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Favourable serum calcification propensity with intraperitoneal as compared with subcutaneous insulin administration in type 1 diabetes.
- Source :
-
Therapeutic advances in endocrinology and metabolism [Ther Adv Endocrinol Metab] 2020 Mar 03; Vol. 11, pp. 2042018820908456. Date of Electronic Publication: 2020 Mar 03 (Print Publication: 2020). - Publication Year :
- 2020
-
Abstract
- Background: Serum calcification propensity can be monitored using the maturation time of calciprotein particles in serum (T <subscript>50</subscript> test). A shorter T <subscript>50</subscript> indicates greater propensity to calcify; this is an independent determinant of cardiovascular disease. As the intraperitoneal (IP) route of insulin administration mimics the physiology more than the subcutaneous (SC) route in persons with type 1 diabetes (T1DM), we hypothesized that IP insulin influences determinants of calcium propensity and therefore result in a longer T <subscript>50</subscript> than SC insulin administration.<br />Methods: Prospective, observational case-control study. Measurements were performed at baseline and at 26 weeks in age and gender matched persons with T1DM.<br />Results: A total of 181 persons, 39 (21.5%) of which used IP and 142 (78.5%) SC insulin were analysed. Baseline T <subscript>50</subscript> was 356 (45) minutes. The geometric mean T <subscript>50</subscript> significantly differed between both treatment groups: 367 [95% confidence interval (CI) 357, 376] for the IP group and 352 (95% CI 347, 357) for the SC group with a difference of -15 (95% CI -25, -4) minutes, in favour of IP treatment. In multivariable analyses, the IP route of insulin administration had a positive relation on T <subscript>50</subscript> concentrations while higher age, triglycerides and phosphate concentrations had an inverse relation.<br />Conclusion: Among persons with T1DM, IP insulin administration results in a more favourable calcification propensity time then SC insulin. It has yet to be shown if this observation translates into improved cardiovascular outcomes.<br />Competing Interests: Conflict of interest statement: AP is an employee and stockholder of Calciscon. All other authors declare they have no conflict of interest.<br /> (© The Author(s), 2020.)
Details
- Language :
- English
- ISSN :
- 2042-0188
- Volume :
- 11
- Database :
- MEDLINE
- Journal :
- Therapeutic advances in endocrinology and metabolism
- Publication Type :
- Academic Journal
- Accession number :
- 32166012
- Full Text :
- https://doi.org/10.1177/2042018820908456