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Published on: September 17, 2015
A comparative study on the effectiveness of losartan/hydrochlorothiazide and telmisartan/hydrochlorothiazide in
Toshihiro Hamada1, Masanari Kuwabara, Arisa Watanabe
1Department of Regional Medicine, Tottori University Faculty of Medicine , Yonago , Japan .
Insights
Losartan/HCTZ combination therapy did not affect uric acid or glucose metabolism in hypertensive patients. However, telmisartan/HCTZ therapy impaired uric acid metabolism and worsened glucose metabolism.
Area of Science:
- Nephrology
- Endocrinology
- Pharmacology
Background:
- Hypertension management often involves combination therapies.
- The metabolic effects of different antihypertensive drug combinations require thorough investigation.
- Understanding the impact on uric acid and glucose metabolism is crucial for patient outcomes.
Purpose of the Study:
- To compare the long-term effects of low-dose hydrochlorothiazide (HCTZ) with losartan (LOS) versus telmisartan (TEL) on uric acid (UA) and glucose metabolism in hypertensive patients.
- To evaluate the impact of LOS+HCTZ and TEL+HCTZ on serum UA levels, UA clearance, and glucose homeostasis markers.
Main Methods:
- A study involving 59 hypertensive patients allocated to either LOS (50 mg/day) + HCTZ (12.5 mg/day) or TEL (40 mg/day) + HCTZ (12.5 mg/day) for one year.
- Assessment of blood pressure and biochemical parameters (blood and urine) before and after treatment.
- Analysis included serum UA, creatinine clearance, fasting plasma glucose, HbA1c, and HOMA-R.
Main Results:
- Both LOS+HCTZ and TEL+HCTZ effectively reduced blood pressure without significant differences.
- LOS+HCTZ did not alter serum UA levels or UA clearance/creatinine clearance (CUA/Ccr), while TEL+HCTZ significantly increased serum UA and reduced CUA/Ccr.
- Neither combination affected fasting glucose, HbA1c, or HOMA-R, except TEL+HCTZ increased HOMA-R in patients with elevated baseline UA.
Conclusions:
- LOS+HCTZ demonstrated a neutral effect on uric acid and glucose metabolism, potentially due to losartan's action on URAT1.
- TEL+HCTZ was associated with impaired uric acid metabolism and worsened glucose metabolism, particularly in patients with higher baseline UA levels.
- These findings suggest differential metabolic impacts of losartan versus telmisartan when combined with HCTZ in hypertensive patients.
Purpose:
Long-term effects of a low-dose hydrochlorothiazide (HCTZ) with losartan (LOS) on uric acid (UA) metabolism as well as glucose metabolism have been studied in hypertensive patients in comparison with those of a low-dose HCTZ with telmisartan (TEL).
Method:
Fifty-nine hypertensive patients were allocated to a combination therapy with either losartan (50 mg/day)/HCTZ (12.5 mg/day) (LOS + HCTZ group: n = 37) or telmisartan (40 mg/day)/HCTZ (12.5 mg/day) (TEL + HCTZ group: n = 22), respectively. Before and 1 year after the treatment, blood pressure and biochemical parameters of blood and urine were evaluated.
Results:
Both systolic and diastolic blood pressures significantly decreased in two groups, without any statistical differences among them. LOS + HCTZ caused no changes in the serum UA level or the ratio of UA clearance to creatinine clearance (CUA/Ccr), whereas TEL + HCTZ significantly increased the serum UA level and reduced CUA/Ccr. LOS + HCTZ did not influence CUA/Ccr in patients with their serum UA below 5.4 mg/dl, while LOS + HCTZ significantly increased CUA/Ccr in patients with their serum UA above 5.5 mg/dl. TEL + HCTZ significantly reduced CUA/Ccr in patients with their serum UA below and above 5.4 mg/dl to increase serum UA level significantly. Neither combination therapies caused any changes in fasting plasma glucose, HbA1c and HOMA-R. In patients with their serum UA level above 5.4 mg/dl, TEL + HCTZ increased HOMA-R, whereas LOS + HCTZ did not.
Conclusions:
LOS + HCTZ did not influence UA metabolism as well as glucose metabolism, likely because of inhibitory action of losartan on URAT1, although TEL + HCTZ were accompanied with impairment of the UA metabolism and glucose metabolism.
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