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C‐peptide and diabetic kidney disease
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| Zeitschriftentitel: | Journal of Internal Medicine |
|---|---|
| Personen und Körperschaften: | |
| In: | Journal of Internal Medicine, 281, 2017, 1, S. 41-51 |
| Format: | E-Article |
| Sprache: | Englisch |
| veröffentlicht: |
Wiley
|
| Schlagwörter: |
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Brunskill, N. J. Brunskill, N. J. |
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Brunskill, N. J. |
| spellingShingle |
Brunskill, N. J. Journal of Internal Medicine C‐peptide and diabetic kidney disease Internal Medicine |
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brunskill, n. j. |
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Brunskill, N. J. 0954-6820 1365-2796 Wiley Internal Medicine http://dx.doi.org/10.1111/joim.12548 <jats:title>Abstract</jats:title><jats:p>Kidney disease is a serious development in diabetes mellitus and poses an increasing clinical problem. Despite increasing incidence and prevalence of diabetic kidney disease, there have been no new therapies for this condition in the last 20 years. Mounting evidence supports a biological role for C‐peptide, and findings from multiple studies now suggest that C‐peptide may beneficially affect the disturbed metabolic and pathophysiological pathways leading to the development of diabetic nephropathy. Studies of C‐peptide in animal models and in humans with type 1 diabetes all suggest a renoprotective effect for this peptide. In diabetic rodents, C‐peptide reduces glomerular hyperfiltration and albuminuria. Cohort studies of diabetic patients with combined islet and kidney transplants suggest that maintained C‐peptide secretion is protective of renal graft function. Further, in short‐term studies of patients with type 1 diabetes, administration of C‐peptide is also associated with a lowered hyperfiltration rate and reduced microalbuminuria. Thus, the available information suggests that type 1 diabetes should be regarded as a dual hormone deficiency disease and that clinical trials of C‐peptide in diabetic nephropathy are both justified and urgently required.</jats:p> C‐peptide and diabetic kidney disease Journal of Internal Medicine |
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C‐peptide and diabetic kidney disease |
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C‐peptide and diabetic kidney disease |
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c‐peptide and diabetic kidney disease |
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Internal Medicine |
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http://dx.doi.org/10.1111/joim.12548 |
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2017 |
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41-51 |
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<jats:title>Abstract</jats:title><jats:p>Kidney disease is a serious development in diabetes mellitus and poses an increasing clinical problem. Despite increasing incidence and prevalence of diabetic kidney disease, there have been no new therapies for this condition in the last 20 years. Mounting evidence supports a biological role for C‐peptide, and findings from multiple studies now suggest that C‐peptide may beneficially affect the disturbed metabolic and pathophysiological pathways leading to the development of diabetic nephropathy. Studies of C‐peptide in animal models and in humans with type 1 diabetes all suggest a renoprotective effect for this peptide. In diabetic rodents, C‐peptide reduces glomerular hyperfiltration and albuminuria. Cohort studies of diabetic patients with combined islet and kidney transplants suggest that maintained C‐peptide secretion is protective of renal graft function. Further, in short‐term studies of patients with type 1 diabetes, administration of C‐peptide is also associated with a lowered hyperfiltration rate and reduced microalbuminuria. Thus, the available information suggests that type 1 diabetes should be regarded as a dual hormone deficiency disease and that clinical trials of C‐peptide in diabetic nephropathy are both justified and urgently required.</jats:p> |
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| description | <jats:title>Abstract</jats:title><jats:p>Kidney disease is a serious development in diabetes mellitus and poses an increasing clinical problem. Despite increasing incidence and prevalence of diabetic kidney disease, there have been no new therapies for this condition in the last 20 years. Mounting evidence supports a biological role for C‐peptide, and findings from multiple studies now suggest that C‐peptide may beneficially affect the disturbed metabolic and pathophysiological pathways leading to the development of diabetic nephropathy. Studies of C‐peptide in animal models and in humans with type 1 diabetes all suggest a renoprotective effect for this peptide. In diabetic rodents, C‐peptide reduces glomerular hyperfiltration and albuminuria. Cohort studies of diabetic patients with combined islet and kidney transplants suggest that maintained C‐peptide secretion is protective of renal graft function. Further, in short‐term studies of patients with type 1 diabetes, administration of C‐peptide is also associated with a lowered hyperfiltration rate and reduced microalbuminuria. Thus, the available information suggests that type 1 diabetes should be regarded as a dual hormone deficiency disease and that clinical trials of C‐peptide in diabetic nephropathy are both justified and urgently required.</jats:p> |
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| spelling | Brunskill, N. J. 0954-6820 1365-2796 Wiley Internal Medicine http://dx.doi.org/10.1111/joim.12548 <jats:title>Abstract</jats:title><jats:p>Kidney disease is a serious development in diabetes mellitus and poses an increasing clinical problem. Despite increasing incidence and prevalence of diabetic kidney disease, there have been no new therapies for this condition in the last 20 years. Mounting evidence supports a biological role for C‐peptide, and findings from multiple studies now suggest that C‐peptide may beneficially affect the disturbed metabolic and pathophysiological pathways leading to the development of diabetic nephropathy. Studies of C‐peptide in animal models and in humans with type 1 diabetes all suggest a renoprotective effect for this peptide. In diabetic rodents, C‐peptide reduces glomerular hyperfiltration and albuminuria. Cohort studies of diabetic patients with combined islet and kidney transplants suggest that maintained C‐peptide secretion is protective of renal graft function. Further, in short‐term studies of patients with type 1 diabetes, administration of C‐peptide is also associated with a lowered hyperfiltration rate and reduced microalbuminuria. Thus, the available information suggests that type 1 diabetes should be regarded as a dual hormone deficiency disease and that clinical trials of C‐peptide in diabetic nephropathy are both justified and urgently required.</jats:p> C‐peptide and diabetic kidney disease Journal of Internal Medicine |
| spellingShingle | Brunskill, N. J., Journal of Internal Medicine, C‐peptide and diabetic kidney disease, Internal Medicine |
| title | C‐peptide and diabetic kidney disease |
| title_full | C‐peptide and diabetic kidney disease |
| title_fullStr | C‐peptide and diabetic kidney disease |
| title_full_unstemmed | C‐peptide and diabetic kidney disease |
| title_short | C‐peptide and diabetic kidney disease |
| title_sort | c‐peptide and diabetic kidney disease |
| title_unstemmed | C‐peptide and diabetic kidney disease |
| topic | Internal Medicine |
| url | http://dx.doi.org/10.1111/joim.12548 |