THE CLINICOPATHOLOGICAL SPECTRUM OF IGA DOMINANT/CO-DOMINANT GLOMERULONEPHRITIS DIAGNOSED AT AN ACADEMIC CENTRE IN SRI LANKA

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THE CLINICOPATHOLOGICAL SPECTRUM OF IGA DOMINANT/CO-DOMINANT GLOMERULONEPHRITIS DIAGNOSED AT AN ACADEMIC CENTRE IN SRI LANKA
Eranga
Wijewickrama
Harshima Wijesinghe harshima@path.cmb.ac.lk University of Colombo Faculty of Medicine Pathology Colombo
Fathima Nuha nuzhamedfac@gmail.com University of Colombo Faculty of Medicine Pathology Colombo
Gayani Ranaweera gayani@path.cmb.ac.lk University of Colombo Faculty of Medicine Pathology Colombo
Priyani Amarathunga priyani@path.cmb.ac.lk University of Colombo Faculty of Medicine Pathology Colombo
Champika Ratnayake champika72r@yahoo.com Medical research institute Pathology Colombo
Dilushi Wijayaratne dilushi_w@yahoo.com University of Colombo Faculty of Medicine Clinical Medicine Colombo
Rushika Lanerolle rushikal@hotmail.com University of Colombo Faculty of Medicine Clinical Medicine Colombo
Vindya Gunasekera vindyaa@hotmail.com Lady Ridgeway Hospital Nephrology Colombo
Chandu de Silva chandu@path.cmb.ac.lk University of Colombo Faculty of Medicine Pathology Colombo
 
 
 
 
 
 

IgA nephropathy is the most common primary glomerular disease in the world. There is limited data on IgA nephropathy in Sri Lanka. 

The records of all kidney biopsies reported at the Department of Pathology, Faculty of Medicine, University of Colombo Sri Lanka from 2018 to 2023 in which light microscopy (LM) and immunofluorescence (IF) results were available were reviewed. The clinicopathological details of cases that showed IgA dominance or co-dominance on IF were analysed. 

Both LM and IF  results were available in 468 of 1975 kidney biopsies handled during this period. 19.3% (n=93) showed IgA dominance/co-dominance which was the commonest IF pattern of the glomerulonephritides. 51.1%(n=47) were male. The median age was 32 years (IQR =24-44 years). Thirteen were below 16 years of age. The presentations included sub nephrotic range proteinuria(n=43;46.2%), nephrotic syndrome/nephrotic range proteinuria(n=36;38.7%), nephrotic/nephritic mixed picture (n=4;4,3%), acute kidney injury (n=5;5.3%), chronic increase in serum creatinine (n=3;3.2%) and nephritic picture (n=2;2.2%). IgA dominant GN was the second commonest cause (13.7%)  for nephrotic syndrome/nephrotic range proteinuria, second to minimal change disease. Co-existing diabetes, hypertension and systemic lupus erythematosus were present in 24.4% (n=12), 47.3% (n=43) and 10.3% (n=5) respectively. 

 

The majority showed a mesangioproliferative pattern(n=45;48.4%) on biopsy with smaller numbers showing minimal changes (n=12;12.9%), mild non-specific changes (n=7; 7.5%), an endocapillary proliferative glomerulonephritis (n=8;8.6%) and chronic changes with moderate to severe glomerulosclerosis, interstitial fibrosis and tubular atrophy (n=7;7.5%). Crescents involving less than 50% of the glomeruli were identified in 18 cases. Three  showed necrotising glomerulonephritis. Four cases were associated with IgA vasculitis and five cases were possibly infection related. Four patients showed an elevated Anti streptolysin-O-titre. The clinical presentation and morphology are summarised in Table 1. 

 

Table 1: The clinical presentation and morphological patterns of IgA dominant/co-dominant glomerulonephritis

Morphological pattern,  n (%)

Clinical presentation

Median age (years)

IQR 

Median serum 

creatinine (µmol/L)(IQR)

 

Median UPCR g/g (IQR)

 

SNP (%)

NRP/NS

(%)

 

Nephritic picture

(%)

Nephrotic/

nephritic mixed (%)

AKI (%)

Chronically increased serum creatinine(%)

Normal on histology, 12 (13.0)

5 (12)

7 (19)

0 (0)

0 (0)

0 (0)

0 (0)

18.5 (15-33.8)

62.3 (29.5-80.4)

2.3

Membranoproliferative, 3 (3.2)

1 (2.3)

2 (5.6)

0 (0)

0 (0)

0 (0)

0 (0)

31

189.2

9.2

Mesangioproliferative , 45 (48.3)

25 (60)

17 (47.2)

1 (50)

1 (25)

0 (0)

1(33.3)

28.0 (24-43)

97.3 (59.2-164.1)

1.9 (0.7-4.9)

Acute diffuse proliferative, 2 (2.2)

0 (0)

1 (2.8)

1 (50)

0 (0)

0 (0)

0 (0)

34.5

132.5

NA

Endocapillary proliferative, 8 (8.6)

3 (7.0)

2 (5.6)

0 (0)

1 (25)

2 (40)

0 (0)

34 (24-39)

88.4(83-148.7)

2.3 (2.0-2.9)*

Crescentic/Necrotising, 

3 (7.0)

2 (4.6)

0 (0)

0 (0)

1 (25)

0 (0)

0 (0)

34

258.0

0.9

Co-existing hypertension, 1 (1.1)

1 (2.3)

0 (0)

0 (0)

0 (0)

0 (0)

0 (0)

48

190.0

NA

Coexisting ATI/TIN/pyelonephritis, 2 (2.2)

0 (0)

0 (0)

0 (0)

0 (0)

2 (40)

0 (0)

39.5

1071.0

NA

Chronic changes, 7(7.5)

0 (0)

3 (8.3)

0 (0)

1 (25)

1 (20)

2 (33.3)

41(33-56)

428.0 (353.7-617.2)

4.0

Mild non-specific changes/Mild mesangial expansion and hypercellularity, 10 (11)

6 (14)

4 (11.2)

0 (0)

0 (0)

0 (0)

0 (0)

33 (21-53)

65(47.7-138)

1.0 (0.58-5.52)

Total, 93 (100)

43 (100)

36 (100)

2 (100)

4 (100)

5 (100)

3 (100)

32 (24-44)

97.0 ( 62.1-189.8)

2.1 (0.7-4.6)

a The cases with IgA dominance included four cases of Henoch-Schoenlein purpura (3  - mesangioproliferative pattern, 1 endocapillary proliferative pattern) 

b The cases with IgA dominance included five cases of possible IRGN (1 - mesangioproliferative pattern, 1 – acute diffuse proliferative glomerulonephritis, 2 – endocapillary proliferative glomerulonephritis, 1 - chronic changes).  *Range. Abbreviations: SNP – sub nephrotic range proteinuria; NRP/NS – nephrotic range proteinuria/nephrotic syndrome; AKI – acute kidney injury; CKD – chronic kidney disease; UPCR – urine protein creatinine ratio; IQ - interquartile 

IgA nephropathy was the most common primary glomerular disease identified among all diagnosed glomerular diseases.  The commonest presentations were nephrotic or sub nephrotic range proteinuria. The majority showed a mesangioproliferative pattern on light microscopy.  


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