Losartan and Eprosartan Induce a Similar Effect on the Acute Rise in Serum Uric Acid Concentration after an Oral Fructose Load in Patients with Metabolic Syndrome

Masajtis-Zagajewska, Anna; Majer, Jacek; Nowicki, Michał

doi:https://doi.org/10.1155/2021/2214978

Journal of the Renin-Angiotensin-Aldosterone System

On this page

Abstract Introduction Methods Results Discussion Conclusion Data Availability Conflicts of Interest Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2021 | Article ID 2214978 | https://doi.org/10.1155/2021/2214978

Losartan and Eprosartan Induce a Similar Effect on the Acute Rise in Serum Uric Acid Concentration after an Oral Fructose Load in Patients with Metabolic Syndrome

Anna Masajtis-Zagajewska,¹Jacek Majer,¹and Michał Nowicki¹

Academic Editor: Lawrence Aderemi Olatunji

Received22 May 2021

Accepted13 Aug 2021

Published26 Aug 2021

Abstract

Introduction. Excessive intake of fructose increases serum uric acid concentration. Hyperuricemia induces a negative effect on atherosclerosis and inflammation. Hyperuricemia is common in patients with arterial hypertension. Several antihypertensive drugs including diuretics increase serum uric acid concentration. In contrast, the angiotensin II receptor antagonist (ARB) losartan was found to lower serum uric acid though it may increase renal excretion while other ARBs showed mostly a neutral effect. In this study, effects of two AT1 receptor antagonists losartan and eprosartan on serum uric acid changes induced by oral fructose load were directly compared. Methods. The randomized, crossover, head-to-head comparative study comprised 16 ambulatory patients (mean age years). The patients fulfilled AHA/NHLBI 2005 criteria of metabolic syndrome. A daily single morning dose of each study drug (50 mg of losartan or 600 mg of eprosartan) was given during two 3-month periods in a random order separated by 2-week washout time. The oral fructose tolerance test (OFTT) was performed at baseline and after each two 3-onth treatment periods. Before and during OFTT, urine excretion of uric acid and creatinine was assessed in the first morning portion of urine. Blood samples for the measurement of serum uric acid and lipids were taken at baseline and 30, 60, and 120 minutes after oral intake of 75 g of fructose. Results. After 3-month treatment with eprosartan and losartan, both systolic and diastolic blood pressure decreased significantly and to a similar extent. After the treatment, serum uric acid and its baseline and postfructose urine excretion were unchanged. No significant changes of plasma lipids before and after OFTT were observed throughout the study. Conclusions. The study showed that in patients with hypertension and metabolic syndrome, both losartan and eprosartan have a neutral effect on fasting and postfructose load serum uric acid concentration and its urinary excretion. This trial is registered with NCT04954560.

1. Introduction

Hyperuricemia is seen in about 20% of adults in the general population [1] and is mostly a consequence of abnormal purine metabolism caused either by an excessive uric acid production or by its impaired elimination by the kidneys [2].

On the one hand, high uric acid concentration may be an important link in the pathogenesis of hypertension, but on the other hand, in mild and moderate hypertension, uric acid excretion is frequently impaired [3]. A study showed that in the hypertensive patients with hyperuricemia, renal blood flow is reduced compared to that in the patients with arterial hypertension but with normal uric acid concentration [4].

Several studies showed that the prevalence of hyperuricemia in patients with hypertension is much higher than that in the general population and may worsen after the onset of antihypertensive treatment [5]. That may indicate that hyperuricemia may be also caused by antihypertensive drugs. In contrast to diuretics and nonselective beta blockers, the agents that block the renin-angiotensin-aldosterone system have had a neutral effect on serum uric acid [5–7]. Several clinical studies showed that losartan in contrast to other AT1 receptor agonists (ARB) may have specific uricosuric properties and thereby can lower uric acid concentration [8–11]. It is not clear whether the effect is clinically relevant and may add to organ protective effects of the drug. It has been speculated that the uricosuric effect could make losartan particularly useful for the treatment of arterial hypertension associated with hyperuricemia and metabolic syndrome [9, 10].

The uricosuric effect of losartan is most likely due to overlapping two different mechanisms regulating the excretion of uric acid. Losartan may increase uric acid tubular secretion in the same way as other inhibitors of the renin-angiotensin-aldosterone system, but in addition, it may specifically inhibit postsecretory resorption of uric acid in the proximal tubule. The effect may be due to a specific structure of the losartan molecule [11]. The urate-anion transporter is a monoammonium-selective transporter, and the losartan molecule is mainly a monoanion at a normal pH range (as opposed to dianion, e.g., eprosartan) and therefore is a good substrate for the exchanger [12]. However, this concept remains speculative since, e.g., irbesartan which is also a monoanion has no consistent uricosuric effect [13].

An increased accessibility of the high-calorie food contributes to the worldwide epidemic of the metabolic syndrome. The rapidly increasing rate of obesity and metabolic syndrome may be partly related to an excessive consumption of fructose added to sweetened beverages and food [14–16]. Fructose, in contrast to other carbohydrates, causes an increase in serum uric acid concentration, which may facilitate the development of the metabolic syndrome [17–19].

The aim of our study was to directly compare the effect of two AT1 receptor antagonists, losartan and eprosartan, on serum uric acid changes stimulated by an oral fructose load.

2. Material and Methods

The study group included 16 patients (15 F, 1 M, mean age years). The patients selected for the study fulfilled the AHA/NHLBI 2005 criteria of the metabolic syndrome [19] and ESC/ESH criteria of arterial hypertension. The exclusion criteria included an antihypertensive therapy with the renin-angiotensin-aldosterone axis blocking agent used anytime during the last 3 months; current or past therapy with the SGLT2 inhibitor, GLP-1 agonist, or DPP4-inhibitor; suspected or confirmed secondary form of hypertension; ; chronic liver disease; acute infection; psychiatric disorders; , or upper range limit. Seven patients had diabetes mellitus of which 4 were treated with insulin. Twelve patients were receiving metformin. Waist circumference was measured on the initial visit. Plasma lipids and blood glucose were measured in a fasting state during the study.

The study was designed as a randomized, crossover, head-to-head comparative study. Randomization was carried out using an MS Excel random number generator. After qualification, each patient was randomly assigned to receive either losartan (Lorista, KRKA, Slovenia) or eprosartan (Teveten, Solvay Pharmaceuticals, Australia). The patients were taking all other previously prescribed drugs in unmodified doses during the whole course of the study. Each study drug was given in a random order as a single morning dose (50 mg of losartan or 600 mg of eprosartan) for two periods each lasting 3 months separated by 2-week washout time.

Losartan (C₂₂H₂₃CIN₆O) is approximately 33% orally bioavailable and has a of 1 hour, and its active metabolite has a of 3-4 hours. The terminal elimination half-life of losartan is 1.5-2.5 hours while the active metabolite has a half-life of 6-9 hours [20].

Eprosartan (C₂₃H₂₄N₂O₄S) has an absolute bioavailability after a single 300 mg oral dose of 13%. Food delays absorption of the drug. Eprosartan is not metabolized by the cytochrome P450 system and is eliminated as unchanged drug. Less than 2% of an oral dose is excreted in the urine. The terminal elimination half-life of eprosartan following oral administration is 5 to 9 hours [21].

Oral fructose tolerance with the administration of 75 g of fructose was conducted 3 times during the study in each patient, i.e., at baseline and after each of the treatment periods. Before the commencement of OFTT, the patients collected the urine for 2 hours for assessment of the urinary excretion of uric acid and creatinine. Other baseline measurements included blood pressure, serum concentration of glucose, uric acid, creatinine and plasma lipids (total, HDL, and LDL cholesterol and triglycerides). Subsequent blood samples were taken three times during each OFTT, i.e., after 30, 60, and 120 minutes from its start to determine serum uric acid concentration. In addition, peripheral blood pressure was measured before the collection of each blood sample. After 120 minutes, blood was also taken to assess plasma lipids. The second timed 2-hour urine collection was obtained during OFTT. The same procedures were repeated after each treatment period. The patients took all their prescribed medication including the study drug in the morning 120 minutes before the beginning of OFTT.

Routine automated laboratory tests were used to assess blood and urine parameters. Blood pressure was taken in a sitting position with the aneroid sphygmomanometer. Blood pressure was measured both at baseline and after 3-month therapy with each study drug. The mean from four measurements obtained between 0 and 120 minutes of OFTT was taken for the analysis. Blood pressure was measured by a designated single member of the staff. Mean blood pressure (MAP) was calculated for all measurements as of pulse pressure ().

The results are expressed as or median with interquartile range depending on each variable distribution. 95% confidence intervals were calculated for the changes of the parameters caused by the treatment. Statistical significance was defined at . The within-group comparisons were analyzed using one-way ANOVA and -test for normally distributed variables or alternatively with the nonparametric Wilcoxon test. The normality of the variable distribution was checked with the Shapiro-Wilk test. The Pearson or Spearman correlation coefficient was used to assess the relations between variables depending on their distribution. The area under the curve (AUC) of serum uric acid during oral fructose tolerance test was calculated using the trapezoidal rule.

3. Results

Twenty-two patients were recruited to the study; after screening, 6 patients did not complete the study procedure and therefore were not included in the final per-protocol data analysis; in total, 16 patients were included. All dropouts were due to gastrointestinal intolerance of oral fructose. No side effects of the study drugs were observed. Baseline clinical characteristics of the study population are presented in Table 1.

Table 2 shows the AHA/NHLBI 2005 criteria for metabolic syndrome and the pass criteria by patients in the study group.

Systolic, diastolic, and mean blood pressure decreased significantly and to a similar extent from baseline after 3 months of eprosartan and losartan administration. Table 3 shows systolic, diastolic, and mean blood pressure values during the study.

No significant changes of blood glucose and serum creatinine were observed throughout the study. Table 4 shows the effect of 3-month treatment with losartan or eprosartan on serum concentration of uric acid and urine uric acid excretion. Serum uric acid concentration and urine uric acid excretion did not significantly change after losartan nor after eprosartan administration.

Serum uric acid increased significantly during OFTT after the therapy with either losartan or eprosartan ( in both study periods). Figure 1 shows the values of serum uric acid concentration on baseline and after 30, 60, and 120 minutes after OFTT and the changes of serum uric acid from baseline after 30, 60, and 120 minutes after ingestion of an acute oral fructose load. The changes of serum acid caused by oral fructose load during OFTT were comparable after both treatment periods. Urinary uric acid excretion after oral fructose load was not changed after treatment with losartan or eprosartan (Figure 2). AUC of serum uric acid concentration during OFTT after treatment with eprosartan () and losartan () and at baseline () was similar.

(a)

(b)

4. Discussion

The main finding of our study was that the angiotensin receptor blocker, losartan—which is believed to lower UA levels—was associated with similar serum uric acid levels to those of a chemically distinct angiotensin receptor antagonist eprosartan. This lack of difference occurred despite the other ARB not attaching to the same renal receptor to which the losartan molecule attaches and supposedly lowers UA serum levels. From these results, we conclude that losartan did not significantly affect serum concentration and urinary excretion of uric acid, as well as the magnitude of the changes of serum uric acid concentration after the oral fructose load in comparison to other ARBs.

Our results contrasting with the findings of several previous studies have not confirmed a class effect of angiotensin receptor blockers (ARB) on serum uric acid [22–25]. While most currently available ARBs appear to have a neutral effect on uricemia, losartan was found to specifically increase the urinary excretion of uric acid and thereby caused a significant reduction of serum uric acid [13, 24–27].

Although some research demonstrated an increased urinary uric acid excretion and a decrease in serum uric acid during losartan therapy, there is only a scarce evidence from head-to-head studies in which the effect of the drug was compared to that of other ARBs in the patients with arterial hypertension [24, 27, 28]. The results of these studies were not concordant. In two small studies [24, 28], losartan significantly increased urinary uric acid excretion, but only in one of them, a simultaneous decrease in serum uric acid was observed [28]. Another randomized study [29] carried out in a group of hypertensive patients after kidney transplantation treated with a cyclosporin-based triple immunosuppressive regimen showed only a small and nonsignificant decrease in serum uric acid after losartan.

Unlike our study, all previous studies investigated only the effect of losartan on a fasting serum level of uric acid but did not assess the effect of this drug on the changes of serum uric acid induced by dietary stimuli. That was also the case in the study [24] which compared the effect of 50 mg daily losartan and 600 mg eprosartan on uric acid metabolism in patients with mild to moderate hypertension. In this study, no significant changes of serum uric acid were reported despite a significant increase in urinary excretion of uric acid seen in the losartan group. The authors hypothesized that a treatment period of only 4 weeks might be a reason for a lack of any significant effect. An additional difficulty in the interpretation of the results was that a low purine diet was observed for only one day before urine was collected.

Our study was designed to address the uncertainty around the effects of different ARBs on uricemia. The crossover design of the study allowed a direct comparison of the effect of both drugs in the same subject and in the same condition [30]. It is of note that several patients, who were qualified to the study, took a small dose of aspirin (75 mg), β-blocker, or diuretic which may have a weak uricosuric activity [7, 31, 32]. These drugs were however administered in an unchanged dose during the whole study and therefore did not have the effect on the comparison between two study drugs.

Schmidt et al. [28] showed that the uricosuric effect of losartan appears to wane over time. In addition, the majority of our patients had only mildly elevated serum uric acid level at baseline which could also limit a potential magnitude of the effect of ARB on its metabolism. The baseline uric acid level in most previous studies was higher than that in our study [23, 25, 28].

Three months of treatment with eprosartan or losartan led to an expected significant decrease in arterial pressure. It should be noted that our patients had a well-controlled blood pressure already at the beginning of the study, so the addition of further antihypertensive drug only had a small effect on blood pressure.

5. Conclusion

Our study demonstrated that losartan did not specifically affect serum concentration and urinary excretion of uric acid, as well as the magnitude of the changes of serum uric acid concentration after the oral fructose load. Therefore, we were not able to confirm the usefulness of losartan compared to other ARBs in the treatment of arterial hypertension in the patients with metabolic syndrome.

Data Availability

The data presented in this study are available on request from the corresponding author.

Conflicts of Interest

The authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Acknowledgments

The authors disclosed the receipt of the following financial support for the research, authorship, and/or publication of this article: the study was funded by the Medical University of Lodz under grant no. 503/1-151-02/503-01.

References

L. Li, Y. Zhang, and C. Zeng, “Update on the epidemiology, genetics, and therapeutic options of hyperuricemia,” American Journal of Translational Research, vol. 12, no. 7, pp. 3167–3181, 2020.
View at: Google Scholar
R. L. Wortmann, “Gout and hyperuricemia,” Current opinion in rheumatology, vol. 14, no. 3, pp. 281–286, 2002.
View at: Publisher Site | Google Scholar
D. J. Stewart, V. Langlois, and D. Noone, “Hyperuricemia and hypertension: links and risks,” Integrated blood pressure control, vol. Volume 12, pp. 43–62, 2019.
View at: Publisher Site | Google Scholar
N. M. Simon, E. Jon, and M. D. Smucker, “Differential uric acid excretion in essential and renal hypertension,” Circulation, vol. 39, no. 1, pp. 121–125, 1969.
View at: Publisher Site | Google Scholar
D. Gill, A. C. Cameron, S. Burgess et al., “Urate, blood pressure, and cardiovascular disease,” Hypertension, vol. 77, no. 2, pp. 383–392, 2021.
View at: Publisher Site | Google Scholar
A. Tykarski and A. Posadzy-Małaczyńska, “Mechanism of hyperuricemic action of angiotensin converting enzyme inhibitors in patients with essential hypertension,” Journal of Hypertension, vol. 14, pp. 219–224, 1996.
View at: Google Scholar
M. Burnier and M. Hagman, “Short-term and sustained renal effects of angiotensin II receptor blockade in healthy subjects,” Hypertension, vol. 25, 4 Part 1, pp. 602–609, 1995.
View at: Publisher Site | Google Scholar
M. Hatch, R. Freel, and N. Vaziri, “Effects of the specific angiotensin II receptor antagonist losartan on urate homeostasis and intestinal urate transport,” Journal of Pharmacology and Experimental Therapeutics, vol. 276, pp. 187–193, 1996.
View at: Google Scholar
I. Tikkanen, P. Omvik, and H. A. Jensen, “Comparison of the angiotensin II antagonist losartan with the angiotensin converting enzyme inhibitor enalapril in patients with essential hypertension,” Journal of Clinical Pharmacology, vol. 36, pp. 403–408, 1996.
View at: Google Scholar
A. I. Goldberg, M. C. Dunlay, and C. S. Sweet, “Safety and tolerability of losartan potassium, an angiotensin II receptor antagonist, compared with hydrochlorothiazide, atenolol, felodipne ER, and angiotensin-converting enzyme inhibitors for the treatment of systemic hypertension,” The American Journal of Cardiology, vol. 75, no. 12, pp. 793–795, 1995.
View at: Publisher Site | Google Scholar
R. M. Edwards, W. Trizna, E. Stack, and J. Weinstock, “Interaction of nonpeptide angiotensin II receptor antagonists with the urate transporter in rat renal brush-border membranes,” The Journal of Pharmacology and Experimental Therapeutics, vol. 276, no. 1, pp. 125–129, 1996.
View at: Google Scholar
O. W. Portman, E. Y. Lawry, and D. Bruno, “Effect of dietary carbohydrate on experimentally induced hypercholesteremia and hyperbetalipoproteinemia in rats,” Proceedings of the Society for Experimental Biology and Medicine, vol. 91, no. 2, pp. 321–323, 1956.
View at: Publisher Site | Google Scholar
F. Roch-Ramel and J. Diezi, “Renal transport of organic ions and uric acid,” in Diseases of the Kidney, R. W. Schrier and C. W. Gottschalk, Eds., pp. 231–249, Little Brown & Co, Boston, 6 edition, 1996.
View at: Google Scholar
S. Al-Nagdy, D. S. Miller, and J. Yudkin, “Changes in body composition and metabolism induced by sucrose in the rat,” Nutrition and Metabolism, vol. 12, pp. 193–219, 2004.
View at: Google Scholar
J. Sleder, Y. D. Chen, M. D. Cully, and G. M. Reaven, “Hyperinsulinemia in fructose-induced hypertriglyceridemia in the rat,” Metabolism, vol. 29, no. 4, pp. 303–305, 1980.
View at: Publisher Site | Google Scholar
J. C. Bode, O. Zelder, H. J. Rumpelt, and U. Wittkamp, “Depletion of liver adenosine phosphates and metabolic effects of intravenous infusion of fructose or sorbitol in man and in the rat,” European Journal of Clinical Investigation, vol. 3, no. 5, pp. 436–441, 1973.
View at: Publisher Site | Google Scholar
S. Nair, P. V. Chacko, C. Arnold, and A. M. Diehl, “Hepatic ATP reserve and efficiency of replenishing: comparison between obese and non-obese normal individuals,” The American Journal of Gastroenterology, vol. 98, no. 2, pp. 466–470, 2003.
View at: Publisher Site | Google Scholar
R. C. Morris Jr., K. Nigon, and E. B. Reed, “Evidence that the severity of depletion of inorganic phosphate determines the severity of the disturbance of adenine nucleotide metabolism in the liver and renal cortex of the fructose-loaded rat,” The Journal of Clinical Investigation, vol. 61, no. 1, pp. 209–220, 1978.
View at: Publisher Site | Google Scholar
S. M. Grundy, J. I. Cleeman, S. R. Daniels et al., “Diagnosis and management of the metabolic syndrome,” Circulation, vol. 112, no. 17, pp. 2735–2752, 2005.
View at: Publisher Site | Google Scholar
X. Chen, Z. L. Ji, and Y. Z. Chen, “TTD: therapeutic target database,” Nucleic Acids Research, vol. 30, no. 1, pp. 412–415, 2002.
View at: Publisher Site | Google Scholar
M. B. Bottorff and D. M. Tenero, “Pharmacokinetics of eprosartan in healthy subjects, patients with hypertension, and special populations,” Pharmacotherapy, vol. 19, no. 4 Part 2, pp. 73S–78S, 1999.
View at: Publisher Site | Google Scholar
A. Dang, Y. Zhang, G. Liu, G. Chen, W. Song, and B. Wang, “Effects of losartan and irbesartan on serum uric acid in hypertensive patients with hyperuricaemia in Chinese population,” Journal of Human Hypertension, vol. 20, no. 1, pp. 45–50, 2006.
View at: Publisher Site | Google Scholar
J. G. Puig, F. Mateos, A. Buño, R. Ortega, F. Rodriguez, and R. Dal-Ré, “Effect of eprosartan and losartan on uric acid metabolism in patients with essential hypertension,” Journal of Hypertension, vol. 17, no. 7, pp. 1033–1039, 1999.
View at: Publisher Site | Google Scholar
B. L. Rayner, Y. A. Trinder, D. Baines, and H. Lionel, “Effect of losartan versus candesartan on uric acid, renal function, and fibrinogen in patients with hypertension and hyperuricemia associated with diuretics,” American Journal of Hypertension, vol. 19, no. 2, pp. 208–213, 2006.
View at: Publisher Site | Google Scholar
W. J. Elliott, D. A. Calhoun, D. L. PT, L. P. Gazdick, D. E. Kerns, and R. K. Zeldin, “Losartan versus valsartan in the treatment of patients with mild to moderate essential hypertension: data from a multicenter, randomized, double-blind, 12-week trial,” Clinical Therapeutics, vol. 23, no. 8, pp. 1166–1179, 2001.
View at: Publisher Site | Google Scholar
T. Hamada, I. Hisatome, Y. Kinugasa et al., “Effect of the angiotensin II receptor antagonist losartan on uric acid and oxypurine metabolism in healthy subjects,” Internal Medicine, vol. 41, no. 10, pp. 793–797, 2002.
View at: Publisher Site | Google Scholar
G. Würzner, J. C. Gerster, A. Chiolero et al., “Comparative effects of losartan and irbesartan on serum uric acid in hypertensive patients with hyperuricaemia and gout,” Journal of Hypertension, vol. 19, no. 10, pp. 1855–1860, 2001.
View at: Publisher Site | Google Scholar
A. Schmidt, U. Gruber, G. Böhmig, E. Köller, and G. Mayer, “The effect of ACE inhibitor and angiotensin II receptor antagonist therapy on serum uric acid levels and potassium homeostasis in hypertensive renal transplant recipients treated with CsA,” Nephrology, Dialysis, Transplantation, vol. 16, no. 5, pp. 1034–1037, 2001.
View at: Publisher Site | Google Scholar
D. Caspi, E. Lubart, E. Graff, B. Habot, M. Yaron, and R. Segal, “The effect of mini-dose aspirin on renal function and uric acid handling in elderly patients,” Arthritis and Rheumatism, vol. 43, no. 1, pp. 103–108, 2000.
View at: Publisher Site | Google Scholar
P. Verdecchia, J. A. Staessen, F. Angeli et al., “Usual versus tight control of systolic blood pressure in non-diabetic patients with hypertension (Cardio-Sis): an open-label randomised trial,” Lancet, vol. 374, no. 9689, pp. 525–533, 2009.
View at: Publisher Site | Google Scholar
Z. Jelic-Ivanovic, S. Spasic, N. Majkic-Singh, and P. Todorovic, “Effects of some anti-inflammatory drugs on 12 blood constituents: protocol for the study of in vivo effects of drugs,” Clinical Chemistry, vol. 31, no. 7, pp. 1141–1143, 1985.
View at: Publisher Site | Google Scholar
C. Bengtsson, “Comparison between alprenolol and chlorthalidone as antihypertensive agents,” Acta Medica Scandinavica, vol. 191, pp. 433–438, 1972.
View at: Google Scholar

Copyright

Copyright © 2021 Anna Masajtis-Zagajewska et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

PDF Download Citation

Download other formats

Order printed copies

Views

1579

Downloads

773

Citations