A clinico-pathological study of lupus nephritis based on the International Society of Nephrology-Renal Pathology Society 2003 classification system.

INTRODUCTION: Lupus nephritis (LN) is a major complication of systemic lupus erythematosus (SLE). Renal involvement is a major determinant of the prognosis of SLE. The histological classification of LN is a key factor in determining the renal survival of patients with LN. Prompt recognition and treatment of renal disease are important, as early response to therapy is correlated with better outcome and renal biopsy plays an important role in achieving this.
OBJECTIVES: The objective of this study was to correlate the clinical and laboratory findings with histopathological classes of LN as per the 2003 International Society of Nephrology-Renal Pathology Society (ISN/RPS) classification system. PATIENTS AND METHODS: Fifty-six patients with SLE, undergoing a renal biopsy for renal dysfunction were studied. The comparison of data from multiple groups was made by Pearson's Chi-square test and between two groups by independent samples t-test. The values of P < 0.05 were considered statistically significant.
RESULTS: Of the 56 cases studied, 51 (91.1%) were females. The most common presenting symptoms were edema, arthralgia, and hypertension. Class IV (55.4%) was the most common class. Thirty-nine (69.6%) cases showed full house immunostaining. Hypertension, hematuria, proteinuria, and tubulo-interstitial disease showed a significant correlation (P < 0.05) with ISN/RPS classification, 2003.
CONCLUSION: Assessment and management of patients with suspected LN are greatly facilitated through information obtained by renal biopsy. Since renal morphology may predict long-term prognosis, and no clinical or laboratory feature uniformly predicts prognosis, it is important to study the constellation of features in LN for better patient management.

Introduction

Lupus nephritis (LN) is one of the most common manifestations of systemic lupus erythematosus (SLE), occurring in about 50%–70% of the patients, and is the major cause of morbidity and mortality in the SLE population. The clinical course of LN is heterogeneous and varies from subclinical disease to an aggressive course that may rapidly progress to end stage renal disease (ESRD). The nature and severity of the clinical features of LN do not always predict the underlying histological severity. Nevertheless, certain histological and clinical parameters have been associated with poor renal survival.[1]

Kidney biopsy is the main-stay for the diagnosis of LN. Material obtained by renal biopsy is evaluated by light microscopy (LM), immunofluorescence (IF), and electron microscopy. In many cases, renal biopsy is instrumental in establishing the diagnosis of LN.[2]

The histopathological manifestations of LN are classified into several categories, originally designated by the WHO in 1982. These have recently evolved under the auspices of both the International Society of Nephrology and the Renal Pathology Society (ISN/RPS).[3] The general structure includes six principal pathological patterns (Classes I–VI).[4]

Although clinical variables such as the elevation of serum creatinine, nephrotic syndrome at presentation, persistent elevations of blood pressure, low hematocrit, hypocomplementemia, and presence of anti-dsDNA antibodies have prognostic value, the histological information obtained from biopsies, the most important of which are the presence of crescents and interstitial fibrosis, continues to be indispensable in enhancing outcome prediction.[4]

Although certain histological and clinical parameters have been associated with poor renal survival, the results have been diverse due to difference in the population studied, sample size, selection criteria, and outcome variables chosen in different studies.[1] It is therefore, relevant to document the clinico-pathological features of various patterns of renal diseases in SLE patients, in a south Indian tertiary care center.

Patients and Methods

This was a cross-sectional study conducted in the Departments of Pathology and Nephrology, JSS Medical college hospital, JSS University, Mysore for a period of 2½ years. A total of 56 patients were studied and included, undergoing a renal biopsy during the course of their clinical care as determined by their treating nephrologists. The definitive diagnosis of LN was based on clinical and laboratory findings and finally by LM and IF study. Ethical clearance from the Institutional Ethical Committee was obtained.

Data were collected as per the case report form. Preliminary investigations were performed as per the standard care at our institute. An informed consent before renal biopsy was taken from all patients. Renal biopsy was performed under local anesthesia using 2% lignocaine with an automated gun (Bard Company) and disposable needles. Two cores were taken. The tissue was placed in 10% formalin for light microscopic (LM) examination and in saline for IF studies. For LM, multiple step serials (32) from renal core were stained and studied using hematoxylin and eosin, periodic acid Schiff, Masson's trichrome stain, and Jones silver methanamine stain. For IF, the biopsy specimens were washed in phosphate-buffered saline (PBS) thrice followed by embedding the tissue for frozen section in optimum cutting temperature medium. Once the tissue was frozen, 2–3 micron thin sections were cut. One to two sections were layered on each slide and were labeled as IgG, IgA, IgM, C3, C1q, kappa, and lambda. The slides were then stained with fluorosceinisothiocynate labeled anti-human antibodies of IgG, IgA, IgM, C3, C1q, kappa, and lambda light chains (DACO), respectively. The slides were then incubated for an hour at 37°C. After incubation the slides were again washed thrice with PBS, mounted with glycerin and viewed under immunofluorescent microscope-Olympus BX 41.

Statistical evaluation

The statistical analyses were performed using statistical package for social sciences (IBM SPSS Statistics for Windows, Version 21.0. Armonk, NY: IBM Corp) computer program. All continuous variables were expressed as mean ± standard deviation and categorical variables were presented as percentage. The comparison of data from multiple groups was made by Pearson's Chi-square test and between two groups by independent samples t-test. P < 0.05 were considered statistically significant. Graphs were generated using Microsoft excel 2013.

Results

During the study, a total of 56 patients with biopsy proven LN were reviewed. The baseline data at the time of renal biopsy is given in Table 1.

Table 1

Baseline data at the time of renal biopsy

In this study, the age range was from 9 to 55 years with a mean age of 28.05 ± 10.30 years. The maximum number of cases was found to be in the range of 21–30 years. Fifty-one out of 56 patients (91.1%) of the patients were females and five patients (8.9%) were males with a male to female ratio of 1:10.2.

The most common clinical features consistent with SLE seen in this study were hematological abnormalities in 34 (60.71%) (anemia [<11 g/dl], leukopenia [<4,000 cells/cumm] or thrombocytopenia [<1 lakh platelets/cumm]), followed by edema in 26 (46.4%) and hypertension in 23 (41%) patients. Skin lesions, malar rash, oral ulcers, joint pains suggestive of arthritis, pregnancy related complications in the form of history of recurrent pregnancy loss, anti-phospholipid antibody syndrome were seen and neurological disorder in the form of optic neuritis was noted. There was a statistically significant association (P = 0.007) of hypertension with ISN/RPS, 2003 classification of LN.

Classes of LN showed statistical significance with proteinuria and hematuria. No statistical significance was seen between classes of LN and anemia, serum creatinine or blood urea nitrogen [Table 2].

Table 2

Renal function values in International Society of Nephrology-Renal Pathology Society classification of lupus nephritis, 2003

Renal function was categorized by the level of serum creatinine (mg/dl) as follows: Normal-mild renal insufficiency (<1.5), moderate renal insufficiency (1.5–3.0), and advanced renal insufficiency (≥3.0). Renal insufficiency did not show any statistical significance (P = 0.095) with classes of LN [Table 3]. However, it showed a statistically significant correlation with hypertension (P = 0.015), with hypertensive patients having poorer renal function.

Table 3

Renal insufficiency-class wise distribution

In this study, information on ANA was available for 55 patients of whom 54 (98.18%) patients were positive. Anti-dsDNA was positive in 39 (88.63%) patients in 44 patients for whom data were available.

Renal biopsies from these patients were studied and on the basis of the histopathological and IF studies, were divided into the Classes I to VI according to the ISN/RPS, 2003 classification of LN [Figure 1]. Majority of the patients, that is, 31 (55.4%) belonged to Class IV [Figure 2 and Table 4]. The class-wise distribution of various histopathological parameters is given in Table 5. Serum creatinine showed a statistical significance with tubular atrophy and interstitial fibrosis (P = 0.032) as well as tubulo-interstitial inflammation (P = 0.000).

Figure 1

(a) Class II lupus nephritis – mesangial cell hypercellularity (periodic acid schiff ×200). (b) Class III lupus nephritis – focal and segmental glomerulonephritis (periodic acid schiff ×100). (c) Class V lupus nephritis – thickened glomerular basement membrane (periodic acid schiff ×100). (d) Class VI lupus nephritis - >90% glomerular sclerosis (Masson's trichrome stain ×100)

Figure 2

(a) Class IV lupus nephritis – endocapillary proliferation with wireloop lesions (periodic acid schiff ×200). (b) Class IV lupus nephritis – circumferential cellular crescent (Jones silver methanamine stain ×200). (c) Class IV lupus nephritis – thrombotic microangiopathy with fibrinoid necrosis of the arterioles (periodic acid schiff ×100). (d) Class IV G (A/C) lupus nephritis – two proliferative glomeruli and three sclerotic glomeruli (Jones silver methanamine stain ×100)

Table 4

International Society of Nephrology-Renal Pathology Society Classification, 2003-class distribution of patients with lupus nephritis

Table 5

Class wise distribution of the various histological parameters

Class IV was further divided into Class IV-S and IV-G. The differences between the two sub-groups are given in Table 6.

Table 6

Class IV-segmental lupus nephritis versus Class IV-global lupus nephritis

Biopsies from all 56 (100%) patients were positive for IgG. Biopsies from 43 (76.7%) patients and 52 (92.8%) patients were positive for IgA and IgM, respectively. Biopsies from 52 (96.3%) patients were positive for complement C3 deposition and for C1q deposition, each.

Thirty-nine (69.6%) biopsies showed full house staining with positivity for immunoglobulins IgG, IgA and IgM, and complements C3 and C1q [Figure 3].

Figure 3

(a) Class IV lupus nephritis – mesangial and capillary loop deposits (IgG ×100). (b) Class IV lupus nephritis – subendothelial deposits and hyaline globules (IgG ×100). (c) Class V lupus nephritis – subepithelial deposits (IgG ×100). (d) Class IV lupus nephritis – tubulo-interstitial deposits (IgG ×100)

Biopsies from 16 (28.5%) patients showed tubulo-interstitial deposits on IF. All the 16 biopsies stained positively for IgG and nine (56.25%) biopsies stained positively for C1q. Two (3.57%) biopsies showed vascular immune deposits.

Discussion

SLE is an autoimmune disease characterized by chronic immune complex formation and variable manifestations that include multiple organ involvement, accompanied by multiple laboratory abnormalities, and frequent exacerbations. Renal involvement is common in SLE and often determines the course of the disease. Nearly 50–70% of all cases of SLE have some clinical manifestation of LN, mostly glomerulonephritis.[5]

In the present study, 51 out of 56 patients (91.1%) were females with a male to female ratio of 1:10.2. This study shows a significant female predominance which is also seen in most of the studies.[1567891011] A female phenotype is the major risk factor for the development of lupus. The female:male ratio increases from 2:1 in prepubertal children up to 4.5:1 in adolescence to the 8–12:1 reported in series of adult onset patients, falling back to 2:1 in patients over 60 years of age. These data are in accord with the theory that estrogens are precipitating factors in the emergence of lupus; whereas androgens are protective.[12] The common clinical features seen in this study were consistent with other studies.[7131415]

In the present study, one patient had optic neuritis. Optic neuritis is uncommon in SLE, but may be the presenting feature of the disease. Ophthalmological and central nervous system manifestations occur in 20%–40% of patients with SLE. Involvement of the optic nerve or chiasm is rare and occurs in only 1% of patients with SLE. It is important to differentiate SLE associated optic neuritis from idiopathic optic neuritis because of the severe visual impairment and steroid dependence associated with the former. Early diagnosis and prompt treatment are important for restoring visual function in these patients.[16]

Hypertension was the most common complication encountered in this study with a significant correlation with renal insufficiency and classes of LN. Studies have shown that hypertension was associated with a poor renal function and poor outcome both at biopsy and follow-up[17] and was found to be a poor prognostic factor.[1718] Furthermore, majority of patients with Class IV LN had hypertension, which corroborates with previous studies which show that hypertension is an added insult on top of severe glomerular inflammation in proliferative LN and may hasten the disease progression.[119] These findings highlight the need for effectively treating this risk factor.

Proteinuria is one of the dominant signs of LN.[6] There was a statistically significant association between proteinuria and classes of LN with patients with Class IV LN having predominantly nephrotic range of proteinuria. Previous studies have shown that nephrotic syndrome has a significant association with Class V LN,[514] but in the present study, only one out of the four patients with Class V LN, presented with nephrotic syndrome. This could be attributed to the small number of patients with Class V LN in our study. Hematuria which showed a positive correlation with classes of LN was seen only in patients having proliferative LN (Class III and IV), a finding which is consistent with previous studies.[11]

An elevated serum creatinine level at the time of renal biopsy is associated with an increased rate of the development of renal failure and is a very strong adverse clinical prognostic indicator.[517] Serum creatinine showed a statistical significance with tubular atrophy and interstitial fibrosis as well as tubulo-interstitial inflammation, although no statistical significance was seen with classes of LN. This finding is in concordance with findings of previous studies which showed that interstitial infiltrates had prognostic value.[82021] Hill et al.[8] found interstitial inflammation to be one of the strongest histologic correlates of serum creatinine.[22]

High serum creatinine and greater degree of proteinuria indicate either severe disease presentation or a delay in the diagnosis of the disease, further emphasizing that early diagnosis, and prompt and aggressive treatment of proliferative LN is essential to improve outcomes of LN.[1]

Tubulo-interstitial inflammation by itself, whether measured in its entirety or confined to areas without atrophy or fibrosis, correlates with both renal function at biopsy and with renal survival. Therefore, the severity of interstitial nephritis serves as an independent prognostic indicator.[22]

The vast majority of patients in this study presented with Class IV LN, as has been seen in other studies and up to 40% of the patients with diffuse proliferative glomerulonephritis die or lose their renal function within 5 years after diagnosis.[5] Because of its relative severity, this is the most important form of renal disease complicating SLE.[23] This form of glomerular disease has a widely variable course[232425] and this has prompted a search for clinical and pathological factors that would enable better prognostication and management of the disease.[23242526] In Class IV LN, the glomerular involvement is diffuse with either segmental or global involvement of the glomerular tuft. This subdivision comes in significant part as the result of a study by Najafi et al.,[9] in which it was found that cases with “severe segmental” glomerular lesions, involving >50% of glomeruli (the equivalent of Class IV-S), had a worse outcome at 10 years than those with diffuse proliferative lesions involving the entire glomerular tuft (the equivalent of Class IV-G).[927] In the present study, we did not find any significant difference (P = 0.228) between classes IV-S and IV-G in terms of the development of renal insufficiency. This is consistent with other studies that have found that there was no significant difference in survival and outcome between the patients with Class IV-S and IV-G lesions at the initial biopsy.[272829]

Studies have shown that patients with LN classified as IV-G tend to have higher blood pressure, higher serum creatinine concentrations, more severe proteinuria, a higher level of anti–double-stranded DNA, lower hemoglobin levels and lower levels of C3 and C4 at baseline than do patients with Class IV-S LN. However, these differences did not always reach statistical significance.[2729] The present study showed Class IV-G patients to have a lower mean hemoglobin and higher mean serum creatinine than Class IV-S patients although there was no statistical significance. Mean proteinuria in both groups were found to be similar, although it showed statistical significance with IV-S, which is inconsistent with previous studies. This could be explained by the small sample size of the Group IV-S.

The highly variable nature of LN has prompted investigation of prognostic features that would permit identification of those at high risk of renal failure.[24] The clinical course of patients with diffuse proliferative glomerular lesions is probably influenced by the variable occurrence of certain histological features not specified by the conventional classification system of LN. Thus, detailed description of active and chronic, irreversible pathologic lesions affecting glomeruli, tubules, interstitium, and vasculature could augment the prognostic information derived from histologic classification and permit recognition of those patients with diffuse proliferative glomerulonephritis at high risk of ESRD.[2430]

In the present study, the mean activity index was 5.48 ± 4.138 and the mean chronicity index was 1.52 ± 2.374. Chronic, sclerotic lesions in glomeruli are thought to be irreversible and refractory to therapy, whereas active lesions are reversible and can respond to therapy. Concordantly, persistent urinary protein was more often observed in the chronic types than in active types. Urinary protein by itself is an important risk factor for the deterioration of renal function, which is in part a result of direct interstitial inflammation. Such a feedback loop between sclerotic lesions and urinary protein can be a mechanism toward chronic renal injury. Even in very active cases of Class IV-G, the patients’ renal outcome is favorable when the chronic lesions are absent, reiterating the importance of recording the activity and chronicity indices.[10]

It is thus recommended that patients with SLE have a kidney biopsy as soon as the clinical features of kidney involvement become evident, to hasten the treatment decisions and to minimize the risk of inflammation induced chronic kidney damage.

As in many other forms of glomerular disease, it is the distribution of deposits in the glomerular tuft that determines the proliferative response, and the glomerular lesions that result are therefore best interpreted in the context of the pattern of immune deposition. The IF staining pattern is often extremely helpful in confirming a diagnosis of LN when the diagnosis of SLE may be in doubt at the time of biopsy.[31]

The staining pattern is called “full house” when deposits containing all three immunoglobulin classes (IgG, IgM, and IgA) and both complement components (C3 and C1q) are present in LN.[31] In the present study, 39 (69.6%) of the biopsies showed full house staining.

Studies have shown that tubulo-interstitial immune deposits can be detected by fluorescence and electron microscopy in approximately 50% of patients. They occur more frequently in diffuse proliferative LN than in the focal proliferative variant, but they may also occur in some patients with membranous and mesangial proliferative forms.[31] In the present study, 16 (28.5%) biopsies showed tubulo-interstitial deposits on IF. Of the 16 biopsies, 13 (81.25%) biopsies were from patients with Class IV LN, which is consistent with previous studies.[31] The composition of the tubulo-interstitial deposits varies. Most have positive staining for IgG, with other immunoglobulins detected less frequently.[31] Complement components are associated with the immunoglobulins in most cases and occasionally may be detected in their absence,[32] suggesting a role for antibody-independent complement activation.[31] In the present study, all the16 cases were positive for IgG and nine (56.25%) biospies were positive for C1q.

Conclusion

Prompt recognition and treatment of renal disease in patients with SLE is important, as early response to therapy is correlated with better outcome. Renal biopsy provides information on the class of LN, tubular and vascular changes, activity, and chronicity indices. Class IV LN, by far has been seen to be the most important poor prognostic factor. Management goals in patients with LN include early diagnosis and appropriate therapy while preserving the overall kidney function without undue side-effects. This study which focuses on renal pathology will be an important addition to the existing literature and also provide information on the clinical utility of renal biopsy among SLE patients. Renal biopsy forms the cornerstone of management of patients with LN, as it provides invaluable information to the clinician, since approach to treatment of patients with different classes of LN is different.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.