ABSTRACT
OBJECTIVE: To incorporate new clusters in the MARCH (Metformin and AcaRbose in Chinese patients as the initial Hypoglycemic treatment) cohort of newly diagnosed type 2 diabetes (T2D) patients and compare the anti-glycemic effects of metformin and acarbose across different clusters. METHODS: K-means cluster analysis was performed based on six clinical indicators. The diabetic clusters in the MARCH cohort were retrospectively associated with the response to metformin and acarbose. RESULTS: A total of 590 newly diagnosed T2D patients were classified by data-driven clusters into the MARD (mild obesity-related diabetes) (34.1 %), MOD (mild obesity-related diabetes) (34.1 %), SIDD (severe insulin-deficient diabetes) (20.3 %) and SIRD (severe insulin-resistant diabetes) (11.5 %) subgroups at baseline. At 24 and 48 weeks, 346 participants had finished the follow-up. After the adjustment of age, gender, weight, baseline HbA1c, baseline fasting glucose and 2-h postprandial blood glucose (2hPG), metformin mainly decreased the fasting glucose (0.07 ± 0.89 vs -0.26 ± 0.83, P = 0.043) in the MARD subgroup presented with OGTT (oral glucose tolerance test) results compared with acarbose group at 24 weeks. Acarbose led to a greater decrease in 2hPG in the MOD subgroup compared with metformin group (0.08 ± 0.86 vs -0.24 ± 0.92, P = 0.037) at 24 weeks. There was a also significant interaction between cluster and treatment efficacy in HbA1c (glycated hemoglobin) reduction in metformin and acarbose groups at 24 and 48 weeks (pinteraction<0.001). CONCLUSIONS: Metformin and acarbose affected different metabolic variables depending on the diabetes subtype.
Subject(s)
Diabetes Mellitus, Type 2 , Metformin , Humans , Acarbose/therapeutic use , Glycated Hemoglobin , Retrospective Studies , Hypoglycemic Agents/therapeutic use , Metformin/therapeutic use , Blood Glucose/metabolism , Insulin , Obesity/drug therapyABSTRACT
The prevalence of diabetes in China has increased rapidly from 0.67% in 1980 to 10.4% in 2013, with the aging of the population and westernization of lifestyle. Since its foundation in 1991, the Chinese Diabetes Society (CDS) has been dedicated to improving academic exchange and the academic level of diabetes research in China. From 2003 to 2014, four versions of Chinese diabetes care guidelines have been published. The guidelines have played an important role in standardizing clinical practice and improving the status quo of diabetes prevention and control in China. Since September 2016, the CDS has invited experts in cardiovascular diseases, psychiatric diseases, nutrition, and traditional Chinese medicine to work with endocrinologists from the CDS to review the new clinical research evidence related to diabetes over the previous 4 years. Over a year of careful revision, this has resulted in the present, new version of guidelines for prevention and care of type 2 diabetes in China. The main contents include epidemiology of type 2 diabetes in China; diagnosis and classification of diabetes; primary, secondary, and tertiary diabetes prevention; diabetes education and management support; blood glucose monitoring; integrated control targets for type 2 diabetes and treatments for hyperglycaemia; medical nutrition therapy; exercise therapy for type 2 diabetes; smoking cessation; pharmacologic therapy for hyperglycaemia; metabolic surgery for type 2 diabetes; prevention and treatment of cardiovascular and cerebrovascular diseases in patients with type 2 diabetes; hypoglycaemia; chronic diabetic complications; special types of diabetes; metabolic syndrome; and diabetes and traditional Chinese medicine.
Subject(s)
Diabetes Complications/therapy , Diabetes Mellitus, Type 2/therapy , Practice Guidelines as Topic/standards , Standard of Care , Blood Glucose Self-Monitoring , China/epidemiology , Diabetes Complications/etiology , Diabetes Mellitus, Type 2/complications , Diabetes Mellitus, Type 2/epidemiology , HumansABSTRACT
Epigallocatechin3gallate (EGCG) is a polyphenolic compound extracted and isolated from green tea, which has a variety of important biological activities in vitro and in vivo, including antitumor, antioxidation, antiinflammation and lowering blood pressure. The aim of the present study was to investigate the protective effect of EGCG against secondary osteoporosis in a mouse model via the Wnt/ßcatenin signaling pathway. Reverse transcriptionquantitative polymerase chain reaction (RTqPCR) and western blotting were used to analyze runtrelated transcription factor 2 and osterix mRNA expression, and the protein expression of cyclin D1, Wnt and ßcatenin, and suppressed peroxisome proliferatoractivated receptor γ protein expression. The protective effect of EGCG against secondary osteoporosis was examined and its potential mechanism was analyzed. Treatment with EGCG significantly decreased serum calcium, urinary calcium, body weight and body fat, and increased leptin levels in mice with secondary osteoporosis. In addition, EGCG treatment significantly inhibited the structure score of articular cartilage and cancellous bone in proximal tibia metaphysis in mice with secondary osteoporosis. Treatment also significantly decreased alkaline phosphatase activity, runtrelated transcription factor 2 and osterix mRNA expression. EGCG also significantly induced the protein expression of cyclin D1, Wnt and ßcatenin, and suppressed peroxisome proliferatoractivated receptor γ protein expression in mice with secondary osteoporosis. Taken together, these results suggest that EGCG may be a possible new drug in clinical settings.
Subject(s)
Catechin/analogs & derivatives , Cell Proliferation/drug effects , Osteoporosis/drug therapy , Tea/chemistry , Wnt Signaling Pathway/drug effects , Animals , Calcium/blood , Calcium/urine , Cartilage/drug effects , Catechin/administration & dosage , Catechin/chemistry , Cyclin D1/genetics , Disease Models, Animal , Humans , Mice , Osteoporosis/blood , Osteoporosis/genetics , Osteoporosis/pathology , PPAR gamma/genetics , beta Catenin/geneticsABSTRACT
: Postprandial hypotension (PPH) is a common condition that occurs primarily in elderly patients with type 2 diabetes mellitus (T2DM). This study aimed to assess the effectiveness of acarbose for PPH; it also investigated possible mechanisms behind PPH development. This single-blind, randomized controlled trial included 91 elderly patients with T2DM, aged between 60 and 80â years, who were inpatients at Beijing Hospital between March 2012 and November 2014. The patients were included into one of three groups: Group A, patients with T2DM without PPH; Group B, patients with T2DM with PPH receiving placebo; and Group C, patients with T2DM with PPH receiving acarbose. After an overnight fast, patients received a single dose of acarbose (100â mg) or placebo and then consumed a standardized 450â kcal meal. Blood pressure, glucose levels, heart rate (HR), and catecholamine levels were evaluated. Acarbose ameliorated PPH as determined by significant improvements in the duration and maximal fall in blood pressure (both p<0.001); however, no differences in HR and blood glucose levels were observed. In patients with PPH, blood pressure was correlated with blood glucose and HR variability values (p<0.05). Correlations between epinephrine and glucagon-like peptide-1 with blood pressure in groups A and C were largely lost in group B. Acarbose reduced postprandial blood pressure fluctuations in elderly patients with diabetes. PPH may be related to impaired autonomic nervous system function, reduced catecholamine secretion, and postprandial fluctuations in blood glucose levels. TRIAL REGISTRATION NUMBER: Chinese Clinical Trial Registry ChiCTR-IPR-15006177.
Subject(s)
Acarbose/therapeutic use , Diabetes Mellitus, Type 2/complications , Diabetes Mellitus, Type 2/drug therapy , Hypotension/complications , Hypotension/drug therapy , Postprandial Period , Acarbose/pharmacology , Aged , Aged, 80 and over , Blood Glucose/metabolism , Blood Glucose Self-Monitoring , Blood Pressure/drug effects , C-Peptide/blood , Catecholamines/blood , Demography , Diabetes Mellitus, Type 2/blood , Diabetes Mellitus, Type 2/physiopathology , Glucagon-Like Peptide 1/blood , Heart Rate/drug effects , Humans , Hypotension/blood , Hypotension/physiopathology , Treatment OutcomeSubject(s)
Diabetes Mellitus, Type 2/therapy , Adult , Aged , Blood Glucose/analysis , China/epidemiology , Diabetes Complications/prevention & control , Diabetes Complications/therapy , Diabetes Mellitus, Type 2/diagnosis , Diabetes Mellitus, Type 2/epidemiology , Exercise , Humans , Hypertension/prevention & control , Hypoglycemic Agents/therapeutic use , Life Style , Middle Aged , Nutrition Therapy , Practice Guidelines as Topic , Risk Factors , Standard of CareABSTRACT
The exchange charge model of crystal field was used to calculate the crystal filed parameters (CFPs) acting upon the V(2+) electrons in the Al(2)O(3) crystals. With those CFPs, the crystal field Hamiltonian was diagonalized in the complete space spanned by all wave functions of the 3d(3) electron configuration of divalent vanadium. The obtained wave functions of the calculated energy levels were used to estimate the zero filed splitting (ZFS) of the ground state and g factors of ground and the first excited states for V(2+) ion in Al(2)O(3) crystals. The theoretical results are in good agreement with the corresponding experimental data. Numerical estimations of the contributions to the ZFS and g factors arising from the nearest ligands and ions from further coordination spheres were performed. It has been shown that consideration of a large cluster around an impurity ion leads to improvement of the calculated results.