Comparison of Insulin Monotherapy and Combination Therapy With Insulin and Metformin or Insulin and Troglitazone in Type 2 Diabetes

Comparison of Insulin Monotherapy and Combination Therapy With Insulin and Metformin or Insulin and Troglitazone in Type 2 Diabetes Suzanne M. Strowig , MSN, RN , M. Larissa Avilés-Santa , MD and Philip Raskin , MD From the University of Texas Southwestern Medical Center at Dallas, Dallas, Texas Abs...

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Veröffentlicht in:Diabetes care 2002-10, Vol.25 (10), p.1691-1698
Hauptverfasser: STROWIG, Suzanne M, LARISSA AVILES-SANTA, M, RASKIN, Philip
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creator STROWIG, Suzanne M
LARISSA AVILES-SANTA, M
RASKIN, Philip
description Comparison of Insulin Monotherapy and Combination Therapy With Insulin and Metformin or Insulin and Troglitazone in Type 2 Diabetes Suzanne M. Strowig , MSN, RN , M. Larissa Avilés-Santa , MD and Philip Raskin , MD From the University of Texas Southwestern Medical Center at Dallas, Dallas, Texas Abstract OBJECTIVE —To evaluate the safety and efficacy of treatment with insulin alone, insulin plus metformin, or insulin plus troglitazone in individuals with type 2 diabetes. RESEARCH DESIGN AND METHODS —A total of 88 type 2 diabetic subjects using insulin monotherapy (baseline HbA lc 8.7%) were randomly assigned to insulin alone ( n = 31), insulin plus metformin ( n = 27), or insulin plus troglitazone ( n = 30) for 4 months. The insulin dose was increased only in the insulin group. Metformin was titrated to a maximum dose of 2,000 mg and troglitazone to 600 mg. RESULTS —HbA lc levels decreased in all groups, the lowest level occurring in the insulin plus troglitazone group (insulin alone to 7.0%, insulin plus metformin to 7.1%, and insulin plus troglitazone to 6.4%, P < 0.0001). The dose of insulin increased by 55 units/day in the insulin alone group ( P < 0.0001) and decreased by 1.4 units/day in the insulin plus metformin group and 12.8 units/day in the insulin plus troglitazone group (insulin plus metformin versus insulin plus troglitazone, P = 0.004). Body weight increased by 0.5 kg in the insulin plus metformin group, whereas the other two groups gained 4.4 kg ( P < 0.0001 vs. baseline). Triglyceride and VLDL triglyceride levels significantly improved only in the insulin plus troglitazone group. Subjects taking metformin experienced significantly more gastrointestinal side effects and less hypoglycemia. CONCLUSIONS —Aggressive insulin therapy significantly improved glycemic control in type 2 diabetic subjects to levels comparable with those achieved by adding metformin to insulin therapy. Troglitazone was the most effective in lowering HbA lc , total daily insulin dose, and triglyceride levels. However, treatment with insulin plus metformin was advantageous in avoiding weight gain and hypoglycemia. ALT, alanine aminotransferase AST, aspartate aminotransferase DCCT, Diabetes Control and Complications Trial UKPDS, U.K. Prospective Diabetes Study Footnotes Address correspondence and reprint requests to Suzanne M. Strowig at University of Texas Southwestern Medical Center at Dallas, 5323 Harry Hines Blvd., Dallas, TX 75390-8858. E-mail: suzanne.strowig{at}UTS
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Strowig , MSN, RN , M. Larissa Avilés-Santa , MD and Philip Raskin , MD From the University of Texas Southwestern Medical Center at Dallas, Dallas, Texas Abstract OBJECTIVE —To evaluate the safety and efficacy of treatment with insulin alone, insulin plus metformin, or insulin plus troglitazone in individuals with type 2 diabetes. RESEARCH DESIGN AND METHODS —A total of 88 type 2 diabetic subjects using insulin monotherapy (baseline HbA lc 8.7%) were randomly assigned to insulin alone ( n = 31), insulin plus metformin ( n = 27), or insulin plus troglitazone ( n = 30) for 4 months. The insulin dose was increased only in the insulin group. Metformin was titrated to a maximum dose of 2,000 mg and troglitazone to 600 mg. RESULTS —HbA lc levels decreased in all groups, the lowest level occurring in the insulin plus troglitazone group (insulin alone to 7.0%, insulin plus metformin to 7.1%, and insulin plus troglitazone to 6.4%, P &lt; 0.0001). The dose of insulin increased by 55 units/day in the insulin alone group ( P &lt; 0.0001) and decreased by 1.4 units/day in the insulin plus metformin group and 12.8 units/day in the insulin plus troglitazone group (insulin plus metformin versus insulin plus troglitazone, P = 0.004). Body weight increased by 0.5 kg in the insulin plus metformin group, whereas the other two groups gained 4.4 kg ( P &lt; 0.0001 vs. baseline). Triglyceride and VLDL triglyceride levels significantly improved only in the insulin plus troglitazone group. Subjects taking metformin experienced significantly more gastrointestinal side effects and less hypoglycemia. CONCLUSIONS —Aggressive insulin therapy significantly improved glycemic control in type 2 diabetic subjects to levels comparable with those achieved by adding metformin to insulin therapy. Troglitazone was the most effective in lowering HbA lc , total daily insulin dose, and triglyceride levels. However, treatment with insulin plus metformin was advantageous in avoiding weight gain and hypoglycemia. ALT, alanine aminotransferase AST, aspartate aminotransferase DCCT, Diabetes Control and Complications Trial UKPDS, U.K. Prospective Diabetes Study Footnotes Address correspondence and reprint requests to Suzanne M. Strowig at University of Texas Southwestern Medical Center at Dallas, 5323 Harry Hines Blvd., Dallas, TX 75390-8858. E-mail: suzanne.strowig{at}UTSouthwestern.edu . Received for publication 8 February 2002 and accepted in revised form 2 July 2002. A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances. 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Endocrine system ; Humans ; Hypoglycemic agents ; Hypoglycemic Agents - therapeutic use ; Insulin ; Insulin - therapeutic use ; Lipids - blood ; Lipoproteins - blood ; Male ; Medical sciences ; Metformin ; Metformin - therapeutic use ; Middle Aged ; Pharmacology. 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Strowig , MSN, RN , M. Larissa Avilés-Santa , MD and Philip Raskin , MD From the University of Texas Southwestern Medical Center at Dallas, Dallas, Texas Abstract OBJECTIVE —To evaluate the safety and efficacy of treatment with insulin alone, insulin plus metformin, or insulin plus troglitazone in individuals with type 2 diabetes. RESEARCH DESIGN AND METHODS —A total of 88 type 2 diabetic subjects using insulin monotherapy (baseline HbA lc 8.7%) were randomly assigned to insulin alone ( n = 31), insulin plus metformin ( n = 27), or insulin plus troglitazone ( n = 30) for 4 months. The insulin dose was increased only in the insulin group. Metformin was titrated to a maximum dose of 2,000 mg and troglitazone to 600 mg. RESULTS —HbA lc levels decreased in all groups, the lowest level occurring in the insulin plus troglitazone group (insulin alone to 7.0%, insulin plus metformin to 7.1%, and insulin plus troglitazone to 6.4%, P &lt; 0.0001). The dose of insulin increased by 55 units/day in the insulin alone group ( P &lt; 0.0001) and decreased by 1.4 units/day in the insulin plus metformin group and 12.8 units/day in the insulin plus troglitazone group (insulin plus metformin versus insulin plus troglitazone, P = 0.004). Body weight increased by 0.5 kg in the insulin plus metformin group, whereas the other two groups gained 4.4 kg ( P &lt; 0.0001 vs. baseline). Triglyceride and VLDL triglyceride levels significantly improved only in the insulin plus troglitazone group. Subjects taking metformin experienced significantly more gastrointestinal side effects and less hypoglycemia. CONCLUSIONS —Aggressive insulin therapy significantly improved glycemic control in type 2 diabetic subjects to levels comparable with those achieved by adding metformin to insulin therapy. Troglitazone was the most effective in lowering HbA lc , total daily insulin dose, and triglyceride levels. However, treatment with insulin plus metformin was advantageous in avoiding weight gain and hypoglycemia. ALT, alanine aminotransferase AST, aspartate aminotransferase DCCT, Diabetes Control and Complications Trial UKPDS, U.K. Prospective Diabetes Study Footnotes Address correspondence and reprint requests to Suzanne M. Strowig at University of Texas Southwestern Medical Center at Dallas, 5323 Harry Hines Blvd., Dallas, TX 75390-8858. E-mail: suzanne.strowig{at}UTSouthwestern.edu . Received for publication 8 February 2002 and accepted in revised form 2 July 2002. A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances. DIABETES CARE</description><subject>Adult</subject><subject>Age of Onset</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Body Mass Index</subject><subject>C-Peptide - blood</subject><subject>Care and treatment</subject><subject>Chromans - therapeutic use</subject><subject>Comparative analysis</subject><subject>Continental Population Groups</subject><subject>Diabetes</subject><subject>Diabetes Mellitus, Type 2 - blood</subject><subject>Diabetes Mellitus, Type 2 - drug therapy</subject><subject>Drug therapy</subject><subject>Drug Therapy, Combination</subject><subject>Evaluation</subject><subject>Female</subject><subject>General and cellular metabolism. Vitamins</subject><subject>Glycated Hemoglobin A - metabolism</subject><subject>Hormones. Endocrine system</subject><subject>Humans</subject><subject>Hypoglycemic agents</subject><subject>Hypoglycemic Agents - therapeutic use</subject><subject>Insulin</subject><subject>Insulin - therapeutic use</subject><subject>Lipids - blood</subject><subject>Lipoproteins - blood</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Metformin</subject><subject>Metformin - therapeutic use</subject><subject>Middle Aged</subject><subject>Pharmacology. Drug treatments</subject><subject>Texas</subject><subject>Thiazoles - therapeutic use</subject><subject>Thiazolidinediones</subject><subject>Troglitazone</subject><subject>Type 2 diabetes</subject><issn>0149-5992</issn><issn>1935-5548</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpt0U2L1DAYB_AgijuufgEPUoT1oh3z2jTHZXxb2MXLiMeSpk9msrTJmLTIePWLmzLFRRl6KP339yRp_wi9JHhNGZPvO6eNjrCmYp0jUinyCK2IYqIUgteP0QoTrkqhFL1Az1K6xxhzXtdP0QWhTBBesRX6vQnDQUeXgi-CLW58mnrni7vgw7iHqA_HQvuuyKp1Xo8us-2Sf3fj_u_AjO5gtCEO-SnEf15sY9j1btS_gociZ9vjAQpafHC6hRHSc_TE6j7Bi-V-ib59-rjdfClvv36-2VzflobTipRc4FYpUK0EgUHaCtdWkbqTAIzamhvLbC1AGskJYy1YUgGzLa84453qKnaJ3pzWPcTwY4I0NoNLBvpeewhTaiQlVEg2w9f_wfswRZ_P1lDKsKBckozendBO99A4b8MYtdmBz3-nzx9qXY6vFZWqroTIvDzD89XB4Mw5T0_exJBSBNscoht0PDYEN3P9zVJ_Q8UczfXnoVfLwad2gO5hZOk7g6sF6GR0b6P2xqUHxxTnXMrs3p7c3u32P13epVvKOrftH8yUyQc</recordid><startdate>200210</startdate><enddate>200210</enddate><creator>STROWIG, Suzanne M</creator><creator>LARISSA AVILES-SANTA, M</creator><creator>RASKIN, Philip</creator><general>American Diabetes Association</general><scope>IQODW</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>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>7X8</scope></search><sort><creationdate>200210</creationdate><title>Comparison of Insulin Monotherapy and Combination Therapy With Insulin and Metformin or Insulin and Troglitazone in Type 2 Diabetes</title><author>STROWIG, Suzanne M ; LARISSA AVILES-SANTA, M ; RASKIN, Philip</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4261-450b99e9b7e50e7f608f918d7ee32f84cf3f85e7c74133bef16e3fb46434d9d63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Adult</topic><topic>Age of Onset</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Body Mass Index</topic><topic>C-Peptide - blood</topic><topic>Care and treatment</topic><topic>Chromans - therapeutic use</topic><topic>Comparative analysis</topic><topic>Continental Population Groups</topic><topic>Diabetes</topic><topic>Diabetes Mellitus, Type 2 - blood</topic><topic>Diabetes Mellitus, Type 2 - drug therapy</topic><topic>Drug therapy</topic><topic>Drug Therapy, Combination</topic><topic>Evaluation</topic><topic>Female</topic><topic>General and cellular metabolism. Vitamins</topic><topic>Glycated Hemoglobin A - metabolism</topic><topic>Hormones. Endocrine system</topic><topic>Humans</topic><topic>Hypoglycemic agents</topic><topic>Hypoglycemic Agents - therapeutic use</topic><topic>Insulin</topic><topic>Insulin - therapeutic use</topic><topic>Lipids - blood</topic><topic>Lipoproteins - blood</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Metformin</topic><topic>Metformin - therapeutic use</topic><topic>Middle Aged</topic><topic>Pharmacology. 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Strowig , MSN, RN , M. Larissa Avilés-Santa , MD and Philip Raskin , MD From the University of Texas Southwestern Medical Center at Dallas, Dallas, Texas Abstract OBJECTIVE —To evaluate the safety and efficacy of treatment with insulin alone, insulin plus metformin, or insulin plus troglitazone in individuals with type 2 diabetes. RESEARCH DESIGN AND METHODS —A total of 88 type 2 diabetic subjects using insulin monotherapy (baseline HbA lc 8.7%) were randomly assigned to insulin alone ( n = 31), insulin plus metformin ( n = 27), or insulin plus troglitazone ( n = 30) for 4 months. The insulin dose was increased only in the insulin group. Metformin was titrated to a maximum dose of 2,000 mg and troglitazone to 600 mg. RESULTS —HbA lc levels decreased in all groups, the lowest level occurring in the insulin plus troglitazone group (insulin alone to 7.0%, insulin plus metformin to 7.1%, and insulin plus troglitazone to 6.4%, P &lt; 0.0001). The dose of insulin increased by 55 units/day in the insulin alone group ( P &lt; 0.0001) and decreased by 1.4 units/day in the insulin plus metformin group and 12.8 units/day in the insulin plus troglitazone group (insulin plus metformin versus insulin plus troglitazone, P = 0.004). Body weight increased by 0.5 kg in the insulin plus metformin group, whereas the other two groups gained 4.4 kg ( P &lt; 0.0001 vs. baseline). Triglyceride and VLDL triglyceride levels significantly improved only in the insulin plus troglitazone group. Subjects taking metformin experienced significantly more gastrointestinal side effects and less hypoglycemia. CONCLUSIONS —Aggressive insulin therapy significantly improved glycemic control in type 2 diabetic subjects to levels comparable with those achieved by adding metformin to insulin therapy. Troglitazone was the most effective in lowering HbA lc , total daily insulin dose, and triglyceride levels. However, treatment with insulin plus metformin was advantageous in avoiding weight gain and hypoglycemia. ALT, alanine aminotransferase AST, aspartate aminotransferase DCCT, Diabetes Control and Complications Trial UKPDS, U.K. Prospective Diabetes Study Footnotes Address correspondence and reprint requests to Suzanne M. Strowig at University of Texas Southwestern Medical Center at Dallas, 5323 Harry Hines Blvd., Dallas, TX 75390-8858. E-mail: suzanne.strowig{at}UTSouthwestern.edu . Received for publication 8 February 2002 and accepted in revised form 2 July 2002. A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances. DIABETES CARE</abstract><cop>Alexandria, VA</cop><pub>American Diabetes Association</pub><pmid>12351463</pmid><doi>10.2337/diacare.25.10.1691</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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identifier ISSN: 0149-5992
ispartof Diabetes care, 2002-10, Vol.25 (10), p.1691-1698
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source MEDLINE; EZB-FREE-00999 freely available EZB journals
subjects Adult
Age of Onset
Aged
Biological and medical sciences
Body Mass Index
C-Peptide - blood
Care and treatment
Chromans - therapeutic use
Comparative analysis
Continental Population Groups
Diabetes
Diabetes Mellitus, Type 2 - blood
Diabetes Mellitus, Type 2 - drug therapy
Drug therapy
Drug Therapy, Combination
Evaluation
Female
General and cellular metabolism. Vitamins
Glycated Hemoglobin A - metabolism
Hormones. Endocrine system
Humans
Hypoglycemic agents
Hypoglycemic Agents - therapeutic use
Insulin
Insulin - therapeutic use
Lipids - blood
Lipoproteins - blood
Male
Medical sciences
Metformin
Metformin - therapeutic use
Middle Aged
Pharmacology. Drug treatments
Texas
Thiazoles - therapeutic use
Thiazolidinediones
Troglitazone
Type 2 diabetes
title Comparison of Insulin Monotherapy and Combination Therapy With Insulin and Metformin or Insulin and Troglitazone in Type 2 Diabetes
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