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Clinical use of the co-formulation of insulin degludec and insulin aspart.

Identifieur interne : 001A13 ( PubMed/Curation ); précédent : 001A12; suivant : 001A14

Clinical use of the co-formulation of insulin degludec and insulin aspart.

Auteurs : A. Kumar [Inde] ; T. Awata [Japon] ; S C Bain [Royaume-Uni] ; A. Ceriello [Espagne] ; G R Fulcher [Australie] ; A G Unnikrishnan ; R. Arechavaleta [Mexique] ; G. Gonzalez-Gálvez [Mexique] ; T. Hirose [Japon] ; P D Home [Royaume-Uni] ; K. Kaku [Japon] ; L. Litwak [Argentine] ; S. Madsbad [Danemark] ; M. Pinget [France] ; R. Mehta [Mexique] ; A. Mithal [Inde] ; M. Tambascia [Brésil] ; J. Tibaldi [États-Unis] ; J S Christiansen [Danemark]

Source :

RBID : pubmed:27384031

Descripteurs français

English descriptors

Abstract

To provide a review of the available data and practical use of insulin degludec with insulin aspart (IDegAsp). Premixed insulins provide basal and prandial glucose control; however, they have an intermediate-acting prandial insulin component and do not provide as effective basal coverage as true long-acting insulins, owing to the physicochemical incompatibility of their individual components, coupled with the inflexibility of adjustment. The molecular structure of the co-formulation of IDegAsp, a novel insulin preparation, allows these two molecules to coexist without affecting their individual pharmacodynamic profiles.

DOI: 10.1111/ijcp.12821
PubMed: 27384031

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pubmed:27384031

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A G Unnikrishnan
<affiliation>
<nlm:affiliation>Chellaram Diabetes Institute, Pune, Maharashtra.</nlm:affiliation>
<wicri:noCountry code="subField">Maharashtra</wicri:noCountry>
</affiliation>

Le document en format XML

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<name sortKey="Hirose, T" sort="Hirose, T" uniqKey="Hirose T" first="T" last="Hirose">T. Hirose</name>
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<nlm:affiliation>Division of Diabetes, Metabolism, and Endocrinology, Department of Medicine, Toho University School of Medicine, Tokyo, Japan.</nlm:affiliation>
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<name sortKey="Home, P D" sort="Home, P D" uniqKey="Home P" first="P D" last="Home">P D Home</name>
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<nlm:affiliation>Newcastle University, Newcastle upon Tyne, UK.</nlm:affiliation>
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<nlm:affiliation>Department of Internal Medicine, Kawasaki Medical School, Kurashiki, Japan.</nlm:affiliation>
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<name sortKey="Christiansen, J S" sort="Christiansen, J S" uniqKey="Christiansen J" first="J S" last="Christiansen">J S Christiansen</name>
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<country xml:lang="fr">Danemark</country>
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<title level="j">International journal of clinical practice</title>
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<term>Blood Glucose</term>
<term>Clinical Trials, Phase II as Topic</term>
<term>Clinical Trials, Phase III as Topic</term>
<term>Diabetes Mellitus, Type 1 (drug therapy)</term>
<term>Diabetes Mellitus, Type 2 (drug therapy)</term>
<term>Drug Administration Schedule</term>
<term>Drug Substitution</term>
<term>Humans</term>
<term>Hypoglycemic Agents (adverse effects)</term>
<term>Hypoglycemic Agents (pharmacology)</term>
<term>Hypoglycemic Agents (therapeutic use)</term>
<term>Insulin Aspart (administration & dosage)</term>
<term>Insulin Aspart (adverse effects)</term>
<term>Insulin Aspart (pharmacology)</term>
<term>Insulin, Long-Acting (administration & dosage)</term>
<term>Insulin, Long-Acting (adverse effects)</term>
<term>Insulin, Long-Acting (pharmacology)</term>
<term>Treatment Outcome</term>
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<term>Diabète de type 1 (traitement médicamenteux)</term>
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<term>Essais cliniques de phase II comme sujet</term>
<term>Essais cliniques de phase III comme sujet</term>
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<term>Hypoglycémiants (pharmacologie)</term>
<term>Hypoglycémiants (usage thérapeutique)</term>
<term>Insuline Asparte (administration et posologie)</term>
<term>Insuline Asparte (effets indésirables)</term>
<term>Insuline Asparte (pharmacologie)</term>
<term>Insuline à longue durée d'action (administration et posologie)</term>
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<term>Hypoglycemic Agents</term>
<term>Insulin Aspart</term>
<term>Insulin, Long-Acting</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en">
<term>Hypoglycemic Agents</term>
<term>Insulin Aspart</term>
<term>Insulin, Long-Acting</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en">
<term>Hypoglycemic Agents</term>
</keywords>
<keywords scheme="MESH" type="chemical" xml:lang="en">
<term>Blood Glucose</term>
</keywords>
<keywords scheme="MESH" qualifier="administration et posologie" xml:lang="fr">
<term>Insuline Asparte</term>
<term>Insuline à longue durée d'action</term>
</keywords>
<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en">
<term>Diabetes Mellitus, Type 1</term>
<term>Diabetes Mellitus, Type 2</term>
</keywords>
<keywords scheme="MESH" qualifier="effets indésirables" xml:lang="fr">
<term>Hypoglycémiants</term>
<term>Insuline Asparte</term>
<term>Insuline à longue durée d'action</term>
</keywords>
<keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr">
<term>Hypoglycémiants</term>
<term>Insuline Asparte</term>
<term>Insuline à longue durée d'action</term>
</keywords>
<keywords scheme="MESH" qualifier="traitement médicamenteux" xml:lang="fr">
<term>Diabète de type 1</term>
<term>Diabète de type 2</term>
</keywords>
<keywords scheme="MESH" qualifier="usage thérapeutique" xml:lang="fr">
<term>Hypoglycémiants</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Clinical Trials, Phase II as Topic</term>
<term>Clinical Trials, Phase III as Topic</term>
<term>Drug Administration Schedule</term>
<term>Drug Substitution</term>
<term>Humans</term>
<term>Treatment Outcome</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Calendrier d'administration des médicaments</term>
<term>Essais cliniques de phase II comme sujet</term>
<term>Essais cliniques de phase III comme sujet</term>
<term>Glycémie</term>
<term>Humains</term>
<term>Résultat thérapeutique</term>
<term>Substitution de médicament</term>
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<front>
<div type="abstract" xml:lang="en">To provide a review of the available data and practical use of insulin degludec with insulin aspart (IDegAsp). Premixed insulins provide basal and prandial glucose control; however, they have an intermediate-acting prandial insulin component and do not provide as effective basal coverage as true long-acting insulins, owing to the physicochemical incompatibility of their individual components, coupled with the inflexibility of adjustment. The molecular structure of the co-formulation of IDegAsp, a novel insulin preparation, allows these two molecules to coexist without affecting their individual pharmacodynamic profiles.</div>
</front>
</TEI>
<pubmed>
<MedlineCitation Status="MEDLINE" Owner="NLM">
<PMID Version="1">27384031</PMID>
<DateCreated>
<Year>2016</Year>
<Month>07</Month>
<Day>28</Day>
</DateCreated>
<DateCompleted>
<Year>2017</Year>
<Month>07</Month>
<Day>31</Day>
</DateCompleted>
<DateRevised>
<Year>2017</Year>
<Month>08</Month>
<Day>17</Day>
</DateRevised>
<Article PubModel="Print-Electronic">
<Journal>
<ISSN IssnType="Electronic">1742-1241</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>70</Volume>
<Issue>8</Issue>
<PubDate>
<Year>2016</Year>
<Month>Aug</Month>
</PubDate>
</JournalIssue>
<Title>International journal of clinical practice</Title>
<ISOAbbreviation>Int. J. Clin. Pract.</ISOAbbreviation>
</Journal>
<ArticleTitle>Clinical use of the co-formulation of insulin degludec and insulin aspart.</ArticleTitle>
<Pagination>
<MedlinePgn>657-67</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1111/ijcp.12821</ELocationID>
<Abstract>
<AbstractText Label="AIMS" NlmCategory="OBJECTIVE">To provide a review of the available data and practical use of insulin degludec with insulin aspart (IDegAsp). Premixed insulins provide basal and prandial glucose control; however, they have an intermediate-acting prandial insulin component and do not provide as effective basal coverage as true long-acting insulins, owing to the physicochemical incompatibility of their individual components, coupled with the inflexibility of adjustment. The molecular structure of the co-formulation of IDegAsp, a novel insulin preparation, allows these two molecules to coexist without affecting their individual pharmacodynamic profiles.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">Clinical evidence in phase 2/3 trials of IDegAsp efficacy and safety in type 1 and type 2 diabetes mellitus (T1DM and T2DM) have been assessed and summarised.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">In people with T2DM, once- and twice-daily dosing provides similar overall glycaemic control (HbA1c ) to current modern insulins, but with lower risk of nocturnal hypoglycaemia. In prior insulin users, glycaemic control was achieved with lower or equal insulin doses vs. other basal+meal-time or premix insulin regimens. In insulin-naïve patients with T2DM, IDegAsp can be started once or twice-daily, based on individual need. People switching from more than once-daily basal or premix insulin therapy can be converted unit-to-unit to once-daily IDegAsp, although this strategy should be assessed by the physician on an individual basis.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">IDegAsp offers physicians and people with T2DM a simpler insulin regimen than other available basal-bolus or premix-based insulin regimens, with stable daytime basal coverage, a lower rate of hypoglycaemia and some flexibility in injection timing compared with premix insulins.</AbstractText>
<CopyrightInformation>© 2016 John Wiley & Sons Ltd.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y">
<Author ValidYN="Y">
<LastName>Kumar</LastName>
<ForeName>A</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Diabetes Care & Research Centre, Patna, India.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Awata</LastName>
<ForeName>T</ForeName>
<Initials>T</Initials>
<AffiliationInfo>
<Affiliation>Department of Diabetes, Endocrinology and Metabolism, International University of Health and Welfare Hospital, Tochigi, Japan.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Bain</LastName>
<ForeName>S C</ForeName>
<Initials>SC</Initials>
<AffiliationInfo>
<Affiliation>Diabetes Research Unit Cymru, Swansea University & ABM University Health Board, Swansea, UK.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Ceriello</LastName>
<ForeName>A</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Insititut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS) and Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM), Barcelona, Spain.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>IRCCS MultiMedica, Milan, Italy.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Fulcher</LastName>
<ForeName>G R</ForeName>
<Initials>GR</Initials>
<AffiliationInfo>
<Affiliation>University of Sydney, Royal North Shore Hospital, Sydney, NSW, Australia.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Unnikrishnan</LastName>
<ForeName>A G</ForeName>
<Initials>AG</Initials>
<AffiliationInfo>
<Affiliation>Chellaram Diabetes Institute, Pune, Maharashtra.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Arechavaleta</LastName>
<ForeName>R</ForeName>
<Initials>R</Initials>
<AffiliationInfo>
<Affiliation>Departamento de Endocrinologia, Universidad Autónoma de Guadalajara, Zapopan, Mexico.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Gonzalez-Gálvez</LastName>
<ForeName>G</ForeName>
<Initials>G</Initials>
<AffiliationInfo>
<Affiliation>Instituto Jalisciense de Investigación en Diabetes y Obesidad S.C. Guadalajara, Jalisco, México.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Hirose</LastName>
<ForeName>T</ForeName>
<Initials>T</Initials>
<AffiliationInfo>
<Affiliation>Division of Diabetes, Metabolism, and Endocrinology, Department of Medicine, Toho University School of Medicine, Tokyo, Japan.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Home</LastName>
<ForeName>P D</ForeName>
<Initials>PD</Initials>
<AffiliationInfo>
<Affiliation>Newcastle University, Newcastle upon Tyne, UK.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Kaku</LastName>
<ForeName>K</ForeName>
<Initials>K</Initials>
<AffiliationInfo>
<Affiliation>Department of Internal Medicine, Kawasaki Medical School, Kurashiki, Japan.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Litwak</LastName>
<ForeName>L</ForeName>
<Initials>L</Initials>
<AffiliationInfo>
<Affiliation>Endocrine, Metabolism and Nuclear Medicine Service, Diabetes Section, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Madsbad</LastName>
<ForeName>S</ForeName>
<Initials>S</Initials>
<AffiliationInfo>
<Affiliation>Department of Endocrinology, Hvidovre Hospital, University of Copenhagen, Copenhagen, Denmark.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Pinget</LastName>
<ForeName>M</ForeName>
<Initials>M</Initials>
<AffiliationInfo>
<Affiliation>Department of Endocrinology, University of Strasbourg, Strasbourg, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Mehta</LastName>
<ForeName>R</ForeName>
<Initials>R</Initials>
<AffiliationInfo>
<Affiliation>Department of Endocrinology, National Institute of Medical Sciences and Nutrition, Salvador Zubirán, México City, Mexico.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Mithal</LastName>
<ForeName>A</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Division of Endocrinology and Diabetes, Medanta the Medicity, Gurgaon, Haryana, India.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Tambascia</LastName>
<ForeName>M</ForeName>
<Initials>M</Initials>
<AffiliationInfo>
<Affiliation>Faculty of Medical Sciences, State University of Campinas, São Paulo, Brazil.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Tibaldi</LastName>
<ForeName>J</ForeName>
<Initials>J</Initials>
<AffiliationInfo>
<Affiliation>Queens Diabetes and Endocrinology Associates, Fresh Meadows, New York, NY, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Christiansen</LastName>
<ForeName>J S</ForeName>
<Initials>JS</Initials>
<AffiliationInfo>
<Affiliation>Department of Clinical Medicine - The Department of Endocrinology and Diabetes, Aarhus University Hospital, NBG, Aarhus C, Denmark.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
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<PublicationType UI="D016428">Journal Article</PublicationType>
<PublicationType UI="D016454">Review</PublicationType>
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</Article>
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<Country>England</Country>
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<ISSNLinking>1368-5031</ISSNLinking>
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<QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName>
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<MeshHeading>
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<Month>11</Month>
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