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One-year treatment with exenatide vs. insulin glargine: effects on postprandial glycemia, lipid profiles, and oxidative stress.

Bunck, Mathijs C (författare)
Cornér, Anja (författare)
Eliasson, Björn, 1959 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicin, avdelningen för molekylär och klinisk medicin,Institute of Medicine, Department of Molecular and Clinical Medicine
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Heine, Robert J (författare)
Shaginian, Rimma M (författare)
Wu, Yan (författare)
Yan, Ping (författare)
Smith, Ulf, 1943 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicin, avdelningen för molekylär och klinisk medicin,Institute of Medicine, Department of Molecular and Clinical Medicine
Yki-Järvinen, Hannele (författare)
Diamant, Michaela (författare)
Taskinen, Marja-Riitta (författare)
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 (creator_code:org_t)
Elsevier BV, 2010
2010
Engelska.
Ingår i: Atherosclerosis. - : Elsevier BV. - 1879-1484 .- 0021-9150. ; 212:1, s. 223-9
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • OBJECTIVE: The objective of the present study was to investigate the effects of one-year treatment with exenatide or Insulin Glargine, followed by a 5-week off-drug period, on postprandial lipidaemia, glycaemia and measures of oxidative stress. METHODS: Sixty-nine metformin-treated patients with type 2 diabetes were randomised (using apermuted block randomisation scheme stratified by site and baseline HbA(1c) stratum (< or = 8.5% or >8.5%) of which 60 completed (exenatide n=30; Insulin Glargine n=30) the pre-treatment and on-drug meal test. Postprandial glucose, lipids and lipoproteins, and oxidative stress markers were studied at week -1, 51, and after a 5-week off-drug period following a breakfast and lunch mixed-meal containing 50 g fat, 75 g carbohydrates, and 35 g protein. RESULTS: 51-Week exenatide treatment resulted in a significant reduction of prandial glucose, triglycerides, apo-B48, calculated VLDL-C, FFA and MDA excursions whereas Insulin Glargine predominantly reduced fasting glucose, FFA and MDA. Changes in markers of oxidative stress were related to changes in postprandial glucose and triglyceride excursions, independent of treatment arm. All postprandial measures returned to pre-treatment values in both groups after 5-week cessation of study treatment. CONCLUSION: Exenatide showed beneficial effects on postprandial glycaemia and lipidaemia, and these effects were related to changes in the oxidative stress markers MDA and oxLDL during one year of treatment as compared to Insulin Glargine. Following cessation of both exenatide and Insulin Glargine measures returned to pre-treatment values, suggesting that ongoing treatment is necessary to maintain the beneficial effects of either therapy.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)

Nyckelord

Apolipoprotein B-48
blood
Biological Markers
blood
Blood Glucose
drug effects
metabolism
Cholesterol
VLDL
blood
Diabetes Mellitus
Type 2
blood
drug therapy
Drug Administration Schedule
Europe
Fatty Acids
Nonesterified
blood
Female
Hemoglobin A
Glycosylated
metabolism
Humans
Hyperlipidemias
blood
etiology
prevention & control
Hypoglycemic Agents
administration & dosage
adverse effects
Insulin
administration & dosage
adverse effects
analogs & derivatives
Lipids
blood
Lipoproteins
LDL
blood
Male
Malondialdehyde
blood
Middle Aged
Oxidative Stress
drug effects
Peptides
administration & dosage
adverse effects
Postprandial Period
Time Factors
Treatment Outcome
Triglycerides
blood
Venoms
administration & dosage
adverse effects

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