Metabolic and cardiovascular effects of early insulin glargin prescription: based on data from ORIGIN study

We discuss results of ORIGIN, a multicenter parallel groups study for efficiency assessment of insulin glargin against polyunsaturatedomega-3 fatty acids or placebo regarding cardiovascular and/or mortality risk reduction in patients with impaired fasting glycemia,impaired glucose tolerance or type...

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Autores principales: Elena Valer'evna Biryukova, Alexander Sergeevich Ametov, Mikhail Borisovich Antsiferov, Alsu Gafurovna Zalevskaya, Galina Afanas'evna Mel'nichenko, Ashot Musaelovich Mkrtumyan, Marina Vladimirovna Shestakova
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Publicado: Endocrinology Research Centre 2012
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spelling oai:doaj.org-article:b7e6d26cdbee4110988b38b6e29a334f2021-11-14T09:00:17ZMetabolic and cardiovascular effects of early insulin glargin prescription: based on data from ORIGIN study2072-03512072-037810.14341/2072-0351-6092https://doaj.org/article/b7e6d26cdbee4110988b38b6e29a334f2012-09-01T00:00:00Zhttps://www.dia-endojournals.ru/jour/article/view/6092https://doaj.org/toc/2072-0351https://doaj.org/toc/2072-0378We discuss results of ORIGIN, a multicenter parallel groups study for efficiency assessment of insulin glargin against polyunsaturatedomega-3 fatty acids or placebo regarding cardiovascular and/or mortality risk reduction in patients with impaired fasting glycemia,impaired glucose tolerance or type 2 diabetes mellitus (T2DM) on its early stage and high risk for cardiovascular events. 12 537 patientstook part in this study; 6 264 were randomized in insulin glargin group, where dosage was adjusted for complete compensationof fasting glycemia (5.3 mmol/l was set as a therapeutic goal). After treatment with glargin therapeutic goal was achieved and furthermaintained for 6.2 years of follow-up. Compensation of fasting glycemia did not affect the outcome of cardiovascular diseases in patientswith early stages of dysglycemia according to primary endpoints. It was not associated with increase in general morbidity and inrisk of hypoglycemic events. Treatment with insulin glargin delayed progression from prediabetes to clinical onset for 28% (OR 0.72,CI 95% 0.58-0.91; p = 0,006), while lowering incidence of DM. Longtime treatment with insulin glargin does not increase incidenceof malignant tumors of different localization, including patients with prediabetes. Due to results of ORIGIN, insulin glargin (Lantus?)has become the most studied human insulin analogue to date.Elena Valer'evna BiryukovaAlexander Sergeevich AmetovMikhail Borisovich AntsiferovAlsu Gafurovna ZalevskayaGalina Afanas'evna Mel'nichenkoAshot Musaelovich MkrtumyanMarina Vladimirovna ShestakovaEndocrinology Research Centrearticleprediabetesdiabetes mellitushypoglycemiaoncologyonsulin glarginorigin studyNutritional diseases. Deficiency diseasesRC620-627ENRUСахарный диабет, Vol 15, Iss 3, Pp 92-100 (2012)
institution DOAJ
collection DOAJ
language EN
RU
topic prediabetes
diabetes mellitus
hypoglycemia
oncology
onsulin glargin
origin study
Nutritional diseases. Deficiency diseases
RC620-627
spellingShingle prediabetes
diabetes mellitus
hypoglycemia
oncology
onsulin glargin
origin study
Nutritional diseases. Deficiency diseases
RC620-627
Elena Valer'evna Biryukova
Alexander Sergeevich Ametov
Mikhail Borisovich Antsiferov
Alsu Gafurovna Zalevskaya
Galina Afanas'evna Mel'nichenko
Ashot Musaelovich Mkrtumyan
Marina Vladimirovna Shestakova
Metabolic and cardiovascular effects of early insulin glargin prescription: based on data from ORIGIN study
description We discuss results of ORIGIN, a multicenter parallel groups study for efficiency assessment of insulin glargin against polyunsaturatedomega-3 fatty acids or placebo regarding cardiovascular and/or mortality risk reduction in patients with impaired fasting glycemia,impaired glucose tolerance or type 2 diabetes mellitus (T2DM) on its early stage and high risk for cardiovascular events. 12 537 patientstook part in this study; 6 264 were randomized in insulin glargin group, where dosage was adjusted for complete compensationof fasting glycemia (5.3 mmol/l was set as a therapeutic goal). After treatment with glargin therapeutic goal was achieved and furthermaintained for 6.2 years of follow-up. Compensation of fasting glycemia did not affect the outcome of cardiovascular diseases in patientswith early stages of dysglycemia according to primary endpoints. It was not associated with increase in general morbidity and inrisk of hypoglycemic events. Treatment with insulin glargin delayed progression from prediabetes to clinical onset for 28% (OR 0.72,CI 95% 0.58-0.91; p = 0,006), while lowering incidence of DM. Longtime treatment with insulin glargin does not increase incidenceof malignant tumors of different localization, including patients with prediabetes. Due to results of ORIGIN, insulin glargin (Lantus?)has become the most studied human insulin analogue to date.
format article
author Elena Valer'evna Biryukova
Alexander Sergeevich Ametov
Mikhail Borisovich Antsiferov
Alsu Gafurovna Zalevskaya
Galina Afanas'evna Mel'nichenko
Ashot Musaelovich Mkrtumyan
Marina Vladimirovna Shestakova
author_facet Elena Valer'evna Biryukova
Alexander Sergeevich Ametov
Mikhail Borisovich Antsiferov
Alsu Gafurovna Zalevskaya
Galina Afanas'evna Mel'nichenko
Ashot Musaelovich Mkrtumyan
Marina Vladimirovna Shestakova
author_sort Elena Valer'evna Biryukova
title Metabolic and cardiovascular effects of early insulin glargin prescription: based on data from ORIGIN study
title_short Metabolic and cardiovascular effects of early insulin glargin prescription: based on data from ORIGIN study
title_full Metabolic and cardiovascular effects of early insulin glargin prescription: based on data from ORIGIN study
title_fullStr Metabolic and cardiovascular effects of early insulin glargin prescription: based on data from ORIGIN study
title_full_unstemmed Metabolic and cardiovascular effects of early insulin glargin prescription: based on data from ORIGIN study
title_sort metabolic and cardiovascular effects of early insulin glargin prescription: based on data from origin study
publisher Endocrinology Research Centre
publishDate 2012
url https://doaj.org/article/b7e6d26cdbee4110988b38b6e29a334f
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