Semicarbazide-sensitive amine oxidase activity and total nitrite and nitrate concentrations in serum: novel biochemical markers for type 2 diabetes?
The aim of this study was to evaluate the activity of semicarbazide-sensitive amine oxidase (SSAO) and the total nitrite and nitrate (NO x ) concentrations in serum from type 2 diabetic patients and control subjects in order to evaluate if they could be used as novel diabetic markers. We studied 38...
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Published in | Acta diabetologica Vol. 46; no. 2; pp. 135 - 140 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Milan
Springer Milan
01.06.2009
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | The aim of this study was to evaluate the activity of semicarbazide-sensitive amine oxidase (SSAO) and the total nitrite and nitrate (NO
x
) concentrations in serum from type 2 diabetic patients and control subjects in order to evaluate if they could be used as novel diabetic markers. We studied 38 type 2 diabetic patients and 35 control subjects. Serum samples from those subjects were evaluated by radiochemical methods for SSAO activity using
14
C-benzylamine. Serum NO
x
concentrations were obtained as an index of nitric oxide production by the Griess reaction. Serum SSAO activity was higher in type 2 diabetic patients than in control group and serum SSAO in type 2 diabetic correlated with age, serum creatinine and total cholesterol. Serum NO
x
levels in type 2 diabetic patients were also significantly higher than those in the control group. Serum NO
x
levels in control group correlated with serum SSAO activity. In conclusion, the increase in the SSAO activity and NO
x
levels observed in type 2 diabetic patients could be parameters to take in account and play relevant role in diabetes development. SSAO and NO
x
are suggested as markers for prognostic of diabetes. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 0940-5429 1432-5233 1432-5233 |
DOI: | 10.1007/s00592-008-0070-7 |