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Journal of Clinical Medicine Research

Review

Volume 10, Number 1, January 2018, pages 1-8

HIV-Associated Nephropathy in Africa: Pathology, Clinical Presentation and Strategy for Prevention

There is a wide geographical variation in the prevalence of HIV-associated nephropathy (HIVAN); it ranges from 38% to 48.5% worldwide [1-4]. However, one of the limitations of this review is that this area is not well researched in Africa and as a result few publications are available about prevalence in African countries [1, 5]. The long use of combined antiretroviral medication (cART) has led to higher incidence of HIVAN in the recent years though a plateau was reached at its start. Middle-aged HIV-positive individuals of African ancestry showed a markedly greater possibility of developing HIVAN than their European descent counterparts [4]. In 2004, Dia reported the first case of HIVAN in Senegal in a 40-year-old black patient with fluid retention with renal edema syndrome and immunosuppressive signs, who was found to be HIV-positive with low CD4 count and no known causes of nephrotic syndrome [6].

The prevalence of HIVAN in South Africa (have the highest rate of HIV worldwide) was estimated to be around 83% among 615 HIV-infected patients screened for proteinuria in a hospital-based study, 24% had microalbuminuria and 86% of the biopsied patients showed HIVAN [5, 7]. Furthermore, the incidence of HIVAN increased from 6.6% in 2000 to 25.7% in 2009 in Cape Town [8]. The prevalence of HIVAN showed significant variation in different African nations especially in young individuals and those with short duration of HIV infection. For instance, about 6.6% out of 863 individuals with end-stage renal disease (ESRD) diagnosed in a general hospital in Cameroon over a period of 10 years were found to be HIV-positive. Importantly, these patients were noticed to be younger, more commonly to be women, to be single and unemployed [9], whilst high prevalence of HIVAN was noted in Nigeria. The estimated prevalence of HIVAN in one locality in Nigeria was estimated to be 77% and 76.7% in the age group of 21 - 40 years [10]. Alarmingly, children with HIV are not protected against HIVAN. For example, it was estimated that the prevalence of HIVAN in children in Nigeria was 31.6% and this can be associated with high mortality. Risk factors in children can be proteinuria, advanced disease, low CD4 count and the use of the highly active antiretroviral therapy (HAART) [11-14]. It seems that genetic factors may also play an important role in the development of HIVAN, as different populations in Africa showed very low prevalence of HIVAN. For instance, HIVAN was seen in only 0.8% of 338 HIV-positive patients of Ethiopian ancestry [15]. Furthermore, no single patient was found to have HIVAN among 176 HIV-infected patients in a study that included 126 Ethiopians and 50 non-Ethiopian Israelis. The authors attributed their findings to population-based differences in host genetic factors rather than to differences in HIV infection control or viral subtype [16].

Chronic kidney disease (CKD) is an important comorbidity during HIV infection. It is predominantly caused by HIVAN that has largely been detected in people of African origin [17] and HIVAN has a broad spectrum of renal manifestations. HIVAN may present with acute renal failure, proteinuria, microalbuminuria, nephrotic syndrome, chronic renal failure or high kidney echogenicity on ultra-sonographic examination. Adults with clinically non-advanced HIV disease, commonly show less severe renal impairment. Out of 526 Malawian ART-naive patients with WHO stages I or II HIV, nearly fourth (23.3%) of them had proteinuria (≥ 1+). More than half (57.4%) had reduced creatinine clearance (CrCl) (< 90 mL/min): 18.8% showed moderate (CrCl 30 - 59 mL/min) and 2.2% showed severe (CrCl < 30 mL/min) renal dysfunction. Renal biopsy studies confirmed HIVAN in 1.8-21.2%. This highlights the high benefit of assessing renal function as a routine test in HIV patients [18].

Proteinuria is commonly detected in HIV-positive patients in Nigeria. Emem et al encountered renal disease (proteinuria and/or elevated serum creatinine) in 38% out of 400 consecutive adult HIV/AIDS patients [19]. In a case-control study, Esezobor et al found that compared with 6% of the 50 controls, 20.5% of the 88 Nigerian children infected with HIV had proteinuria (P = 0.026) [14]. In another Nigerian case-control study, the mean protein excretion/24 h was significantly greater in 79 AIDS group compared to 57 controls (2.99 ± 54 g and 0.56 ± 0.12 g, respectively, P = 0.001). Inversely, controls demonstrated high levels of glomerular filtration rate (GFR) when correlated to the study group (103.30 ± 37.78 and 68.03 ± 37.55, respectively, P = 0.004). Interestingly, subjects in the AIDS group with renal disease had a significantly longer duration of illness when matched to those un-diseased (12.33 ± 8.67 months and 7.28 ± 7.78 months, respectively, P = 0.008) [20].

Moreover, microalbuminuria was detected in 28.8% of Tanzanian HIV-infected children at a medical center. Microalbuminuria was considerably connected to the degree of HIV disease progression according to WHO disease stage (P = 0.0015) and a reduced amount of CD4 count, below 350 cells/µL (P = 0.044). Therefore, to decrease the risk of emerging ESRD, early screening and treatment of microalbuminuria is required, especially for those at high risk (advanced HIV disease and those with a CD4 count below 350 cells/µL). Urinary albumin screening can be done in a situation where routine screening for microalbuminuria is not available [21].

Nonetheless, the nephrotic syndrome represented the most common clinical manifestations of HIVAN in childhood in KwaZulu-Natal, South Africa [22]. Hematological, electrolyte abnormalities and renal impairment were documented in 86.4%, 69.4% and 41% of patients, respectively on initial presentation [22]. However, ESRD was present in only 4% of these patients [22]. HIV nephropathy was also reported in 15% of nephrotic Black African adults in a hospital in Abidjan [23]. At a University Hospital in South West Nigeria, out of 10 kidney disease HIV-infected children, four presented with acute kidney injury (AKI), three with nephrotic syndrome and two with chronic renal failure. One patient had left renal artery stenosis [24]. Moreover, HIVAN was seen in 42.8% of 294 adult black South Africans with the biopsy-proven cause of nephrotic syndrome in Cape Town in 10 years duration and thought to be accountable for the growing prevalence of ESRD in Africa [25]. Furthermore, proteinuria in the nephrotic range was the predominant clinical indication for a renal biopsy at a single hospital in Cape Town, representing 52.5% out of 1,284 renal biopsies, followed by acute renal failure (21.3%), and then asymptomatic urinary abnormalities (13.6%). Other indications included chronic renal failure (6.4%), acute nephritic syndrome (5.8%) and hematuria (0.3%) [25]. Nevertheless, non-nephrotic proteinuria was the initial clinical presentation of HIV-associated renal disease in 54% and nephrotic syndrome in 23% of African HIV patients. The other clinical manifestations were acute kidney injury and chronic kidney disease in 28% and 22%, respectively as stated in that study [26].

Using sonographic characterization of 302 HIV/AIDS subjects prospectively for 22 months in Plateau State, Nigeria, 77.7% of them showed augmented renal echogenicity displaying a high rate of renal disease among them, and 76.7% of the patients were in the age group 21 - 40 years [10]. Table 1 [10, 14, 18-22, 25, 26] provides summary of common presentations of HIVAN. Therefore, regular monitoring of renal function should be part of routine investigation for HIV patients.

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Table 1. Different Clinical, Radiological and Biochemical Presentations of HIVAN [10, 14, 18-22, 25, 26]

CKD in HIV patients may take place as a consequence of HIV infection, other co-morbid illnesses as well as a result of therapy-related complications. Regardless of the cause, a variety of renal pathological lesions are seen in renal biopsies obtained from patients with HIV-CKD; commonly HIVAN, the aggressive collapsing form; HIV-immune complex disease; focal segmental glomerulosclerosis (FSGS) and rarely thrombotic microangiopathy [1, 26]. Membranous nephropathy has also been described [24]. The introduction of antiretroviral therapy (ART) leads to a change in the pattern of CKD with an increasing prevalence of FSGS and decline in the incidence of HIVAN [1].

The main renal pathological lesions of 61 HIV patients were found to be FSGS, mainly the collapsing form HIVAN in 28%, acute interstitial nephritis (AIN) in 26% and immune complex-mediated glomerulonephritis (ICGN) in 25% of the cases in Brazil. Baseline CD4 cell count ≥ 200 cells/mm³ proved to be a protective factor against CKD (hazard ratio = 0.997; 95% confidence interval (CI): 0.994 - 0.999; P = 0.012) after 24 months follow-up [27].

Similarly, FSGS was the most common histopathological finding which was seen in 32 (65.3%) HIV-infected South African children; 13 (26.5%) had collapsing glomerulopathy and 19 (38.8%) had classic FSGS [22].

Acute kidney injury seems to have mostly acute tubular necrosis owing to sepsis, dehydration, and nephrotoxic drugs [5]. Chronic granulomatous tubulo-interstitial nephritis has also been reported in a patient infected with HIV type-1 and receiving ritonavir-boosted atazanavir [28]. Acute kidney injury in HIV-positive patients, mainly as a consequence of acute tubular necrosis, is thought to arise from a combination of hemodynamic, immunological, and toxic insult [29].

In Uganda, eosinophilic endocapillary proliferative glomerulonephritis (GN) was found to be the most frequent histological finding. It was reported in 27/41 cases [30].

Biopsy findings of seven patients with persistent microalbuminuria in a South African single center showed HIVAN in 86%, membranoproliferative nephropathy in two (7%) and interstitial nephritis in three (10%), while membranous nephropathy was seen in four patients with HIVAN [7].

In a retrospective study of 99 biopsies for HIV-positive patients in South Africa, the leading histologic types were “classic HIVAN” (27%) and HIV immune complex kidney disease (HIVICK) (21%). Other glomerulonephritides encompassed membranous, post-infectious disease, mesangial hyperplasia, and immunoglobulin A nephropathy. While in the HIV-negative group collapsing FSGS and non-specific immune complex disease were not seen, but increased cases of minimal change and membranoproliferative disease [31].

HIVAN is mediated by factors related to the virus, host genetic predisposition and environmental factors. The mechanisms responsible for HIVAN include HIV infection of podocytes and tubular epithelial cells, the molecules accountable for HIV entry, and diverse mechanisms of cell injury [26]. Disease phenotype may be influenced by host response to HIV infection through activation of cytokine pathways [1].

Viral replication and interstitial inflammation play central roles in the pathogenesis of HIVAN. To understand how HIV replication initiates HIVAN, Chen et al in 2016 determined the cellular response of renal tubule epithelial cells (RTECs) to HIV by inspecting the transcriptional profiles of primary RTECs when exposed to T cells, some infected and others not infected with HIV. An innate response to HIV, which further was sub-classified by gene ontology biological process terms, was noticed when HIV-induced gene expression in hRTECs was examined in vitro by Illumina RNA deep sequencing. Their results showed that as compared with cell-free virus infection, exposure to HIV-infected T cells elicited a stronger upregulation of genes responsible for inflammation and immune response, largely the chemokine/cytokine families. They include inflammatory cytokines CCL20, IL6 and IL8-related chemokines: IL8, CXCL1, CXCL2, CXCL3, CXCL5 and CXCL6. They concluded that interactions between primary RTECs and HIV-infected T cells result in the potent induction of inflammatory response genes and release of cytokines/chemokines from RTECs that can invite extra T cells. Triggering of these genes means an innate response to HIV by non-immune cells [32].

Recently, pyroptosis, a new type of programed cell death, was thought to be induced by HIV in T lymphocytes through the generation of Nod-like receptor protein 3 (NLRP3) inflammasome complexes. Hague et al (2016) assessed the role of HIV in podocyte NLRP3 inflammasome formation both in vivo and in vitro. Their results revealed that renal cortical slices of HIV-transgenic mice (Tg26) demonstrated amplified expression of NLRP3, ASC (a CARD protein), caspase-1, and IL-1beta proteins, approving the formation of NLRP3 inflammasome complex in podocytes of Tg26 mice. Boosted mRNA levels and protein expressions of inflammasome markers (NLRP3, ASC, and caspase-1, and IL-1beta) were also demonstrated in renal tissues of Tg26 mice. Serum of Tg26 mice also showed elevated concentrations of IL-1beta cytokine compared with FVBN mice. Pyroptosis was induced within podocytes by HIV in a dose- and time-dependent way, representing a phenotype of inflammasome activation. They found that caspase-1 inhibitor not only reduced podocyte expression of caspase-1 and IL-1beta but further provided protection against pyroptosis. This suggests that HIV-induced podocyte injury was facilitated by caspase-1 activation. Interestingly, they instituted that podocyte pyroptosis induced by HIV could be partially inhibited by Tempol (a superoxide dismutase-mimetic agent) and by glyburide (an inhibitor of potassium efflux). Therefore, generation of reactive oxygen species and potassium efflux play a role in HIV-induced pyroptosis and activation of the NLRP3 inflammasome in podocytes [33].

Experimental studies mapped a major HIVAN susceptibility locus (HIVAN1) to chromosome 3A1-A3 in a cross between HIV-1 transgenic mice on the FVB/NJ background (TgFVB) which is a documented model of HIVAN and CAST/EiJ (CAST) strains, and introgression of a 51.9 Mb segment covering HIVAN1 from CAST into TgFVB caused enhanced progress of nephropathy. So, dormant molecular disorders may lead to nephropathy when exposed to HIV-1 [34].

It has been suggested that genetic factors play a crucial role in the pathogenesis of HIVAN [4, 35]. Purswani et al reported a 3.5-fold higher odds of CKD in patients carrying high-risk APOL1 genotypes in a nested case-control study of 451 PHIV contributors in the Pediatric HIV/AIDS Cohort Study. They also reported a unadjusted incidence of 1.2 CKD cases/100 person-years (95% CI: 0.5 - 2.5) in PHIV youth carrying APOL1 high-risk variants, with imperative connotations for sub-Saharan Africa [36]. The alleles that were more implicated as risk factors for CKD in individuals of African descent are APOL1 G1 and G2 rather than the previously examined MYH9 E1 risk haplotype.

About half of African Americans with two APOL1 risk alleles, if untreated, would develop HIVAN. However, it has been perceived that these two variants are not enough to cause disease. The predominant faith is that modifying factors or second hits (including genetic hits) lie beneath the pathogenesis of kidney disease [35].

In 120 patients with HIVAN and CKD and 108 controls from a South-African black population, Kasembeli et al found that 79% of patients with HIVAN and 2% of the controls carried two risk alleles (APOL1 G1 and G2 variants). Their study exposed that individuals possessing any combination of two APOL1 risk alleles had 89-fold increased odds (95% CI: 18 - 912; P < 0.001) of developing HIVAN when related to HIV-positive controls [37].

Although the two risk alleles were significantly connected to higher odds of HIVAN, APOL1 genotype did not predict confidently this specific histopathology and cannot eliminate the important role of kidney biopsy in the clinical care of HIV-positive blacks who are with proteinuria more than 3.5 mg/24 h urine or unexplained kidney disease [38]. The findings of Da Silva et al in 2016 also strengthen the importance of renal biopsy in HIV patients with kidney impairment and/or proteinuria [27].

Nevertheless, the rates of the APOL1 G1 and G2 variants among Ethiopians are significantly and dramatically lower than those observed among HIV-infected African-Americans, African-Americans and West Africans explaining the lack of HIVAN among HIV patients of Ethiopian ancestry [15]. On the other hand, even though birth in a sub-Saharan African (SSA) country was ominously related to baseline CKD, Schoffelen et al reported that it had no influence on newly evolving CKD upon a time. In their large Dutch AIDS Therapy Evaluation in the Netherlands (ATHENA) cohort, authors found that patients of SSA origin and those born in Western Europe, Australia, or New Zealand had a similar risk of newly emerging CKD (adjusted hazard ratio, 1.00; 95% CI: 0.63 - 1.59). However, they followed the patients for a median duration of only 4.7 years [17].

Booth et al described the renal pathology of HIV-associated immune complex kidney (HIVICK) disease and compared the clinical characteristics of patients with HIVICK (65 patients) with those with IgA nephropathy (27 patients) and HIVAN (70 patients) in a multicenter study. Their results revealed that black ethnic background and HIV RNA were related to HIVICK, use of ART with IgA nephropathy and black ethnicity and CD4 cell count with HIVAN. It also showed that HIVICK was linked to lower rates of end-stage kidney disease progression in comparison with HIVAN and IgA nephropathy (P < 0.0001). They suggested a pathogenic role for HIV replication in the development of HIVICK and that ART may recover kidney function in patients who have noticeable HIV RNA at the time of HIVICK diagnosis [39].

The epidemiology of HIV-related CKD has been changed with the advent of cART in the mid-1990s. With the era of prevalent use of cART and the aging of HIV population, a change has been observed in the scales of HIV-related CKD. HIVAN is becoming rare in patients under medical care, and the problem of comorbid disease is growing [5, 40].

Surprisingly, HIV-1 particles were detected into continuous ambulatory peritoneal dialysis effluents of HIV-positive patients with ESRD on HAART in South Africa even in patients with suppressed plasma viral load without equivalent recognition in the paired plasma [41]. This may justify the presence of ongoing emerging kidney disease in spite of the use of HAART; however, these findings need to be taken seriously with the further assessment.

The severity of the HIV infection (based on CD4⁺ count), anemia, malnutrition and increasing age were suggested as possible risk factors for renal disease [19]. Anemia and malnutrition are widely encountered in an African population. The combination of HIV infection and poorly controlled diabetes mellitus (DM) which is common in Africa exacerbates the complications and leads frequency to nephropathy. Pillay et al reported substantial variations in the incidence of nephropathy when reviewed HIV-infected and uninfected diabetic patients with evident proteinuria (25.66% vs. 15.43%) [42].

Furthermore, the unusual pattern of CKD of the black race was partly attributed to renal lesions related to tropical diseases and they were suggested to play a significant role in the increased frequency of the CKD in sub-Saharan Africa [43]. In addition to epidemics of HIV, tuberculosis, and non-communicable disease, predominantly hypertension and diabetes have implications on the development of both CKD and acute kidney injury. This increased frequency of HIVAN in SSA may be justified by the late presentation and lack of effective screening for renal disease in HIV-positive patients. Furthermore, the definitive diagnosis necessitates a renal biopsy, which is often not possible in many regions of sub-Saharan Africa [44].

In a recent study, a small but significant decline in kidney function has been detected in patients on tenofovir with baseline estimated glomerular filtration rate (eGFR) ≥ 90 mL/min/1.73 m² [45]. In the same study, CD4 count < 200 cells/µL was shown to be significantly linked to low eGFR [45].

Govender et al determined the independent clinical risk factors for in-hospital mortality (IHM) for 690 older (aged ≥ 50 years old) HIV-infected adults from a hospital administrative database using logistic regression. Male gender (P = 0.005), CD4 count < 350 cells/mm³ (P = 0.035), unknown CD4 count (P = 0.048), tuberculosis (P = 0.033) and renal failure (P = 0.013) were considered potential risk factors for IHM [46]. Focused assessment with sonography for HIV-associated TB was considered one of the most relevant point-of-care ultrasound applications in SSA settings [47]. Management of HIVAN and other non-comunicable diseases in Africa and in low-income and middle-income countries, in general, necessitates combined clinicopathological clinics that will enable early screening, diagnosis and monitoring [48].

Prevention and management of HIVAN is summarized in Figures 1 and 2. The benefit of screening for HIVAN should be part of the routine follow tests for individuals with HIV on basis of 4 - 6 months. This should include urine for albuminuria, proteinuria and plasma test for creatinine and eGFR. Presence of proteinuria and decline in renal function should prompt treating HIV physicians to refer the patient to nephrologists according to guidelines in place. The management of risk factors that lead to HIVAN cannot be over-emphasized (Figs. 1 and 2). Therefore, researchers in the future may be able to address the following interesting points about HIVAN in Africa: 1) Prevalence and risk factors of HIVAN in other African countries. 2) Role of ethnicity in HIVAN. 3) Why the incidence of HIVAN is low in Ethopia and high in Nigeria and South Africa. 4) What is incidence and risk factors of HIVAN of African population living in Western countries. 5) Multi-center research studies will yield significant observations and help in increasing our understanding of pathognesis, management and prevention of HIVAN in African populations.

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Figure 1. Some of the risk factors that may lead to HIVAN in Africa.

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Figure 2. Possible valid strategies in management and prevention of HIVAN in Africa.

HIVAN prevalence in Africa is high. The first and common manifestation of this syndrome is proteinuria. Definite diagnosis is achieved by renal biopsy. Several risk factors were identified including diabetes, hypertension, low CD4 count, high viral load, anemia, infectious disease and malnutrition. Routine screening is important to treat and manage those at risk and risk factors like diabetes and hypertension at an early phase of the disease. Therefore, Ahmed et al suggested that metabolic clinic should be integral part of HIV services; further information about HIV metabolic clinic in Milton Keynes University Hospital, UK can be obtained from reference [49]. Further research is needed in order to enhance our understanding about how to manage and design strategy for management of HIVAN (Fig. 2).

Competing Interests

The authors declare that they have no competing interests.

Abbreviations

HIVAN: HIV-associated nephropathy; WHO: World Health Organization

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