LOW-DENSITY LIPOPROTEIN-APHERESIS IN CHILDREN WITH MULTI-DRUG RESISTANT NEPHROTIC SYNDROME: PROSPECTIVE, SINGLE-ARM, INTERVENTIONAL STUDY FROM A SINGLE CENTER IN A DEVELOPING COUNTRY- INTERIM ANALYSIS

 

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LOW-DENSITY LIPOPROTEIN-APHERESIS IN CHILDREN WITH MULTI-DRUG RESISTANT NEPHROTIC SYNDROME: PROSPECTIVE, SINGLE-ARM, INTERVENTIONAL STUDY FROM A SINGLE CENTER IN A DEVELOPING COUNTRY- INTERIM ANALYSIS

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Kinnari
Vala
Kinnari Vala kbvala@gmail.com Institute of Kidney Diseases and Research Center- Institute of Pediatric Nephrology Ahmedabad India *
Amit Prajapati amitikdrc@gmail.com Institute of Kidney Diseases and Research Center- Institute of Transfusion Medicine Ahmedabad India -
Shahenaz Kapadia kp.shahenaz@gamil.com Institute of Kidney Diseases and Research Center- Institute of Pediatric Nephrology Ahmedabad India -
Disha Bhatt disha2291@gmail.com Institute of Kidney Diseases and Research Center- Institute of Pediatric Nephrology Ahmedabad India -
Pooja Modi poojaroxx27@gmail.com Institute of Kidney Diseases and Research Center- Institute of Transfusion Medicine Ahmedabad India -
Anshuman Saha drasaha1980@gmail.com Institute of Kidney Diseases and Research Center- Institute of Pediatric Nephrology Ahmedabad India -
Rupesh Raina rraina@akronchildrens.org Akron Children's Pediatric Nephrology Ohio United States -
Pranjal Modi drpranjalmodi@gmail.com Institute of Kidney Diseases and Research Center- Institute of Urology and Abdominal Organ Transplant Ahmedabad India -
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Multi-drug resistant nephrotic syndrome (MDR-NS) in children is associated with high morbidity and risk of progression to kidney failure. Low-density lipoprotein apheresis (LDL-A) has emerged as a potential adjunctive therapy, but data from developing countries remain scarce.

We conducted a prospective, single-arm, interventional study at a public-sector tertiary referral center over two years. Children <18 years with MDR-NS (eGFR >45 ml/min/1.73m²) or post-transplant focal segmental glomerulosclerosis (FSGS) recurrence refractory to plasma exchange and rituximab were enrolled. Each patient underwent 12 LDL-A sessions (double filtration or immunoadsorption) over nine weeks, in combination with corticosteroids and optimized immunosuppression. Clinical and laboratory parameters [urine protein–creatinine ratio (UPCR), serum albumin, lipid profile, and serum creatinine] were assessed at baseline, post-treatment, and during follow-up. Safety outcomes and adverse events were documented.

Ten children (median age 9.3 years, 7 males) received 11 cycles of LDL-A. Complete remission was observed in 4/11 at 1 month, 3/6 at 3 months, 3/5 at 6 months, and 1/2 at 12 months; partial remission occurred in 1/11 at 1 month and 1/5 at 6 months (median follow-up 4.5 months, IQR 8). LDL levels reduced by 50% post-treatment. No major procedure-related adverse events occurred; minor events included transient hypotension and hypocalcemia, managed conservatively. At 18 months, 1/2 patients with initial complete remission maintained sustained response.

LDL-apheresis appears safe and effective in inducing remission in children with MDR-NS and refractory post-transplant FSGS. Larger multicenter studies with longer follow-up are needed to validate efficacy and identify predictors of sustained remission.

Kewords