Published in IJCP March 2024
Review Article
Pattern of Glomerulonephritis in Nigeria and Challenges Faced in Treating It
March 11, 2024 | Sotubo Sotomiwa, Sourabh Sharma, Amisu Mumuni, Odeyemi Ayoola
Nephrology
     


Abstract

Glomerulonephritis is one of the leading causes of chronic kidney disease in Nigeria. The pattern of glomerulonephritis is said to be different from other parts of the world which can be attributed to the prevalence of APOL1 gene in the black population and prevalence of tropical diseases. Treating glomerulonephritis in Nigeria can be challenging due to poor awareness and understanding of the disease, limited access to health care facility and lack of trained nephrologist. Possible solutions to this problems include creating awareness and education of the populace, partnering with NGOs to subsidize treatment and training of Nephrologist.

Keywords: Challenges, patterns, glomerulonephritis, Nigeria

Glomerulonephritis (GN) is a disease that affects the kidneys, specifically the glomeruli, which are the tiny blood vessels that filter waste and excess fluids from the blood.1 The disease is common in Nigeria, where it is one of the leading causes of chronic kidney disease (CKD).2,3 The pattern of GN in Nigeria is distinct from that in other parts of the world, and treating it presents several challenges. Here is what you need to know.

PATTERN OF GLOMERULONEPHRITIS IN NIGERIA

Glomerulonephritis in Nigeria has a unique pattern compared to other parts of the world. According to studies, the most common type of GN in Nigeria is focal segmental glomerulosclerosis (FSGS).3,4 In contrast, IgA nephropathy is the most common type of GN in many other parts of the world.5,6

There are several factors that contribute to the unique pattern of GN in Nigeria. These include genetic factors, infectious diseases and environmental factors such as exposure to toxins and pollutants.4

More than 600 genes have been implicated in kidney diseases such as FSGS, IgA nephropathy and membra­nous nephropathy just to mention a few.7

Of note is the APOL1 gene, which is associated with increased risk of CKD and is predominantly higher in Blacks.7,8

In a study done by Kopp et al, it was seen that APOL1 gene increased the risk of FSGS by 17 folds, risk of human immunodeficiency virus-associated nephro­pathy (HIVAN) by 29-fold along with rapid progression to end-stage kidney disease (ESKD).9

Infections like HIV, tuberculosis, hepatitis B and C are said to be endemic in Africa, especially in Nigeria,10-12 which can lead to HIVAN, renal amyloidosis, membra­nous and membranoproliferative GN, respectively.13-16 Tropical diseases like schistosomiasis, onchocerciasis and lymphatic filariasis have also been associated with membranoproliferative GN.17,18

In some areas of Nigeria like Yobe, exposure to toxins and heavy metals has been shown to correlate with the incidence of CKD in the region.19 Ojo et al20 found the same trend among CKD patients attending outpatient clinic at Owo; hence, advocating that the sources of this exposure be identified and eliminated.

CHALLENGES FACED IN TREATING GLOMERULONEPHRITIS IN NIGERIA

Treating GN in Nigeria presents several challenges. The following are some of the most significant challenges (Table 1).

Table 1. Challenges Faced in Treating GN in Nigeria

Challenges

Limited access to health care

Lack of trained nephrologists

Limited availability of medications

Poor awareness and understanding of the disease

Poor infrastructure

  • Limited access to health care: Access to health care is limited in many parts of Nigeria, particularly in rural areas.21,22 This makes it difficult for patients with GN to receive timely and appropriate care, which can lead to complications and worsen the prognosis.23
  • Lack of trained nephrologists: There is a severe shortage of trained nephrologists in Nigeria, which makes it challenging to provide specialized care for patients with GN.24 Many patients are treated by general practitioners who may not have the expertise or experience to manage the disease effectively.25
  • Limited availability of medications: The cost of medications is a significant barrier to treatment in Nigeria. Many patients cannot afford to buy the drugs they need, and even when the medications are available, they may be of poor quality or counterfeit.26 Drugs like tacrolimus, mycophenolate mofetil (MMF), cyclosporine and rituximab used in some cases of GN, are expensive for the average Nigerian patients, who need it for treatment.
  • Poor awareness and understanding of the disease: There is limited awareness and understanding of GN among the general population and even some health care professionals in Nigeria. This can lead to delayed diagnosis and inappropriate treatment, which can worsen the prognosis.25,27
  • Poor infrastructure: The health care infrastructure in Nigeria is inadequate, with many hospitals lacking the necessary equipment, facilities and personnel to provide quality care.28

Kidney biopsy is critical in the diagnosis of GN; unfortu­nately the cost of procedure and standard histologic analysis makes it impossible for many patients to be able to afford it.29 This can hinder the delivery of appropriate treatment for patients with GN.

Genetic testing should be considered in patients with a positive family history, early age of onset of renal impairment and presence of extrarenal symptoms as they have a high likelihood of having a monogenic kidney disease.7

However, genetic testing facilities are not readily available and expensive in our environment.30 Early diagnosis with genetic testing has been shown to be helpful in showing down progression of CKD and also donor workup in high-risk families; however, our patients are not able to benefit from its advantages.7

WHAT IS THE WAY FORWARD?

Kidney Biopsy

With political will and relationship with sister organiza­tions, standard local laboratories that can analyze kidney biopsy samples using at least 2 out of the 3 recommended methods (light microscope, immunofluorescence, elec­tron microscope), will go a long way in reducing cost. This will put a stop to sending samples out of Nigeria for analysis, which comes with a huge cost.

Government should encourage local industries to make the biopsy needles locally to also reduce cost. Increasing the number of biopsies done yearly will go a long way in improving the skills of the nephrologists and also presents an opportunity to train nephrology trainees.

Immunosuppressive Medications

Till date, drugs like tacrolimus, MMF, rituximab and many more, are shipped into Nigeria as it is not yet locally manufactured by pharmaceutical companies in Nigeria. Because of the increasing use of these medications and the increasing number of kidney transplants,31 govern­ment should support local pharmaceutical companies in partnering with international organizations to set up companies that can manufacture these drugs locally.28

Inaxaplin, a novel small molecule inhibitor of APOL1 channel has been demonstrated to reduce proteinuria in patients with APOL1-associated FSGS.32

This is likely to have impact on the incidence of GN; however, cost will remain a major barrier in getting it across to patients in Nigeria that will benefit from it.

AWARENESS AND TARGETED EDUCATION

Awareness and education by the nephrology community is key so as to improving health seeking behavior of the population and raise the index of suspicion of non-nephrologist for prompt referral of GN patients to the nephrologist.

CONCLUSION

In conclusion, the pattern of GN in Nigeria is distinct from that in other parts of the world, and treating it presents several challenges. Limited access to health care, a shortage of trained nephrologists, limited availa­bility of medications, poor awareness and under­standing of the disease and poor infrastructure are some of the challenges that need to be addressed to improve the management of GN in Nigeria. Addressing these challenges will require a concerted effort from policymakers, health care professionals and the general public.

REFERENCES

  1. Stahl RA, Hoxha E. Glomerulonephritis. Dtsch Med Wochenschr. 2016;141(13):960-8.
  2. Odubanjo MO, Oluwasola AO, Kadiri S. The epidemiology of end-stage renal disease in Nigeria: the way forward. Int Urol Nephrol. 2011;43(3):785-92.
  3. Umeizudike TI, Awobusuyi JO, Amira CO, Bello TB, Mabayoje MO, Adekoya AO, et al. Renal histology patterns in a prospective study of nephrology clinics in Lagos, Nigeria. Clin Nephrol. 2016 Suppl 1;86(2016)(13):119-22.
  4. Ekrikpo UE, Obiagwu PN, Udo AI, Chukwuonye II, Noubiap JJ, Okpechi-Samuel US, et al. Prevalence and distribution of primary glomerular diseases in Africa: a systematic review and meta-analysis of observational studies. Pan Afr Med J. 2023;45:153.
  5. Soares MF, Roberts IS. IgA nephropathy: an update. Curr Opin Nephrol Hypertens. 2017;26(3):165-71.
  6. Schena FP, Nistor I. Epidemiology of IgA nephropathy: a global perspective. Semin Nephrol. 2018;38(5):435-42.
  7. KDIGO Conference Participants. Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference. Kidney Int. 2022;101(6):1126-41.
  8. Freedman BI, Moxey-Mims MM, Alexander AA, Astor BC, Birdwell KA, Bowden DW, et al. APOL1 Long-term Kidney Transplantation Outcomes Network (APOLLO): Design and Rationale. Kidney Int Rep. 2020;5(3):278-88.
  9. Kopp JB, Nelson GW, Sampath K, Johnson RC, Genovese G, An P, et al. APOL1 genetic variants in focal segmental glomerulosclerosis and HIV-associated nephropathy. J Am Soc Nephrol. 2011;22(11):2129-37.
  10. Awofala AA, Ogundele OE. HIV epidemiology in Nigeria. Saudi J Biol Sci. 2018;25(4):697-703.
  11. Ugwu KO, Agbo MC, Ezeonu IM. Prevalence of tuberculosis, drug-resistant tuberculosis and HIV/TB co-infection in Enugu, Nigeria. Afr J Infect Dis. 2021;15(2):24-30.
  12. Odukoya OO, Odeyemi KA, Odubanjo OM, Isikekpei BC, Igwilo UU, Disu YM, et al. Hepatitis B and C seroprevalence among residents in Lagos State, Nigeria: apopulation-based survey. Niger Postgrad Med J. 2022;29(2):75-81.
  13. Husain NE, Ahmed MH, Almobarak AO, Noor SK, Elmadhoun WM, Awadalla H, et al. HIV-associated nephropathy in Africa: pathology, clinical presentation and strategy for prevention. J Clin Med Res. 2018;10(1):1-8.
  14. Yoo JJ, Lee JH, Yoon JH, Lee M, Lee DH, Cho Y, et al. Hepatitis B virus-related glomerulonephritis: not a predo­minant cause of proteinuria in Korean patients with chronic hepatitis B. Gastroenterol Res Pract. 2015;2015:126532.
  15. Muneer A, Macrae B, Krishnamoorthy S, Zumla A. Urogenital tuberculosis - epidemiology, pathogenesis and clinical features. Nat Rev Urol. 2019;16(10):573-98.
  16. Nayak S, Kataria A, Sharma MK, Rastogi A, Gupta E, Singh A, et al. Hepatitis C virus-associated membranopro­liferative glomerulonephritis treated with directly acting antiviral therapy. Indian J Nephrol. 2018;28(6):462-4.
  17. Seck SM, Sarr ML, Dial MC, Ka EF. Schistosoma hemato­bium-associated glomerulopathy. Indian J Nephrol. 2011;
    21(3):201-3.
  18. van Velthuysen ML, Florquin S. Glomerulopathy asso­ciated with parasitic infections. Clin Microbiol Rev. 2000;13(1):55-66, table of contents.
  19. Amshi SA, Iliya I, Adamu A. Chronic kidney disease associated with heavy metals (Cr, Pb, Cd) analyzed from irrigation water of Gashua, Yobe, Nigeria. IOSR J Appl Chem. 2019;12(5):43-8.
  20. Ojo O, Adenuga A, Ojo OA, Ariyo O, Arogundade F, Balogun R. WCN23-1150 Evaluation of toxic metals and essential elements in CKD patients from Owo a semi urban city in Southern Nigeria. Kidney Int Rep. 2023;8(3):S183.
  21. McKing IA, Ifunanya CE. Improving access, quality and efficiency in health care delivery in Nigeria: a perspective. PAMJ-OH. 2021;5(3).
  22. Vivien OA. Poor Health care access in nigeria: a function of fundamental misconceptions and misconstruction of the health system. In: Ayse Emel Ö (Ed.). Healthcare Access. Rijeka: IntechOpen; 2022. p. Ch. 8.
  23. Lewis G, Maxwell AP. Timely diagnosis and treatment essential in glomerulonephritis. Practitioner. 2015;259
    (1779):13-7, 2.
  24. Okoye O, Mamven M. Global dialysis perspective: Nigeria. Kidney 360. 2022;3(9):1607-10.
  25. Agaba EI, Agaba PA, Dankyau M, Akanbi MO, Daniyam CA, Okeke EN, et al. Specialist physician know­ledge of chronic kidney disease: acomparison of internists and family physicians in West Africa. Afr J Prim Health Care Fam Med. 2012;4(1):319.
  26. Johnston A, Holt DW. Substandard drugs: a potential crisis for public health. Br J Clin Pharmacol. 2014;78(2):218-43.
  27. Oluyombo R, Ayodele OE, Akinwusi PO, Okunola OO, Gbadegesin BA, Soje MO, et al. Awareness, knowledge and perception of chronic kidney disease in a rural community of South-West Nigeria. Niger J Clin Pract. 2016;19(2):161-9.
  28. Sotubosotomiwa O, Olugbenga Awobusuyi J, Sharma S. Etiology of chronic kidney disease in Nigeria and management challenges. Indian J Clin Pract. 2023;33(9):10-4.
  29. Okani CO, Ekrikpo UE, Okolo CA, Asinobi AO, Salako B, Akang EE. Is the art of renal biopsy on the decline in Nigeria? Ann Ibadan Postgrad Med. 2014;12(1):38-41.
  30. Adeyemo AA, Amodu OK, Ekure EE, Omotade OO. Medical genetics and genomic medicine in Nigeria. Mol Genet Genomic Med. 2018;6(3):314-21.
  31. Arogundade FA. Kidney transplantation in a low-resource setting: Nigeria experience. Kidney Int Suppl (2011). 2013;3(2):241-5.
  32. Vasquez-Rios G, De Cos M, Campbell KN. Novel therapies in APOL1-mediated kidney disease: from molecular pathways
    to therapeutic options. Kidney Int Rep. 2023;8(11):2226-34.