Nusinersen or risdiplam treatment did not improve eGFR in SMA patients, with 19% showing impaired renal function and 51.7% having symptoms of tubular dysfunction.
Does treatment with genetic therapies (nusinersen or risdiplam) improve renal function in patients with spinal muscular atrophy?
Patients with spinal muscular atrophy have a high prevalence of impaired renal and tubular function, which is only partially mitigated (hypokalemia improves, but eGFR decline continues) by SMN2-splicing modifying therapies.
Absolute Event Rate: 0% vs 0%
Background Spinal muscular atrophy (SMA) is caused by loss-of-function of the survival motor neuron 1 ( SMN1 ) gene and deficiency of the ubiquitously expressed SMN protein. Genetic therapies can partially rescue motor units and improve prognosis of SMA, but effects of SMN shortage in other tissues has not been studied in detail. Methods We longitudinally assessed renal function in a cohort of patients with SMA before and after the start of genetic therapies. Results We enrolled 263 patients with SMA types 1c-4. Median age was 33 years (IQR: 22–49). Fifty (19%) patients had serum cystatin C based eGFR rates <90 ml/min/1.73m 2 , indicating increased risk of developing chronic kidney failure, 9 (3.5%) patients had eGFR compatible with chronic kidney failure (eGFR <60 ml/min/1.73m 2 ) and 2 patients showed end-stage renal failure based on eGFR <15 ml/min/1.73m 2 . Symptoms of tubular dysfunction (abnormal low serum potassium levels (<3.8 mmol/L) and proteinuria) were present in 134 (51.7%) and 53 patients (22%), respectively. Forty-two (16%) patients had a history of kidney stones or nephrocalcinosis. Treatment with nusinersen or risdiplam resulted in reduction of the number of patients with hypokalaemia, but not of those with proteinuria. Cystatin C eGFR continued to decline during treatment. Conclusions Patients with SMA are at risk of impaired renal clearance, which does not improve after treatment with SMN2 -splicing modifying therapies. Tubular function may improve partially following the start of treatment. These data indicate that SMN protein deficiency affects kidneys and that this will probably cause health problems in later life.
Asselman et al. (Fri,) reported a other. Nusinersen or risdiplam treatment did not improve eGFR in SMA patients, with 19% showing impaired renal function and 51.7% having symptoms of tubular dysfunction.