Literature DB >> 34295040

Renal function in children infected with Schistosoma haematobium: a case-control study of an endemic Ghanaian community.

Richard K D Ephraim1, Ruth C Brenyah2, Prince Adoba1, Hope Agbodjakey1, Larissa E Allotey1, Patrick Korang1, Evans Duah1, Isaac Bogoch3, Albert Abaka-Yawson4, Christian Hotorvi1, Precious Kwablah Kwadzokpui4.   

Abstract

Schistosomiasis has been associated with kidney diseases leading to serious health problems especially in advanced cases. Most studies have used renal biopsy, and ultrasonography in the diagnosis of renal damage among urogenital schistosomiasis affected individuals. This study assessed serum urea, creatinine, and eGFR as biochemical markers of renal abnormalities in children with urogenital schistosomiasis (Schistosoma haematobium) at a resource limited setting in Sorodofo-Abaasa in the Central Region of Ghana. A case-control study was conducted among 116 basic school children aged 9 to 17 years from January 2015 to May 2015 at Sorodofo-Abaasa in the Abura Asebu Kwamankese District of the Central Region of Ghana. A pre-tested questionnaire was used to obtain information on age, sex, guardian's occupation, water contact activities, history of gross haematuria and history of medication. Participants weight and height were measured using a bathroom scale (Zhongshan Camry Electronic Co. Ltd, Guangdong-China) and a wall-mounted ruler to the nearest 0.1 kg and 0.1 cm respectively. Approximately 4 ml of venous blood sample was collected from the median cubital vein of the study participants and used for the estimation of serum urea and creatinine levels. eGFR (mL/min/1.73 m2) was calculated using the Schwartz equation. The average ages of the cases and the controls recruited in this study were 12.7 ± 1.0 and 12. ± 2.6 years respectively. The median (minimum-maximum) did not differ between cases and controls with regards to eGFR [115.92(62.40-164.98) vs 112.50(51.82-170.36; p = 0.806], serum creatinine [57.20(28.91-84.67) vs 58.19(25.17-90.21); p = 0.876], and urea [9.82(5.80-13.74) vs 10.21(7.29-13.03); p = 0.586]. Hyperfiltration though statistically similar (p = 0.787), was observed among a higher proportion of the controls (20.5%) than observed among the cases (18.4%). This study documented no significant differences between children with light (less than 50 ova per 10 ml urine) and heavy (more than 50 ova per 10 ml urine) infection. This study documented no significant variation in the biochemical markers of renal function between the cases and controls. S. haematobium Infection intensity did not significantly alter the renal physiology of the school children studied. © Indian Society for Parasitology 2020.

Entities:  

Keywords:  Renal abnormalities; Schistosoma haematobium; Urogenital schistosomiasis

Year:  2020        PMID: 34295040      PMCID: PMC8254696          DOI: 10.1007/s12639-020-01313-6

Source DB:  PubMed          Journal:  J Parasit Dis        ISSN: 0971-7196


  13 in total

1.  A population-based comparison of BMI percentiles and waist-to-height ratio for identifying cardiovascular risk in youth.

Authors:  Henry S Kahn; Giuseppina Imperatore; Yiling J Cheng
Journal:  J Pediatr       Date:  2005-04       Impact factor: 4.406

2.  On the relationship between glomerular filtration rate and serum creatinine in children.

Authors:  Hans Pottel; Felix M Mottaghy; Zahur Zaman; Frank Martens
Journal:  Pediatr Nephrol       Date:  2009-12-15       Impact factor: 3.714

Review 3.  Imaging techniques in the evaluation of morbidity in schistosomiasis mansoni.

Authors:  José Roberto Lambertucci; Luciana Cristina dos Santos Silva; Luciene Mota Andrade; Leonardo Campos de Queiroz; Vinicius Tostes Carvalho; Izabela Voieta; Carlos Maurício Antunes
Journal:  Acta Trop       Date:  2008-08-08       Impact factor: 3.112

Review 4.  Evolution of schistosomiasis-induced pathology after therapy and interruption of exposure to schistosomes: a review of ultrasonographic studies.

Authors:  J Richter
Journal:  Acta Trop       Date:  2000-10-23       Impact factor: 3.112

5.  Praziquantel treatment of school children from single and mixed infection foci of intestinal and urogenital schistosomiasis along the Senegal River Basin: monitoring treatment success and re-infection patterns.

Authors:  Bonnie L Webster; Oumar T Diaw; Mohmoudane M Seye; Djibril S Faye; J Russell Stothard; Jose C Sousa-Figueiredo; David Rollinson
Journal:  Acta Trop       Date:  2012-09-26       Impact factor: 3.112

6.  Urinary schistosomiasis in Maiduguri, north east Nigeria.

Authors:  K S Chugh; A D Harries; M H Dahniya; A C Nwosu; A Gashau; J Thomas; T D Thaliza; S Hogger; Z Ajewski; A C Onwuchekwa
Journal:  Ann Trop Med Parasitol       Date:  1986-12

7.  Comparative performance of the CKD Epidemiology Collaboration (CKD-EPI) and the Modification of Diet in Renal Disease (MDRD) Study equations for estimating GFR levels above 60 mL/min/1.73 m2.

Authors:  Lesley A Stevens; Christopher H Schmid; Tom Greene; Yaping Lucy Zhang; Gerald J Beck; Marc Froissart; Lee L Hamm; Julia B Lewis; Michael Mauer; Gerjan J Navis; Michael W Steffes; Paul W Eggers; Josef Coresh; Andrew S Levey
Journal:  Am J Kidney Dis       Date:  2010-06-16       Impact factor: 8.860

Review 8.  Schistosomiasis chemotherapy.

Authors:  Sophie A-L Thétiot-Laurent; Jérôme Boissier; Anne Robert; Bernard Meunier
Journal:  Angew Chem Int Ed Engl       Date:  2013-06-27       Impact factor: 15.336

Review 9.  Schistosomiasis and the kidney.

Authors:  Rashad S Barsoum
Journal:  Semin Nephrol       Date:  2003-01       Impact factor: 5.299

10.  Bacteriuria and urinary schistosomiasis in primary school children in rural communities in Enugu State, Nigeria, 2012.

Authors:  Okechukwu Paulinus Ossai; Raymond Dankoli; Chimezie Nwodo; Dahiru Tukur; Peter Nsubuga; Daniel Ogbuabor; Osaeloka Ekwueme; Godwin Abonyi; Echezona Ezeanolue; Patrick Nguku; Douglas Nwagbo; Suleiman Idris; George Eze
Journal:  Pan Afr Med J       Date:  2014-07-21
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