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1.
Diabetes Obes Metab ; 19(11): 1635-1639, 2017 11.
Article in English | MEDLINE | ID: mdl-28417527

ABSTRACT

Youth with type 1 diabetes (T1D) infrequently achieve HbA1c targets. Therefore, this placebo-controlled, randomized, crossover study was set up to assess the safety, effect and pharmacokinetics of a single dose of 10 mg dapagliflozin (DAPA) as add-on to insulin in relationship to HbA1c in youth. A total of 33 youths (14 males, median age 16 years, diabetes duration 8 years) were included and stratified into 3 baseline HbA1c categories (<7.5%, 7.5%-9.0% or >9.0; n = 11 each). During the study period of 24 hours, intravenous insulin administration and glucose-infusion kept blood glucose levels at 160 to 220 mg/dL. DAPA reduced mean insulin dose by 13.6% ( P < .0001 by ANOVA) and increased urinary glucose excretion by 610% (143.4 vs 22.4 g/24 h; P < .0001), both irrespective of baseline HbA1c. Six independent episodes in 6 patients with plasma ß-hydroxybutyrate levels between ≥0.6 and <1.0 mmol/L were observed after liquid meal challenges, 5 episodes in the DAPA group and 1 in the placebo group. This study provides a proof-of-concept, irrespective of preexisting HbA1c levels, for adjunct SGLT2-inhibitor therapy in the paediatric age group by lowering insulin dose and increasing glucose excretion.


Subject(s)
3-Hydroxybutyric Acid/blood , Benzhydryl Compounds/pharmacology , Diabetes Mellitus, Type 1/drug therapy , Glucosides/pharmacology , Glycated Hemoglobin/metabolism , Glycosuria/chemically induced , Insulin/administration & dosage , Adolescent , Adult , Benzhydryl Compounds/administration & dosage , Benzhydryl Compounds/pharmacokinetics , Child , Cross-Over Studies , Diabetes Mellitus, Type 1/blood , Diabetes Mellitus, Type 1/complications , Diabetes Mellitus, Type 1/urine , Dose-Response Relationship, Drug , Double-Blind Method , Drug Therapy, Combination , Female , Glucosides/administration & dosage , Glucosides/pharmacokinetics , Glycated Hemoglobin/drug effects , Glycosuria/epidemiology , Humans , Insulin/pharmacokinetics , Male , Pilot Projects , Young Adult
2.
Article in English | MEDLINE | ID: mdl-27217742

ABSTRACT

BACKGROUND: Maintaining and improving physical functioning is key to mitigating the cycle of deconditioning associated with chronic obstructive pulmonary disease (COPD). We evaluated the impact of free combination of the long-acting anticholinergic tiotropium plus the long-acting ß2-agonist olodaterol on physical functioning in a real-world clinical setting. METHODS: In this open-label noninterventional study, Global initiative for chronic Obstructive Lung Disease (GOLD) B-D patients with COPD aged ≥40 years were treated for 4-6 weeks with either tiotropium 5 µg + olodaterol 5 µg (both via Respimat(®) inhaler) or tiotropium 18 µg (HandiHaler(®)) + olodaterol 5 µg (Respimat(®)) once daily. Physical functioning was assessed by the self-reported 10-item Physical Functioning Questionnaire (PF-10). The primary end point was the percentage of patients achieving therapeutic success, defined as a 10-point increase in the PF-10 between baseline (visit 1) and weeks 4-6 (visit 2). Secondary end points included absolute PF-10 scores, Physicians' Global Evaluation, satisfaction with Respimat(®) and adverse events. RESULTS: A total of 1,858 patients were treated: 1,298 (69.9%) with tiotropium 5 µg + olodaterol 5 µg and 560 (30.1%) with tiotropium 18 µg + olodaterol 5 µg. At study end, 1,683 (92.6%) and 1,556 patients (85.6%) continued using tiotropium and olodaterol, respectively; 48.9% (95% confidence interval: 46.5, 51.3) achieved the primary end point. Therapeutic success rates were significantly higher for maintenance-naïve patients compared to those who had received prior therapy (59.1% vs 44.5%; P<0.0001), largely driven by maintenance-treatment-naïve GOLD B (59.8%) and C (63.0%) patients. Absolute physical functioning scores increased from an average baseline of 44.0 (standard deviation: 25.2) to 54.2 (standard deviation: 26.9) at visit 2. Patients' general condition improved from baseline to visit 2, and patients were largely satisfied with the Respimat(®) inhaler. Adverse events were reported by 7.5% of patients; the most common were respiratory in nature. CONCLUSION: Tiotropium + olodaterol improved physical functioning within 4-6 weeks in patients with moderate-to-very severe COPD. GOLD B and C patients with no prior maintenance treatment demonstrated the greatest benefit.


Subject(s)
Adrenergic beta-2 Receptor Agonists/administration & dosage , Benzoxazines/administration & dosage , Bronchodilator Agents/administration & dosage , Cholinergic Antagonists/administration & dosage , Lung/drug effects , Pulmonary Disease, Chronic Obstructive/drug therapy , Tiotropium Bromide/administration & dosage , Administration, Inhalation , Adrenergic beta-2 Receptor Agonists/adverse effects , Aged , Benzoxazines/adverse effects , Bronchodilator Agents/adverse effects , Cholinergic Antagonists/adverse effects , Drug Combinations , Female , Health Status , Humans , Lung/physiopathology , Male , Middle Aged , Nebulizers and Vaporizers , Prospective Studies , Pulmonary Disease, Chronic Obstructive/diagnosis , Pulmonary Disease, Chronic Obstructive/physiopathology , Recovery of Function , Severity of Illness Index , Surveys and Questionnaires , Time Factors , Tiotropium Bromide/adverse effects , Treatment Outcome
4.
Funct Neurol ; 21(1): 21-9, 2006.
Article in English | MEDLINE | ID: mdl-16734998

ABSTRACT

We aimed to investigate attentional resources distribution in traumatic brain injury (TBI) patients. Auditory event-related potentials (ERPs) were recorded from 35 severe TBI patients in post-acute care, and 35 age- and gender-matched controls using an auditory oddball paradigm under passive (ignore stimuli) and active (count deviants) conditions. Six components (P1, N1, P2, N2, P3, N3) in four waveforms were studied, i.e., the waveforms elicited by standard and by deviant tones in the passive and active task, respectively. In addition to alterations of latency and/or amplitude of single components, particularly of the late components N2 and P3, we observed in patients a different response pattern to task condition. We found evidence of deficits in the early stages of information processing and allocation of attentional resources. The analysis of the response to standards was crucial for detecting new aspects of attentional impairments.


Subject(s)
Attention/physiology , Brain Injuries/physiopathology , Evoked Potentials, Auditory/physiology , Field Dependence-Independence , Reaction Time/physiology , Adolescent , Adult , Aged , Female , Humans , Male , Matched-Pair Analysis , Middle Aged , Reference Values , Severity of Illness Index
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