Lispro is superior to regular insulin in transient intensive insulin therapy in type 2 diabetes
スポンサーリンク
概要
- 論文の詳細を見る
Objective. The optimal approach to relatively recent onset type 2 diabetes patients is still unknown. We speculated that the use of short-acting insulin analogs might be of particular benefit in this context. Patients and Methods. To explore this possibility, we compared the effect on β- and α-cell function of transient intensive insulin therapy using lispro versus human regular insulin in a total of 21 type 2 diabetic patients who were randomly assigned to 14-days intensive insulin therapy consisting of bedtime NPH insulin plus three injections of mealtime lispro (n=11) or regular insulin (n=10). The dosages of both types of insulin were adjusted to attain preprandial glucose levels of <6.1 mmol/l within 1 week with similar rates of glucose decline. An oral glucose tolerance test (OGTT) was performed at day 0 (baseline), 7, and 14; plasma glucose, serum insulin, and plasma glucagon responses over 0-120 minutes were measured, and calculated as the area under the curve (AUC). Results. Lispro led to a significant reduction in glucose-AUC and also an increase in insulin-AUC versus regular insulin on day 7. Glucagon secretion following OGTT was well suppressed with lispro on day 14 compared to regular insulin. Conclusion. Two-week intensive insulin therapy with lispro appeared to be more effective than that with regular insulin in type 2 diabetes in attaining both more rapid β-cell rest and greater suppression of glucagon. These changes may provide significant long-term benefits.
- 日本内科学会の論文
- 2004-09-01
著者
-
Mabuchi Hiroshi
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
-
Mabuchi Hiroshi
Departments Of Lipidology Kanazawa University Graduate School Of Medical Science
-
Yagi Kunimasa
Department of Internal Medicine, Kanazawa University Graduate School of Medical Science
-
Yagi Kunimasa
金沢大学 医学系研究科循環医科学専攻臓器機能制御学
-
Yagi Kunimasa
Department Of Internal Medicine Kanazawa University Graduate School Of Medical Science
-
Yagi Kunimasa
Department Of Internal Medicine Kanazawa University Hospital
-
MURAMOTO Hiroaki
Kanazawa Social Insurance Hospital
-
MURASE Yuko
Department of Lifestyle-related disease, Kanazawa University Graduate School of Medical Science
-
Murase Yuko
Department Of Lifestyle-related Disease Kanazawa University Graduate School Of Medical Science
-
Murase Yuko
Molecular Genetics Of Cardiovascular Disorders Graduate School Of Medical Science Kanazawa Universit
-
YAGI Kunimasa
Molecular Genetics of Cardiovascular Disorders, Graduate School of Medical Science, Kanazawa Univers
-
SUGIHARA Masako
Department of Internal Medicine, Kanazawa Social Insurance Hospital
-
CHUJO Daisuke
Molecular Genetics of Cardiovascular Disorders, Graduate School of Medical Science, Kanazawa Univers
-
OTSUJI Michio
Molecular Genetics of Cardiovascular Disorders, Graduate School of Medical Science, Kanazawa Univers
-
MURAMOTO Hiroaki
Department of Internal Medicine, Kanazawa Social Insurance Hospital
-
Otsuji Michio
Molecular Genetics Of Cardiovascular Disorders Graduate School Of Medical Science Kanazawa Universit
-
Chujo Daisuke
Department Of Internal Medicine Kanazawa University Hospital
-
Yagi Kunimasa
Division Of Cardiovascular Medicine Kanazawa University Graduate School Of Medicine
-
Yagi Kunimasa
Molecular Genetics Of Cardiovascular Disorders Graduate School Of Medical Science Kanazawa Universit
-
Mabuchi Hiroshi
Molecular Genetics Of Cardiovascular Disorders Graduate School Of Medical Science Kanazawa Universit
-
Mabuchi Hiroshi
Molecular Genetics Of Cardiovascular Disorders Vascular Medicine Division Of Cardiovascular Medicine
-
Sugihara Masako
Department Of Internal Medicine Kanazawa Social Insurance Hospital
-
Mabuchi Hiroshi
Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Graduate School O
-
Otsuji Michiko
Molecular Genetics of Cardiovascular Disorders, Graduate School of Medical Science, Kanazawa University
関連論文
- FRS-048 Temporal Assessment of Tenascin-C Expression after Myocardial Ischemia and Reperfusion using I-125-anti Tenascin-C Antibody(FRS10,Updates in Nuclear Cardiology (I),Featured Research Session (English),The 73rd Annual Scientific Meeting of The Japan
- Cardiac Sympathetic Nerve Activity and Left Ventricular Remodeling in Hypertrophic Cardiomyopathy(Cardiomyopathy, Clinical 3 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- PJ-424 Cardiac Sympathetic Nerve Activity in Patients with Hypertrophic Cardiomyopathy Caused by Thin Filament Gene Mutations(Cardiomyopathy, Clinical 5 (M) : PJ71)(Poster Session (Japanese))
- PE-502 Impact of Acceleration of Post-prandial Remnant Lipoprotein Clearance in Autosomal Recessive Hypercholesterolemia (ARH)(PE084,Lipid Disorders 2 (H),Poster Session (English),The 73rd Annual Scientific Meeting of the Japanese Circulation Society)
- Diabetes Progression from "High-Normal" Glucose in School Teachers
- Difference between Fasting and Nonfasting Triglyceridemia ; the Influence of Waist Circumference
- 2 Visceral Adipose Tissue vs. HOMA-R as a Predictor for Metabolic Abnormalities(Key Players of Metabolic Syndrome,Symposium 4 (SY-04) (M),The 73rd Annual Scientific Meeting of The Japanese Circulation Society)
- Telmisartan treatment decreases Visceral Fat Accumulation and improves Serum Levels of Adiponectin and Vascular Inflammation Markers in Japanese Hypertensive Patients.
- Effect of Walking with a Pedometer on Serum Lipid and Adiponectin Levels in Japanese Middle-aged Men
- 1144 The Importance of Coronary Vasospasm in Heterozygous Familial Hypercholesterolemia.
- -1113- Myocardial glucose metabolism in vasospastic angina(VSA)assessed by positron emission tomography(PET)(PROCEEDINGS OF THE 59th ANNUAL SCIENTIFIC MEETING OF THE JAPANESE CIRCULATION SOCIETY)
- -0435- RENAL ARTERIAL SCLEROSIS IN HETEROZYGOUS PATIENTS WITH FH(PROCEEDINGS OF THE 59th ANNUAL SCIENTIFIC MEETING OF THE JAPANESE CIRCULATION SOCIETY)
- Lispro is superior to regular insulin in transient intensive insulin therapy in type 2 diabetes
- Abnormal sympathetic innervation of the heart in a patient with Emery-Dreifuss muscular dystrophy
- Risk Evaluation of Coronary Heart Disease and Cerebrovascular Disease by the Japan Atherosclerosis Society Guidelines 2002 Using the Cohort of the Holicos-PAT Study
- Differentiation between patients with takotsubo cardiomyopathy and those with anterior acute myocardial infarction
- PE-279 High Incidence of Sudden Cardiac Death with Conduction Disturbances and Atrial Cardiomyopathy Caused by a Mutation in the STA Gene(Cardiomyopathy, Clinical 3 (M) : PE48)(Poster Session (English))
- Reduction of hemolysis without reoperation following mitral valve repair
- Identification of two novel missense mutations (p.R1221C and p.R1357W) in the ABCC6 (MRP6) gene in a Japanese patient with pseudoxanthoma elasticum (PXE)
- Type III hyperlipoproteinemia exaggerated by Sheehan's syndrome with advanced systemic atherosclerosis - A 28-year clinical course
- Japan Lipid Intervention Trial (J-LIT) Chart Predicts the Absence of Coronary Artery Disease More Accurately Than Symptom Limited Exercise Stress Electrocardiography
- In-hospital Outcome in Octogenarians with Acute Coronary Syndrome Undergoing Emergent Coronary Angiography
- Gene mutations in adult Japanese patients with dilated cardiomyopathy
- Oxidative Stress Correlates with Left Ventricular Volume after Acute Myocardial Infarction
- OE-007 Transient Overexpression of Heme Oxygenase-1 Promotes Cardioprotection in Ischemic Myocardial Injury through Antioxidative Stress and -apoptotic Activities(OE02,ACS/AMI (Basic) (IHD),Oral Presentation (English),The 73rd Annual Scientific Meeting of
- PJ-564 Transient Overexpression of Heme Oxygenage-1 Promotes Tolerance of Transplanted Mesenchymal Stem Cells to Oxidative Stress(Regeneration (angiogenesis/myocardial regeneration)(05)(M),Poster Session(Japanese),The 72nd Annual Scientific Meeting of the
- PE-493 Impact of Insulin Resistance on Coronary Ectasia : Results from Study on Heterozygous Familial Hypercholesterolemia with Common LDL Receptor Mutation(Diabetes/Obesity/Metabolic syndrome-08, The 71st Annual Scientific Meeting of the Japanese Circula
- Double deletions and missense mutations in the first nucleotide-binding fold of the ATP-binding cassette transporter A1 (ABCA1) gene in Japanese patients with Tangier disease
- Difference in the risk factors for coronary, renal and other peripheral arteriosclerosis in heterozygous familial hypercholesterolemia
- FRS-128 Mutations in Phospholamban Gene Cause Hypertrophic and Dilated Cardiomyopathy(Myocardial Disease (M) : FRS16)(Featured Research Session (English))
- Coronary Atherosclerosis and Apolipoprotein(a)phenotype
- -532- CORONARY ANGIOGRAPHIC CHARACTERISTICS IN PATIENTS WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA
- Retinoid X Receptor Heterodimer Variants and Cardiovascular Risk Factors
- The Relationship of Percent Body Fat by Bioelectrical Impedance Analysis with Blood Pressure, and Glucose and Lipid Parameters
- Association of Genetic Variation of the Adiponectin gene with Body Fat Distribution and Carotid Atherosclerosis in Japanese Obese Subjects
- CAUSES OF DEATH IN PATIENTS WITH FAMILIAL HYPERCHOLESTEROLEMIA : RATE OF DEATH FROM CORONARY HEART DISEASE : Atherosclerosis : PROCEEDINGS OF THE 50th ANNUAL SCIENTIFIC MEETING OF THE JAPANESE CIRCULATION SOCIETY
- Increased Circulating Matrix Metalloproteinase-2 in Patients with Hypertrophic Cardiomyopathy with Systolic Dysfunction
- Scintigraphic evaluation of regression of abnormal Q waves in myocardial infarction
- PJ-425 Early Development of Dilated Cardiomyopathy in Subjects with Mutations in the Cardiac Troponin Complex Genes(Cardiomyopathy, Clinical 5 (M) : PJ71)(Poster Session (Japanese))
- OJ-511 Missense Mutations in Cardiac Ryanodine Receptor Gene Cause Hypertrophic Cardiomyopathy Associated with Ventricular Arrhythmia or Massive Hypertrophy(Cardiomyopathy, Basic (M) : OJ62)(Oral Presentation (Japanese))
- OJ-229 Atrial Fibrillation in Patients with Hypertrophic Cardiomyopathy with Different Genotypes(Cardiomyopathy, Clinical 1 (M) : OJ26)(Oral Presentation (Japanese))
- OJ-078 Usefulness of Q-T Peak Dispersion for Diagnosis of KCNH2 Gene Mutations in Patients with Long QT Syndrome(Arrhythmia, Basic 1 (A) : OJ10)(Oral Presentation (Japanese))
- FRS-129 Mutations Responsible for Dilated Cardiomyopathy in Japan(Myocardial Disease (M) : FRS16)(Featured Research Session (English))
- PJ-596 Exercise-induced Systolic Dysfunction in Patients with Non-obstructive Hypertrophic Cardiomyopathy and Mutations in the Cardiac Troponin Genes(Cardiomyopathy, Clinical 7 (M) : PJ100)(Poster Session (Japanese))
- OJ-335 PRKAR1A Gene Mutation in Patients with Cardiac Myxoma(Valvular Heart Disease/Pericarditis/Cardiac Tumor 2 (M) : OJ40)(Oral Presentation (Japanese))
- Alterations in Echocardiographic Tissue Characterization in Patients with Cardiac Troponin I Gene Mutation a Possible Indicator of Preclinical Hypertrophic Cardiomyopathy
- Cardiac Actin and Alpha-Tropomyosin Genes Are Associated with Neither Hypertrophic Nor Dilated Cardiomyopathy in Patients from Hokuriku District in Japan
- PE-280 Missense Mutations in the MYBPC3 Gene are Responsible for Hypertrophic Cardiomyopathy with Left Ventricular Systolic Dysfunction and Dilatation(Cardiomyopathy, Clinical 3 (M) : PE48)(Poster Session (English))
- PE-278 Electrocardiography Shows Preferable Diagnostic Value Even in Carriers of Hypertrophic Cardiomyopathy who do not Manifest Ventricular Wall Hypertrophy on Echocardiography(Cardiomyopathy, Clinical 3 (M) : PE48)(Poster Session (English))
- OJ-237 KCNJ2 Gene Mutation is a Rare Cause of Long QT Syndrome(Arrhythmia, Diagnosis/Pathophysiology/EPS 9 (A) : OJ27)(Oral Presentation (Japanese))
- FRS-132 Phenotypic Discrepancies Between Electrocardiography and Echocardiography for Hypertrophic Cardiomyopathy in Genetically Affected Subjects(Myocardial Disease (M) : FRS16)(Featured Research Session (English))
- Left ventricular dysfunction and dilatation in elderly patients with hypertrophic cardiomyopathy associated with a novel missense mutation in MyBP-C gene
- Relationship between QT Variables and Disproportion of Left Ventricular Wall in Patients with Hypertrophic Cardiomyopathy
- Fluctuation of T-peak to T-end before and after ventricular tachycardia
- Q-T peak dispersion in congenital long QT syndrome ; increased lag of T wave peak as a new marker of HERG
- Pathophysiological Roles of the Adrenal Renin-Angiotensin System in Patients with Primary Aldosteronism
- Effects of Aldosterone Blockade on Cardiac Renin-Angiotensin-Aldosterone System in Salt-Sensitive Hypertension (Hypertension, Basic 5 (H), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Probucol-Induced Long QT Syndrome Associated with a Novel Missense Mutation M124T in the N Terminus of HERG
- Long QT Syndrome Mutations in Different Sites of HERG Elicit a Variety of Functional Changes
- Double Missense Mutations (D611Y in KCNQ1 and D609G in HERG) in a Japanese Family with Long QT Syndrome
- Characterization of a Novel Missense Mutation E637K in the Pore-S6 Loop of HERG in a Patient with Long QT Syndrome
- Clinical and electrophysiological characterization of a novel mutation (F193L) in the KCNQ1 gene associated with long QT syndrome
- Effects of Angiotensin-Converting Enzyme Inhibitor and Aldosterone Antagonist on Myocardial Collagen in Cardiomyopathic Hamsters
- -0954-ABDOMINAL ARTIC ANEURYSM OF FAMILIAL HYPERCHOLESTEROLEMIA : THE 54th ANNUAL SCIENTIFIC MEETING OF THE JAPANESE CIRCULATION SOCIETY
- Clinical features and prognosis of Japanese patients with anomalous origin of the coronary artery
- A Forced Burgers Turbulence in the Inviscid Limit
- Sixteen-slice computed tomography, transthoracic real-time 3-dimensional echocardiography and magnetic resonance imaging assessment of a long-term survivor of rupture of sinus of valsalva aneurysm
- Increased matrix metalloproteinase-2 in patients with hypertrophic cardiomyopathy with systolic dysfunction
- OE-234 Impact of Genetic Variation of the Adiponectin Gene and Body Fat Distribution on Development of Atherosclerosis in Metabolic Subjects(Metabolism/Biochemistry/Energetics(01)(M),Oral Presentation(English),The 72nd Annual Scientific Meeting of the Jap
- OJ-415 Electrocardiographic Events and Cholesterol Reduction with Pravastatin in Patients with Hypercholesterolemia : Hokuriku Lipid Coronary Heart Disease Study-Pravastatin Atherosclerosis Trial(Preventive Medicine/Epidemiology/Education 3 (H) : OJ50)(Or
- Effect of Pravastatin-Induced LDL-Cholesterol Reduction on Coronary Heart Disease and Cerebrovascular Disease in Japanese : Hokuriku Lipid Coronary Heart Disease Study-Pravastatin Atherosclerosis Trial(Holicos-PAT)
- PCSK9 Gene Mutation is Less Frequent in Clinically Diagnosed FH Patients without LDLR and ApoB-100 Gene Mutation in Japan(Lipid Disorders 1 (H), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Usefulness of Acoustic Densitometry Method for Detection of Myocardial Changes in Preclinical Patients with Hypertrophic Cardiomyopathy
- Prevalence of Long QT Syndrome in Japanese Children(ECG/Body Surface Potential Mapping/Holter 1 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Difference in Coronary Blood Flow Dynamics between Patients with Hypertension and Those with Hypertrophic Cardiomyopathy
- Quantitative evaluation of the rate of myocardial interstitial fibrosis using a personal computer
- Q-T peak dispersion in congenital long QT syndrome: Possible marker of mutation of HERG
- Cardiac Manifestations and Long-Term Course in Emery-Dreifuss Muscular Dystrophy Caused by a Nonsense Mutation in the STA Gene
- Effects of gender on the number of diseased vessels and clinical outcome in Japanese patients with acute coronary syndrome
- A novel de novo mutation in the cardiac β - myosin heavy chain gene in patients with dilated cardiomyopathy
- Mitochondrial DNA mutations in hypertrophic cardiomyopathy
- Novel KCNQ1 missense mutation (D611Y) in a Japanese long QT family
- Whole and regional variation of cardiac sympathetic nervous activity in patients with hypertrophic cardiomyopathy with malignant tachyarrthythmias and sudden death
- Age-related Changes in Abdominal Fat Distribution in Japanese Adults in the General Population
- Association between Single Nucleotide Polymorphisms (SNPs) of Cardiac Potassium Channel Genes and Drug-Induced Long QT Syndrome in Japanese
- A Novel Mutation (lnt21DSG+1A) in the MyBP-C Gene Shows Hypertrophic Cardiomyopathy with a High Degree of Penetrance in Adult Patients
- Microvascular ischemia in patients with myotonic dystrophy
- Diagnostic Values of Abnormal Q Waves for Hypertrophic Cardiomyopathy Based on the Genetic Information
- QT Variables in Preclinical Patients with Hypertrophic Cardiomyopathy
- QT Variables in Various Genotyped Patients with Hypertrophic Cardiomyopathy
- Mitochondrial DNA Mutations in Hypertrophic Cardiomyopathy
- Frequency of Asymmetric Septal Hypertrophy in Patients with Hypertrophic Cardiomyopathy : Difference in Genotypes
- Differences in Diagnostic Values of Abnormal Q Waves between Hypertrophic Cardiomyopathy with a cTnl Gene Mutation and MyBP-C Gene Mutations
- Spontaneous Development of Left Ventricular Aneurysm in a Patient With Untreated Cardiac Sarcoidosis
- Clinical and Electrophysiological Characteristics of Brugada Syndrome Caused by a Missense Mutation in the S5-pore site of SCN5A(Arrhythmia, Diagnosis/Pathophysiology/EPS 5 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- FRS-144 A Novel Missense Mutation of SCN5A Gene Associated with Brugada Syndrome by Bidirectional Effects on Blocking Actions of Antiarrhythmic Drugs(Sudden Cardiac Death (A) : FRS18)(Featured Research Session (English))
- Comparison of the effects of losartan vs. ramipril on several adipocytokines and vascular remodeling biomarkers
- Successful pregnancy and delivery in a patient with adult GH deficiency : role of GH replacement therapy
- Insulin secretion and insulin sensitivity on the oral glucose tolerance test (OGTT) in middle-aged Japanese
- Insulin Autoimmune Syndrome Caused by an Adhesive Skin Patch Containing Loxoprofen-Sodium