Insulin Therapy to Improve BMI in Cystic Fibrosis-Related Diabetes Without Fasting Hyperglycemia: Results of the Cystic Fibrosis Related Diabetes Therapy Trial

OBJECTIVE: Cystic fibrosis-related diabetes (CFRD) without fasting hyperglycemia (CFRD FH-) is not associated with microvascular or macrovascular complications, leading to controversy about the need for treatment. The Cystic Fibrosis Related Diabetes Therapy (CFRDT) Trial sought to determine whether...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Diabetes care 2009-10, Vol.32 (10), p.1783-1788
Hauptverfasser: Moran, Antoinette, Pekow, Penelope, Grover, Patricia, Zorn, Martha, Slovis, Bonnie, Pilewski, Joseph, Tullis, Elizabeth, Liou, Theodore G, Allen, Holley
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1788
container_issue 10
container_start_page 1783
container_title Diabetes care
container_volume 32
creator Moran, Antoinette
Pekow, Penelope
Grover, Patricia
Zorn, Martha
Slovis, Bonnie
Pilewski, Joseph
Tullis, Elizabeth
Liou, Theodore G
Allen, Holley
description OBJECTIVE: Cystic fibrosis-related diabetes (CFRD) without fasting hyperglycemia (CFRD FH-) is not associated with microvascular or macrovascular complications, leading to controversy about the need for treatment. The Cystic Fibrosis Related Diabetes Therapy (CFRDT) Trial sought to determine whether diabetes therapy improves BMI in these patients. RESEARCH DESIGN AND METHODS: A three-arm multicenter randomized trial compared 1 year of therapy with premeal insulin aspart, repaglinide, or oral placebo in subjects with cystic fibrosis who had abnormal glucose tolerance. RESULTS: One hundred adult patients were enrolled. Eighty-one completed the study, including 61 with CFRD FH- and 20 with severly impaired glucose tolerance (IGT). During the year before therapy, BMI declined in all groups. Among the group with CFRD FH-, insulin-treated patients lost 0.30 ± 0.21 BMI units the year before therapy. After 1 year of insulin therapy, this pattern reversed, and they gained 0.39 ± 21 BMI units (P = 0.02). No significant change in the rate of BMI decline was seen in placebo-treated patients (P = 0.45). Repaglinide-treated patients had an initial significant BMI gain (0.53 ± 0.19 BMI units, P = 0.01), but this effect was not sustained. After 6 months of therapy they lost weight so that by 12 months there was no difference in the rate of BMI change during the study year compared with the year before (P = 0.33). Among patients with IGT, neither insulin nor repaglinide affected the rate of BMI decline. No significant differences were seen in the rate of lung function decline or the number of hospitalizations in any group. CONCLUSIONS: Insulin therapy safely reversed chronic weight loss in patients with CFRD FH-.
doi_str_mv 10.2337/dc09-0585
format Article
fullrecord <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2752940</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A210368295</galeid><sourcerecordid>A210368295</sourcerecordid><originalsourceid>FETCH-LOGICAL-f423t-c1e5a0f9ef4e5c27a351b0288e8df11ac90f4325b2a95e81da2276b178d3896e3</originalsourceid><addsrcrecordid>eNptkV1rFDEUhgdR7Fq98A9oELycms-ZxAuhrq5dqAh1i5dDJnMymzI7GZNsYX6Nf9XAbosfJReBnCfPeU9SFC8JPqOM1e86g1WJhRSPigVRTJRCcPm4WGDCVSmUoifFsxhvMMacS_m0OCFKKFoxuih-rce4H9yINlsIeppR8mi9m4K_BfTx6xrlynKOyRm0cm3w0cXyCgadoEOfnG4hQUQ_XNr6fUIrncGxRxfzBKEfZgM7p9-jK8gdUkTeorSFf3XoP91dkk1wenhePLF6iPDiuJ8W16vPm-VFefnty3p5fllaTlkqDQGhsVVgOQhDa80EaTGVEmRnCdFGYcsZFS3VSoAknaa0rlpSy45JVQE7LT4cvNO-3UFnYExBD80U3E6HufHaNX9XRrdten_b0FpQxXEWvDkKgv-5h5iaG78PY87cUMpw7s1IhsoD1OsBGjdan12mhzFPPPgRrMvH55RgVkmqRObPHuDz6vLTmgcvvPpzjPv8dx-egbdHQEejBxv0aFy85yhRqq4rnrnXB85q3-g-ZOb6O8WEYVLJivOa_QbkrsRO</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>223032531</pqid></control><display><type>article</type><title>Insulin Therapy to Improve BMI in Cystic Fibrosis-Related Diabetes Without Fasting Hyperglycemia: Results of the Cystic Fibrosis Related Diabetes Therapy Trial</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>Moran, Antoinette ; Pekow, Penelope ; Grover, Patricia ; Zorn, Martha ; Slovis, Bonnie ; Pilewski, Joseph ; Tullis, Elizabeth ; Liou, Theodore G ; Allen, Holley</creator><creatorcontrib>Moran, Antoinette ; Pekow, Penelope ; Grover, Patricia ; Zorn, Martha ; Slovis, Bonnie ; Pilewski, Joseph ; Tullis, Elizabeth ; Liou, Theodore G ; Allen, Holley ; Cystic Fibrosis Related Diabetes Therapy Study Group</creatorcontrib><description>OBJECTIVE: Cystic fibrosis-related diabetes (CFRD) without fasting hyperglycemia (CFRD FH-) is not associated with microvascular or macrovascular complications, leading to controversy about the need for treatment. The Cystic Fibrosis Related Diabetes Therapy (CFRDT) Trial sought to determine whether diabetes therapy improves BMI in these patients. RESEARCH DESIGN AND METHODS: A three-arm multicenter randomized trial compared 1 year of therapy with premeal insulin aspart, repaglinide, or oral placebo in subjects with cystic fibrosis who had abnormal glucose tolerance. RESULTS: One hundred adult patients were enrolled. Eighty-one completed the study, including 61 with CFRD FH- and 20 with severly impaired glucose tolerance (IGT). During the year before therapy, BMI declined in all groups. Among the group with CFRD FH-, insulin-treated patients lost 0.30 ± 0.21 BMI units the year before therapy. After 1 year of insulin therapy, this pattern reversed, and they gained 0.39 ± 21 BMI units (P = 0.02). No significant change in the rate of BMI decline was seen in placebo-treated patients (P = 0.45). Repaglinide-treated patients had an initial significant BMI gain (0.53 ± 0.19 BMI units, P = 0.01), but this effect was not sustained. After 6 months of therapy they lost weight so that by 12 months there was no difference in the rate of BMI change during the study year compared with the year before (P = 0.33). Among patients with IGT, neither insulin nor repaglinide affected the rate of BMI decline. No significant differences were seen in the rate of lung function decline or the number of hospitalizations in any group. CONCLUSIONS: Insulin therapy safely reversed chronic weight loss in patients with CFRD FH-.</description><identifier>ISSN: 0149-5992</identifier><identifier>EISSN: 1935-5548</identifier><identifier>DOI: 10.2337/dc09-0585</identifier><identifier>PMID: 19592632</identifier><identifier>CODEN: DICAD2</identifier><language>eng</language><publisher>Alexandria, VA: American Diabetes Association</publisher><subject>Adult ; Biological and medical sciences ; Body Mass Index ; Care and treatment ; Clinical trials ; Cystic fibrosis ; Cystic Fibrosis - complications ; Dextrose ; Diabetes ; Diabetes Mellitus - drug therapy ; Diabetes Mellitus - etiology ; Diabetes. Impaired glucose tolerance ; Endocrine pancreas. Apud cells (diseases) ; Endocrinopathies ; Errors of metabolism ; Etiopathogenesis. Screening. Investigations. Target tissue resistance ; Female ; Fibrosis ; Glucose ; Humans ; Hyperglycemia ; Hyperglycemia - complications ; Hypoglycemia ; Hypoglycemic Agents - adverse effects ; Hypoglycemic Agents - therapeutic use ; Insulin ; Insulin - adverse effects ; Insulin - therapeutic use ; Male ; Medical sciences ; Metabolic diseases ; Miscellaneous ; Miscellaneous hereditary metabolic disorders ; Original Research ; Public health. Hygiene ; Public health. Hygiene-occupational medicine</subject><ispartof>Diabetes care, 2009-10, Vol.32 (10), p.1783-1788</ispartof><rights>2009 INIST-CNRS</rights><rights>COPYRIGHT 2009 American Diabetes Association</rights><rights>Copyright American Diabetes Association Oct 2009</rights><rights>2009 by the American Diabetes Association. 2009</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=21997764$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19592632$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Moran, Antoinette</creatorcontrib><creatorcontrib>Pekow, Penelope</creatorcontrib><creatorcontrib>Grover, Patricia</creatorcontrib><creatorcontrib>Zorn, Martha</creatorcontrib><creatorcontrib>Slovis, Bonnie</creatorcontrib><creatorcontrib>Pilewski, Joseph</creatorcontrib><creatorcontrib>Tullis, Elizabeth</creatorcontrib><creatorcontrib>Liou, Theodore G</creatorcontrib><creatorcontrib>Allen, Holley</creatorcontrib><creatorcontrib>Cystic Fibrosis Related Diabetes Therapy Study Group</creatorcontrib><title>Insulin Therapy to Improve BMI in Cystic Fibrosis-Related Diabetes Without Fasting Hyperglycemia: Results of the Cystic Fibrosis Related Diabetes Therapy Trial</title><title>Diabetes care</title><addtitle>Diabetes Care</addtitle><description>OBJECTIVE: Cystic fibrosis-related diabetes (CFRD) without fasting hyperglycemia (CFRD FH-) is not associated with microvascular or macrovascular complications, leading to controversy about the need for treatment. The Cystic Fibrosis Related Diabetes Therapy (CFRDT) Trial sought to determine whether diabetes therapy improves BMI in these patients. RESEARCH DESIGN AND METHODS: A three-arm multicenter randomized trial compared 1 year of therapy with premeal insulin aspart, repaglinide, or oral placebo in subjects with cystic fibrosis who had abnormal glucose tolerance. RESULTS: One hundred adult patients were enrolled. Eighty-one completed the study, including 61 with CFRD FH- and 20 with severly impaired glucose tolerance (IGT). During the year before therapy, BMI declined in all groups. Among the group with CFRD FH-, insulin-treated patients lost 0.30 ± 0.21 BMI units the year before therapy. After 1 year of insulin therapy, this pattern reversed, and they gained 0.39 ± 21 BMI units (P = 0.02). No significant change in the rate of BMI decline was seen in placebo-treated patients (P = 0.45). Repaglinide-treated patients had an initial significant BMI gain (0.53 ± 0.19 BMI units, P = 0.01), but this effect was not sustained. After 6 months of therapy they lost weight so that by 12 months there was no difference in the rate of BMI change during the study year compared with the year before (P = 0.33). Among patients with IGT, neither insulin nor repaglinide affected the rate of BMI decline. No significant differences were seen in the rate of lung function decline or the number of hospitalizations in any group. CONCLUSIONS: Insulin therapy safely reversed chronic weight loss in patients with CFRD FH-.</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Body Mass Index</subject><subject>Care and treatment</subject><subject>Clinical trials</subject><subject>Cystic fibrosis</subject><subject>Cystic Fibrosis - complications</subject><subject>Dextrose</subject><subject>Diabetes</subject><subject>Diabetes Mellitus - drug therapy</subject><subject>Diabetes Mellitus - etiology</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Errors of metabolism</subject><subject>Etiopathogenesis. Screening. Investigations. Target tissue resistance</subject><subject>Female</subject><subject>Fibrosis</subject><subject>Glucose</subject><subject>Humans</subject><subject>Hyperglycemia</subject><subject>Hyperglycemia - complications</subject><subject>Hypoglycemia</subject><subject>Hypoglycemic Agents - adverse effects</subject><subject>Hypoglycemic Agents - therapeutic use</subject><subject>Insulin</subject><subject>Insulin - adverse effects</subject><subject>Insulin - therapeutic use</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Metabolic diseases</subject><subject>Miscellaneous</subject><subject>Miscellaneous hereditary metabolic disorders</subject><subject>Original Research</subject><subject>Public health. Hygiene</subject><subject>Public health. Hygiene-occupational medicine</subject><issn>0149-5992</issn><issn>1935-5548</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptkV1rFDEUhgdR7Fq98A9oELycms-ZxAuhrq5dqAh1i5dDJnMymzI7GZNsYX6Nf9XAbosfJReBnCfPeU9SFC8JPqOM1e86g1WJhRSPigVRTJRCcPm4WGDCVSmUoifFsxhvMMacS_m0OCFKKFoxuih-rce4H9yINlsIeppR8mi9m4K_BfTx6xrlynKOyRm0cm3w0cXyCgadoEOfnG4hQUQ_XNr6fUIrncGxRxfzBKEfZgM7p9-jK8gdUkTeorSFf3XoP91dkk1wenhePLF6iPDiuJ8W16vPm-VFefnty3p5fllaTlkqDQGhsVVgOQhDa80EaTGVEmRnCdFGYcsZFS3VSoAknaa0rlpSy45JVQE7LT4cvNO-3UFnYExBD80U3E6HufHaNX9XRrdten_b0FpQxXEWvDkKgv-5h5iaG78PY87cUMpw7s1IhsoD1OsBGjdan12mhzFPPPgRrMvH55RgVkmqRObPHuDz6vLTmgcvvPpzjPv8dx-egbdHQEejBxv0aFy85yhRqq4rnrnXB85q3-g-ZOb6O8WEYVLJivOa_QbkrsRO</recordid><startdate>20091001</startdate><enddate>20091001</enddate><creator>Moran, Antoinette</creator><creator>Pekow, Penelope</creator><creator>Grover, Patricia</creator><creator>Zorn, Martha</creator><creator>Slovis, Bonnie</creator><creator>Pilewski, Joseph</creator><creator>Tullis, Elizabeth</creator><creator>Liou, Theodore G</creator><creator>Allen, Holley</creator><general>American Diabetes Association</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>7RV</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BEC</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0K</scope><scope>M0R</scope><scope>M0S</scope><scope>M0T</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>S0X</scope><scope>5PM</scope></search><sort><creationdate>20091001</creationdate><title>Insulin Therapy to Improve BMI in Cystic Fibrosis-Related Diabetes Without Fasting Hyperglycemia: Results of the Cystic Fibrosis Related Diabetes Therapy Trial</title><author>Moran, Antoinette ; Pekow, Penelope ; Grover, Patricia ; Zorn, Martha ; Slovis, Bonnie ; Pilewski, Joseph ; Tullis, Elizabeth ; Liou, Theodore G ; Allen, Holley</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-f423t-c1e5a0f9ef4e5c27a351b0288e8df11ac90f4325b2a95e81da2276b178d3896e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Body Mass Index</topic><topic>Care and treatment</topic><topic>Clinical trials</topic><topic>Cystic fibrosis</topic><topic>Cystic Fibrosis - complications</topic><topic>Dextrose</topic><topic>Diabetes</topic><topic>Diabetes Mellitus - drug therapy</topic><topic>Diabetes Mellitus - etiology</topic><topic>Diabetes. Impaired glucose tolerance</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>Errors of metabolism</topic><topic>Etiopathogenesis. Screening. Investigations. Target tissue resistance</topic><topic>Female</topic><topic>Fibrosis</topic><topic>Glucose</topic><topic>Humans</topic><topic>Hyperglycemia</topic><topic>Hyperglycemia - complications</topic><topic>Hypoglycemia</topic><topic>Hypoglycemic Agents - adverse effects</topic><topic>Hypoglycemic Agents - therapeutic use</topic><topic>Insulin</topic><topic>Insulin - adverse effects</topic><topic>Insulin - therapeutic use</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Metabolic diseases</topic><topic>Miscellaneous</topic><topic>Miscellaneous hereditary metabolic disorders</topic><topic>Original Research</topic><topic>Public health. Hygiene</topic><topic>Public health. Hygiene-occupational medicine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Moran, Antoinette</creatorcontrib><creatorcontrib>Pekow, Penelope</creatorcontrib><creatorcontrib>Grover, Patricia</creatorcontrib><creatorcontrib>Zorn, Martha</creatorcontrib><creatorcontrib>Slovis, Bonnie</creatorcontrib><creatorcontrib>Pilewski, Joseph</creatorcontrib><creatorcontrib>Tullis, Elizabeth</creatorcontrib><creatorcontrib>Liou, Theodore G</creatorcontrib><creatorcontrib>Allen, Holley</creatorcontrib><creatorcontrib>Cystic Fibrosis Related Diabetes Therapy Study Group</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Agricultural Science Collection</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Database</collection><collection>Agricultural &amp; Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>eLibrary</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Agricultural Science Database</collection><collection>Consumer Health Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Diabetes care</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Moran, Antoinette</au><au>Pekow, Penelope</au><au>Grover, Patricia</au><au>Zorn, Martha</au><au>Slovis, Bonnie</au><au>Pilewski, Joseph</au><au>Tullis, Elizabeth</au><au>Liou, Theodore G</au><au>Allen, Holley</au><aucorp>Cystic Fibrosis Related Diabetes Therapy Study Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Insulin Therapy to Improve BMI in Cystic Fibrosis-Related Diabetes Without Fasting Hyperglycemia: Results of the Cystic Fibrosis Related Diabetes Therapy Trial</atitle><jtitle>Diabetes care</jtitle><addtitle>Diabetes Care</addtitle><date>2009-10-01</date><risdate>2009</risdate><volume>32</volume><issue>10</issue><spage>1783</spage><epage>1788</epage><pages>1783-1788</pages><issn>0149-5992</issn><eissn>1935-5548</eissn><coden>DICAD2</coden><abstract>OBJECTIVE: Cystic fibrosis-related diabetes (CFRD) without fasting hyperglycemia (CFRD FH-) is not associated with microvascular or macrovascular complications, leading to controversy about the need for treatment. The Cystic Fibrosis Related Diabetes Therapy (CFRDT) Trial sought to determine whether diabetes therapy improves BMI in these patients. RESEARCH DESIGN AND METHODS: A three-arm multicenter randomized trial compared 1 year of therapy with premeal insulin aspart, repaglinide, or oral placebo in subjects with cystic fibrosis who had abnormal glucose tolerance. RESULTS: One hundred adult patients were enrolled. Eighty-one completed the study, including 61 with CFRD FH- and 20 with severly impaired glucose tolerance (IGT). During the year before therapy, BMI declined in all groups. Among the group with CFRD FH-, insulin-treated patients lost 0.30 ± 0.21 BMI units the year before therapy. After 1 year of insulin therapy, this pattern reversed, and they gained 0.39 ± 21 BMI units (P = 0.02). No significant change in the rate of BMI decline was seen in placebo-treated patients (P = 0.45). Repaglinide-treated patients had an initial significant BMI gain (0.53 ± 0.19 BMI units, P = 0.01), but this effect was not sustained. After 6 months of therapy they lost weight so that by 12 months there was no difference in the rate of BMI change during the study year compared with the year before (P = 0.33). Among patients with IGT, neither insulin nor repaglinide affected the rate of BMI decline. No significant differences were seen in the rate of lung function decline or the number of hospitalizations in any group. CONCLUSIONS: Insulin therapy safely reversed chronic weight loss in patients with CFRD FH-.</abstract><cop>Alexandria, VA</cop><pub>American Diabetes Association</pub><pmid>19592632</pmid><doi>10.2337/dc09-0585</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0149-5992
ispartof Diabetes care, 2009-10, Vol.32 (10), p.1783-1788
issn 0149-5992
1935-5548
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2752940
source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects Adult
Biological and medical sciences
Body Mass Index
Care and treatment
Clinical trials
Cystic fibrosis
Cystic Fibrosis - complications
Dextrose
Diabetes
Diabetes Mellitus - drug therapy
Diabetes Mellitus - etiology
Diabetes. Impaired glucose tolerance
Endocrine pancreas. Apud cells (diseases)
Endocrinopathies
Errors of metabolism
Etiopathogenesis. Screening. Investigations. Target tissue resistance
Female
Fibrosis
Glucose
Humans
Hyperglycemia
Hyperglycemia - complications
Hypoglycemia
Hypoglycemic Agents - adverse effects
Hypoglycemic Agents - therapeutic use
Insulin
Insulin - adverse effects
Insulin - therapeutic use
Male
Medical sciences
Metabolic diseases
Miscellaneous
Miscellaneous hereditary metabolic disorders
Original Research
Public health. Hygiene
Public health. Hygiene-occupational medicine
title Insulin Therapy to Improve BMI in Cystic Fibrosis-Related Diabetes Without Fasting Hyperglycemia: Results of the Cystic Fibrosis Related Diabetes Therapy Trial
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-06T23%3A19%3A43IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Insulin%20Therapy%20to%20Improve%20BMI%20in%20Cystic%20Fibrosis-Related%20Diabetes%20Without%20Fasting%20Hyperglycemia:%20Results%20of%20the%20Cystic%20Fibrosis%20Related%20Diabetes%20Therapy%20Trial&rft.jtitle=Diabetes%20care&rft.au=Moran,%20Antoinette&rft.aucorp=Cystic%20Fibrosis%20Related%20Diabetes%20Therapy%20Study%20Group&rft.date=2009-10-01&rft.volume=32&rft.issue=10&rft.spage=1783&rft.epage=1788&rft.pages=1783-1788&rft.issn=0149-5992&rft.eissn=1935-5548&rft.coden=DICAD2&rft_id=info:doi/10.2337/dc09-0585&rft_dat=%3Cgale_pubme%3EA210368295%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=223032531&rft_id=info:pmid/19592632&rft_galeid=A210368295&rfr_iscdi=true