Effects of exenatide on measures of diabetic neuropathy in subjects with type 2 diabetes: results from an 18-month proof-of-concept open-label randomized study
Experimental studies have reported potential benefit of glucagon-like peptide-1(GLP-1) receptor agonists in preventing diabetic peripheral neuropathy (DPN). We therefore performed a proof-of-concept pilot study to evaluate the effect of exenatide, a GLP-1 agonist, on measures of DPN and cardiovascul...
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Published in | Journal of diabetes and its complications Vol. 29; no. 8; pp. 1287 - 1294 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier Inc
01.11.2015
Elsevier Limited |
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Abstract | Experimental studies have reported potential benefit of glucagon-like peptide-1(GLP-1) receptor agonists in preventing diabetic peripheral neuropathy (DPN). We therefore performed a proof-of-concept pilot study to evaluate the effect of exenatide, a GLP-1 agonist, on measures of DPN and cardiovascular autonomic neuropathy (CAN) in patients with type 2 diabetes (T2D).
Forty-six T2D subjects (age 54±10years, diabetes duration 8±5years, HbA1c 8.2±1.3%) with mild to moderate DPN at baseline were randomized to receive either twice daily exenatide (n=22) or daily insulin glargine (n=24). The subjects, with similar HbA1c levels, were followed for 18months. The primary end point was the prevalence of confirmed clinical neuropathy (CCN). Changes in measures of CAN, other measures of small fiber neuropathy such as intra-epidermal nerve fiber density (IENFD), and quality of life were also analyzed.
Glucose control was similar in both groups during the study. There were no statistically significant treatment group differences in the prevalence of CCN, IENFD, measures of CAN, nerve conductions studies, or quality of life indices.
In this pilot study of patients with T2D and mild to moderate DPN, 18months of exenatide treatment had no significant effect on measures of neuropathy compared with glargine treatment. |
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AbstractList | Experimental studies have reported potential benefit of glucagon-like peptide-1(GLP-1) receptor agonists in preventing diabetic peripheral neuropathy (DPN). We therefore performed a proof-of-concept pilot study to evaluate the effect of exenatide, a GLP-1 agonist, on measures of DPN and cardiovascular autonomic neuropathy (CAN) in patients with type 2 diabetes (T2D).
Forty-six T2D subjects (age 54±10years, diabetes duration 8±5years, HbA1c 8.2±1.3%) with mild to moderate DPN at baseline were randomized to receive either twice daily exenatide (n=22) or daily insulin glargine (n=24). The subjects, with similar HbA1c levels, were followed for 18months. The primary end point was the prevalence of confirmed clinical neuropathy (CCN). Changes in measures of CAN, other measures of small fiber neuropathy such as intra-epidermal nerve fiber density (IENFD), and quality of life were also analyzed.
Glucose control was similar in both groups during the study. There were no statistically significant treatment group differences in the prevalence of CCN, IENFD, measures of CAN, nerve conductions studies, or quality of life indices.
In this pilot study of patients with T2D and mild to moderate DPN, 18months of exenatide treatment had no significant effect on measures of neuropathy compared with glargine treatment. Abstract Objective Experimental studies have reported potential benefit of glucagon-like peptide-1(GLP-1) receptor agonists in preventing diabetic peripheral neuropathy (DPN). We therefore performed a proof-of-concept pilot study to evaluate the effect of exenatide, a GLP-1 agonist, on measures of DPN and cardiovascular autonomic neuropathy (CAN) in patients with type 2 diabetes (T2D). Research Design and Methods Forty-six T2D subjects (age 54 ± 10 years, diabetes duration 8 ± 5 years, HbA1c 8.2 ± 1.3%) with mild to moderate DPN at baseline were randomized to receive either twice daily exenatide (n = 22) or daily insulin glargine (n = 24). The subjects, with similar HbA1c levels, were followed for 18 months. The primary end point was the prevalence of confirmed clinical neuropathy (CCN). Changes in measures of CAN, other measures of small fiber neuropathy such as intra-epidermal nerve fiber density (IENFD), and quality of life were also analyzed. Results Glucose control was similar in both groups during the study. There were no statistically significant treatment group differences in the prevalence of CCN, IENFD, measures of CAN, nerve conductions studies, or quality of life indices. Conclusions In this pilot study of patients with T2D and mild to moderate DPN, 18 months of exenatide treatment had no significant effect on measures of neuropathy compared with glargine treatment. ObjectiveExperimental studies have reported potential benefit of glucagon-like peptide-1(GLP-1) receptor agonists in preventing diabetic peripheral neuropathy (DPN). We therefore performed a proof-of-concept pilot study to evaluate the effect of exenatide, a GLP-1 agonist, on measures of DPN and cardiovascular autonomic neuropathy (CAN) in patients with type 2 diabetes (T2D).Research Design and MethodsForty-six T2D subjects (age 54±10years, diabetes duration 8±5years, HbA1c 8.2±1.3%) with mild to moderate DPN at baseline were randomized to receive either twice daily exenatide (n=22) or daily insulin glargine (n=24). The subjects, with similar HbA1c levels, were followed for 18months. The primary end point was the prevalence of confirmed clinical neuropathy (CCN). Changes in measures of CAN, other measures of small fiber neuropathy such as intra-epidermal nerve fiber density (IENFD), and quality of life were also analyzed.ResultsGlucose control was similar in both groups during the study. There were no statistically significant treatment group differences in the prevalence of CCN, IENFD, measures of CAN, nerve conductions studies, or quality of life indices.ConclusionsIn this pilot study of patients with T2D and mild to moderate DPN, 18months of exenatide treatment had no significant effect on measures of neuropathy compared with glargine treatment. Objective Experimental studies have reported potential benefit of glucagon-like peptide-1(GLP-1) receptor agonists in preventing diabetic peripheral neuropathy (DPN). We therefore performed a proof-of-concept pilot study to evaluate the effect of exenatide, a GLP-1 agonist, on measures of DPN and cardiovascular autonomic neuropathy (CAN) in patients with type 2 diabetes (T2D). Research Design and Methods Forty-six T2D subjects (age 54 plus or minus 10years, diabetes duration 8 plus or minus 5years, HbA1c 8.2 plus or minus 1.3%) with mild to moderate DPN at baseline were randomized to receive either twice daily exenatide (n=22) or daily insulin glargine (n=24). The subjects, with similar HbA1c levels, were followed for 18months. The primary end point was the prevalence of confirmed clinical neuropathy (CCN). Changes in measures of CAN, other measures of small fiber neuropathy such as intra-epidermal nerve fiber density (IENFD), and quality of life were also analyzed. Results Glucose control was similar in both groups during the study. There were no statistically significant treatment group differences in the prevalence of CCN, IENFD, measures of CAN, nerve conductions studies, or quality of life indices. Conclusions In this pilot study of patients with T2D and mild to moderate DPN, 18months of exenatide treatment had no significant effect on measures of neuropathy compared with glargine treatment. |
Author | Jaiswal, Mamta Feldman, Eva L. Callaghan, Brian Pop-Busui, Rodica Martin, Catherine L. Albers, James W. Brown, Morton B. |
AuthorAffiliation | 2 Division of Metabolism, Endocrinology and Diabetes, Department of Internal Medicine, University of Michigan, Ann Arbor, MI 3 Department of Biostatistics, University of Michigan, Ann Arbor, MI 1 Department of Neurology, University of Michigan, Ann Arbor, MI |
AuthorAffiliation_xml | – name: 2 Division of Metabolism, Endocrinology and Diabetes, Department of Internal Medicine, University of Michigan, Ann Arbor, MI – name: 3 Department of Biostatistics, University of Michigan, Ann Arbor, MI – name: 1 Department of Neurology, University of Michigan, Ann Arbor, MI |
Author_xml | – sequence: 1 givenname: Mamta surname: Jaiswal fullname: Jaiswal, Mamta organization: Department of Neurology, University of Michigan, Ann Arbor, MI – sequence: 2 givenname: Catherine L. surname: Martin fullname: Martin, Catherine L. organization: Division of Metabolism, Endocrinology and Diabetes, Department of Internal Medicine, University of Michigan, Ann Arbor, MI – sequence: 3 givenname: Morton B. surname: Brown fullname: Brown, Morton B. organization: Department of Biostatistics, University of Michigan, Ann Arbor, MI – sequence: 4 givenname: Brian surname: Callaghan fullname: Callaghan, Brian organization: Department of Neurology, University of Michigan, Ann Arbor, MI – sequence: 5 givenname: James W. surname: Albers fullname: Albers, James W. organization: Department of Neurology, University of Michigan, Ann Arbor, MI – sequence: 6 givenname: Eva L. surname: Feldman fullname: Feldman, Eva L. organization: Department of Neurology, University of Michigan, Ann Arbor, MI – sequence: 7 givenname: Rodica surname: Pop-Busui fullname: Pop-Busui, Rodica email: rpbusui@med.umich.edu organization: Division of Metabolism, Endocrinology and Diabetes, Department of Internal Medicine, University of Michigan, Ann Arbor, MI |
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Keywords | Clinical trial GLP-1receptor agonist Diabetic peripheral neuropathy Exenatide Cardiovascular autonomic neuropathy Glargine |
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Snippet | Experimental studies have reported potential benefit of glucagon-like peptide-1(GLP-1) receptor agonists in preventing diabetic peripheral neuropathy (DPN). We... Abstract Objective Experimental studies have reported potential benefit of glucagon-like peptide-1(GLP-1) receptor agonists in preventing diabetic peripheral... ObjectiveExperimental studies have reported potential benefit of glucagon-like peptide-1(GLP-1) receptor agonists in preventing diabetic peripheral neuropathy... Objective Experimental studies have reported potential benefit of glucagon-like peptide-1(GLP-1) receptor agonists in preventing diabetic peripheral neuropathy... |
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SubjectTerms | Aged Cardiac arrhythmia Cardiovascular autonomic neuropathy Clinical trial Cohort Studies Colleges & universities Diabetes Diabetes Mellitus, Type 2 - blood Diabetes Mellitus, Type 2 - complications Diabetes Mellitus, Type 2 - drug therapy Diabetes Mellitus, Type 2 - metabolism Diabetic Neuropathies - epidemiology Diabetic Neuropathies - physiopathology Diabetic Neuropathies - prevention & control Diabetic neuropathy Diabetic peripheral neuropathy Endocrinology & Metabolism Exenatide Female Glargine GLP-1receptor agonist Glucagon-Like Peptide-1 Receptor - agonists Glucagon-Like Peptide-1 Receptor - metabolism Glycated Hemoglobin A - analysis Heart rate Humans Hyperglycemia Hyperglycemia - prevention & control Hypoglycemia Hypoglycemic Agents - adverse effects Hypoglycemic Agents - therapeutic use Incretins - adverse effects Incretins - therapeutic use Infections Insulin Insulin Glargine - adverse effects Insulin Glargine - therapeutic use Male Michigan - epidemiology Middle Aged Nausea Neural Conduction - drug effects Peptides - adverse effects Peptides - therapeutic use Pilot Projects Prevalence Quality of Life Severity of Illness Index Venoms - adverse effects Venoms - therapeutic use |
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Title | Effects of exenatide on measures of diabetic neuropathy in subjects with type 2 diabetes: results from an 18-month proof-of-concept open-label randomized study |
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