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Chlorthalidone

Generic Name
Chlorthalidone
Brand Names
Edarbyclor, Tenoretic, Thalitone
Drug Type
Small Molecule
Chemical Formula
C14H11ClN2O4S
CAS Number
77-36-1
Unique Ingredient Identifier
Q0MQD1073Q
Background

Chlorthalidone is a thiazide-like diuretic used for the treatment of hypertension and for management of edema caused by conditions such as heart failure or renal impairment. Chlorthalidone improves blood pressure and swelling by preventing water absorption from the kidneys through inhibition of the Na+/Cl− symporter in the distal convoluted tubule cells in the kidney. The exact mechanism of chlorthalidone's anti-hypertensive effect is under debate, however, it is thought that increased diuresis results in decreased plasma and extracellular fluid volume, decreased cardiac output and therefore overall reduction in blood pressure.

Chlorthalidone is considered first-line therapy for management of uncomplicated hypertension as there is strong evidence from meta-analyses that thiazide diuretics such as chlorthalidone reduce the risk of stroke, myocardial infarction, heart failure, and cardiovascular all-cause mortality in patients with hypertension. In particular, the ALLHAT trial confirmed the role of thiazide diuretics as first-line therapy and demonstrated that chlorthalidone had a statistically significant lower incidence of stroke and heart failure when compared to Lisinopril, Amlodipine, or Doxazosin. Further studies have indicated that low-dose thiazides are as good as, and in some secondary endpoints, better than β-blockers, ACE inhibitors, Calcium Channel Blockers or ARBs.

Chlorthalidone has been shown to have a number of pleiotropic effects that differentiate it from other diuretics such as Hydrochlorothiazide. In addition to its antihypertensive effects, chlorthalidone has also been shown to decrease platelet aggregation and vascular permeability, as well as promote angiogenesis in vitro, which is thought to be partly the result of reductions in carbonic anhydrase–dependent pathways. These pathways may play a role in chlorthalidone's cardiovascular risk reduction effects.

Indication

Chlorthalidone is indicated in the management of hypertension either as the sole therapeutic agent or to enhance the effect of other antihypertensive drugs in the more severe forms of hypertension.

Chlorthalidone is indicated as adjunctive therapy in edema associated with congestive heart failure, hepatic cirrhosis, and corticosteroid and estrogen therapy.

Chlorthalidone has also been found useful in edema due to various forms of renal dysfunction, such as nephrotic syndrome, acute glomerulonephritis, and chronic renal failure.

Associated Conditions
Calcium Nephrolithiasis, Edema, Hypertension

FDA Approves HemiClor: First Low-Dose Chlorthalidone Tablet for Hypertension Management

• The FDA has approved HemiClor (12.5 mg chlorthalidone), the first low-dose formulation of this thiazide-like diuretic available in the U.S. for treating hypertension in adults. • The 12.5 mg dosage aligns with current ACC/AHA guideline recommendations and landmark clinical trials like ALLHAT and SHEP, which demonstrated cardiovascular outcome benefits with this starting dose. • HemiClor may help clinicians better individualize therapy and potentially reduce dose-related adverse effects such as hypokalemia and hyperuricemia, particularly beneficial for elderly patients.

Hanmi Pharm Seeks Approval for Triple-Combination Hypertension Drug Amosartan PLUS-L

• Hanmi Pharm has filed for domestic approval of Amosartan PLUS-L, a triple-combination hypertension therapy containing amlodipine, losartan, and chlorthalidone at one-third the standard dose. • Phase 3 clinical trials (HM-APOLLO-301) demonstrated comparable efficacy to standard-dose single agents in adults with mild to moderate hypertension over eight weeks. • The low-dose combination therapy showed similar efficacy with improved tolerability, potentially reducing medication-switching rates and enhancing patient convenience. • Hanmi Pharm aims to launch Amosartan PLUS-L in 2025, positioning it as a potential paradigm shift in early hypertension treatment by targeting multiple pathways.

Genetic Risk Score Predicts Hypertension Treatment Response in Black Individuals

• A new study reveals a genetic risk score (ΔSBP) can predict Black individuals' response to chlorthalidone for hypertension. • Individuals with lower ΔSBP scores experienced a greater reduction in systolic blood pressure with chlorthalidone treatment. • Higher ΔSBP scores were associated with a significantly increased risk of developing treatment-resistant hypertension. • The ΔSBP score shows potential for personalizing hypertension treatment, guiding selection between chlorthalidone and lisinopril.

Genetic Risk Score Predicts Blood Pressure Response to Chlorthalidone in Black Individuals

• A systolic blood pressure polygenic risk score (SBP PRS) was evaluated for its association with blood pressure response to hypertension treatment in Black individuals. • Individuals in the lowest SBP PRS quintile experienced a 3.5 mm Hg greater reduction in systolic blood pressure with chlorthalidone compared to the median quintile. • A high SBP PRS was associated with an increased risk of apparent treatment-resistant hypertension, suggesting potential for personalized treatment. • The SBP PRS may help identify individuals who could benefit most from chlorthalidone, warranting further research to inform treatment decisions.
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