Drug products: Aprovel, CoAprovel, Ifirmacombi, Ifirmasta, Irbesartan Accord, Irbesartan Actavis, Irbesartan Aurobindo, Irbesartan Bluefish, Irbesartan Hydrochlorothiazide Zentiva, Irbesartan Jubilant, Irbesartan Mylan, Irbesartan Ranbaxy, Irbesartan Sandoz, Irbesartan STADA, Irbesartan Teva, Irbesartan Zentiva, Irbesartan/Hydrochlorothiazide Sandoz, Irbesartan/Hydrochlorothiazide STADA, Irbesartan/Hydrochlorothiazide Teva, Irbesartan/Hydroklortiazid Actavis, Karvea, Karvezide
ATC code: C09CA04, C09DA04
Substances: irbesartan, irbesartan hydrochloride (anhydrous), irbesartan hydrochloride sesquihydrate
No major sex-related differences in the pharmacokinetics of irbesartan have been observed and adjustment of the dose is not necessary with respect to the patient’s sex.
Overall, the effect on blood pressure is stated to be the same regardless of the patient’s sex and the risk of sudden death was twice as common for men and therefore women had a better overall prognosis. Non-fatal myocardial infarction was more common in women than men. The baseline characteristics of women in some heart failure studies have shown more severe illness but women had similar rates of hospitalization and better survival than men.
Clinical and epidemiologic evidence suggests that women with renal disease have a slower progression to end stage compared with men, but the underlying mechanisms remain unknown. A possible contributing phenomenon is physiologic sex-based difference in the function of the renin-angiotensin system (RAS). In a study (15 men, 15 women) with incremental dosages of irbesartan, blood pressure declined in both men and women. Women, but not men, achieved a significant reduction of angiotensin II sensitivity. Men, but not women, continued to show pressor response with increasing doses of irbesartan. Receptor expression at baseline was similar in men and women but by week eight there was a significant decrease in women and unchanged in men. This suggests that men may require larger doses of angiotensin receptor blocker than women and the blood pressure response cannot be used as a surrogate marker for adequate RAS blockade of the renal microvasculature .
Polymorphism in the kininogen 1 gene has shown a sex-specific association with plasma irbesartan concentrations in Chinese patients (488 men, 612 women) with essential hypertension. Male, but not female, GG allele carriers had significantly lower irbesartan concentrations relative to TT genotype .
No sex-related differences in pharmacokinetics are observed in healthy elderly (age 65-80 years) or in healthy young (age 18-40 years) patients treated with irbesartan. In studies of hypertensive patients, there is no sex difference in half-life or accumulation, but somewhat higher plasma concentrations of irbesartan are observed in women (11% to 44%) .
In a small study (12 young men, 12 young women, 12 elderly men, 12 elderly women) with irbesartan, no statistically sex-effects were observed in peak plasma concentration, AUC and terminal elimination half-life of irbesartan. No adjustment in irbesartan is necessary with respect to the patient’s sex [3, 4], which is also concluded in other pharmacokinetic studies .
There is some conflicting evidence regarding the effects of irbesartan depending on the patient’s sex. Some sources claim that the efficacy of irbesartan is not affected by the patient’s sex .In an observational study (8317 men, 7906 women), the effect of irbesartan in reducing cardiovascular risk in hypertensive type 2 diabetic patients was examined. No important differences were noted between men and women in mean 10-year cardiovascular risk as calculated with SCORE [7, 8]. In a subgroup analysis of antihypertensive effi acy of irbesartan/hydrochlorothiazide (HCTZ) in patients with metabolic syndrome and type 2 diabetes, no significant differences between the sexes were found in blood pressure change from baseline to week 18 .
Other sources state differences in the effects depending on the patient’s sex. The effects of irbesartan on cardiovascular and renal events in patients with hypertension, diabetes type 2 and renal disease, seemed lower in women . Nonfatal myocardial infarction was increased in women while it decreased in men when compared to placebo. No proper explanation for these findings has been identified .In heart failure with preserved ejection fraction there are significant differences between men and women treated with irbesartan. Despite worse symptoms, more congestion, and lower quality of life, women had similar rates of hospitalization and better survival than men. Their risk of sudden death was half that of men  and therefore women had better overall prognosis .Blood pressure control rates with irbesartan/HCTZ treatment were slightly better for women compared to men (58% vs 45%) in a study (252 men, 197 women) where valsartan/HCTZ was compared to irbesartan/HCTZ .
One study (67 men, 35 women) found a sex-specific association between preproendothelin-1 genotype and reduction of systolic blood pressure during treatment with irbesartan or atenolol. Men, but not women, with the T-allele responded on average with a more than two-fold greater reduction than those with the G/G genotype .
No studies with a clinically relevant sex analysis regarding non-cardiovascular adverse effects of irbesartan have been found.
Angiotensin II-antagonists should not be used during pregnancy, especially not during the second or third trimester. Treatment during this period has been associated with complications during pregnancy and the neonatal period . Regarding teratogenic aspects, please consult Janusmed Drugs and Birth Defects (in Swedish, Janusmed fosterpåverkan).
Date of litterature search: 2021-01-22
Reviewed by: Diana Rydberg
Approved by: Karin Schenck-Gustafsson