Glucose-6-Phosphate Dehydrogenase (G-6-PD) Status and Kidney Functions Evaluation in Patients with Acute Kidney Injury in Two Tertiary Hospitals, Sokoto
Asian Journal of Research in Nephrology, Volume 5, Issue 3,
Page 47-53
Abstract
Background: Glucose-6-phosphate dehydrogenase deficiency has been implicated in the pathogenesis of a number of common diseases, including acute kidney injury. G6PD deficient individuals are prone to developing acute kidney injury if exposed to certain medication, food or infection. There is high prevalence of G6PD deficiency in Sokoto.
Aim: To determine the G6PD status and evaluate kidney function in patients with acute kidney injury (AKI).
Methodology: This was a case control study involving 206 participants comprising of 106 patients with acute kidney injury and 100 apparently healthy control subjects. The AKI patients were grouped into two; group A: AKI patients with G6PD deficiency, and group B: AKI patients with normal G6PD status. Their blood samples were collected and G6PD status determined by methaemoglobin reduction method, full blood count using Sysmex auto analyser, electrolytes by Ion Selective Electrode, cystatin C by ELISA technique, urea, creatinine and bilirubin using Diacetyl monoxime, Jaffe and Diazo methods respectively.
Results: G6PD deficiency was established in patients with acute kidney injury. The values of Cystatin C, microalbumin, creatinine, urea were significantly higher in AKI patients compared with control, their values were higher in AKI patients with G6PD deficiency. There was no significant difference in bilirubin, and electrolytes values between the patients and control with the exception of bicarbonate which was significantly lower in the patients than the control. Haematocrit was lower while white cell count was higher in the patients than in the control.
Conclusion: AKI patients with G6PD deficiency had impaired kidney function profiles which was more pronounced than in AKI with normal G6PD status. Since it is recognized that certain medications can precipitate AKI, and because of high G6PD prevalence, there is need for G6PD screening before commencement of drug to patient whose G6PD is unknown.
- G6PD
- acute kidney injury
- medication
How to Cite
References
Wisnumurti DA, Sribudiani Y, Porch RM, Maskoen AM, Rahayuninsih SE, Asni EK et al. G6PD genetic variations in neonatal hyperbilirubinaemia in indonesian deutromalay population. BMC Paediatrics. 2019;19: 506.
Nassef YE, Fathy HA, Ni A, Hamed MA, Fathy GA. Evaluation of G6PD activity and antioxidants status in jaundiced egyptian neonates. Int. J. Med. Med. Sci. 2013;5 (12):550-559.
Ogunkanbi SO, Adedoyin OT, Biliaminu SA, Ernest ST. Prevalence of Glucose–6–phosphate dehydrogenase deficiency among steady– state sickle cell disease children at University of Ilorin Teaching Hospital, Ilorin. Open Journal of Paediatrics. 2019;9:29-38.
Kim SY, Lee SM, Tak JK, Choi KS, Kwon TK, Park JW. Regulation of singlet oxygen induced apoptosis by cytosolic NADP+dependent is ocitrate dehydrogenase. Mol. Cell Biochem. 2007;302:27-34.
Bhutani VK. Jaundice due to glucose-6-phosphate dehydrogenase deficiency. Neoreviews. 2012;13;e166.
Filosa S, Fico A, Paglialunga F, Balestrieri M, Crooke A, Verde P et al. Failure to increase glucose consumption through the pentose phosphate pathway results in the death of glucose-6-phosphate dehydrogenase gene- deleted mouse embryonic stem cells subjected to oxidative stress. Biochem J. 2003;370: 935-943.
Leong A. Is there need for neonatal screening of glucose-phosphate dehydrogenase deficiency in Canada? McGill Journal of Medicine. 2007;10(1): 31-34.
Alli N. Frequency of glucose-6- phosphate dehydrogenase deficiency in some ethnic groups in Pakistan. Journal of the College of Physician and Surgeon. 2005; 15:137-141.
Oduola T, Thomas KD, Falana CO. Prevalence and pattern of glucose-6phosphate dehydrogenase deficiency in different haemoglobin types in Ile-Ife, Nigeria. Journal of Medical Laboratory Science. 2004;13(2):67-71.20
Oduola1T, Jelani I, Bolarin DM, Ndakotsu MA, Dallatu MK. Prevalence of glucose-6-phosphate dehydrogenase (G-6-PD) deficiency in Sokoto: Liver function and oxidative stress biomarkers in deficient individual. BJMMR. 2016;13(11):1-6.
Oduola T, Bunza F, Yusuf MT, Dallatu MK, Ndakotsu MA, Panti A et al. Prevalence of glucose-6-phosphate dehydrogenase deficiency among neonates in Usmanu Danfodiyo University Teaching Hospital (UDUTH), Sokoto, Nigeria: Oxidative stress markers in G6pd Deficient Neonates. IBRR. 2018;8(2):1-6.
Muhammad MA, Liman HM, Yakubu A, Isah MD, Abdullahi S, Chijioke A. Clinical pattern and outcome of acute kidney injury patients from a Tertiary Health Institution in Northwestern Nigeria. Sahel Medical Journal. 2016;19:142-5.
Anigilaje EA, Adebayo AI, Ocheni SA. Acute kidney injury in children: A study of etiology, clinical profile, and short-term outcomes at the University of Abuja Teaching Hospital, Gwagwalada, Abuja, Nigeria. Saudi Journal of Kidney Diseases and Transplantation. 2019;30(2):421-439.
Rahman M, Shad F, Smith MC. Acute kidney injury: A guide to diagnosis and management. American Family Physician. 2012;86(7):632-639.
Okunola OO, Arogundade FA, Sanusi AA, Akinsola A. Acute renal failure in the intensive care unit: Aetiological and predisposing factors and outcome. West African Journal of Medicine. 2009;28: 240-4.
Arogundade FA, Sanusi AA, Okunola OO, Soyinka FO, Ojo OE, Akinsola A. Acute renal failure (ARF) in developing countries: Which factors actually influence survival?. Central African Journal of Medicine. 2007; 53:34-9.
Hakeem GLA, Naheem EAA, Swelam SH, Fotoh LMA, ElMazary AAM, Fadil AMA, et al. Detection of occult acute kidney injury in G-6-PD deficient anaemia. Mediterr J. Hematol Infect Dis. 2016; 8(1):e2016038.
Kaul A, Prasad P, Kumari N, Bhaduaria D, Sharma RK, Prasad N et al. G6PD deficiency is not an uncommon cause of pigment nephropathy. Saudi Journal of Kidney Diseases and Transplantation. 2018;29(6):1371-1375.
Xin JAO, Majid M, Utama H, Taib F. Acute haemolysis precipitating rhabdomyolysis and acute kidney injury in a newly diagnosed glucose-6-phosphate dehydrogenase deficiency: A case report. Bangladesh Journal of Medical Science. 2022;21(3):741-744.
Ruan P, Qiu H, Chen H. Acute haemolytic anaemia and acute kidney injury induced by non-high dose ascorbic acid in a child with G-6-PD deficiency. Paediatrics and Neonatology. 2022;63:103-104.
Katibi OS, Adedoyin OT, Anoba S, Sowunmi FO, Folorunsho BO, Ibrahim OR. Current trends in the management of acute kidney injury in children. Nigerian Journal of Paediatrics. 2013;40(3):314-320.
Monica C. Methaemoglobin reduction method for G6PD screening. Discrete laboratory practice in tropical countries. Part 2.Cambridge, 2nd Edn. Press Syndicate of the University of Cambridge. 2006;333-334.
Mohammad R, Boyde TRC. Improvements in the determination of urea using diacetyl monoxime; Methods with and without deproteinisation. Clinical Chimica Acta. 1980;107:3-9.
Spierto FW, McNeil ML, Burtis CA. The effect of temperature and wavelength on the measurement of creatinine with Jaffe’s procedure. Clinical Biochemistry. 1979;12: 18-21.
Elving LD, Bakkeren JA, Jansen MJ, Angelino, CM K, Nobel E, Van Munster PJ. Screening for Microalbuminuria in patients with diabetes mellitus: Frozen storage of urine samples decreases their albumin content. Clinical Chemistry. 1989;35(2): 308-310.
Durmus ME, Yalcin IS, Sahinturk Y. Glucose-6-phosphate dehydrogenase deficiency resulting in massive haemolysis and acute renal failure. Dahuder Medical Journal. 2021;1(1):25-29.
Khandelia V, Pyarsabadi P, Nama U, Chittora S, Swami Y, Richariya H. The potential nephrotoxic effect of single tablet of 15 mg primaquine in G-6-PD deficient Hadoti region population of India. Int J Adv Med. 2017;4:605-608.
Torres CD, Chandia CM. Favism presenting as an acute renal failure: Report of one case. Revista medica de Chile. 2012;140:1043-1045.
Symvoulidis A, Voudiclaris S, Mountokalakis T, Pougounias H. Acute renal failure in glucose-6-phosphate dehydrogenase. Lancet. 1972;2:819-820.
Capellini MD, Fiorelli G. Glucose-6-phosphate dehydrogenase deficiency. Lancet. 2018;371:64-74.
-
Abstract View: 88 times
PDF Download: 31 times