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Medizinische Klinik A, Klinikum der Stadt Ludwigshafen, Ludwigshafen, Germany
Correspondence: Dr. Raoul Bergner, Medizinische Klinik A, Klinikum der Stadt Ludwigshafen GmbH, Bremserstraße 79, 67063 Ludwigshafen, Germany. E-mail: bergnerr{at}klilu.de
The authors of this brief publication report on newly diagnosed myeloma patients with renal failure. They define the renal failure as serum creatinine
2mg/dL. The reason for this definition is to exclude patients with mild renal impairment that can be easily corrected with hydration. The authors however did not calculate the creatinine clearance, thereby overestimating the renal function. Serum creatinine levels are not only dependent from renal function but also from the muscle mass. In our own study in multiple myeloma patients with different stages of renal insufficiancy we included 40 patients with creatinine clearance from 8–138 mL/min (clearance
80 mL/min n=10; 79–50 mL/min n=11; 30–49 mL/min n=10; <30 mL/min n=9) only 18 patients had serum creatinine levels > 1.3 mg/dL (normal range) and only 9 >2.0 mg/dL, respectively (Figure 1).1 To minimize the error the creatinine clearance has been calculated as a mean from 3 methods: creatinine clearance with 24 hour collected urine, MDRD-formula2 and Cockcroft and Gault formula.3 The age of the patients ranged from 41–83 years (mean 67.4±9.9 years). Included were patients with biopsy proven kidney disease from multiple myeloma but also patients with reduced kidney function due to nephroan-giosclerosis or other renal disease. Because of the wide spectrum of renal diseases associated with multiple myeloma and their different prognosis,4 the definiton of elevated serum creatinine for renal involvement in multiple myeloma is more than questionable. Patients with cast nephropathy (CN) had a worse prognosis than patients with interstitial nephritis or nephrocalcinosis, whereas patients with light chain deposit disease (LCDD) or AL-amyloidosis (ALA) had an intermediate prognosis regarding their kidney function. Without kidney biopsy it is impossible to distinguish between this different kidney disease. We could show that patients with high free light chain excretion in the urine had predominantly cast nephropathy (unpublished data). In our study about free light chain excretion (FLCurine) in urine in patients with biopsy proven CN had FLCUrine of 329.5±334.5 mg/dL, patients with LCDD 17.4±21.6 mg/dL and patients with ALA 7.5±10.0 mg/dL respectively (p<0.05) In a series of 35 patients patients with monoclonal light chain disease, who underwent a kidney biopsy cast nephropathy was diagnosed in 13 patients, LCDD in 3 patients and AL-amyloidosis in 8 patients. Eleven patients had other renal involvement such as nephrocalcinosis or interstitial nephritis, which were easly treatable with corticosteroids and bisphosphonates.5 Only about one third of our patients had cast nephropathy with unfavorable prognosis. Knudsen et al. also describe that the reversibility of renal failure was more frequently observed in patients with moderate renal failure, hypercalcaemia and low Bence-Jones protein excretion.6 The observation of the authors that patients with light chain myeloma or Bence-Jones proteinuria had a lower probability of recovery of the renal failure is in accordance with this.
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Figure 1. Serum creatinine levels are ploted with the according calculated creatinine clearance. The creatinine clearance was calculated as the mean value of three different methods to calculate the creatinine clearance (collecting urine-method, MDRD-method, Cockcroft & Gault-method).
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