averrhoa bilimbi ingestion and acute kidney injury: a case series

Averrhoa bilimbi (Irumban puli) is commonly used in South India for variety of household preparations and also as a remedy for hypertension, diabetes and dyslipidemia. The fruit has very high oxalate content which, when consumed in large quantities, forms calcium oxalate crystals in the renal tubules. These crystals get adhered to the tubular cells and cause cell necrosis resulting in acute kidney injury. We describe a series of 4 such cases who presented to us in acute renal failure after consumption of Averrhoa bilimbi in excess. 3 out of 4 patients required hemodialysis. There was recovery of renal function at the end of 2-6 weeks.

introduction Averrhoa bilimbi is one of the important medicinal plants of many tropical and subtropical countries of the world. Averrhoa bilimbi is closely related to Averrhoa carambola (starfruit). It is cultivated throughout Malaysia, Indonesia, Singapore, Philippines, Thailand, Bangladesh, Myanmar, and India [1]. The fruits of the tree are greenish in colour with a firm and juicy flesh which becomes soft on ripening. The fruit juice is sour and extremely acidic [2]. The fruit is rich in vitamin C and oxalic acid [3]. It is known to cause acute kidney injury (AKI) due to calcium oxalate crystal deposition in renal tubules, acute tubular necrosis, acute interstitial nephritis and chronically may cause interstitial fibrosis [4]. We describe a series of four cases who presented to us with AKI after consumption of Averrhoa bilimbi (also called Irumban puli).

case series case 1
A 34-year-old male presented with complaints of swelling of both lower limbs, abdominal distension and facial puffiness of 3 days duration. He also had decreased urine output over last 2 days, but no history of hematuria or abdominal pain. He reported nausea, but there were no episodes of vomiting or loose stools. No history of any co-morbidities or hospital admissions till the present visit. He had consumed about 500 ml of wine prepared from Averrhoa bilimbi 5 days earlier at his house. On examination, his pulse rate: 85/min and regular, BP: 170/100 mm Hg, afebrile, respiratory rate (RR): 24/min. There was bilateral pitting pedal edema extending upto two-thirds of both the legs, periorbital puffiness and evidence of free fluid in the abdomen. Investigations revealed severe AKI with serum creatinine: 9.8 mg/dl, with normal hemogram and liver function tests. Urine microscopy showed trace proteinuria, 3-4 WBCs and plenty of oxalate crytals. Ultrasound abdomen showed normal sized kidneys with well maintained cortico-medullary differentiation (CMD). No evidence of calculi/ hydronephrosis. ABG showed partially compensated metabolic acidosis. He was started on furosemide and nitroglycerin IV infusion. However, in view of persistent oliguria, fluid overload and acidosis, he was started on hemodialysis. Symptoms improved after 2 sessions following which a left percutaneous kidney biopsy was done which showed acute tubular necrosis with intra-tubular calcium oxalate crystals ( Figure 1). He required about 8 hemodialysis sessions. His renal function tests returned to normal (1.3 mg/dl) in 6 weeks.

case 2
A 48-year-old male, with history of type 2 diabetes mellitus and dyslipidemia on medications presented with excessive fatigue, nausea, loss of appetite and vomiting for the last 1 week. There was no history of fever/ abdominal pain/ loose stools/ decreased urine output. He gave history of consumption of Averrhoa bilimbi fruit juice for about 5 days to control the serum cholesterol levels, one week prior to the visit to our centre. On examination, he was afebrile, BP was 140/90 mm Hg, RR: 18/min. He had normal complete hemogram, serum creatinine: 8.5 mg/dl, normal liver function tests, total cholesterol: 240 mg/dl, LDL: 145 mg/dl, HbA1c: 7.1% and urine microscopy showed 1+ proteinuria with plenty of oxalate crystals ( Figure 2). Ultrasound abdomen showed slightly bulky kidneys but CMD was well maintained. He underwent left percutaneous kidney biopsy which showed acute tubular necrosis with many polarizable fractured crystals in the tubular lumina (calcium oxalate crystals). He was initiated on hemodialysis. He improved symptomatically with time. Around 6 sessions of hemodialysis were done and his serum creatinine returned to baseline of 1.2 mg/dl at the end of 4 weeks.

case 3
A 39-year-old male presented with nausea, vomiting and excessive fatigue for the last 2 days. No fever or abdominal pain or dysuria. He had no other significant co-morbidities. He gave history of consumption of about 250 ml of wine made of Averrhoa bilimbi fruit 4 days before the visit. On examination, he was afebrile, no edema, BP was 130/80 mmHg, RR was 16/min. Serum creatinine was 5.6 mg/dl. Urine microscopy showed plenty of oxalate crystals. Ultrasound abdomen was normal. Patient was managed conservatively with fluid management. Kidney biopsy and hemodialysis were not carried out in view of symptomatic improvement of patient. His renal function returned to normal (Serum creatinine: 0.8 mg/dl) at the end of 2 weeks.

case 4
A 42-year-old male presented with swelling of both lower limbs and abdominal distension for last 5 days, decreased urine output for 2 days and breathlessness of 1 day duration. No history of fever, vomiting, pain abdomen, chest discomfort or alcohol intake. No significant co-morbidities. He had returned from abroad 15 days back and had consumed Averrhoa bilimbi fruit juice of about 200 ml every day, for about 4-5 days. On examination, Pulse was 102/ min, BP was 220/110 mm Hg, RR was 35/min, sp02 was 90% on room air. He had bilateral pitting pedal edema, bilateral basal crepitations and evidence of free fluid in the abdomen. Investigations showed severe renal failure with serum creatinine: 12.5 mg/ dl, normal hemogram, slightly elevated liver enzymes and plenty of oxalate crystals in urine microscopy. Bedside ultrasound showed normal sized kidneys without any evidence of calculi/hydronephrosis. In view of oliguria, accelerated hypertension and acute pulmonary edema, he was initiated on hemodialysis. Kidney biopsy was deferred in view of poor general condition of the patient. However, he showed symptomatic improvement after 2-3 sessions of hemodialysis, urine output slowly improved, chest congestion was relieved and edema started subsiding. He required about 12 sessions of hemodialysis. Serum creatinine at the end of 6 weeks was 2.3 mg/dl and he was advised regular nephrology follow-up.
Primary hyperoxaluria is a rare inborn error of glyoxylate metabolism characterized by the overproduction of oxalate, which deposits as calcium oxalate in various organs as kidney function declines. Secondary hyperoxaluria is more common and is usually the result of increased dietary oxalate intake, increased intestinal oxalate availability, decreased intestinal oxalate degradation, or increased colonic permeability to oxalate. Excessive dietary consumption accounts for 30.6% cases of secondary oxalate nephropathy [8].
The initial event in the development of oxalate nephropathy is the formation of calcium oxalate crystals in the lumen of proximal tubules followed by adhesion of calcium oxalate crystals to the surface of tubular epithelial cells. Calcium oxalate binding proteins that promote oxalate nephropathy have also been identified [9]. Inflammasomes represent large multimolecular cytosolic complexes that assemble into a platform for the activation of pro-inflammatory caspase-1. Inflammasomes are important mediators of apoptosis, interstitial inflammation and fibrosis in various types of renal disease. Of great importance in the context of oxalate nephropathy is the nucleotidebinding domain, leucine-rich repeat inflammasome (NALP3 or NLRP3). When activated, NALP3 proteins oligomerize and form a protein complex with caspase-1. This process activates caspase-1 which cleaves the inactive precursors of IL-1β and IL-18 to generate active cytokines that promote interstitial inflammation and fibrosis, as well as progression of renal failure, in oxalate nephropathy [10,11]. Extensive tubular damage with epithelial necrosis and dilatation of tubular lumen is the cardinal characteristic of oxalate nephropathy. Crystal deposition can also occur in walls of the renal vessels, while the involvement of glomeruli is inconsistent. conclusion Averrhoa bilimbi (Irumban puli) is used as an ingredient in fruit juice, wine and pickles in South India. It is also traditionally used as a remedy for ailments like hyperlipidemia, hypertension and diabetes. When consumed in excess, it can lead to AKI secondary to acute tubular necrosis, due to its high oxalate content. Therefore, we recommend not to consume oxalate-rich food in excess, which may cause life threatening consequences.

Conflicts of interest
Authors declare no conflicts of interest.