkable negative association with [[Alzheimer's disease]] (AD).  A retrospective analysis of five million patient records with the US [[United States Department of Veterans Affairs|Department of Veterans Affairs]] system found different types of commonly used antihypertensive medications had very different AD outcomes.  Those patients taking angiotensin receptor blockers (ARBs) were 35 to 40% less likely to develop AD than those using other antihypertensives.

A retrospective study of 1968 stroke patients revealed that prestroke treatment with ARB may be associated with both reduced stroke severity and better outcome. This finding agrees with experimental data that suggest that ARB's exert a cerebral protective effect.

This class of drugs is usually well tolerated. Common [[adverse drug reaction]]s (ADRs) include: dizziness, headache, and/or [[hyperkalemia]]. Infrequent ADRs associated with therapy include: first dose [[orthostatic hypotension]], rash, diarrhea, [[dyspepsia]], abnormal liver function, muscle cramp, [[myalgia]], back pain, [[insomnia]], decreased [[hemoglobin]] levels, [[renal impairment]], [[pharyngitis]], and/or nasal congestion. A 2014 Cochrane systematic review based on randomized controlled trials reported that when comparing patients taking ACE inhibitors to patients taking ARBs, fewer ARB patients withdrew from the study due to adverse events compared to ACE inhibitor patients.

While one of the main rationales for the use of this class is the avoidance of a persistent dry cough and/or angioedema associated with ACE inhibitor therapy, rarely they may still occur. In addition, there is also a small risk of cross-reactivity in patients having experienced [[angioedema]] with ACE inhibitor therapy.

The issue of whether angiotensin II receptor antagonists slightly increase the risk of [[myocardial infarction]] (MI or heart attack) is currently being investigated. Some studies suggest ARBs can increase the risk of MI. However, other studies have found ARBs do not increase the risk of MI. To date, with no consensus on whether ARBs have a tendency to increase the risk of myocardial infarction, further investigations are underway.

Indeed, as a consequence of AT₁ blockade, ARBs increase angiotensin II levels several-fold above baseline by uncoupling a [[negative-feedback]] loop. Increased levels of circulating angiotensin II result in unopposed stimulation of the AT₂ receptors, which are, in addition, upregulated. However, recent data suggest AT₂ receptor stimulation may be less beneficial than previously proposed, and may even be harmful under certain circumstances through mediation of growth promotion, [[fibrosis]], and [[hypertrophy]], as well as eliciting [[atherogenesis|proatherogenic]] and [[proinflammatory]] effects.

A study published in 2010 determined that "...meta-analysis of randomised controlled trials suggests that ARBs are associated with a modestly increased risk of new cancer diagnosis. Given the limited data, it is not possible to draw conclusions about the exact risk of cancer associated with each particular drug. These findings warrant further investigation."  A later meta-analysis by the U.S. [[Food and Drug Administration]] (FDA) of 31 randomized controlled trials comparing ARBs to other treatment found no evidence of an increased risk of incident (new) cancer, cancer-related death, breast cancer, lung cancer, or prostate cancer in patients receiving ARBs. In 2013, [[comparative effectiveness research]] from the [[United States Department of Veterans Affairs]] on the experience of more than a million [[veterans]] found no increased risks for either [[lung cancer]] or [[prostate cancer]]. The researchers concluded: "In this large nationwide cohort of United States Veterans, we found no evidence to support any concern of increased risk of lung cancer among new users of ARBs compared with nonusers. Our findings were consistent with a protective effect of ARBs."

In May 2013, a senior regulator at the Food & Drug Administration, Medical Team Leader Thomas A. Marciniak, revealed publicly that contrary to the FDA's official conclusion that there was no increased cancer risk, after a patient-by-patient examination of the available FDA data he had concluded that there was a lung-cancer risk increase of about 24% in ARB patients, compared with patients taking a placebo or other drugs. One of the criticisms Marciniak made was that the earlier FDA meta-analysis did not count lung [[carcinomas]] as cancers. In ten of the eleven studies he examined, Marciniak said that there were more lung cancer cases in the ARB group than the control group. Ellis Unger, chief of the drug-evaluation division that includes Marciniak, was quoted as calling the complaints a "diversion," and saying in an interview, "We have no reason to tell the public anything new." In an article about the dispute, the Wall Street Journal interviewed three other doctors to get their views; one had "no doubt" ARBs increased cancer risk, one was concerned and wanted to see more data, and the third thought there was either no relationship or a hard to detect, low-frequency relationship.

A 2016 meta-analysis including 148,334 patients found no significant differences in cancer incidence associated with ARB use.

Although ARBs have protective effects against developing kidney diseases for patients with [[diabetes]] and previous [[hypertension]] without administration of ARBs, ARBs may worsen [[kidney function]]s such as reducing [[glomerular filtration rate]] associated with a rise of [[serum creatinine]] in patients with pre-existing [[proteinuria]], [[renal artery stenosis]], [[hypertensive nephrosclerosis]], [[heart failure]], [[polycystic kidney disease]], [[chronic kidney disease]], [[Fibrosis#Heart|interstitial fibrosis]], [[focal segmental glomerulosclerosis]], or any conditions such as ARBs-treated but still clinically present [[hypertension]] that lead to abnormal narrowing of blood vessels to the kidney that interrupts oxygen and nutrient supply to the organ.

{{further|Discovery and development of angiotensin receptor blockers}}

[[Losartan]], [[irbesartan]], [[olmesartan]], [[candesartan]], [[valsartan]], [[fimasartan]] include the [[tetrazole]] group (a ring with four nitrogen and one carbon). Losartan, irbesartan, olmesartan, candesartan, and [[telmisartan]] include one or two [[imidazole]] groups.

These substances are AT₁-receptor antagonists; that is, they block the activation of [[Angiotensin receptor|angiotensin II AT₁ receptors]]. AT₁ receptors are found in [[smooth muscle]] cells of vessels, cortical cells of the [[adrenal gland]], and [[adrenaline|adrenergic]] nerve synapses. Blockage of AT₁ receptors directly causes [[vasodilation]], reduces secretion of [[vasopressin]], and reduces production and secretion of [[aldosterone]], among other actions. The combined effect reduces blood pressure.

The specific efficacy of each ARB within this class depends upon a combination of three [[pharmacodynamic]] (PD) and [[pharmacokinetic]] (PK) parameters. Efficacy requires three key PD/PK areas at an effective level; the parameters of the three characteristics will need to be compiled into a table similar to one below, eliminating duplications and arriving at consensus values; the latter are at variance now.

[[Pressor]] inhibition at [[trough level]] {{emdash}} this relates to the degree of blockade or inhibition of the blood pressure-raising ("pressor") effect of angiotensin II.  However, pressor inhibition is not a measure of blood pressure-lowering (BP) efficacy ''per se''.  The rates as listed in the U.S. [[Food and Drug Administration]] (FDA) Package Inserts (PIs) for inhibition of this effect at the 24th hour for the ARBs are as follows:

* [[Valsartan]]{{snd}} 30% at 80&nbsp;mg

* [[Olmesartan]]{{snd}} 61% at 20&nbsp;mg; 74% at 40&nbsp;mg

The ratios of AT₁ to AT₂ in binding affinities of the specific ARBs are shown as follows. However, AT₁ affinity vs AT₂ is not a meaningful indicator of blood pressure response.

* [[Losartan]]{{snd}} 1000-fold

* [[Saprisartan]] – ???

Nearly all ARBs contain [[biphenyltetrazole moiety]] except [[telmisartan]] and [[eprosartan]].

Losartan carries a [[heterocycle imidazole]] while valsartan carries a nonplanar acylated [[amino acid]].

{| class="wikitable"

|+ Table 1: Comparison of ARB [[pharmacokinetics]]

| 4–32

| [[Moderate sensitive substrate]]: [[CYP2C9]]

|-

| [[Valsartan]]

|}

{{further|Discovery and development of angiotensin receptor blockers}}

===Longevity===

Knockout of the Agtr1a gene that encodes AT₁ results in marked prolongation of the life-span of mice, by 26% compared to controls.  The likely mechanism is reduction of oxidative damage (especially to mitochondria) and overexpression of renal prosurvival genes. The ARBs seem to have the same effect.

ARBs, such as losartan, have been shown to curb or reduce muscular, liver, cardiac, and kidney fibrosis.

A 2003 study using candesartan and valsartan demonstrated an ability to regress dilated [[Ascending aorta|aortic root]] size.

{{Anchor|recalls}}

{{See also|Ranitidine#impurities}}

In 2018 and in 2019, the U.S [[Food and Drug Administration]] (FDA) found traces of NDMA and NDEA impurities in the angiotensin II receptor blocker (ARB) drug products [[valsartan]], [[losartan]], and [[irbesartan]]. The FDA stated "In June 2018, FDA was informed of the presence of an impurity, identified as [[N-Nitrosodimethylamine]] (NDMA), from one [[active ingredient|API]] producer. Since then, FDA has determined that other types of [[nitrosamine]] compounds, e.g., [[N-Nitrosodiethylamine]] (NDEA), are present at unacceptable levels in APIs from multiple API producers of valsartan and other drugs in the ARB class." In 2018, the FDA issued guidance to the industry on how to assess and control the impurities.

In August 2020, the [[European Medicines Agency]] (EMA) provided guidance to marketing authorization holders on how to avoid the presence of nitrosamine impurities in human medicines and asked them to review all chemical and biological human medicines for the possible presence of nitrosamines and to test the products at risk.

In November 2020, the [[Committee for Medicinal Products for Human Use]] (CHMP) of the EMA aligned recommendations for limiting nitrosamine impurities in sartan medicines with recommendations it issued for other classes of medicines. The main change concerns the limits for nitrosamines, which previously applied to the active ingredients but now apply instead to the finished products (e.g. tablets). These limits, based on internationally agreed standards (ICH M7(R1)), should ensure that the excess risk of cancer from nitrosamines in any sartan medicines is below 1 in 100,000 for a person taking the medicine for lifelong treatment.

These sartan medicines have a specific ring structure (tetrazole) whose synthesis could potentially lead to the formation of nitrosamine impurities. Other sartan medicines which do not have this ring, such as azilsartan, eprosartan and telmisartan, were not included in this review but are covered by the subsequent review of other medicines.

{{multiple image | width1 = 200 | image1 = Losartan azide.svg | alt1 = Skeletal formula of losartan azide | width2 = 180 | image2 = AZBT.svg | alt2 = Skeletal formula of azidomethyl-biphenyl-tetrazole | footer = Losartan azide (left) and AZBT (right), two azido process impurities detected in sartans. Losartan azide occurs exclusively during manufacture of losartan, while AZBT can be found in several drugs in the class.}}

In April 2021, the [[European Directorate for the Quality of Medicines & HealthCare|European Directorate for the Quality of Medicines]] (EDQM) warned of the risk of contamination with non-nitrosamine impurities (specifically, [[azide|azido]] compounds) in tetrazole-containing sartans. In September 2021, the EDQM announced that investigations had revealed a novel azido contaminant which occurs only in losartan (losartan azide or losartan azido impurity) and which was found to be mutagenic on [[Ames test]]ing.

Later in 2021 and 2022, several cases of contamination with azido impurities were detected in losartan, irbesartan, and valsartan, prompting regulatory responses ranging from investigation to market withdrawals and precautionary recalls in [[Australia]], [[Brazil]], and Europe (including Switzerland).

[[Teva Pharmaceuticals]] announced that it would change its losartan manufacturing process to prevent future contamination with these impurities, and the Indian API manufacturer IOL Chemicals and Pharmaceuticals applied for a patent on a new synthesis of losartan designed to be free of azido contaminants.

{{clear}}

* {{MeshName|Angiotensin II Type 1 Receptor Blockers}}

* {{cite web | title=Nitrosamine impurities in medications: Guidance | website=Health Canada | date=4 April 2022 | url=https://www.canada.ca/en/health-canada/services/drugs-health-products/compliance-enforcement/information-health-product/drugs/nitrosamine-impurities/medications-guidance.html }}

{{Major drug groups}}

{{Receptor agonists and antagonists}}

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{{二次利用|date=4 March 2024}}

{{DEFAULTSORT:Angiotensin Ii Receptor Blocker}}

[[Category:Angiotensin II receptor antagonists| ]]

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