529358JRA0010.1177/1470320314529358Journal of the Renin Angiotensin Aldosterone SystemShiga et al. research-article2014 Original Article Efficacy and safety of combination therapy of high-dose losartan and hydrochlorothiazide in patients with hypertension Journal of the Renin-Angiotensin- Aldosterone System 2015, Vol. 16(4) 1078 1084 The Author(s) 2014 Reprints and permissions: sagepub.co.uk/journalspermissions.nav DOI: 10.1177/1470320314529358 jra.sagepub.com Yuhei Shiga 1,2,3,4, Shin-ichiro Miura 1,6, Kenji Norimatsu 1, Yuka Hitaka 1,2, Itsuki Nagata 1,5, Rie Koyoshi 1, Joji Morii 1,5, Takashi Kuwano 1, Yoshinari Uehara 1,6, Asao Inoue 2, Tetsuro Shirotani 3, Kazuaki Fujisawa 4, Eiyu Matsunaga 5 and Keijiro Saku 1,6 Abstract Objective: We analyzed the efficacy and safety of combination therapy of high-dose losartan (100 mg/day) and hydrochlorothiazide (HCTZ, 12.5 mg/day) compared with those of the combination of high-dose telmisartan (80 mg/ day) and HCTZ (12.5 mg/day). Methods: Forty hypertensive patients who received a combination of high-dose telmisartan and HCTZ were enrolled. We applied a changeover strategy with switching from a combination of high-dose telmisartan and HCTZ to highdose losartan and HCTZ. We divided the patients into two groups; those who achieved the target blood pressure (controlled group) and those who did not reach the target blood pressure (uncontrolled group) before the changeover and performed further analysis. Results: The uncontrolled group showed a significant decrease in systolic blood pressure (SBP) (143±12 mmhg to 126±11 mmhg at three months). In addition, serum uric acid significantly decreased in all subjects, and in each of the controlled and uncontrolled groups. There were no significant changes in other biochemical parameters, such as potassium and hemoglobin A1c, at three months after the changeover in all subjects. Conclusion: Combination therapy with high-dose losartan and HCTZ was superior to the combination of telmisartan and HCTZ with respect to significant decreases in systolic blood pressure and serum uric acid in hypertensive patients. Keywords Blood pressure, angiotensin II type 1 receptor blocker, losartan, hydrochlorothiazide, uric acid Introduction Combinations of angiotensin II type 1 receptor blockers (ARBs) and thiazide diuretics are recommended by various guidelines for the treatment of high blood pressure. 1,2 Most patients with hypertension require two or more drugs to achieve their target blood pressure (BP). 3 In fact, largescale clinical trials have shown that thiazide diuretics and/ or calcium channel blockers are frequently added to ARBs to achieve adequate BP control. 4 Nine kinds of single-pill fixed-dose combinations of ARBs and diuretics are available for clinical use in Japan (Table 1). The combination of high-dose telmisartan (80 mg/day) and hydrochlorothiazide (HCTZ, 12.5 mg/day) (Micombi BP) has the strongest BP-lowering effect. 5 We previously used a changeover design in which the patients were switched from high-dose ARBs or a combination of medium-dose losartan (50 mg/ day) and HCTZ to high-dose telmisartan and HCTZ. 6 Although we found that high-dose telmisartan and HCTZ induced a significant reduction of BP at three months after changeover, the combination therapy resulted in a 1 Department of Cardiology, Fukuoka University School of Medicine, Japan 2 Inoue Hospital, Fukuoka, Japan 3 Shirotani Hospital, Fukuoka, Japan 4 Fujisawa Clinic, Fukuoka, Japan 5 Matsunaga Hospital, Fukuoka, Japan 6 Department of Molecular Cardiovascular Therapeutics, Fukuoka University School of Medicine, Japan Corresponding author: Shin-ichiro Miura, Department of Cardiology, Fukuoka University School of Medicine, 7-45-1 Nanakuma, Jonan-ku, Fukuoka, 814-0180, Japan. Email: miuras@cis.fukuoka-u.ac.jp Creative Commons CC-BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (http://www.uk.sagepub.com/aboutus/openaccess.htm).
Shiga et al. 1079 Table 1. Nine kinds of single-pill, fixed-dose combination of angiotensin II receptor blockers (ARBs) and diuretics in Japan. ARBs Diuretics Hydrochlorothiazide 6.25 mg 12.5 mg Losartan 50mg Preminent Valsartan 80mg Codio MD Codio EX Candesartan 8mg Ecard HD 4mg Ecard LD Telmisartan 80mg Micombi BP 40mg Micombi AP Trichlormethiazide 1mg Irbesartan 200mg Irtra HD 100mg Irtra LD significant increase in serum uric acid (UA). In particular, an elevation of serum UA was observed in patients who were switched from a combination of medium-dose losartan and HCTZ to high-dose telmisartan and HCTZ. It is still controversial whether a higher level of serum UA is a risk factor for arteriosclerosis and coronary artery disease. Although a relationship between serum UA and cardiovascular events was not observed in the Framingham study, 7 such relationships have been demonstrated in some studies. 8,9 Moreover, in a subanalysis of data from the Japanese Coronary Artery Disease Study, a high level of UA was shown to be an independent predictor of all events, including cardiovascular events and all-cause mortality. 10 In a prospective, randomized trial, allopurinol was shown to decrease C-reactive protein and reduce cardiovascular and hospitalization risk in patients with estimated GFR (egfr) <60 ml/min. 11 Among ARBs, although both losartan and telmisartan significantly blocked urate transporter 1 (URAT1) in in vitro experiments, 12,13 only losartan showed uricosuric action through the inhibition of URAT1 in humans. 14 We hypothesized that a combination of high-dose losartan and HCTZ could produce similar reduction in BP and significant decrease in serum UA compared with a combination of high-dose telmisartan and HCTZ. Therefore, we analyzed whether a changeover with switching from a combination of high-dose telmisartan and HCTZ to highdose losartan (100 mg/day) and HCTZ would be more efficacious and safe for hypertensive patients. Methods Study design Forty hypertensive patients who received a combination of high-dose telmisartan and HCTZ were enrolled. We applied a changeover strategy with switching from Micombi BP (a single-pill fixed-dose combination of telmisartan (80 mg/day) and HCTZ (12.5 mg/day)) to Preminent (a single-pill fixed-dose combination of losartan (50 mg/day) and HCTZ (12.5 mg/day)) + losartan (50 mg/day). Twenty-four patients (60%) received Micombi BP in the morning and the rest of patients (40%) received it in the evening. After changeover, we did not change the administration time in all patients. We divided the patients into two groups: those who achieved the target BP (controlled group) and those who did not reach the target BP (uncontrolled group) before the changeover, and performed further analysis according to the Japanese Society of Hypertension Guidelines 2009. 1 We excluded patients with secondary hypertension, heart failure of NYHA grade III or IV, moderate to severe liver dysfunction (defined as aspartate aminotransferase and alanine aminotransferase levels of more than three-fold the normal ranges), renal dysfunction (defined as a serum creatinine (Cr) level of more than 2.0 mg/dl), pregnancy, or a history of allergy to losartan. The protocol in this study was approved by the ethics committee of Fukuoka University Hospital, and all subjects gave their informed consent to participate. Evaluation of clinical parameters We analyzed seated office systolic BP (SBP), diastolic BP (DBP) and pulse rate (PR), body weight (BW), and blood and urinary levels of biochemical parameters at baseline and at three months after changeover. BP was determined as the mean of two measurements obtained in an office setting by the conventional cuff method using a mercury sphygmomanometer after at least 5 min of rest. All of the blood and urinary samples were collected in the morning after the patients had fasted overnight. Data regarding serum levels of biochemical parameters, such as highdensity lipoprotein-cholesterol (HDL-C), low-density lipoprotein-cholesterol (LDL-C), triglycerides (TG), UA, Cr, egfr, brain natriuretic peptide (BNP), fasting blood glucose (FBS), hemoglobin A1c (HbA1c), sodium (Na), potassium (K), albumin (Alb), urinary (U)-UA, U-Cr, the ratio of U-UA to U-Cr (U-UA/U-Cr), and the fractional excretion of UA (FEUA, U-UA serum Cr/serum UA U-Cr) were collected in all patients. Body mass index (BMI) was calculated as weight (kg)/height (m) 2. The characteristics of the patients, with regard to history of dyslipidemia (DL), diabetes mellitus (DM), hyperuricemia (HU), smoking status and medication use, were obtained from medical records. Patients who had a current SBP/DBP 140/90mmHg or who were receiving antihypertensive therapy were considered to have hypertension. Patients with LDL-C 140 mg/dl, TG 150 mg/dl and/or HDL-C < 40 mg/dl, or who were receiving lipid-lowering therapy were considered to have DL. DM was defined using the American Diabetes Association criteria or the use of a glucose-lowering drug. HU was defined as a
1080 Journal of the Renin-Angiotensin-Aldosterone System 16(4) Table 2. Baseline patient characteristics. All subjects (n=40) Controlled group (n=27) Uncontrolled group (n=13) Age, years 71±13 73±12 68±14 Sex (male), % 23 22 23 BMI, kg/m 2 24±4 24±4 25±4 Smoking, % 38 26 62 WC, cm 86±9 86±10 85±8 DL, % 63 67 54 DM, % 13 7 23 HU, % 35 26 54 CAD, % 10 11 8 CKD, % 40 44 31 Medications CCB, % 98 96 100 β-blocker, % 35 41 23 α-blocker, % 10 15 0 Continuous variables are expressed as mean ± standard deviation. BMI: body mass index; WC: waist circumference; DL: dyslipidemia; DM: diabetes mellitus; HU: hyperuricemia; CAD: coronary artery disease; CKD: chronic kidney disease; CCB: calcium channel blocker serum UA level of 7.0 mg/dl. Chronic kidney disease (CKD) was defined as an egfr level of < 60 ml/min per 1.73 m 2. Statistical analysis Statistical analysis was performed using the StatView statistical software package (StatView 5; SAS Institute Inc., Cary, NC, USA). Data are shown as the mean ± standard deviation (SD). Categorical variables were compared between groups by a chi-square analysis. The significance of differences between mean values was evaluated by paired and unpaired t-tests or one-way analysis of variance followed by Fisher s protected-least-significant-difference test, as appropriate. Results Patient characteristics Table 2 shows the characteristics of the 40 patients, who included nine (23%) males. No patients withdrew from the study. The prevalence of DL, DM, HU and CKD was 63%, 13%, 35% and 40%, respectively. In addition, the percentage use of calcium channel blocker (CCB), β-blocker and α-blocker was 98%, 35% and 10%, respectively. There were no significant differences in the baseline patient characteristics between the controlled and uncontrolled groups. We did not change these medications throughout the study period. Changes in BP and PR In all patients, SBP/DBP and PR at baseline were 126±17/69±11 mmhg and 69±9 beats/min, respectively (Figure 1). SBP significantly decreased from 126±17 mmhg at baseline to 119±13 at three months after changeover in all subjects. In particular, the uncontrolled group showed a significant decrease in SBP (143±12 mmhg to 126±11 mmhg at three months). There were no significant changes in DBP or PR during the study period. Changes in biochemical parameters As shown in Table 3, there were no significant changes in biochemical parameters such as serum blood urea nitrogen (BUN), Cr, K, HbA1c, BNP and lipid profile in all subjects, or in the controlled and uncontrolled groups. Changes in serum UA, U-UA/U-Cr and FEUA in all subjects, and in the controlled and uncontrolled groups The combination of high-dose losartan and HTCZ significantly decreased serum UA after three months in all subjects, and in the controlled and uncontrolled groups (Figure 2), whereas there were no changes in U-UA/U-Cr or FEUA in all subjects, or in the controlled and uncontrolled groups (Table 3). Changes in serum UA, K and HbA1c between sub-groups The normal UA, K and HbA1c values at our University Hospital are 5.0 7.0 mg/dl, 3.5 5.0 meq/l and 4.6 5.6%, respectively. Therefore, we divided all of the patients into two groups according to each normal range described as previously. 6 Our relatively high UA group was defined as
Shiga et al. 1081 Figure 1. Changes in systolic blood pressure (SBP)/diastolic blood pressure (DBP) and pulse rate (PR) in all subjects (n=40), and in the controlled (n=27) and uncontrolled groups (n=13) at zero and three months. *p<0.01 vs. zero months. HR: heart rate Figure 2. Changes in serum uric acid (UA) in all subjects (n=40), and in the controlled (n=27) and uncontrolled groups (n=13) at zero and three months. *p<0.01 vs. zero months. ***p<0.0001 vs. zero months. UA > 6.0 mg/dl, and the relatively low UA group was defined as 6.0 mg/dl UA. Our relatively high K group was defined as K > 4.3 meq/l, and the relatively low K group was defined as 4.3 meq/l K. Our relatively high HbA1c group was defined as HbA1c > 5.1%, and the relatively low HbA1c group was defined as 5.1% HbA1c. In the relatively low and high UA groups, their values at three months were significantly less than those at baseline (Figure 3). In the relatively high K group, although the level of K at three months was significantly less than
1082 Journal of the Renin-Angiotensin-Aldosterone System 16(4) Table 3. Change in biochemical parameters in all subjects, controlled and uncontrolled groups. All subjects (n=40) Controlled group (n=27) Uncontrolled group (n=13) 0 months 3 months 0 months 3 months 0 months 3 months BUN, mg/dl 18.8±6.3 19.0±5.8 19.5±7.0 19.6±6.1 17.1±4.1 17.9±5.3 Cr, mg/dl 0.8±0.2 0.8±0.2 0.8±0.2 0.9±0.3 0.8±0.2 0.8±0.2 egfr, ml/min per 1.73 m 2 62±15 61±18 59±15 59±18 66±15 65±18 Na, meq/l 140±4 141±3 140±4 140±3 141±3 142±2 K, meq/l 4.2±0.4 4.1±0.5 4.2±0.4 4.1±0.4 4.1±0.3 4.2±0.5 TG, mg/dl 125±96 121±57 108±47 116±59 160±151 131±55 LDL-C, mg/dl 106±29 97±22 106±31 99±23 105±26 95±22 HDL-C, mg/dl 56±15 57±17 57±15 57±15 54±16 56±21 FPG, mg/dl 100±20 96±13 101±19 96±12 100±21 97±14 HbA1c, % 5.2±0.4 5.3±0.5 5.2±0.4 5.3±0.4 5.3±0.5 5.4±0.7 BNP, pg/ml 47±57 56±100 57±66 70±117 27±17 23±15 U-Alb, mg/g Cr 33±78 33±88 20±28 18±26 61±130 65±148 U-UA/U-Cr 0.5±0.2 0.5±0.4 0.5±0.2 0.5±0.2 0.5±0.2 0.5±0.2 FEUA, % 7.4±4.8 7.8±5.0 9.0±4.2 8.8±3.0 7.0±7.2 7.6±7.6 BUN: blood urea nitrogen; Cr: creatinine; egfr: estimated glomerular filtration rate; Na: sodium; K: potassium; TG: triglyceride; LDL-C: low density lipoprotein cholesterol; HDL-C: high density lipoprotein cholesterol; FPG: fast plasma glucose; HbA1c: hemoglobin A1c; BNP: brain natriuretic peptide; U-Alb: urinary albumin; UA: uric acid; FEUA: fractional excretion of UA. Figure 3. Changes in uric acid (UA) (a) (UA > 6.0 mg/dl vs. 6.0 mg/dl UA), potassium (K) (b) (K > 4.3 meq/l vs. 4.3 meq/l K) and hemoglobin A1c (HbA1c) (c) (HbA1c > 5.1% vs. 5.1% HbA1c). p<0.05 vs. zero months ***p<0.0001 that at baseline, the average value was still within the normal range (K=4.3 meq/l at three months). Moreover, there were no significant changes after three months in either the relatively low K group or the low and high HbA1c groups. Discussion In the present study, the combination of high-dose losartan and HTCZ significantly reduced SBP and serum UA after the switch from high-dose telmisartan and HTCZ. Moreover, there were no serious adverse effects in any of the patients. High-dose losartan and HTCZ significantly reduced SBP. BP control is the best strategy for achieving remarkable clinical benefits with regard to cardiovascular and renal protection. Since the change in SBP using highdose losartan and HTCZ was 7 mmhg in all subjects, SBP reduction should provide tremendous clinical
Shiga et al. 1083 benefits. For example, a 2 mmhg reduction in SBP should provide a 10% lower incidence of stroke mortality and about a 7% lower incidence of mortality from coronary artery disease or other vascular causes in middle age. 15 The synergistic effect of the combination of high-dose losartan and HTCZ may be stronger than that with highdose telmisartan and HTCZ. In a previous study, 12.5 mg/day of HCTZ significantly increased plasma renin activity (PRA). 16 In this case, the blockade of the activation of PRA induced by HTCZ with high-dose losartan may be stronger than that with high-dose telmisartan. Since the combination of medium-dose losartan (50 mg/ day) and HTCZ had the same depressor effect as that of medium-dose telmisartan (40 mg/day) and HCTZ, 17 we did not expect that a changeover from high-dose telmisartan and HTCZ to high-dose losartan and HTCZ would be a useful strategy for inducing a more significant reduction in SBP. In this study, high-dose losartan and HTCZ significantly decreased serum UA after a switch from high-dose telmisartan and HCTZ. Losartan has been shown to have uricosuric action via URAT1 in hypertensive patients. 14 Hamada et al. reported that losartan and HCTZ increased the ratio of UA clearance to creatinine clearance (CUA/ Ccr) in patients with a serum UA above 5.5 mg/dl, whereas telmisartan and HCTZ significantly reduced CUA/Ccr. 17 Unexpectedly, U-UA/U-Cr and FEUA did not change after the changeover to high-dose losartan and HTCZ. The classification of HU into one of two types (i.e. the overproduction of UA or a decrease in the urinary excretion of UA) based on a 60-min spot urine or 24-h urine collection in outpatients is important for determining the treatment strategy, 18 but there are no standardized methods available. Thus, further studies will be needed to resolve this issue. Benson et al. indicated that telmisartan activated peroxisome proliferator-activated receptor (PPAR)-γ, which may improve insulin sensitivity, 19 whereas losartan did not activate PPAR-γ. 20 Telmisartan may be useful in hypertensive patients with insulin resistance or DM. 21 Nonetheless, in this study, the levels of HbA1c and FBS did not change at three months after a changeover from high-dose telmisartan and HTCZ to high-dose losartan and HTCZ. Telmisartan-induced activation of PPAR-γ may not be clinically important in this study, and this result was consistent with a previous report. 22 Zillich et al. reported that the treatment of thiazideinduced hypokalemia might reverse glucose intolerance. 23 Although the level of K at three months after changeover was significantly decreased in the relatively high K group, the average value (K=4.3 meq/l at three months) was still within the normal range and was clinically ignorable. Therefore, the level of K may not influence glucose intolerance. Study limitations This study has three important limitations. First, the sample size is relatively small, which limits our ability to determine significance. Second, we applied a changeover with switching from high-dose telmisartan and HTCZ to high-dose losartan and HTCZ. However, a crossover study would be preferable. Third, we applied a changeover strategy with switching from one tablet (Micombi BP) to two tablets (Preminent + losartan). Twenty-four patients received Micombi BP in the morning and the rest of patients received it in the evening before changeover, whereas we did not change the administration time in all patients after changeover. The numbers of tablets and administration time may affect drug adherence and BP lowering effects. Conclusions The combination of high-dose losartan and HTCZ significantly reduced SBP and decreased serum UA after three months. In addition, there were no serious adverse effects in any of the patients. Conflict of interest KS, SM and YU have received grants and lecture honoraria from MSD, Co. Ltd. KS is a Chief Director and SM is a Director of NPO Clinical and Applied Science, Fukuoka, Japan. KS has an Endowed Department of Department of Molecular Cardiovascular Therapeutics supported by MSD, Co. Ltd. SM and YU belong to the Department of Molecular Cardiovascular Therapeutics supported by MSD, Co. Ltd. Funding This research received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors. References 1. Ogihara T, Kikuchi K, Matsuoka H, et al.; Japanese Society of Hypertension Committee. The Japanese Society of Hypertension Guidelines for the Management of Hypertension (JSH 2009). Hypertens Res 2009; 32: 3 107. 2. Mancia G, De Backer G, Dominiczak A, et al.; Management of Arterial Hypertension of the European Society of Hypertension; European Society of Cardiology. 2007 Guidelines for the management of arterial hypertension: The Task Force for the Management of Arterial Hypertension of the European Society of Hypertension (ESH) and of the European Society of Cardiology (ESC). J Hypertens 2007; 25: 1105 1187. 3. Dahlöf B, Sever PS, Poulter NR, et al.; ASCOT Investigators. Prevention of cardiovascular events with an antihypertensive regimen of amlodipine adding perindopril as required versus atenolol adding bendroflumethiazide as required, in the Anglo-Scandinavian Cardiac Outcomes Trial Blood Pressure Lowering Arm (ASCOT-BPLA): A multicentre randomized controlled trial. Lancet 2005; 366: 895 906.
1084 Journal of the Renin-Angiotensin-Aldosterone System 16(4) 4. Kato J and Eto T. Diuretics in the LIFE study. Lancet 2004; 364: 413. 5. Sharma AM, Davidson J, Koval S, et al. Telmisartan/ hydrochlorothiazide versus valsartan/hydrochlorothiazide in obese hypertensive patients with type 2 diabetes: The SMOOTH study. Cardiovasc Diabetol 2007; 6: 28. 6. Shiga Y, Miura S, Mitsutake R, et al. Efficacy and safety of a single-pill fixed-dose combination of high-dose telmisartan/hydrochlorothiazide in patients with uncontrolled hypertension. J Renin Angiotensin Aldosterone Syst 2012; 13: 394 400. 7. Culleton BF, Larson MG, Kannel WB, et al. Serum uric acid and risk for cardiovascular disease and death: The Framingham heart study. Ann Intern Med 1999; 131: 7 13. 8. Alderman MH, Cohen H, Madhavan S, et al. Serum uric acid and cardiovascular events in successfully treated hypertensive patients. Hypertension 1999; 34: 144 150. 9. Verdecchia P, Schillaci G, Reboldi G, et al. Relation between serum uric acid and risk of cardiovascular disease in essential hypertension: The PIUMA study. Hypertension 2000; 36: 1072 1078. 10. Okura T, Higaki J, Kurata M, et al.; Japanese Coronary Artery Disease Study Investigators. Elevated serum uric acid is an independent predictor for cardiovascular events in patients with severe coronary artery stenosis: Subanalysis of the Japanese Coronary Artery Disease (JCAD) Study. Circ J 2009; 73: 885 891. 11. Goicoechea M, de Vinuesa SG, Verdalles U, et al. Effect of allopurinol in chronic kidney disease progression and cardiovascular risk. Clin J Am Soc Nephrol 2010; 5: 1388 1393. 12. Edwards RM, Trizna W, Stack EJ, et al. Interaction of nonpeptide angiotensin II receptor antagonists with the urate transporter in rat renal brush-border membranes. J Pharmacol Exp Ther 1996; 276: 125 129. 13. Enomoto A, Kimura H, Chairoungdua A, et al. Molecular identification of a renal urate anion exchanger that regulates blood urate levels. Nature 2002; 417: 447 452. 14. Hamada T, Ichida K, Hosoyamada M, et al. Uricosuric action of losartan via the inhibition of urate transporter 1 (URAT 1) in hypertensive patients. Am J Hypertens 2008; 21: 1157 1162. 15. Lewington S, Clarke R, Qizilbash N, et al.; Prospective Studies Collaboration. Age-specific relevance of usual blood pressure to vascular mortality: A meta-analysis of individual data for one million adults in 61 prospective studies. Lancet 2002; 360: 1903 1913. 16. Villamil A, Chrysant SG, Calhoun D, et al. Renin inhibition with aliskiren provides additive antihypertensive efficacy when used in combination with hydrochlorothiazide. J Hypertens 2007; 25: 217 226. 17. Hamada T, Kuwabara M, Watanabe A, et al. A comparative study on the effectiveness of losartan/hydrochlorothiazide and telmisartan/hydrochlorothiazide in patients with hypertension. Clin Exp Hypertens 2014; 36: 251 257. 18. Ohta Y, Tsuchihashi T and Kiyohara K. Usefulness of conventional methods of the classification of hyperuricemia in hypertensive patients with hyperuricemia. Gout and Nucleic Acid Metabolism 2012; 36: 9 13. 19. Benson SC, Pershadsingh HA, Ho CI, et al. Identification of telmisartan as a unique angiotensin II receptor antagonist with selective PPARgamma-modulating activity. Hypertension 2004; 43: 993 1002. 20. Morii J, Miura S, Shiga Y, et al. Comparison of the efficacy and safety of irbesartan and olmesartan in patients with hypertension (EARTH study). Clin Exp Hypertens 2012; 34: 342 349. 21. Suksomboon N, Poolsup N and Prasit T. Systematic review of the effect of telmisartan on insulin sensitivity in hypertensive patients with insulin resistance or diabetes. J Clin Pharm Ther 2012; 37: 319 327. 22. Minami J, Furukata S, Ishimitsu T, et al. Comparison of therapies between fixed-dose telmisartan/hydrochlorothiazide and losartan/hydrochlorothiazide in patients with mild to moderate hypertension. Int Heart J 2009; 50: 85 93. 23. Zillich AJ, Garg J, Basu S, et al. Thiazide diuretics, potassium, and the development of diabetes: A quantitative review. Hypertension 2006; 48: 219 224.