Skip to main content
Top
Published in: BMC Complementary Medicine and Therapies 1/2020

Open Access 01-12-2020 | Febuxostat | Research article

A randomized, double-blind, positive-controlled, prospective, dose-response clinical study to evaluate the efficacy and tolerability of an aqueous extract of Terminalia bellerica in lowering uric acid and creatinine levels in chronic kidney disease subjects with hyperuricemia

Authors: Usharani Pingali, Chandrasekhar Nutalapati, Niranjan Koilagundla, Gangadhar Taduri

Published in: BMC Complementary Medicine and Therapies | Issue 1/2020

Login to get access

Abstract

Background

Hyperuricemia is an independent risk factor in chronic kidney disease (CKD). Allopurinol and febuxostat are prescription medicines used to treat hyperuricemia but suffer side-effects. Earlier clinical study has shown that an aqueous extract of Terminalia bellerica (TBE), significantly reduced uric acid levels with no serious adverse effects in hyperuricemic subjects. The objective of this study is to determine the efficacy and tolerability of TB in reducing uric acid and creatinine levels in CKD subjects.

Methods

59-subjects were randomized to three groups-40 mg-once-daily febuxostat, 500 mg-twice-daily and 1000 mg-twice-daily of TBE. Serum uric acid, creatinine levels and estimated-glometular-filtration-rate were measured at baseline, 4, 8, 12, 16, 20, 24-weeks. Biomarkers of oxidative-stress, endothelial function, systemic inflammation, and platelet-aggregation were evaluated at baseline, 4, 8, 12, 24-weeks. Adverse drug reactions were recorded. Statistical analysis evaluated using GraphPadPrism4.

Results

55-subjects completed 24-week study. Starting at 4-weeks, all treatment groups showed a significant decrease in serum uric acid levels from baseline (p ≤ 0.0001). At 24-weeks, febuxostat, T.bellerica 500 mg-twice-daily, and T.bellerica 1000 mg-twice-daily doses decreased mean-percentage serum uric acid by 63.70 ± 4.62, 19.84 ± 6.43 and 33.88% ± 4.95% respectively (p ≤ 0.0001). Significant decrease in serum creatinine with all the groups starting at 16-weeks was seen (p ≤ 0.005-p ≤ 0.0001). At 24-weeks, the mean-percentage change in creatinine levels was 23.71 ± 12.50, 11.70 ± 9.0, and 24.42 ± 8.14, respectively with febuxostat, T.bellerica 500 mg-twice-daily and T.bellerica 1000 mg-twice-daily. Statistically significant (p ≤ 0.05) increase in estimated glomerular filtration rate-(eGFR) was seen at 20 (p ≤ 0.05) and 24-weeks (p ≤ 0.01) for both febuxostat vs T.bellerica 500 mg-twice-daily and T.bellerica 1000 mg-twice-daily vs T.bellerica 500 mg-twice-daily. There was no statistically significant difference between febuxostat and T.bellerica 1000 mg-twice-daily, with an increase of eGFR of 41.38 and 40.39 ml/min/1.73m2 respectively, with the inference that T.bellerica at 1000 mg-twice-daily dose is as good as febuxostat 40 mg-once-daily. Positive improvements were made by all the groups in endothelial function and the related biomarkers and high-sensitivity C-reactive protein. None of the products showed effect on platelet aggregation.

Conclusion

In this 24-week study Febuxostat 40 mg, T. bellerica 500 mg-twice-daily and 1000 mg-twice-daily, significantly decreased the serum uric acid and creatinine levels, increased eGFR in CKD subjects. T. bellerica 500 mg-twice-daily and 1000 mg-twice-daily were one-third and more than half as effective at 24-weeks, respectively. T. bellerica extract may be considered a natural alternative for reducing serum uric acid levels.

Trial registration

This study was registered with the Clinical Trials Registry – India (CTRI) with the registration number: CTRI/​2019/​11/​022093 [Registered on: 21/11/2019] Trial Registered Retrospectively.
Appendix
Available only for authorised users
Literature
1.
go back to reference Levey AS, Atkins R, Coresh J, et al. Chronic kidney disease as a global public health problem: approaches and initiatives—a position statement from kidney disease improving global outcomes. Kidney Int. 2007;72(3):247–59.PubMed Levey AS, Atkins R, Coresh J, et al. Chronic kidney disease as a global public health problem: approaches and initiatives—a position statement from kidney disease improving global outcomes. Kidney Int. 2007;72(3):247–59.PubMed
2.
go back to reference Fried LF. Higher incidence of ESRD than mortality in the AASK study. J Am Soc Nephrol. 2010;21(8):1244–6.PubMed Fried LF. Higher incidence of ESRD than mortality in the AASK study. J Am Soc Nephrol. 2010;21(8):1244–6.PubMed
3.
go back to reference Levey AS, Stevens LA, Coresh J. Conceptual model of CKD: applications and implications. Am J Kidney Dis. 2009;53(3):S4–16.PubMed Levey AS, Stevens LA, Coresh J. Conceptual model of CKD: applications and implications. Am J Kidney Dis. 2009;53(3):S4–16.PubMed
4.
go back to reference Eijkelkamp WB, Zhang Z, Remuzzi G, et al. Albuminuria is a target for renoprotective therapy independent from blood pressure in patients with type 2 diabetic nephropathy: post hoc analysis from the reduction of endpoints in NIDDM with the angiotensin II antagonist losartan (RENAAL) trial. J Am Soc Nephrol. 2007;18(5):1540–6.PubMed Eijkelkamp WB, Zhang Z, Remuzzi G, et al. Albuminuria is a target for renoprotective therapy independent from blood pressure in patients with type 2 diabetic nephropathy: post hoc analysis from the reduction of endpoints in NIDDM with the angiotensin II antagonist losartan (RENAAL) trial. J Am Soc Nephrol. 2007;18(5):1540–6.PubMed
5.
go back to reference Renal Data System US. USRDS 2011 annual Data report: atlas of chronic kidney disease and end-stage Renal disease in the United States. Am J Kidney Dis. 2012;59(1):e1–420. Renal Data System US. USRDS 2011 annual Data report: atlas of chronic kidney disease and end-stage Renal disease in the United States. Am J Kidney Dis. 2012;59(1):e1–420.
6.
go back to reference Sanchez-Lozada LG, Tapia E, Lopez-Molina R, et al. Effects of acute and chronic L-arginine treatment in experimental hyperuricemia. Am J Phys. 2007;292(4):F1238–44. Sanchez-Lozada LG, Tapia E, Lopez-Molina R, et al. Effects of acute and chronic L-arginine treatment in experimental hyperuricemia. Am J Phys. 2007;292(4):F1238–44.
7.
go back to reference Weiner DE, Tighiouart H, Elsayed EF, Griffith JL, Salem DN, Levey AS. Uric acid and incident kidney disease in the community. J Am Soc Nephrol. 2008;19(6):1204–11.PubMedPubMedCentral Weiner DE, Tighiouart H, Elsayed EF, Griffith JL, Salem DN, Levey AS. Uric acid and incident kidney disease in the community. J Am Soc Nephrol. 2008;19(6):1204–11.PubMedPubMedCentral
8.
go back to reference Johnson RJ, Kang DH, Feig D, et al. Is there a pathogenetic role for uric acid in hypertension and cardiovascular and renal disease? Hypertension. 2003;41:1183–90.PubMed Johnson RJ, Kang DH, Feig D, et al. Is there a pathogenetic role for uric acid in hypertension and cardiovascular and renal disease? Hypertension. 2003;41:1183–90.PubMed
9.
go back to reference Kosugi T, Nakayama T, Heinig M, et al. The effect of lowering uric acid on renal disease in the type 2 diabetic db/db mice. Am J Physiol Ren Physiol. 2009;297(2):F481–8. Kosugi T, Nakayama T, Heinig M, et al. The effect of lowering uric acid on renal disease in the type 2 diabetic db/db mice. Am J Physiol Ren Physiol. 2009;297(2):F481–8.
10.
go back to reference Jalal DI, Chonchol M, Chen W, Targher G. Uric acid as a target of therapy in CKD. Am J Kidney Dis. 2013;61(1):134–46.PubMed Jalal DI, Chonchol M, Chen W, Targher G. Uric acid as a target of therapy in CKD. Am J Kidney Dis. 2013;61(1):134–46.PubMed
11.
go back to reference Usharani P, Nutalapati C, Pokuri VK, Kumar CU, Taduri G. A randomized, double-blind, placebo-, and positive-controlled clinical pilot study to evaluate the efficacy and tolerability of standardized aqueous extracts of Terminalia chebula and Terminalia bellerica in subjects with hyperuricemia. Clin Pharm. 2016;22(8):51–9. Usharani P, Nutalapati C, Pokuri VK, Kumar CU, Taduri G. A randomized, double-blind, placebo-, and positive-controlled clinical pilot study to evaluate the efficacy and tolerability of standardized aqueous extracts of Terminalia chebula and Terminalia bellerica in subjects with hyperuricemia. Clin Pharm. 2016;22(8):51–9.
12.
go back to reference Chowienezyk PJ, Kelly RP, MacCallum H, Millasseau SC, Andersson TL, Gosling RG, et al. Photoplethysmographic assessment of pulse wave reflection: blunted response to endothelium-dependent beta 2-adrenergic vasodilation in type II diabetes mellitus. J Am Coll Cardiol. 1999;34:2007–14. Chowienezyk PJ, Kelly RP, MacCallum H, Millasseau SC, Andersson TL, Gosling RG, et al. Photoplethysmographic assessment of pulse wave reflection: blunted response to endothelium-dependent beta 2-adrenergic vasodilation in type II diabetes mellitus. J Am Coll Cardiol. 1999;34:2007–14.
13.
go back to reference Naidu MUR, Sridhar Y, Usha Rani P, Mateen AA. Comparison of two β2 adrenoceptor agonists by different routes of administration to assess human endothelial function. Indian J Pharm. 2007;39:168–9. Naidu MUR, Sridhar Y, Usha Rani P, Mateen AA. Comparison of two β2 adrenoceptor agonists by different routes of administration to assess human endothelial function. Indian J Pharm. 2007;39:168–9.
14.
go back to reference Millaesseau SC, Kelly RP, Ritter JM, Chowienczyk PJ. Determination of age-related increases in large artery stiffness by digital pulse contour analysis. Clin Sci. 2002;103:371–7. Millaesseau SC, Kelly RP, Ritter JM, Chowienczyk PJ. Determination of age-related increases in large artery stiffness by digital pulse contour analysis. Clin Sci. 2002;103:371–7.
15.
go back to reference Vidyasagar J, Karunaka N, Reddy MS, Rajnarayan K, Surender T, Krishna DR. Oxidative stress and antioxidant status in acute organophosphorus insecticide poisoning. Indian J Pharm. 2004;36:76–9. Vidyasagar J, Karunaka N, Reddy MS, Rajnarayan K, Surender T, Krishna DR. Oxidative stress and antioxidant status in acute organophosphorus insecticide poisoning. Indian J Pharm. 2004;36:76–9.
16.
go back to reference Yao D, Vlessidis AG, Evmiridis NP. Determination of nitric oxide in biological samples. Microchim Acta. 2004;147:1–20. Yao D, Vlessidis AG, Evmiridis NP. Determination of nitric oxide in biological samples. Microchim Acta. 2004;147:1–20.
17.
go back to reference Verma S, Buchanan MR, Anderson TJ. Endothelial function testing as a biomarker of vascular disease. Circulation. 2003;108(17):2054–9.PubMed Verma S, Buchanan MR, Anderson TJ. Endothelial function testing as a biomarker of vascular disease. Circulation. 2003;108(17):2054–9.PubMed
18.
go back to reference Elman GL. Tissue sulfhydryl groups. Arch Biochem Biophys. 1959;82:70–7. Elman GL. Tissue sulfhydryl groups. Arch Biochem Biophys. 1959;82:70–7.
19.
go back to reference Kishan PV, Kumar U, Shobha JC, Usharani P. Effect of Oral anti-platelet regimens on platelet aggregation using Chronolog light transmittance Aggregometry in coronary heart disease patients: an observational study. J Clin Diagn Res. 2013;7(11):2478–82. Kishan PV, Kumar U, Shobha JC, Usharani P. Effect of Oral anti-platelet regimens on platelet aggregation using Chronolog light transmittance Aggregometry in coronary heart disease patients: an observational study. J Clin Diagn Res. 2013;7(11):2478–82.
20.
go back to reference Rajendran P, Rengarajan T, Thangavel J, Nishigaki Y, Sakthisekaran D, Sethi G, et al. The vascular endothelium and human diseases. Int J Biol Sci. 2013;9(10):1057–69.PubMedPubMedCentral Rajendran P, Rengarajan T, Thangavel J, Nishigaki Y, Sakthisekaran D, Sethi G, et al. The vascular endothelium and human diseases. Int J Biol Sci. 2013;9(10):1057–69.PubMedPubMedCentral
21.
go back to reference Schnabel RB, Schulz A, Wild PS, Sinning CR, Wilde S, Eleftheriadis M, et al. Noninvasive vascular function measurement in the community. Circulation. 2011;4:371–80.PubMed Schnabel RB, Schulz A, Wild PS, Sinning CR, Wilde S, Eleftheriadis M, et al. Noninvasive vascular function measurement in the community. Circulation. 2011;4:371–80.PubMed
22.
go back to reference Pirinccioglu AG, Gökalp D, Pirinccioglu M, Kizil G, Kizil M. Malondialdehyde (MDA) and protein carbonyl (PCO) levels as biomarkers of oxidative stress in subjects with familial hypercholesterolemia. Clin Biochem. 2010;43(15):1220–4.PubMed Pirinccioglu AG, Gökalp D, Pirinccioglu M, Kizil G, Kizil M. Malondialdehyde (MDA) and protein carbonyl (PCO) levels as biomarkers of oxidative stress in subjects with familial hypercholesterolemia. Clin Biochem. 2010;43(15):1220–4.PubMed
23.
go back to reference Khoubnasabjafari M, Ansarin K, Jouyban A. Reliability of malondialdehyde as a biomarker of oxidative stress in psychological disorders. Bioimpacts. 2015;5(3):123–7.PubMedPubMedCentral Khoubnasabjafari M, Ansarin K, Jouyban A. Reliability of malondialdehyde as a biomarker of oxidative stress in psychological disorders. Bioimpacts. 2015;5(3):123–7.PubMedPubMedCentral
24.
go back to reference Jin RC, Loscalzo J. Vascular nitric oxide: formation and function. J Blood Med. 2010;1:147–62.PubMedCentral Jin RC, Loscalzo J. Vascular nitric oxide: formation and function. J Blood Med. 2010;1:147–62.PubMedCentral
25.
go back to reference Kurutas EB. The importance of antioxidants which play the role in cellular response against oxidative/nitrosative stress: current state. Nutr J. 2016;15:71.PubMedPubMedCentral Kurutas EB. The importance of antioxidants which play the role in cellular response against oxidative/nitrosative stress: current state. Nutr J. 2016;15:71.PubMedPubMedCentral
26.
go back to reference Nimse SB, Pal D. Free radicals, natural antioxidants, and their reaction mechanisms. RSC Adv. 2015;5(35):27986–8006. Nimse SB, Pal D. Free radicals, natural antioxidants, and their reaction mechanisms. RSC Adv. 2015;5(35):27986–8006.
27.
go back to reference Gowdaiah PK, Mamatha TR, Nirgude D, Hosamani PB. High sensitivity C-reactive protein in metabolic syndrome. Int J Adv Med. 2016;3(3):607–10. Gowdaiah PK, Mamatha TR, Nirgude D, Hosamani PB. High sensitivity C-reactive protein in metabolic syndrome. Int J Adv Med. 2016;3(3):607–10.
28.
go back to reference Kimura K, Hosoya T, Uchida S, Inaba M, Makino H, Maruyama S, et al. Febuxostat therapy for patients with stage 3 CKD and asymptomatic Hyperuricemia: a randomized trial. Am J Kidney Dis. 2018;72(6):798–10.PubMed Kimura K, Hosoya T, Uchida S, Inaba M, Makino H, Maruyama S, et al. Febuxostat therapy for patients with stage 3 CKD and asymptomatic Hyperuricemia: a randomized trial. Am J Kidney Dis. 2018;72(6):798–10.PubMed
29.
go back to reference Sircar D, Chatterjee S, Waikhom R, Golay V, Raychaudhury A, Chatterjee S, et al. Efficacy of Febuxostat for slowing the GFR decline in patients with CKD and asymptomatic Hyperuricemia: a 6-month, double-blind, randomized, placebo-controlled trial. Am J Kidney Dis. 2015;66(6):945–50.PubMed Sircar D, Chatterjee S, Waikhom R, Golay V, Raychaudhury A, Chatterjee S, et al. Efficacy of Febuxostat for slowing the GFR decline in patients with CKD and asymptomatic Hyperuricemia: a 6-month, double-blind, randomized, placebo-controlled trial. Am J Kidney Dis. 2015;66(6):945–50.PubMed
30.
go back to reference Tsuruta Y, Mochizuki T, Moriyama T, Itabashi M, Takei T, Tsuchiya K, et al. Switching from allopurinol to febuxostat for the treatment of hyperuricemia and renal function in patients with chronic kidney disease. Clin Rheumatol. 2014;33(11):1643–8.PubMedPubMedCentral Tsuruta Y, Mochizuki T, Moriyama T, Itabashi M, Takei T, Tsuchiya K, et al. Switching from allopurinol to febuxostat for the treatment of hyperuricemia and renal function in patients with chronic kidney disease. Clin Rheumatol. 2014;33(11):1643–8.PubMedPubMedCentral
31.
go back to reference Lin CS, Hung YJ, Chen GY, Tzeng TF, Lee DY, Chen CY, et al. A multicenter study of the association of serum uric acid, serum creatinine, and diuretic use in hypertensive patients. Int J Cardiol. 2011;148(3):325–30.PubMed Lin CS, Hung YJ, Chen GY, Tzeng TF, Lee DY, Chen CY, et al. A multicenter study of the association of serum uric acid, serum creatinine, and diuretic use in hypertensive patients. Int J Cardiol. 2011;148(3):325–30.PubMed
32.
go back to reference Kim AH, Seo Y, Song YW. Four-week effects of allopurinol and Febuxostat treatments on blood pressure and serum Creatinine level in gouty men. J Korean Med Sci. 2014;29:1077–81.PubMedPubMedCentral Kim AH, Seo Y, Song YW. Four-week effects of allopurinol and Febuxostat treatments on blood pressure and serum Creatinine level in gouty men. J Korean Med Sci. 2014;29:1077–81.PubMedPubMedCentral
33.
go back to reference Jalal D, Decker E, Perrenoud L, Nowak KL, Bispham N, Mehta T, et al. Vascular function and uric acid-lowering in stage 3 CKD. J Am Soc Nephrol. 2017;28(3):943–52.PubMed Jalal D, Decker E, Perrenoud L, Nowak KL, Bispham N, Mehta T, et al. Vascular function and uric acid-lowering in stage 3 CKD. J Am Soc Nephrol. 2017;28(3):943–52.PubMed
34.
go back to reference Ling XC, Kuo KL. Oxidative stress in chronic kidney disease. Renal Replace Ther. 2018;4:53. Ling XC, Kuo KL. Oxidative stress in chronic kidney disease. Renal Replace Ther. 2018;4:53.
35.
go back to reference Tsuruta Y, Kikuchi K, Tsuruta Y, Sasaki Y, Moriyama T, Itabashi M, et al. Febuxostat improves endothelial function in hemodialysis patients with hyperuricemia: a randomized controlled study. Hemodial Int. 2015;19(4):514–20.PubMed Tsuruta Y, Kikuchi K, Tsuruta Y, Sasaki Y, Moriyama T, Itabashi M, et al. Febuxostat improves endothelial function in hemodialysis patients with hyperuricemia: a randomized controlled study. Hemodial Int. 2015;19(4):514–20.PubMed
36.
go back to reference Fahmi AN, Shehatou GS, Shebl AM, Salem HA. Febuxostat exerts dose-dependent renoprotection in rats with cisplatin-induced acute renal injury. Naunyn Schmiedeberg's Arch Pharmacol. 2016;389(8):819–30. Fahmi AN, Shehatou GS, Shebl AM, Salem HA. Febuxostat exerts dose-dependent renoprotection in rats with cisplatin-induced acute renal injury. Naunyn Schmiedeberg's Arch Pharmacol. 2016;389(8):819–30.
37.
go back to reference Hwang SJ, Lee KH, Jang HH, Lee SR, Woo JS, Lee HJ, et al. Febuxostat contributes to improvement of endothelial dysfunction in an experimental model of streptozocin-induced diabetic rats. Int J Cardiol. 2014;171(3):e110–2.PubMed Hwang SJ, Lee KH, Jang HH, Lee SR, Woo JS, Lee HJ, et al. Febuxostat contributes to improvement of endothelial dysfunction in an experimental model of streptozocin-induced diabetic rats. Int J Cardiol. 2014;171(3):e110–2.PubMed
38.
go back to reference Shirakura T, Nomura J, Matsui C, Kobayashi T, Tamura M, Masuzaki H. Febuxostat, a novel xanthine oxidoreductase inhibitor, improves hypertension and endothelial dysfunction in spontaneously hypertensive rats. Naunyn Schmiedeberg's Arch Pharmacol. 2016;389(8):831–8. Shirakura T, Nomura J, Matsui C, Kobayashi T, Tamura M, Masuzaki H. Febuxostat, a novel xanthine oxidoreductase inhibitor, improves hypertension and endothelial dysfunction in spontaneously hypertensive rats. Naunyn Schmiedeberg's Arch Pharmacol. 2016;389(8):831–8.
39.
go back to reference Sezai A, Soma M, Nakata KI, Osaka S, Ishii Y, Yaoita H, et al. Comparison of febuxostat and allopurinol for hyperuricemia in cardiac surgery patients with chronic kidney disease (NU-FLASH trial for CKD). J Cardiol. 2015;66(4):298–303.PubMed Sezai A, Soma M, Nakata KI, Osaka S, Ishii Y, Yaoita H, et al. Comparison of febuxostat and allopurinol for hyperuricemia in cardiac surgery patients with chronic kidney disease (NU-FLASH trial for CKD). J Cardiol. 2015;66(4):298–303.PubMed
Metadata
Title
A randomized, double-blind, positive-controlled, prospective, dose-response clinical study to evaluate the efficacy and tolerability of an aqueous extract of Terminalia bellerica in lowering uric acid and creatinine levels in chronic kidney disease subjects with hyperuricemia
Authors
Usharani Pingali
Chandrasekhar Nutalapati
Niranjan Koilagundla
Gangadhar Taduri
Publication date
01-12-2020
Publisher
BioMed Central
Published in
BMC Complementary Medicine and Therapies / Issue 1/2020
Electronic ISSN: 2662-7671
DOI
https://doi.org/10.1186/s12906-020-03071-7

Other articles of this Issue 1/2020

BMC Complementary Medicine and Therapies 1/2020 Go to the issue