Effect of Artemisinin Based Combination Therapy on the Liver and Kidney of Patient Attending University Health Centre

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Matthew Ajulo Olugbenga
Onyong-Offiok Akpan Obot
Hephzibah Ajulo Oluwatoyin

Abstract

African countries due to resistance to conventional antimalarial drugs adopted use of artemisinin-based combination therapy (ACTs). This study aimed at evaluating the effect of ACTs on liver and renal functions. Upon approval, patients attending the University Health Centre for treatment of uncomplicated malaria after receiving prescription for ACTs were recruited for the study following their consent. A 3ml blood was collected from the participants immediately after recruitment (Day 0) and seven days later. The participants started ACTs on the day of recruitment. The blood was analysed in the laboratory for alanine aminotransferase (ALT) and aspartate aminotransferase (AST) and creatinine respectively. The data obtained at day 0 and 7 were compared by using descriptive analysis such as mean and standard deviation; t-test was used for statistical analysis and significance was considered at p ? 0.05. Seventy-four (74) patients participated including twenty-six (26) males and forty-eight (48) females with mean age of 37.56±13.96years and mean body mass index (BMI) of 25.92±2.99kg/m2. ALT was elevated in participants from 6.66±5.27IU/L to 6.71±5.48IU/L while creatinine clearance of male participants reduced from 139.10±69.11mL/min to134.25±23.87mL/min. The study showed that ACTs were associated with elevated ALT in participants and reduced renal function in males.

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Olugbenga , M. A., Obot , O.-O. A., & Oluwatoyin , H. A. (2020). Effect of Artemisinin Based Combination Therapy on the Liver and Kidney of Patient Attending University Health Centre. Nigerian Journal of Pharmaceutical and Applied Science Research, 7(2), 28–32. Retrieved from https://nijophasr.net/index.php/nijophasr/article/view/216
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Author Biographies

Matthew Ajulo Olugbenga

Department of Clinical Pharmacy and Biopharmacy, Faculty of Pharmacy, University of Uyo, Uyo. AkwaIbom State. Nigeria.

Onyong-Offiok Akpan Obot

Department of Clinical Pharmacy and Biopharmacy, Faculty of Pharmacy, University of Uyo, Uyo. AkwaIbom State. Nigeria.

Hephzibah Ajulo Oluwatoyin

Veterinary Section, Department of Animal Science Faculty of Agriculture, University of Uyo, Uyo. AkwaIbom State. Nigeria.

References

Adjei A, Narh-Bana S, Amu A, Kukula V, Nagai RA, Owusu-Agyei S, Oduro A et al., (2016). Treatment outcomes in a safety observational study of dihydroartemisinin/piperaquine (Eurartesim®) in the treatment of uncomplicated malaria at public health facilities in four African countries. Malaria Journal, 15:43.

Ajulo MO, Omole MK, Moody JO (2014). Impact of Highly Active Antiretroviral Therapy (HAART) on organs of HIV-infected Children in Abia State, Nigeria. British Journal of Pharmaceutical Research, 4(7): 837-848.

Autino B, Noris A, Russo R and Castelli F (2012). Epidemiology of Malaria in Endemic Areas. Mediterranean Journal of Hematology and Infectious Diseases, 4(1): e2012060, DOI 10.4084/MJHID.2012.060

Beales PF and Gillies HM (2002). Rationale and technique of malaria control. In:Warrell Da, Gilles HM, editors. Essential malariology. 4th Edition, Arnold; London, pp107-190.

Cheesbrough (2006). District laboratory practice in tropical countries. New York, Cambridge press. Part 1, 2nd edition; 249-258.

Cockcroft DW and Gault MH (1976). Prediction of creatinine clearance from serum creatinine. Nephron, 16(1):31-41.

Kremsner PG, and Krishna S (2004). Antimalarial combinations. Lancet, 364:285–294.

National Institute of Health (2018). Artemisinin Derivatives: Clinical and research information on drug induced liver injury. www.livertox.nih.gov/artemisininderivatives. accessed on February 25.

Orrell C, Taylor WR, Olliaro P (2001). Acute asymptomatic hepatitis in a healthy normal volunteer exposed to 2 oral doses of amodiaquine and artesunate. Transactions of the Royal Society of Tropical Medicine and Hygiene, 95: 517-518.

Otuechere CA, Edewor G, Kale OE, Ekor M (2012). Subacute therapeutic dosing of Artemisinin-Lumefantrine and Artesunate-Amodiaquine combination preserved plasma cholesterol, renal antioxidants status and organ weight in rats. Malaria research and treatment. Article ID 257986.

Price R, van Vugt M, Phaipun L, Luxemburger C, Simpson J, Mcgready R, Ter Kuile F, Kham A, Chongsuphajaisiddhi T, White NJ, and Nosten FO (1999). Adverse effects in patients with acute falciparum malaria treated with artemisinin derivatives. American Journal of Tropical Medicine and Hygiene, 60(4): 547–555.

Taylor WR, White NJ (2004). Antimalarial drug toxicity: a review. Drug Safety, 27: 25-61

Thwing J, Eisele TP, Steketee RW (2011). Protective efficacy of malaria case management and intermittent preventive treatment for preventing malaria mortality in children: a systematic review for the Lives Saved Tool. BMC Public Health; 11:S14 (http://

www.ncbi.nlm.nih.gov/pubmed/21501431, (Accessed November 19, 2017).

Toovey S, and Jamieson A (2004). Audiometric changes associated with the treatment of uncomplicated falciparum malaria with co-artemether. Transactions of the Royal Society of Tropical Medicine and Hygiene, 98:261–267.

WHO (2015a). World malaria report.www.who.int/malaria (Accessed January 20, 2018)

WHO (2015b). Guideline for the treatment of malaria, Third Edition. www.who.int/malaria/publication (Accessed January 27, 2018)

WHO (2016). World Malaria Report. Geneva: World Health Organization. www.who.int (Accessed February 1, 2018).