859
Views
2
CrossRef citations to date
0
Altmetric
Letter to the Editor

Outcomes of living kidney donors with monoclonal gammopathy of undetermined significance

, &

Here, we report outcomes of four cases of living kidney donors with history of monoclonal gammopathy of undetermined significance (MGUS) at Mayo Clinic, Rochester, Rochester, MN between January 2000 and September 2014.

The number of patients with end-stage kidney disease (ESRD) awaiting transplantation in the United States (U.S.) has increased over time, by 3000 to 4000 patients each year.Citation1 Data on safety outcomes of living kidney donors are required to increase public confidence in the transplantation system. MGUS is a common asymptomatic premalignant clonal plasma cell or lymphoplasmacytic proliferative disorder, occurring in more than 3% of the general population over the age of 50.Citation2 Since patients with MGUS can progress to more advanced diseases (multiple myeloma, immunoglobulin light chain (AL) amyloidosis, light chain deposition disease in non-IgM MGUS and Waldenström macroglobulinemia in IgM MGUS) approximately at rate of 1% per year],Citation2,Citation3 the outcome data on of living kidney donors with MGUS are needed. Thus, we report outcomes of living kidney donors with history of MGUS prior to donation.

A total of 1776 kidney donors were screened. Four living kidney donors with MGUS were identified using ICD-9 code of 273.1. Donors’ mean age was 57 ± 11 years. Three of the four donors were females. Mean baseline serum creatinine was 1.0 ± 0.1 mg/dL with a mean eGFR of 66 ± 7 mL/min/1.73 m2 using the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI).Citation4 Two donors had monoclonal IgG kappa, one donor had IgM kappa and another donor’s monoclonal protein was detected, but not classified (). At median follow-up time of 5 years (IQR 0.7–9 years), none of the donors were diagnosed with multiple myeloma or other lymphoplasmacytic proliferative disorders. There were no evidences of anemia, hypercalcemia or detected bone lytic lesions. Mean serum creatinine was 1.2 ± 0.2 mg/dL with a mean eGFR of 57 ± 13 mL/min/1.73 m2. None of the donors with MGUS developed end stage renal disease or died.

Table 1. Baseline characteristics of donors with MGUS.

In summary, these findings are reassuring for the safety of healthy living kidney donors with MGUS.

Declaration of interest

The authors declare no conflicts of interest. No financial support has been received for this work.

References

  • Gaston RS, Danovitch GM, Adams PL, et al. The report of a national conference on the wait list for kidney transplantation. Am J Transplant. 2003;3(7):775–785
  • Kyle RA, Durie BG, Rajkumar SV, et al. Monoclonal gammopathy of undetermined significance (MGUS) and smoldering (asymptomatic) multiple myeloma: IMWG consensus perspectives risk factors for progression and guidelines for monitoring and management. Leukemia. 2010;24(6):1121–1127
  • Cheungpasitporn W, Leung N, Sethi S, et al. Refractory atypical hemolytic uremic syndrome with monoclonal gammopathy responsive to bortezomib-based therapy. Clin Nephrol. 2014 . [Epub ahead of print]. doi: 10.5414/CN108363
  • Kilbride HS, Stevens PE, Eaglestone G, et al. Accuracy of the MDRD (Modification of Diet in Renal Disease) study and CKD-EPI (CKD Epidemiology Collaboration) equations for estimation of GFR in the elderly. Am J Kidney Dis. 2013;61(1):57–66

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.