Insulin Therapy for Type 2 Diabetes
Insulin Therapy for Type 2 Diabetes Sanne G. Swinnen , MD , Joost B. Hoekstra , PHD and J. Hans DeVries , PHD From the Department of Internal Medicine, Academic Medical Center, Amsterdam, the Netherlands. Corresponding author: Sanne G. Swinnen, s.g.swinnen{at}amc.uva.nl . A number of landmark random...
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description | Insulin Therapy for Type 2 Diabetes
Sanne G. Swinnen , MD ,
Joost B. Hoekstra , PHD and
J. Hans DeVries , PHD
From the Department of Internal Medicine, Academic Medical Center, Amsterdam, the Netherlands.
Corresponding author: Sanne G. Swinnen, s.g.swinnen{at}amc.uva.nl .
A number of landmark randomized clinical trials established that insulin therapy reduces microvascular complications ( 1 , 2 ). In addition, recent follow-up data from the U.K. Prospective Diabetes Study (UKPDS) suggest that early insulin treatment
also lowers macrovascular risk in type 2 diabetes ( 3 ). Whereas there is consensus on the need for insulin, controversy exists on how to initiate and intensify insulin therapy.
The options for the practical implementation of insulin therapy are many. In this presentation, we will give an overview of
the evidence on the various insulin regimens commonly used to treat type 2 diabetes.
Secondary analyses of the aforementioned landmark trials endeavored to establish a glycemic threshold value below which no
complications would occur. The UKPDS found no evidence for such a threshold for A1C, but instead showed that better glycemic
control was associated with reduced risks of complications over the whole glycemic range (“the lower the better”) ( 4 ). For the management of type 2 diabetes, this resulted in the recommendation to “maintain glycemic levels as close to the
nondiabetic range as possible” ( 5 ). However, in contrast to the UKPDS, the Kumamoto study observed a threshold, with no exacerbation of microvascular complications
in patients with type 2 diabetes whose A1C was |
doi_str_mv | 10.2337/dc09-S318 |
format | Article |
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Sanne G. Swinnen , MD ,
Joost B. Hoekstra , PHD and
J. Hans DeVries , PHD
From the Department of Internal Medicine, Academic Medical Center, Amsterdam, the Netherlands.
Corresponding author: Sanne G. Swinnen, s.g.swinnen{at}amc.uva.nl .
A number of landmark randomized clinical trials established that insulin therapy reduces microvascular complications ( 1 , 2 ). In addition, recent follow-up data from the U.K. Prospective Diabetes Study (UKPDS) suggest that early insulin treatment
also lowers macrovascular risk in type 2 diabetes ( 3 ). Whereas there is consensus on the need for insulin, controversy exists on how to initiate and intensify insulin therapy.
The options for the practical implementation of insulin therapy are many. In this presentation, we will give an overview of
the evidence on the various insulin regimens commonly used to treat type 2 diabetes.
Secondary analyses of the aforementioned landmark trials endeavored to establish a glycemic threshold value below which no
complications would occur. The UKPDS found no evidence for such a threshold for A1C, but instead showed that better glycemic
control was associated with reduced risks of complications over the whole glycemic range (“the lower the better”) ( 4 ). For the management of type 2 diabetes, this resulted in the recommendation to “maintain glycemic levels as close to the
nondiabetic range as possible” ( 5 ). However, in contrast to the UKPDS, the Kumamoto study observed a threshold, with no exacerbation of microvascular complications
in patients with type 2 diabetes whose A1C was <6.5%, suggesting no additional benefit in lowering A1C below this level ( 2 ). Moreover, the intensive glycemia treatment arm of the Action to Control Cardiovascular Risk in Diabetes (ACCORD) study,
targeting A1C <6.0%, was discontinued because of higher mortality in this group compared with the standard therapy group targeting
A1C from 7.0 to 7.9% ( 6 ). Therefore, the American Diabetes Association (ADA) recommendation of an A1C target <7.0% seems the most balanced compromise
at present ( 7 ).
Another important conclusion of the UKPDS was that the risk reductions in long-term complications were related to the levels
of glycemic control …
[Full Text of this Article]</description><identifier>ISSN: 0149-5992</identifier><identifier>EISSN: 1935-5548</identifier><identifier>DOI: 10.2337/dc09-S318</identifier><identifier>PMID: 19875560</identifier><identifier>CODEN: DICAD2</identifier><language>eng</language><publisher>United States: American Diabetes Association</publisher><subject>Care and treatment ; Clinical trials ; Diabetes ; Diabetes Mellitus, Type 2 - blood ; Diabetes Mellitus, Type 2 - drug therapy ; Diabetes Progression, Prevention, and Treatment ; Diabetes therapy ; Disease management ; Glycated Hemoglobin A - metabolism ; Humans ; Hyperglycemia - prevention & control ; Hypoglycemia - chemically induced ; Hypoglycemia - prevention & control ; Hypoglycemic Agents - adverse effects ; Hypoglycemic Agents - therapeutic use ; Insulin ; Insulin - adverse effects ; Insulin - analogs & derivatives ; Insulin - therapeutic use ; Patient Satisfaction ; Quality of Life ; Therapy ; Type 2 diabetes</subject><ispartof>Diabetes care, 2009-11, Vol.32 (suppl 2), p.S253-S259</ispartof><rights>COPYRIGHT 2009 American Diabetes Association</rights><rights>Copyright American Diabetes Association Nov 2009</rights><rights>2009 by the American Diabetes Association. 2009</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c583t-8b1f8d6e63fc4d7376f2e6438e0b04c0e724feb915b4b8fe689802336d4a461f3</citedby><cites>FETCH-LOGICAL-c583t-8b1f8d6e63fc4d7376f2e6438e0b04c0e724feb915b4b8fe689802336d4a461f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19875560$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Swinnen, Sanne G</creatorcontrib><creatorcontrib>Hoekstra, Joost B</creatorcontrib><creatorcontrib>DeVries, J. Hans</creatorcontrib><title>Insulin Therapy for Type 2 Diabetes</title><title>Diabetes care</title><addtitle>Diabetes Care</addtitle><description>Insulin Therapy for Type 2 Diabetes
Sanne G. Swinnen , MD ,
Joost B. Hoekstra , PHD and
J. Hans DeVries , PHD
From the Department of Internal Medicine, Academic Medical Center, Amsterdam, the Netherlands.
Corresponding author: Sanne G. Swinnen, s.g.swinnen{at}amc.uva.nl .
A number of landmark randomized clinical trials established that insulin therapy reduces microvascular complications ( 1 , 2 ). In addition, recent follow-up data from the U.K. Prospective Diabetes Study (UKPDS) suggest that early insulin treatment
also lowers macrovascular risk in type 2 diabetes ( 3 ). Whereas there is consensus on the need for insulin, controversy exists on how to initiate and intensify insulin therapy.
The options for the practical implementation of insulin therapy are many. In this presentation, we will give an overview of
the evidence on the various insulin regimens commonly used to treat type 2 diabetes.
Secondary analyses of the aforementioned landmark trials endeavored to establish a glycemic threshold value below which no
complications would occur. The UKPDS found no evidence for such a threshold for A1C, but instead showed that better glycemic
control was associated with reduced risks of complications over the whole glycemic range (“the lower the better”) ( 4 ). For the management of type 2 diabetes, this resulted in the recommendation to “maintain glycemic levels as close to the
nondiabetic range as possible” ( 5 ). However, in contrast to the UKPDS, the Kumamoto study observed a threshold, with no exacerbation of microvascular complications
in patients with type 2 diabetes whose A1C was <6.5%, suggesting no additional benefit in lowering A1C below this level ( 2 ). Moreover, the intensive glycemia treatment arm of the Action to Control Cardiovascular Risk in Diabetes (ACCORD) study,
targeting A1C <6.0%, was discontinued because of higher mortality in this group compared with the standard therapy group targeting
A1C from 7.0 to 7.9% ( 6 ). Therefore, the American Diabetes Association (ADA) recommendation of an A1C target <7.0% seems the most balanced compromise
at present ( 7 ).
Another important conclusion of the UKPDS was that the risk reductions in long-term complications were related to the levels
of glycemic control …
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Hans</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Insulin Therapy for Type 2 Diabetes</atitle><jtitle>Diabetes care</jtitle><addtitle>Diabetes Care</addtitle><date>2009-11-01</date><risdate>2009</risdate><volume>32</volume><issue>suppl 2</issue><spage>S253</spage><epage>S259</epage><pages>S253-S259</pages><issn>0149-5992</issn><eissn>1935-5548</eissn><coden>DICAD2</coden><abstract>Insulin Therapy for Type 2 Diabetes
Sanne G. Swinnen , MD ,
Joost B. Hoekstra , PHD and
J. Hans DeVries , PHD
From the Department of Internal Medicine, Academic Medical Center, Amsterdam, the Netherlands.
Corresponding author: Sanne G. Swinnen, s.g.swinnen{at}amc.uva.nl .
A number of landmark randomized clinical trials established that insulin therapy reduces microvascular complications ( 1 , 2 ). In addition, recent follow-up data from the U.K. Prospective Diabetes Study (UKPDS) suggest that early insulin treatment
also lowers macrovascular risk in type 2 diabetes ( 3 ). Whereas there is consensus on the need for insulin, controversy exists on how to initiate and intensify insulin therapy.
The options for the practical implementation of insulin therapy are many. In this presentation, we will give an overview of
the evidence on the various insulin regimens commonly used to treat type 2 diabetes.
Secondary analyses of the aforementioned landmark trials endeavored to establish a glycemic threshold value below which no
complications would occur. The UKPDS found no evidence for such a threshold for A1C, but instead showed that better glycemic
control was associated with reduced risks of complications over the whole glycemic range (“the lower the better”) ( 4 ). For the management of type 2 diabetes, this resulted in the recommendation to “maintain glycemic levels as close to the
nondiabetic range as possible” ( 5 ). However, in contrast to the UKPDS, the Kumamoto study observed a threshold, with no exacerbation of microvascular complications
in patients with type 2 diabetes whose A1C was <6.5%, suggesting no additional benefit in lowering A1C below this level ( 2 ). Moreover, the intensive glycemia treatment arm of the Action to Control Cardiovascular Risk in Diabetes (ACCORD) study,
targeting A1C <6.0%, was discontinued because of higher mortality in this group compared with the standard therapy group targeting
A1C from 7.0 to 7.9% ( 6 ). Therefore, the American Diabetes Association (ADA) recommendation of an A1C target <7.0% seems the most balanced compromise
at present ( 7 ).
Another important conclusion of the UKPDS was that the risk reductions in long-term complications were related to the levels
of glycemic control …
[Full Text of this Article]</abstract><cop>United States</cop><pub>American Diabetes Association</pub><pmid>19875560</pmid><doi>10.2337/dc09-S318</doi><oa>free_for_read</oa></addata></record> |
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subjects | Care and treatment Clinical trials Diabetes Diabetes Mellitus, Type 2 - blood Diabetes Mellitus, Type 2 - drug therapy Diabetes Progression, Prevention, and Treatment Diabetes therapy Disease management Glycated Hemoglobin A - metabolism Humans Hyperglycemia - prevention & control Hypoglycemia - chemically induced Hypoglycemia - prevention & control Hypoglycemic Agents - adverse effects Hypoglycemic Agents - therapeutic use Insulin Insulin - adverse effects Insulin - analogs & derivatives Insulin - therapeutic use Patient Satisfaction Quality of Life Therapy Type 2 diabetes |
title | Insulin Therapy for Type 2 Diabetes |
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