Abstract
Sustained and rapid loss of glomerular filtration rate (GFR) is the predominant clinical feature of diabetic kidney disease and a requisite for the development of end-stage renal disease. Although GFR trajectories have been studied in several cohorts with diabetes and without diabetes, whether rapid renal decline clusters in families with diabetes has not been examined. To determine this, we estimated GFR (eGFR) from serum creatinine measurements obtained from 15,612 patients with diabetes at the University of Utah Health Sciences Center and established their renal function trajectories. Patients with rapid renal decline (eGFR slope < 25 mL/min/1.73 m 2 /year) were then mapped to pedigrees using extensive genealogical records from the Utah Population Database to identify high-risk rapid renal decline pedigrees. We identified 2,127 (13.6%) rapid decliners with a median eGFR slope of 28.0 mL/ min/1.73 m 2 /year and 51 high-risk pedigrees (ranging in size from 1,450 to 24,501 members) with excess clustering of rapid renal decline. Familial analysis showed that rapid renal decline aggregates in these families and is associated with its increased risk among first-degree relatives. Further study of these families is necessary to understand the magnitude of the influence of shared familial factors, including environmental and genetic factors, on rapid renal decline in diabetes.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 420-429 |
| Number of pages | 10 |
| Journal | Diabetes |
| Volume | 68 |
| Issue number | 2 |
| DOIs | |
| State | Published - Feb 1 2019 |
Funding
Funding. The authors received grant support from the National Institute of Diabetes and Digestive and Kidney Disease’s Diabetic Complications Consortium (DiaComp) (32307-1/U24-DK-115255 to M.G.P.), the National Kidney Foundation of Utah and Idaho (to M.G.P.), and Driving Out Diabetes, a Larry H. Miller Family Wellness Initiative (to M.G.P.). Duality of Interest. No potential conflicts of interest relevant to this article were reported. Author Contributions. S.G.F., Z.Y., and M.H.P. researched the data. S.G.F. and M.G.P. conceived the idea and designed the study. S.G.F. and M.G.P. analyzed the data with assistance from Z.Y., A.M.L., A.A., J.Y., and T.G. S.G.F. and M.G.P. drafted the manuscript with assistance from A.A., T.R.S., K.L.R., and K.R.S. S.G.F., Z.Y., A.M.L., A.A., M.H.P., L.D., T.R.S., J.Y., T.G., K.L.R., K.R.S., and M.G.P. revised the manuscript and approved the final version. M.G.P. is the guarantor of this work and, as such, had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of its analysis.
| Funders | Funder number |
|---|---|
| National Kidney Foundation of Utah | |
| National Institute of Diabetes and Digestive and Kidney Diseases | U24DK115255 |
ASJC Scopus subject areas
- Internal Medicine
- Endocrinology, Diabetes and Metabolism
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