Baseline factors associated with glycaemic response to treatment with once-weekly dulaglutide in patients with type 2 diabetes

Dulaglutide glycaemic efficacy has been demonstrated in the AWARD clinical trial programme. The objective of the present analysis was to determine the major baseline factors associated with the reduction in glycated haemoglobin (HbA1c) in response to dulaglutide. Baseline covariates from patients re...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Diabetes, obesity & metabolism obesity & metabolism, 2016-11, Vol.18 (11), p.1138-1142
Hauptverfasser: Wysham, Carol, Guerci, Bruno, D'Alessio, David, Jia, Nan, Botros, Fady T.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1142
container_issue 11
container_start_page 1138
container_title Diabetes, obesity & metabolism
container_volume 18
creator Wysham, Carol
Guerci, Bruno
D'Alessio, David
Jia, Nan
Botros, Fady T.
description Dulaglutide glycaemic efficacy has been demonstrated in the AWARD clinical trial programme. The objective of the present analysis was to determine the major baseline factors associated with the reduction in glycated haemoglobin (HbA1c) in response to dulaglutide. Baseline covariates from patients receiving dulaglutide in six phase III studies (n = 2806) were analysed using a gradient‐boosting method to assess their relative influence on the change in HbA1c after 26 weeks of treatment. Influential variables (relative influence >5%) were further evaluated in univariate and multivariable modelling. The gradient‐boosting analysis showed that the top influential baseline factors associated with HbA1c reduction were: HbA1c (48.8%), age (9.1%), fasting serum glucose (FSG; 8.2%), fasting serum insulin (FSI; 6.7%) and estimated glomerular filtration rate (eGFR; 5.4%). Multivariable regression showed that higher baseline HbA1c was the major factor associated with greater HbA1c reduction [coefficient estimates: −0.6% (−6.6 mmol/mol); p < 0.0001]. Age ≤65 years, lower FSG level, FSI level ≤55 pmol/L and eGFR ≤100 mL/min/1.73 m2 were associated with greater decreases in HbA1c, but the effect was very small [coefficient estimates: −0.05% to −0.2% (−0.6 to −2.2 mmol/mol)]. These data indicate that higher baseline HbA1c, reflecting poor glycaemic status, is the major factor associated with greater reduction in HbA1c in response to dulaglutide treatment.
doi_str_mv 10.1111/dom.12702
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1837309472</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1835381583</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4522-59ccd516af7945fb1f932e8f15b4d1a73dc3e6920e9382c16f3e2db0a6622a373</originalsourceid><addsrcrecordid>eNqN0Ttv1jAUBuAIgWgpDPwBZIkFhrS-xI4zQqFfi1q6cBktxz4pbpM42I4-svDbcZu2QyUQXo6H57zS0VsULwneJ_kdWD_sE1pj-qjYJZVgJWFUPL7501I2mO4Uz2K8xBhXTNZPix1aU8Flw3aL3-91hN6NgDptkg8R6Ri9cTqBRVuXfqCLfjEaBmdQgDj5MQJKHqUAOg0wphX50UC5BbjqF2TnXl_0c3IWkBvRpJPLLq4wLRMgiqzTLSSIz4snne4jvLide8XXo49fDo_L0_PNyeG709JUnNKSN8ZYToTu6qbiXUu6hlGQHeFtZYmumTUMREMxNExSQ0THgNoWayEo1axme8WbNXcK_ucMManBRQN9r0fwc1REZoSbqqb_QzmThEuW6esH9NLPYcyHKIZ5U1WCs38qInMTjNCKZPV2VSb4GAN0agpu0GFRBKvrllVuWd20nO2r28S5HcDey7taMzhYwdb1sPw9SX04P7uLLNcNFxP8ut_Q4UqJmtVcff-8UXRzfCS-kU9Ksj8JOr-w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1827231241</pqid></control><display><type>article</type><title>Baseline factors associated with glycaemic response to treatment with once-weekly dulaglutide in patients with type 2 diabetes</title><source>MEDLINE</source><source>Access via Wiley Online Library</source><creator>Wysham, Carol ; Guerci, Bruno ; D'Alessio, David ; Jia, Nan ; Botros, Fady T.</creator><creatorcontrib>Wysham, Carol ; Guerci, Bruno ; D'Alessio, David ; Jia, Nan ; Botros, Fady T.</creatorcontrib><description>Dulaglutide glycaemic efficacy has been demonstrated in the AWARD clinical trial programme. The objective of the present analysis was to determine the major baseline factors associated with the reduction in glycated haemoglobin (HbA1c) in response to dulaglutide. Baseline covariates from patients receiving dulaglutide in six phase III studies (n = 2806) were analysed using a gradient‐boosting method to assess their relative influence on the change in HbA1c after 26 weeks of treatment. Influential variables (relative influence &gt;5%) were further evaluated in univariate and multivariable modelling. The gradient‐boosting analysis showed that the top influential baseline factors associated with HbA1c reduction were: HbA1c (48.8%), age (9.1%), fasting serum glucose (FSG; 8.2%), fasting serum insulin (FSI; 6.7%) and estimated glomerular filtration rate (eGFR; 5.4%). Multivariable regression showed that higher baseline HbA1c was the major factor associated with greater HbA1c reduction [coefficient estimates: −0.6% (−6.6 mmol/mol); p &lt; 0.0001]. Age ≤65 years, lower FSG level, FSI level ≤55 pmol/L and eGFR ≤100 mL/min/1.73 m2 were associated with greater decreases in HbA1c, but the effect was very small [coefficient estimates: −0.05% to −0.2% (−0.6 to −2.2 mmol/mol)]. These data indicate that higher baseline HbA1c, reflecting poor glycaemic status, is the major factor associated with greater reduction in HbA1c in response to dulaglutide treatment.</description><identifier>ISSN: 1462-8902</identifier><identifier>EISSN: 1463-1326</identifier><identifier>DOI: 10.1111/dom.12702</identifier><identifier>PMID: 27265893</identifier><identifier>CODEN: DOMEF6</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adolescent ; Adult ; Aged ; Blood Glucose - drug effects ; Blood Glucose - metabolism ; Diabetes ; Diabetes mellitus (non-insulin dependent) ; Diabetes Mellitus, Type 2 - blood ; Diabetes Mellitus, Type 2 - drug therapy ; Drug Administration Schedule ; dulaglutide ; Epidermal growth factor receptors ; Fasting ; Fasting - blood ; Female ; Glomerular filtration rate ; Glucagon-Like Peptides - administration &amp; dosage ; Glucagon-Like Peptides - adverse effects ; Glucagon-Like Peptides - analogs &amp; derivatives ; Glycated Hemoglobin A - drug effects ; Glycated Hemoglobin A - metabolism ; Hemoglobin ; Humans ; Hypoglycemia - blood ; Hypoglycemia - chemically induced ; Immunoglobulin Fc Fragments - administration &amp; dosage ; Immunoglobulin Fc Fragments - adverse effects ; Laboratory testing ; Male ; Metformin - administration &amp; dosage ; Metformin - adverse effects ; Middle Aged ; Patients ; Recombinant Fusion Proteins - administration &amp; dosage ; Recombinant Fusion Proteins - adverse effects ; Treatment Outcome ; type 2 diabetes ; Young Adult</subject><ispartof>Diabetes, obesity &amp; metabolism, 2016-11, Vol.18 (11), p.1138-1142</ispartof><rights>2016 John Wiley &amp; Sons Ltd</rights><rights>2016 John Wiley &amp; Sons Ltd.</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4522-59ccd516af7945fb1f932e8f15b4d1a73dc3e6920e9382c16f3e2db0a6622a373</citedby><cites>FETCH-LOGICAL-c4522-59ccd516af7945fb1f932e8f15b4d1a73dc3e6920e9382c16f3e2db0a6622a373</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fdom.12702$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fdom.12702$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27926,27927,45576,45577</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27265893$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wysham, Carol</creatorcontrib><creatorcontrib>Guerci, Bruno</creatorcontrib><creatorcontrib>D'Alessio, David</creatorcontrib><creatorcontrib>Jia, Nan</creatorcontrib><creatorcontrib>Botros, Fady T.</creatorcontrib><title>Baseline factors associated with glycaemic response to treatment with once-weekly dulaglutide in patients with type 2 diabetes</title><title>Diabetes, obesity &amp; metabolism</title><addtitle>Diabetes Obes Metab</addtitle><description>Dulaglutide glycaemic efficacy has been demonstrated in the AWARD clinical trial programme. The objective of the present analysis was to determine the major baseline factors associated with the reduction in glycated haemoglobin (HbA1c) in response to dulaglutide. Baseline covariates from patients receiving dulaglutide in six phase III studies (n = 2806) were analysed using a gradient‐boosting method to assess their relative influence on the change in HbA1c after 26 weeks of treatment. Influential variables (relative influence &gt;5%) were further evaluated in univariate and multivariable modelling. The gradient‐boosting analysis showed that the top influential baseline factors associated with HbA1c reduction were: HbA1c (48.8%), age (9.1%), fasting serum glucose (FSG; 8.2%), fasting serum insulin (FSI; 6.7%) and estimated glomerular filtration rate (eGFR; 5.4%). Multivariable regression showed that higher baseline HbA1c was the major factor associated with greater HbA1c reduction [coefficient estimates: −0.6% (−6.6 mmol/mol); p &lt; 0.0001]. Age ≤65 years, lower FSG level, FSI level ≤55 pmol/L and eGFR ≤100 mL/min/1.73 m2 were associated with greater decreases in HbA1c, but the effect was very small [coefficient estimates: −0.05% to −0.2% (−0.6 to −2.2 mmol/mol)]. These data indicate that higher baseline HbA1c, reflecting poor glycaemic status, is the major factor associated with greater reduction in HbA1c in response to dulaglutide treatment.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Blood Glucose - drug effects</subject><subject>Blood Glucose - metabolism</subject><subject>Diabetes</subject><subject>Diabetes mellitus (non-insulin dependent)</subject><subject>Diabetes Mellitus, Type 2 - blood</subject><subject>Diabetes Mellitus, Type 2 - drug therapy</subject><subject>Drug Administration Schedule</subject><subject>dulaglutide</subject><subject>Epidermal growth factor receptors</subject><subject>Fasting</subject><subject>Fasting - blood</subject><subject>Female</subject><subject>Glomerular filtration rate</subject><subject>Glucagon-Like Peptides - administration &amp; dosage</subject><subject>Glucagon-Like Peptides - adverse effects</subject><subject>Glucagon-Like Peptides - analogs &amp; derivatives</subject><subject>Glycated Hemoglobin A - drug effects</subject><subject>Glycated Hemoglobin A - metabolism</subject><subject>Hemoglobin</subject><subject>Humans</subject><subject>Hypoglycemia - blood</subject><subject>Hypoglycemia - chemically induced</subject><subject>Immunoglobulin Fc Fragments - administration &amp; dosage</subject><subject>Immunoglobulin Fc Fragments - adverse effects</subject><subject>Laboratory testing</subject><subject>Male</subject><subject>Metformin - administration &amp; dosage</subject><subject>Metformin - adverse effects</subject><subject>Middle Aged</subject><subject>Patients</subject><subject>Recombinant Fusion Proteins - administration &amp; dosage</subject><subject>Recombinant Fusion Proteins - adverse effects</subject><subject>Treatment Outcome</subject><subject>type 2 diabetes</subject><subject>Young Adult</subject><issn>1462-8902</issn><issn>1463-1326</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqN0Ttv1jAUBuAIgWgpDPwBZIkFhrS-xI4zQqFfi1q6cBktxz4pbpM42I4-svDbcZu2QyUQXo6H57zS0VsULwneJ_kdWD_sE1pj-qjYJZVgJWFUPL7501I2mO4Uz2K8xBhXTNZPix1aU8Flw3aL3-91hN6NgDptkg8R6Ri9cTqBRVuXfqCLfjEaBmdQgDj5MQJKHqUAOg0wphX50UC5BbjqF2TnXl_0c3IWkBvRpJPLLq4wLRMgiqzTLSSIz4snne4jvLide8XXo49fDo_L0_PNyeG709JUnNKSN8ZYToTu6qbiXUu6hlGQHeFtZYmumTUMREMxNExSQ0THgNoWayEo1axme8WbNXcK_ucMManBRQN9r0fwc1REZoSbqqb_QzmThEuW6esH9NLPYcyHKIZ5U1WCs38qInMTjNCKZPV2VSb4GAN0agpu0GFRBKvrllVuWd20nO2r28S5HcDey7taMzhYwdb1sPw9SX04P7uLLNcNFxP8ut_Q4UqJmtVcff-8UXRzfCS-kU9Ksj8JOr-w</recordid><startdate>201611</startdate><enddate>201611</enddate><creator>Wysham, Carol</creator><creator>Guerci, Bruno</creator><creator>D'Alessio, David</creator><creator>Jia, Nan</creator><creator>Botros, Fady T.</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7TK</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>201611</creationdate><title>Baseline factors associated with glycaemic response to treatment with once-weekly dulaglutide in patients with type 2 diabetes</title><author>Wysham, Carol ; Guerci, Bruno ; D'Alessio, David ; Jia, Nan ; Botros, Fady T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4522-59ccd516af7945fb1f932e8f15b4d1a73dc3e6920e9382c16f3e2db0a6622a373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Blood Glucose - drug effects</topic><topic>Blood Glucose - metabolism</topic><topic>Diabetes</topic><topic>Diabetes mellitus (non-insulin dependent)</topic><topic>Diabetes Mellitus, Type 2 - blood</topic><topic>Diabetes Mellitus, Type 2 - drug therapy</topic><topic>Drug Administration Schedule</topic><topic>dulaglutide</topic><topic>Epidermal growth factor receptors</topic><topic>Fasting</topic><topic>Fasting - blood</topic><topic>Female</topic><topic>Glomerular filtration rate</topic><topic>Glucagon-Like Peptides - administration &amp; dosage</topic><topic>Glucagon-Like Peptides - adverse effects</topic><topic>Glucagon-Like Peptides - analogs &amp; derivatives</topic><topic>Glycated Hemoglobin A - drug effects</topic><topic>Glycated Hemoglobin A - metabolism</topic><topic>Hemoglobin</topic><topic>Humans</topic><topic>Hypoglycemia - blood</topic><topic>Hypoglycemia - chemically induced</topic><topic>Immunoglobulin Fc Fragments - administration &amp; dosage</topic><topic>Immunoglobulin Fc Fragments - adverse effects</topic><topic>Laboratory testing</topic><topic>Male</topic><topic>Metformin - administration &amp; dosage</topic><topic>Metformin - adverse effects</topic><topic>Middle Aged</topic><topic>Patients</topic><topic>Recombinant Fusion Proteins - administration &amp; dosage</topic><topic>Recombinant Fusion Proteins - adverse effects</topic><topic>Treatment Outcome</topic><topic>type 2 diabetes</topic><topic>Young Adult</topic><toplevel>online_resources</toplevel><creatorcontrib>Wysham, Carol</creatorcontrib><creatorcontrib>Guerci, Bruno</creatorcontrib><creatorcontrib>D'Alessio, David</creatorcontrib><creatorcontrib>Jia, Nan</creatorcontrib><creatorcontrib>Botros, Fady T.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Diabetes, obesity &amp; metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wysham, Carol</au><au>Guerci, Bruno</au><au>D'Alessio, David</au><au>Jia, Nan</au><au>Botros, Fady T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Baseline factors associated with glycaemic response to treatment with once-weekly dulaglutide in patients with type 2 diabetes</atitle><jtitle>Diabetes, obesity &amp; metabolism</jtitle><addtitle>Diabetes Obes Metab</addtitle><date>2016-11</date><risdate>2016</risdate><volume>18</volume><issue>11</issue><spage>1138</spage><epage>1142</epage><pages>1138-1142</pages><issn>1462-8902</issn><eissn>1463-1326</eissn><coden>DOMEF6</coden><abstract>Dulaglutide glycaemic efficacy has been demonstrated in the AWARD clinical trial programme. The objective of the present analysis was to determine the major baseline factors associated with the reduction in glycated haemoglobin (HbA1c) in response to dulaglutide. Baseline covariates from patients receiving dulaglutide in six phase III studies (n = 2806) were analysed using a gradient‐boosting method to assess their relative influence on the change in HbA1c after 26 weeks of treatment. Influential variables (relative influence &gt;5%) were further evaluated in univariate and multivariable modelling. The gradient‐boosting analysis showed that the top influential baseline factors associated with HbA1c reduction were: HbA1c (48.8%), age (9.1%), fasting serum glucose (FSG; 8.2%), fasting serum insulin (FSI; 6.7%) and estimated glomerular filtration rate (eGFR; 5.4%). Multivariable regression showed that higher baseline HbA1c was the major factor associated with greater HbA1c reduction [coefficient estimates: −0.6% (−6.6 mmol/mol); p &lt; 0.0001]. Age ≤65 years, lower FSG level, FSI level ≤55 pmol/L and eGFR ≤100 mL/min/1.73 m2 were associated with greater decreases in HbA1c, but the effect was very small [coefficient estimates: −0.05% to −0.2% (−0.6 to −2.2 mmol/mol)]. These data indicate that higher baseline HbA1c, reflecting poor glycaemic status, is the major factor associated with greater reduction in HbA1c in response to dulaglutide treatment.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>27265893</pmid><doi>10.1111/dom.12702</doi><tpages>5</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1462-8902
ispartof Diabetes, obesity & metabolism, 2016-11, Vol.18 (11), p.1138-1142
issn 1462-8902
1463-1326
language eng
recordid cdi_proquest_miscellaneous_1837309472
source MEDLINE; Access via Wiley Online Library
subjects Adolescent
Adult
Aged
Blood Glucose - drug effects
Blood Glucose - metabolism
Diabetes
Diabetes mellitus (non-insulin dependent)
Diabetes Mellitus, Type 2 - blood
Diabetes Mellitus, Type 2 - drug therapy
Drug Administration Schedule
dulaglutide
Epidermal growth factor receptors
Fasting
Fasting - blood
Female
Glomerular filtration rate
Glucagon-Like Peptides - administration & dosage
Glucagon-Like Peptides - adverse effects
Glucagon-Like Peptides - analogs & derivatives
Glycated Hemoglobin A - drug effects
Glycated Hemoglobin A - metabolism
Hemoglobin
Humans
Hypoglycemia - blood
Hypoglycemia - chemically induced
Immunoglobulin Fc Fragments - administration & dosage
Immunoglobulin Fc Fragments - adverse effects
Laboratory testing
Male
Metformin - administration & dosage
Metformin - adverse effects
Middle Aged
Patients
Recombinant Fusion Proteins - administration & dosage
Recombinant Fusion Proteins - adverse effects
Treatment Outcome
type 2 diabetes
Young Adult
title Baseline factors associated with glycaemic response to treatment with once-weekly dulaglutide in patients with type 2 diabetes
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-18T06%3A13%3A01IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Baseline%20factors%20associated%20with%20glycaemic%20response%20to%20treatment%20with%20once-weekly%20dulaglutide%20in%20patients%20with%20type%202%20diabetes&rft.jtitle=Diabetes,%20obesity%20&%20metabolism&rft.au=Wysham,%20Carol&rft.date=2016-11&rft.volume=18&rft.issue=11&rft.spage=1138&rft.epage=1142&rft.pages=1138-1142&rft.issn=1462-8902&rft.eissn=1463-1326&rft.coden=DOMEF6&rft_id=info:doi/10.1111/dom.12702&rft_dat=%3Cproquest_cross%3E1835381583%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1827231241&rft_id=info:pmid/27265893&rfr_iscdi=true