全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Insulin Therapy with Personal Insulin Pumps and Early Angiopathy in Children with Type 1 Diabetes Mellitus

DOI: 10.1155/2013/791283

Full-Text   Cite this paper   Add to My Lib

Abstract:

Objective. Assessment of the effect of a treatment method change from multiple daily insulin injection (MDI) to continuous subcutaneous insulin infusion (CSII) on the development of early angiopathy in children with T1DM with or without retinopathy. Methods. The study pump group involved 32 diabetic children aged 14.8, with the initial HbA1c level of 8.3%, previously treated by MDI. The patients were examined before pump insertion and after 3 and 6 months of CSII. We assessed HbA1c level, carotid artery intima-media thickness (c-IMT), and flow-mediated dilatation (FMD) of the brachial artery. The pump group was compared to a group of eight teenagers with diagnosed nonproliferative retinopathy, treated with MDI. Results. HbA1c in the entire group was found to improve in the second and in the third examination. During 6 months of CSII, FMD increased and IMT decreased. Retinopathic adolescents had significantly thicker IMT and lower FMD compared to baseline results of the pump group. Treatment intensification in the retinopathy-free children enhanced these differences. Conclusions. CSII is associated with lower IMT and higher FMD. Whether on the long-run CSII is superior to MDI to delay the occurrence of diabetes late complications remains to be explained. 1. Introduction Insulin pump therapy in the form of continuous subcutaneous insulin infusion (CSII) was introduced in the 1970s and turned out to ensure better metabolic control of diabetes compared to traditional insulin therapy approaches. It is currently considered to be the optimal method of insulin administration, since it imitates the pancreatic activity in the best possible way, ensures precise dosage, and at the same time offers a high level of ease and comfort. Patients that experience the advantages are above all children and adolescents with type 1 diabetes mellitus (T1DM) [1–3]. Compared to the traditional methods of insulin therapy by means of multiple daily insulin injections (MDI), CSII can significantly decrease glycated hemoglobin (HbA1C), reduce 24-hour glucose variability, decrease incidence of severe hypoglycemia, and eliminate dawn phenomenon. Moreover, the use of CSII is associated with improved quality of life and precise insulin administration with respect to physical effort and diet [1, 4]. A long-term effect of CSII on the development of late complications of diabetes in the form of microangiopathy or macroangiopathy needs to be explained [5]. T1DM increases the risk of developing micro- and macrovascular complications which in turn will have a devastating impact on quality of

References

[1]  D. Bruttomesso, S. Costa, and A. Baritussio, “Continuous subcutaneous insulin infusion (CSII) 30 years later: still the best option for insulin therapy,” Diabetes/Metabolism Research and Reviews, vol. 25, no. 2, pp. 99–111, 2009.
[2]  T. Danne, T. Battelino, P. Jarosz-Chobot et al., “Establishing glycaemic control with continuous subcutaneous insulin infusion in children and adolescents with type 1 diabetes: experience of the PedPump Study in 17 countries,” Diabetologia, vol. 51, no. 9, pp. 1594–1601, 2008.
[3]  M. Phillip, T. Battelino, H. Rodriguez, T. Danne, and F. Kaufman, “Use of insulin pump therapy in the pediatric age-group: consensus statement from the European Society for Paediatric Endocrinology, the Lawson Wilkins Pediatric Endocrine Society, and the International Society for Pediatric and Adolescent Diabetes, endorsed by the American Diabetes Association and the European Association for the Study of Diabetes,” Diabetes Care, vol. 30, no. 6, pp. 1653–1662, 2007.
[4]  K. Jeitler, K. Horvath, A. Berghold et al., “Continuous subcutaneous insulin infusion versus multiple daily insulin injections in patients with diabetes mellitus: systematic review and meta-analysis,” Diabetologia, vol. 51, no. 6, pp. 941–951, 2008.
[5]  P. Hammond, “Continuous subcutaneous insulin infusion: short-term benefits apparent, long-term benefits speculative,” The British Journal of Diabetes and Vascular Disease, vol. 4, no. 2, pp. 104–108, 2004.
[6]  M. Mauer and K. Drummond, “The early natural history of nephropathy in type 1 diabetes: I. Study design and baseline characteristics of the study participants,” Diabetes, vol. 51, no. 5, pp. 1572–1579, 2002.
[7]  H. Shamoon, H. Duffy, N. Fleischer et al., “The effect of intensive treatment of diabetes on the development and progression of long-term complications in insulin-dependent diabetes mellitus,” The New England Journal of Medicine, vol. 329, no. 14, pp. 977–986, 1993.
[8]  C. Giannini, A. Mohn, F. Chiarelli, and C. J. H. Kelnar, “Macrovascular angiopathy in children and adolescents with type 1 diabetes,” Diabetes/Metabolism Research and Reviews, vol. 27, no. 5, pp. 436–460, 2011.
[9]  R. B. Goldberg, “Cytokine and cytokine-like inflammation markers, endothelial dysfunction, and imbalanced coagulation in development of diabetes and its complications,” Journal of Clinical Endocrinology and Metabolism, vol. 94, no. 9, pp. 3171–3182, 2009.
[10]  K. Kaul, A. Hodgkinson, J. M. Tarr, E. M. Kohner, and R. Chibber, “Is inflammation a common retinal-renal-nerve pathogenic link in diabetes?” Current diabetes reviews, vol. 6, no. 5, pp. 294–303, 2010.
[11]  P. Libby, P. M. Ridker, and A. Maseri, “Inflammation and atherosclerosis,” Circulation, vol. 105, no. 9, pp. 1135–1143, 2002.
[12]  D. S. Celermajer, “Noninvasive detection of atherosclerosis,” The New England Journal of Medicine, vol. 339, no. 27, pp. 2014–2015, 1998.
[13]  J. To?wińsko, B. G?owińska-Olszewska, M. Urban, B. Florys, and J. Peczyńska, “Ultrasonographic evaluation of selected parameters of the endothelial function in brachial arterferies and IMT measurments in carotid arteries in children with diabetes type 1 dependent using personal insulin pumps. Preliminary report,” Endokrynologia, Diabetologia i Choroby Przemiany Materii Wieku Rozwojowego, vol. 12, no. 3, pp. 200–204, 2006.
[14]  B. G?owińska-Olszewska, M. Urban, B. Urban, J. To?wińska, and A. Szadkowska, “The association of early atherosclerosis and retinopathy in adolescents with type 1 diabetes: preliminary report,” Acta Diabetologica, vol. 44, no. 3, pp. 131–137, 2007.
[15]  P. Pignoli, E. Tremoli, and A. Poli, “Intimal plus medial thickness of the arterial wall: a direct measurement with ultrasound imaging,” Circulation, vol. 74, no. 6, pp. 1399–1406, 1986.
[16]  D. S. Celermajer, K. E. Sorensen, V. M. Gooch et al., “Non-invasive detection of endothelial dysfunction in children and adults at risk of atherosclerosis,” The Lancet, vol. 340, no. 8828, pp. 1111–1115, 1992.
[17]  K. Dahl-J?rgensen, J. R. Larsen, and K. F. Hanssen, “Atherosclerosis in childhood and adolescent type 1 diabetes: early disease, early treatment?” Diabetologia, vol. 48, no. 8, pp. 1445–1453, 2005.
[18]  K. O. Schwab, J. Doerfer, W. Hecker et al., “Spectrum and prevalence of atherogenic risk factors in 27,358 children, adolescents, and young adults with type 1 diabetes: cross-sectional data from the German diabetes documentation and quality management system (DPV),” Diabetes Care, vol. 29, no. 2, pp. 218–225, 2006.
[19]  M. J. J?rvisalo, A. Putto-Laurila, L. Jartti et al., “Carotid artery intima-media thickness in children with type 1 diabetes,” Diabetes, vol. 51, no. 2, pp. 493–498, 2002.
[20]  M. J. J?rvisalo, M. Raitakari, J. O. Toikka et al., “Endothelial dysfunction and increased arterial intima-media thickness in children with type 1 diabetes,” Circulation, vol. 109, no. 14, pp. 1750–1755, 2004.
[21]  J. To?wińska, M. Urban, B. Florys, B. Pieclukiewicz, M. Krawczuk-Rybak, and J. Peczynska, “Ultrasonographic evaluation of common carotid artery wall in children with type 1 diabetes,” Medical Science Monitor, vol. 4, no. 1, pp. 72–80, 1998.
[22]  H. Tamura, T. Suzue, F. Jitsunari, and T. Hirao, “Evaluation of carotid arterial intima-media thickness (IMT) and its relation to clinical parameters in Japanese children,” Acta Medica Okayama, vol. 65, no. 1, pp. 21–26, 2011.
[23]  R. D. Pozza, H. Netz, H.-P. Schwarz, and S. Bechtold, “Subclinical atherosclerosis in diabetic children: results of a longitudinal study,” Pediatric Diabetes, vol. 11, no. 2, pp. 129–133, 2010.
[24]  W. ?uczyński, A. Szypowska, B. G?owińska-Olszewska, and A. Bossowski, “Overweight, obesity and features of metabolic syndrome in children with diabetes treated with insulin pump therapy,” European Journal of Pediatrics, vol. 170, no. 7, pp. 891–898, 2011.
[25]  H. D. Margeirsdottir, J. R. Larsen, C. Brunborg, N. C. ?verby, and K. Dahl-J?rgensen, “High prevalence of cardiovascular risk factors in children and adolescents with type 1 diabetes: a population-based study,” Diabetologia, vol. 51, no. 4, pp. 554–561, 2008.
[26]  The Diabetes Control and Complications Trial Research Group, “Effect of intensive diabetes treatment on the development and progression of long term complications in adolescents with insulin-dependent diabetes mellitus: Diabetes Control and Complications Trial,” Journal of Pediatrics, vol. 125, no. 2, pp. 177–188, 1994.
[27]  E. Downie, M. E. Craig, S. Hing, J. Cusumano, A. K. F. Chan, and K. C. Donaghue, “Continued reduction in the prevalence of retinopathy in adolescents with type 1 diabetes: role of insulin therapy and glycemic control,” Diabetes Care, vol. 34, no. 11, pp. 2368–2373, 2011.
[28]  A. Ceriello, K. Esposito, L. Piconi et al., “Oscillating glucose is more deleterious to endothelial function and oxidative stress than mean glucose in normal and type 2 diabetic patients,” Diabetes, vol. 57, no. 5, pp. 1349–1354, 2008.
[29]  I. M. E. Wentholt, W. Kulik, R. P. J. Michels, J. B. L. Hoekstra, and J. H. DeVries, “Glucose fluctuations and activation of oxidative stress in patients with type 1 diabetes,” Diabetologia, vol. 51, no. 1, pp. 183–190, 2008.
[30]  R. Hernández-Marco, P. Codo?er-Franch, S. Pons Morales, C. del Castillo Villaescusa, L. Boix García, and V. Valls Bellés, “Oxidant/antioxidant status and hyperfiltration in young patients with type 1 diabetes mellitus,” Pediatric Nephrology, vol. 24, no. 1, pp. 121–127, 2009.
[31]  R. Shamir, H. Kassis, M. Kaplan, T. Naveh, and N. Shehadeh, “Glycemic control in adolescents with type 1 diabetes mellitus improves lipid serum levels and oxidative stress,” Pediatric Diabetes, vol. 9, no. 2, pp. 104–109, 2008.
[32]  D. Bruttomesso, D. Crazzolara, A. Maran et al., “In Type 1 diabetic patients with good glycaemic control, blood glucose variability is lower during continuous subcutaneous insulin infusion than during multiple daily injections with insulin glargine,” Diabetic Medicine, vol. 25, no. 3, pp. 326–332, 2008.
[33]  J. C. Pickup, J. Kidd, S. Burmiston, and N. Yemane, “Determinants of glycaemic control in type 1 diabetes during intensified therapy with multiple daily insulin injections or continuous subcutaneous insulin infusion: importance of blood glucose variability,” Diabetes/Metabolism Research and Reviews, vol. 22, no. 3, pp. 232–237, 2006.
[34]  M. Phillip, T. Battelino, H. Rodriguez, et al., “Use of insulin pump therapy in the pediatric age group,” Diabetes Care, vol. 30, pp. 1653–1662, 2007.
[35]  C. Schreiver, U. Jacoby, B. Watzer, A. Thomas, D. Haffner, and D. C. Fischer, “Glycaemic variability in paediatric patients with type 1 diabetes on continuous subcutaneous insulin infusion (CSII) or multiple daily injections (MDI): a cross-sectional cohort study,” Clinical Endocrinology, vol. 79, no. 5, pp. 641–647, 2013.
[36]  M. Giménez, J. J. López, C. Castell, and I. Conget, “Hypoglycaemia and cardiovascular disease in Type 1 Diabetes. Results from the Catalan National Public Health registry on insulin pump therapy,” Diabetes Research and Clinical Practice, vol. 96, no. 2, pp. e23–e25, 2012.
[37]  Y.-H. Noh, S.-M. Lee, E.-J. Kim et al., “Improvement of cardiovascular risk factors in patients with type 2 diabetes after long-term continuous subcutaneous insulin infusion,” Diabetes/Metabolism Research and Reviews, vol. 24, no. 5, pp. 384–391, 2008.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133