Welcome to Open Science
Contact Us
Home Books Journals Submission Open Science Join Us News
Immunopathology of Urinary Schistosomiasis in Relation to Serum Urea, Creatinine, Protein, Sodium and Potassium Among Infected Individuals
Current Issue
Volume 5, 2018
Issue 2 (June)
Pages: 14-17   |   Vol. 5, No. 2, June 2018   |   Follow on         
Paper in PDF Downloads: 19   Since Jun. 5, 2018 Views: 1006   Since Jun. 5, 2018
Authors
[1]
Imarenezor Edobor Peter Kenneth, Tropical Diseases Unit, Department of Microbiology, Faculty of Pure and Applied Sciences, Federal University, Wukari, Nigeria.
[2]
Brown Samuel Tamunoiyowuna Cockeye, Tropical Diseases Unit, Department of Microbiology, Faculty of Pure and Applied Sciences, Federal University, Wukari, Nigeria.
Abstract
Schistosoma haematobium, a fluke worm causes urinary schistosomiasis which poses serious health hazard in tropical Africa, Asia and North America. The infection progressions require an understanding of the profile levels of some electrolytes in immune responses. Therefore, the study aims at determining the profiles level of some serum electrolytes (urea, creatinine, protein, sodium and potassium). The profile level serum electrolytes were determined using standard methods in accordance to World health organization (WHO). The results show that the electrolytes profile of infected individuals when compared with the control individuals shows that urea 1.26±0.17mg/dl, creatinine 1.33±0.05mg/dl, protein 53±2.25mg/dl, sodium 129±2.25mg/dl, Potassium 4.20±0.2md/dl and urea 2.4±0.42mg/dl, creatinine 1.2±0.44mg/dl, protein 66±1.41mg/dl, sodium 135±1.41mg/dl, potassium 4.10±0.19mg/dl respectively. Proteinuria profile level was statistically significant (x2=13.40, p<0.05), when infected was compared with non-infected. The infected individuals had higher mean concentration of serum urea (4.49±0.88Mmol/l) and these differences were statistically significant at P<0.05 when compared with the control (3.86±0.32Mmol/l). The mean concentration of serum creatinine (110.76±10.40Mmol/l) and protein in urine (22.46±3.01Mmol/l) in the infected volunteers were significantly at P<0.05 when compared with the control volunteers (101.66±4.77Mmol/l and 13.66±1.42Mmol/l) respectively. The relationship between Schistosoma parasitaemia, serum creatinine and protein in urine were positively correlated with r=0.61 and r=0.47 respectively. The serum profile level of urea was negatively correlated with Schistosoma parasitaemia. The profile levels of serum electrolytes and intensity of infection of infected and control individuals showed no significant difference (P=0.05). To this end, this researched data deduce that these electrolytes are major immunological indicators in the immunopathology of S. haematobium infection. Furthermore, it is proposed that raised profile levels of these electrolytes should aid as a bio - marker of schistosomes diagnosis in positive individuals in our locality.
Keywords
Immunopathology, Serum, Electrolytes, Schistosoma haematobium, Individuals, Parasitaemia
Reference
[1]
Imarenezor Edobor Peter Kenneth, Iyamu Mercy Itohan, Nmorsi Onyebiguwa Patrick Goddey (2017). Interleukin (IL) - 1α, IL – 7 and IL – 13 Profile Among Enwan Community, Edo State, Nigeria with Schistosoma haematobium Infection. International Journal of Clinical Medicine Research. 4 (3): 21-25.
[2]
Imarenezor EPK., Brown STC., Yakubu OE., Abhadionmhen OA. (2016). Interleukin (IL)- 10 Profile among Nigerians with Schisotoma haematobium infection. FUW Trends in Science and Technology Journal. 1 (1): 24-25.
[3]
World Health Organisation (2013). The control of schistosomiasis second report of the WHO expert committee. WHO technical reports Series, No. 830: Geneva.
[4]
Imarenezor Edobor Peter Kenneth, Iyamu Mercy Itohan, Nmorsi Onyebiguwa Patrick Goddey (2017). Bacteriuria and Urinary Schistosomiasis among Individuals in Ewean Community Akoko – Edo, Edo State, Nigeria. American Journal of Microbiology and Biotechnology. 4 (3): 27-30.
[5]
Das BS. (2008). Renal failure in schistosomiasis: a review. Journal of Vector Borne Disease. 45: 83-89.
[6]
World Health Organisation (2015). Parasitic notes. Report of a rotto expert committee with the participation of FAO. WHO technical reports services. No. 637.
[7]
Nmorsi OPG., Ukwandu NC., Ogoinja S., Blackie HO., Odike MA. (2007). Urinary tract pathology in Schistosoma haematobium infected rural Nigerians. Southeast Asian Journal of Tropical Medicine and Public Health. 38 (1): 32-37.
[8]
Imarenezor EPK., Nmorsi OPG., Eghafona NO., Esumeh FI., Ekozien MI., Isaac C. (2013). Prevalence of Urinary Schistosomiasis in Enwan a Rural Community in Akoko – Edo Local Government Area, Edo State, Nigeria. International Journal of Basic and Applied Sciences. 2: 60-65.
[9]
Imarenezor Edobor Peter Kenneth, Nmorsi Onyebiguwa Patrick Goddey, Ihimire Inegbenose Godwin, Isaac Clement (2017). Mean Profile of Selected Electrolytes in Individuals with Schistosoma haematobium Infection in Enwan Community, Edo State, Nigeria. AASCIT Journal of Health. 4 (4): 31-37.
[10]
Arora DR., Arora B. (2005). Trematodes or Flukes” in Review of Medical Parasitolgy (2nd edition). CBS publishers and distributions New Delhi, India Pp 151-155.
[11]
Abath FG., Morais CN., Montenegro CE., Wynn YA., Montenegro SM. (2006). Immunopathogenic mechanisms in schistosomiasis: what can be learnt from human studies? Trends. Parasitology 22: 85-91.
[12]
Brant SV., Morgans JAT., Mkoyi GM., Snyder SD., Rajapakse RPVJ., Lokers ES. (2006). “An approach to revealing blood fluke life cycles, taxonomy and diversity” Journal of Parasitology. 92 (1): 77-88.
[13]
Chessbrough M. (2005). Medical Laboratory Manual for tropical Countries. Cambridge University press. 221-251.
[14]
Doenhoff MJ., Cioli D., Utzinger J. (2008). Praziquantel mechanisms of action, resistance and new derivatives for schistosomiasis. Current Opinion Infectious Diseases. 21: 659-667.
[15]
Nagvi R., Ahmed E., Akhtar F., Nagvi A., Rizvi A. (2003). Outcome in severe acute renal failure associated with schistosomiasis. Nephrology Dialysis Transplantation. 18: 1820-1823.
Open Science Scholarly Journals
Open Science is a peer-reviewed platform, the journals of which cover a wide range of academic disciplines and serve the world's research and scholarly communities. Upon acceptance, Open Science Journals will be immediately and permanently free for everyone to read and download.
CONTACT US
Office Address:
228 Park Ave., S#45956, New York, NY 10003
Phone: +(001)(347)535 0661
E-mail:
LET'S GET IN TOUCH
Name
E-mail
Subject
Message
SEND MASSAGE
Copyright © 2013-, Open Science Publishers - All Rights Reserved