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1.
J Diabetes Complications ; 34(9): 107671, 2020 09.
Article in English | MEDLINE | ID: mdl-32651031

ABSTRACT

The COVID-19 pandemic has added an enormous toll to the existing challenge of diabetes care world-wide. A large proportion of patients with COVID-19 requiring hospitalization and/or succumbing to the disease have had diabetes and other chronic conditions as underlying risk factors. In particular, individuals belonging to racial/ethnic minorities in the U.S. and other countries have been significantly and disproportionately impacted. Multiple and complex socioeconomic factors have long played a role in increasing the risk for diabetes and now for COVID-19. Since the pandemic began, the global healthcare community has accumulated invaluable clinical experience on providing diabetes care in the setting of COVID-19. In addition, understanding of the pathophysiological mechanisms that link these two diseases is being developed. The current clinical management of diabetes is a work in progress, requiring a shift in patient-provider interaction beyond the walls of clinics and hospitals: the use of tele-medicine when feasible, innovative patient education programs, strategies to ensure medication and glucose testing availability and affordability, as well as numerous ideas on how to improve meal plans and physical activity. Notably, this worldwide experience offers us the possibility to not only prepare better for future disasters but also transform diabetes care beyond the COVID-19 era.


Subject(s)
Betacoronavirus , Coronavirus Infections/complications , Coronavirus Infections/epidemiology , Diabetes Mellitus/epidemiology , Diabetes Mellitus/therapy , Pneumonia, Viral/complications , Pneumonia, Viral/epidemiology , COVID-19 , Coronavirus Infections/therapy , Diabetes Mellitus/virology , Humans , Pandemics , Pneumonia, Viral/therapy , SARS-CoV-2
2.
Int J Obes (Lond) ; 39(3): 495-501, 2015 Mar.
Article in English | MEDLINE | ID: mdl-25179244

ABSTRACT

OBJECTIVES: To examine the specific distribution of liver fat content, visceral and subcutaneous adiposity in normal glucose tolerance (NGT/NGT), isolated impaired fasting glucose (iIFG), isolated impaired glucose tolerance (iIGT) and combined conditions (IFG+IGT), as well as with newly diagnosed type 2 diabetes (nT2D). DESIGN: Multicenter, international observational study: cross-sectional analysis. SUBJECTS: Two thousand five hundred and fifteen patients (50.0% women, 54.5% non-Caucasian) without previously known diabetes were recruited from 29 countries. Abdominal fat distribution was measured by computed tomography (CT). Liver fat was estimated using the CT-liver mean attenuation. RESULTS: Compared with NGT/NGT patients, increased visceral adiposity was found in iIFG, iIGT, IFG+IGT and nT2D; estimated liver fat progressively increased across these conditions. A one-s.d. increase in visceral adiposity was associated with an increased risk of having iIFG (men: odds ratio (OR) 1.41 (95% confidence interval (CI) 1.15-1.74), women: OR 1.62 (1.29-2.04)), iIGT (men: OR 1.59 (1.15-2.01), women: OR 1.30 (0.96-1.76)), IFG+IGT (men: OR 1.64 (1.27-2.13), women: OR 1.83 (1.36-2.48)) and nT2D (men: OR 1.80 (1.35-2.42), women: OR 1.73 (1.25-2.41)). A one-s.d. increase in estimated liver fat was associated with iIGT (men: OR 1.46 (1.12-1.90), women: OR 1.81 (1.41-2.35)), IFG+IGT (men: OR 1.42 (1.14-1.77), women: OR 1.74 (1.35-2.26)) and nT2D (men: OR 1.77 (1.40-2.27), women: OR 2.38 (1.81-3.18)). Subcutaneous abdominal adipose tissue showed an inverse relationship with nT2D in women (OR 0.63 (0.45-0.88)). CONCLUSIONS: Liver fat was associated with iIGT but not with iIFG, whereas visceral adiposity was associated with both. Liver fat and visceral adiposity were associated with nT2D, whereas subcutaneous adiposity showed an inverse relationship with nT2D in women.


Subject(s)
Blood Glucose/metabolism , Glucose Intolerance/metabolism , Intra-Abdominal Fat/metabolism , Liver/metabolism , Prediabetic State/metabolism , Body Mass Index , Cross-Sectional Studies , Fasting , Female , Glucose Intolerance/blood , Glucose Tolerance Test , Humans , Insulin Resistance , Male , Middle Aged , Prediabetic State/blood , Predictive Value of Tests
3.
Int J Clin Pract ; 67(12): 1261-6, 2013 Dec.
Article in English | MEDLINE | ID: mdl-24246207

ABSTRACT

AIMS: To implement a patient registry and collect data related to the care provided to people with type 2 diabetes in six specialized centers of three Latin American countries, measure the quality of such care using a standardized form (QUALIDIAB) that collects information on different quality of care indicators, and analyze the potential of collecting this information for improving quality of care and conducting clinical research. METHODS: We collected data on clinical, metabolic and therapeutic indicators, micro- and macrovascular complications, rate of use of diagnostic and therapeutic elements and hospitalization of patients with type 2 diabetes in six diabetes centers, four in Argentina and one each in Colombia and Peru. RESULTS: We analyzed 1157 records from patients with type 2 diabetes (Argentina, 668; Colombia, 220; Peru, 269); 39 records were discarded because of data entry errors or inconsistencies. The data demonstrated frequency performance deficiencies in several procedures, including foot and ocular fundus examination and various cardiovascular screening tests. In contrast, HbA1c and cardiovascular risk factor assessments were performed with a greater frequency than recommended by international guidelines. Management of insulin therapy was sub-optimal, and deficiencies were also noted among diabetes education indicators. CONCLUSIONS: Patient registry was successfully implemented in these clinics following an interactive educational program. The data obtained provide useful information as to deficiencies in care and may be used to guide quality of care improvement efforts.


Subject(s)
Delivery of Health Care/standards , Diabetes Mellitus, Type 2/therapy , Quality of Health Care , Argentina , Chronic Disease , Clinical Laboratory Techniques/statistics & numerical data , Colombia , Diabetes Mellitus, Type 2/complications , Dyslipidemias/prevention & control , Female , Hospitalization/statistics & numerical data , Humans , Hyperglycemia/prevention & control , Hypertension/prevention & control , Male , Middle Aged , Patient Education as Topic , Peru , Registries
4.
Diabetes Obes Metab ; 15(7): 629-41, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23356633

ABSTRACT

AIM: Visceral adipose tissue (VAT) and liver fat (LF) are strongly associated with type 2 diabetes. It is not known, however, how diabetes treatment and/or risk factor management modulates the association between VAT, LF and diabetes. The aim was to determine the level of VAT and LF in patients with type 2 diabetes according to their treatment status and achievement of the American Diabetes Association's (ADA) diabetes management goals. METHODS: We performed a cross-sectional analysis of the baseline data of the International Study of the Prediction of Intra-Abdominal Adiposity and its Relationship with Cardiometabolic risk/Intra-Abdominal Adiposity (INSPIRE ME IAA), a 3-year prospective cardiometabolic imaging study conducted in 29 countries. Patients (n = 3991) were divided into four groups: (i) those without type 2 diabetes (noT2D n = 1003 men, n = 1027 women); (ii) those with type 2 diabetes but not treated with diabetes medications (T2Dnomeds n = 248 men, n = 198 women); (iii) those with type 2 diabetes and treated with diabetes medications but not yet using insulin (T2Dmeds-ins n = 591 men, n = 484 women) and (iv) those with type 2 diabetes and treated with insulin (T2Dmeds+ins n = 233 men, n = 207 women). Abdominal and liver adiposity were measured by computed tomography. RESULTS: Fewer patients with high VAT or LF achieved the ADA's goals for high-density lipoprotein cholesterol (HDL-C) or triglycerides compared to patients with low VAT or LF. Visceral adiposity (p = 0.02 men, p = 0.003 women) and LF (p = 0.0002 men, p = 0.0004 women) increased among patients who met fewer of the ADA treatment criteria, regardless of type 2 diabetes treatment. CONCLUSION: Residual cardiometabolic risk exists among patients with type 2 diabetes characterized by elevated VAT and LF.


Subject(s)
Diabetes Mellitus, Type 2/drug therapy , Hypoglycemic Agents/therapeutic use , Insulin/therapeutic use , Metabolic Syndrome/prevention & control , Adiposity , Adult , Aged , Cohort Studies , Combined Modality Therapy , Cross-Sectional Studies , Diabetes Mellitus, Type 2/blood , Diabetes Mellitus, Type 2/pathology , Diabetes Mellitus, Type 2/therapy , Drug Therapy, Combination , Female , Humans , Hyperlipidemias/etiology , Hyperlipidemias/prevention & control , Intra-Abdominal Fat/diagnostic imaging , Intra-Abdominal Fat/pathology , Lipid Metabolism , Liver/diagnostic imaging , Liver/pathology , Male , Medication Adherence , Metabolic Syndrome/epidemiology , Metabolic Syndrome/physiopathology , Middle Aged , Practice Guidelines as Topic , Radiography , Risk Factors
5.
Diabetes Metab ; 38(2): 128-34, 2012 Apr.
Article in English | MEDLINE | ID: mdl-22019715

ABSTRACT

AIM: To evaluate the impact of diabetes education provided to patients with type 2 diabetes mellitus (T2DM) in non-controlled studies ("real-world conditions") on quality of care, resource consumption and conditions of employment. METHODS: This cross-sectional study and longitudinal follow-up describe the data (demographic and socioeconomic profiles, clinical characteristics, treatment of hyperglycaemia and associated cardiovascular risk factors, resource consumption) collected during the second phase (2006) of the International Diabetes Management Practices Study (IDMPS). Patients received diabetes education directly from the practice nurse, dietitian or educator, or were referred to ad hoc group-education programmes; all programmes emphasized healthy lifestyle changes, self-care and active participation in disease control and treatment. Educated vs non-educated T2DM patients (n=5692 in each group), paired by age, gender and diabetes duration, were randomly recruited for the IDMPS by participating primary-care physicians from 27 countries in Eastern Europe, Asia, Latin America and Africa. Outcome measures included clinical (body weight, height, waist circumference, blood pressure, foot evaluation), metabolic (HbA(1c) levels, blood lipid profile) and biochemical control measures. Treatment goals were defined according to American Diabetes Association guidelines. RESULTS: T2DM patients' education significantly improved the percentage of patients achieving target values set by international guidelines. Educated patients increased their insulin use and self-care performance, had a lower rate of chronic complications and a modest increase in cost of care, and probably higher salaries and slightly better productivity. CONCLUSION: Diabetes education is an efficient tool for improving care outcomes without having a major impact on healthcare costs.


Subject(s)
Diabetes Mellitus, Type 1/epidemiology , Diabetes Mellitus, Type 2/epidemiology , Employment/statistics & numerical data , Patient Education as Topic , Self Care/statistics & numerical data , Africa/epidemiology , Asia/epidemiology , Blood Glucose/metabolism , Cross-Sectional Studies , Diabetes Mellitus, Type 1/blood , Diabetes Mellitus, Type 1/therapy , Diabetes Mellitus, Type 2/blood , Diabetes Mellitus, Type 2/therapy , Educational Status , Europe, Eastern/epidemiology , Female , Follow-Up Studies , Humans , Latin America/epidemiology , Longitudinal Studies , Male , Middle Aged , Outcome Assessment, Health Care , Patient Acceptance of Health Care
6.
Int J Clin Pract ; 64(3): 305-15, 2010 Feb.
Article in English | MEDLINE | ID: mdl-20456170

ABSTRACT

The Diabetes Control and Complications Trial (DCCT) led to considerable improvements in the management of type 1 diabetes, with the wider adoption of intensive insulin therapy to reduce the risk of complications. However, a large gap between evidence and practice remains, as recently shown by the Pittsburgh Epidemiology of Diabetes Complications (EDC) study, in which 30-year rates of microvascular complications in the 'real world' EDC patients were twice that of DCCT patients who received intensive insulin therapy. This gap may be attributed to the many challenges that patients and practitioners face in the day-to-day management of the disease. These barriers include reaching glycaemic goals, overcoming the reality and fear of hypoglycaemia, and appropriate insulin therapy and dose adjustment. As practitioners, the question remains: how do we help patients with type 1 diabetes manage glycaemia while overcoming barriers? In this article, the Global Partnership for Effective Diabetes Management provides practical recommendations to help improve the care of patients with type 1 diabetes.


Subject(s)
Diabetes Mellitus, Type 1/drug therapy , Diabetic Angiopathies/drug therapy , Hypoglycemic Agents/therapeutic use , Insulin/therapeutic use , Adult , Blood Glucose/metabolism , Blood Glucose Self-Monitoring , Diabetes Mellitus, Type 1/blood , Diabetic Angiopathies/blood , Glycated Hemoglobin/metabolism , Humans , Hypoglycemia/prevention & control , Insulin/administration & dosage , Insulin/analogs & derivatives , Mental Disorders/etiology , Patient Education as Topic , Practice Guidelines as Topic , Risk Factors
7.
Av. diabetol ; 26(2): 95-100, mar.-abr. 2010. tab
Article in Spanish | IBECS | ID: ibc-85852

ABSTRACT

En Colombia la prevalencia de diabetes mellitus tipo 2 oscila entre el 4 y el8%, en función del rango de edad de la población estudiada. En las zonasrurales es menor del 2%. El mestizaje, el envejecimiento y los factores asociadosa la urbanización son los principales determinantes de la epidemia dediabetes que se observa en la región. Entre estos últimos destaca la alta frecuenciade sobrepeso (más del 30%) y de síndrome metabólico (entre 20 y35%). La intolerancia a la glucosa es casi tan frecuente como la diabetes. Estaenfermedad se encuentra entre las primeras cinco causas de muerte enColombia y su morbilidad también es considerable. El sistema integrado deseguridad social ha permitido que la mayoría de los colombianos tengan accesoa una atención diabetológica aceptable en cuanto al alcance de metas,aunque todavía existen importantes limitaciones. El gasto en salud es 7 vecesmás bajo que el de España. La incidencia de diabetes mellitus tipo 1 en Colombiaes relativamente baja (de 3-4 por 100.000 niños menores de 15años) y la prevalencia se estima en un 0,07%(AU)


Prevalence of type 2 diabetes in Colombia varies between 4 and 8% dependingon the age range of the studied population. In the rural area it is less tan2%. Ethnic admixture, ageing process and risk factors associated with urbanizationare the main determinants of the diabetes epidemic observed in ourregion. Among the latter, the high frequency of overweight (more than 30%)and metabolic syndrome (20-35%) are the most important. Impaired glucosetolerance is almost as frequent as diabetes. This disease ranks among the firstfive causes of death in Colombia and its morbidity is also high. Thanks to theintegrated health care system, most Colombian citizens have access to an acceptablediabetes care in terms of reaching goals, but there are still importantlimitations. Health care expenditure is 7 times lower than in Spain. Incidence oftype 1 diabetes is relatively low in Colombia (3 to 4 per 100,000 childrenaged lower than 15) and the estimated overall prevalence is 0.07%(AU)


Subject(s)
Humans , Diabetes Mellitus/epidemiology , Diabetes Mellitus, Type 1/epidemiology , Diabetes Mellitus, Type 2/epidemiology , Colombia/epidemiology , Risk Factors , Age and Sex Distribution , Body Mass Index , Obesity/epidemiology , Mortality/trends
8.
Diabetes Obes Metab ; 12(3): 252-61, 2010 Mar.
Article in English | MEDLINE | ID: mdl-20070351

ABSTRACT

AIM: To compare the efficacy and safety of monotherapy with sitagliptin and metformin in treatment-naïve patients with type 2 diabetes. METHODS: In a double-blind study, 1050 treatment-naïve patients (i.e. not taking an antihyperglycaemic agent for > or =16 weeks prior to study entry) with type 2 diabetes and an HbA(1c) 6.5-9% were randomized (1:1) to treatment with once-daily sitagliptin 100 mg (N = 528) or twice-daily metformin 1000 mg (N = 522) for 24 weeks. Metformin was up-titrated from 500 to 2000 mg per day (or maximum tolerated daily dose > or =1000 mg) over a period of 5 weeks. The primary analysis used a per-protocol (PP) approach to assess whether sitagliptin was non-inferior to metformin based on HbA(1c) change from baseline at week 24. Non-inferiority was to be declared if the upper boundary of the 95% confidence interval (CI) for the between-group difference in this endpoint was <0.40%. RESULTS: From a mean baseline HbA(1c) of 7.2% in the PP population, HbA(1c) change from baseline was -0.43% with sitagliptin (n = 455) and -0.57% with metformin (n = 439). The between-group difference (95% CI) was 0.14% (0.06, 0.21), thus confirming non-inferiority. Baseline HbA(1c) influenced treatment response, with larger reductions in HbA(1c) observed in patients with baseline HbA(1c)> or =8% in the sitagliptin (-1.13%; n = 74) and metformin (-1.24%; n = 73) groups. The proportions of patients at week 24 with HbA(1c) values at the goals of <7 or <6.5% were 69 and 34% with sitagliptin and 76 and 39% with metformin, respectively. Fasting plasma glucose changes from baseline were -11.5 mg/dL (-0.6 mmol/l) and -19.4 mg/dl (-1.1 mmol/l) with sitagliptin and metformin, respectively (difference in LS mean change from baseline [95% CI] = 8.0 mg /dl [4.5,11.4]). Both treatments led to similar improvements from baseline in measures of homeostasis model assessment-beta cell function (HOMA-beta) and insulin resistance (HOMA-IR). The incidence of hypoglycaemia was 1.7% with sitagliptin and 3.3% with metformin (p = 0.116). The incidence of gastrointestinal-related adverse experiences was substantially lower with sitagliptin (11.6%) compared with metformin (20.7%) (difference in incidence [95% CI] = -9.1% [-13.6,-4.7]), primarily because of significantly decreased incidences of diarrhoea (3.6 vs. 10.9%; p < 0.001) and nausea (1.1 vs. 3.1%; p = 0.032). Body weight was reduced from baseline with both sitagliptin (LS mean change [95% CI] = -0.6 kg [-0.9,-0.4]) and metformin (-1.9 kg [-2.2, -1.7]) (p < 0.001 for sitagliptin vs. metformin). CONCLUSIONS: In this 24-week monotherapy study, sitagliptin was non-inferior to metformin in improving HbA(1c) in treatment-naïve patients with type 2 diabetes. Although both treatments were generally well tolerated, a lower incidence of gastrointestinal-related adverse experiences was observed with sitagliptin.


Subject(s)
Diabetes Mellitus, Type 2/drug therapy , Hypoglycemic Agents/administration & dosage , Metformin/administration & dosage , Pyrazines/administration & dosage , Triazoles/administration & dosage , Adolescent , Adult , Aged , Diabetes Mellitus, Type 2/blood , Double-Blind Method , Female , Glycated Hemoglobin/metabolism , Humans , Hypoglycemic Agents/adverse effects , Male , Metformin/adverse effects , Middle Aged , Pyrazines/adverse effects , Sitagliptin Phosphate , Treatment Outcome , Triazoles/adverse effects , Young Adult
10.
Int J Clin Pract Suppl ; (157): 22-30, 2007 Dec.
Article in English | MEDLINE | ID: mdl-17991188

ABSTRACT

The recent United Nations (UN) Resolution on diabetes calls for action to curb the severe risks posed by diabetes and its complications, and encourages member states to improve awareness, treatment and care of diabetes worldwide. Overcoming barriers to good glycaemic control is a pressing need as we work towards fulfilling the UN resolution. In this article, the Global Partnership for Effective Diabetes Management highlights diabetes care strategies worldwide which employ a patient-centered approach that has improved patient care and health outcomes. Examples include implementation of multidisciplinary teams and forging of effective patient partnerships to motivate and empower individuals with type 2 diabetes to take control of their condition. These real-world case studies provide practical ways to facilitate effective diabetes care across the spectrum of resource settings worldwide.


Subject(s)
Diabetes Mellitus/therapy , Patient-Centered Care/organization & administration , Humans , Patient Care Team/organization & administration , Patient Education as Topic , Professional-Patient Relations , Self Care/methods
11.
Diabetes Obes Metab ; 5(3): 180-8, 2003 May.
Article in English | MEDLINE | ID: mdl-12681025

ABSTRACT

AIM: To determine if obese non-insulin-dependent diabetic patients lose more weight when treated for 24 weeks (6 months) with orlistat (120 mg t.i.d.), in conjunction with a hypocaloric diet plus behavioural counselling, than when treated by placebo (t.i.d.) plus similar instructions. The secondary objectives were to evaluate the effects on glucose profile and to determine the tolerability and safety of orlistat. DESIGN: Double-blind, parallel, randomized, placebo-controlled, multicentre study. SUBJECTS: Obese, non-insulin-dependent diabetic patients, aged 18-70 years old, with BMI > 27 kg/m2, evaluated at 10 Latin-American centres, in five countries. EFFICACY AND TOLERABILITY MEASUREMENTS: After screened, eligible patients passed by a 2-week placebo run-in period receiving a hypocaloric diet. On day 0, patients were randomized to orlistat or placebo for 24 weeks. At each visit, body weight, blood pressure and waist circumference were measured. At the screening visit, baseline visit (week 0), and at weeks 8, 16 and 24, a central laboratory was in charge of measuring fasting glucose and insulin, HbA1c, postprandial glucose and insulin, fasting total cholesterol, HDL-cholesterol, LDL-cholesterol, triglycerides, and postprandial triglycerides. Other safety laboratory assessments were measured locally at the screening visit, baseline visit and at the end of the study. Adverse events were assessed at each visit from baseline. RESULTS: After 24 weeks of treatment, the orlistat group lost an average of 4.7% of initial body weight vs. 3.0% in the placebo group (p = 0.0003). A greater weight loss was achieved in the orlistat compared with the placebo group (4.24 +/- 0.23 vs. 2.58 +/- 1.46 kg, p = 0.0003). Almost twice as many patients receiving orlistat (30% vs. 17%) lost > or = 5% of initial body weight (p = 0.003). Orlistat treatment plus diet compared to placebo plus diet was associated with significant improvement in glycaemic control, as reflected in decreases in HbA1c (p = 0.04), fasting plasma glucose (p = 0.036) and postprandial glucose (p = 0.05). Orlistat-treated patients had a mean decrease in glucose levels of 1.00 +/- 0.34 mmol/l [3.7%] vs. 0.01 +/- 0.30 mmol/l for placebo group, at week 24 and an absolute decrease of HbA1c of 0.61 +/- 0.15 vs. a decrease of 0.22 +/- 0.14% in the placebo group. Orlistat therapy also resulted in significantly greater improvements than placebo in lipid profile, with reductions in total cholesterol (p = 0.0001) and LDL-cholesterol (p = 0.002). Mild to moderate transient gastrointestinal events were reported, mainly with orlistat treatment, but their association with withdrawal from the study was low. CONCLUSION: Orlistat is a useful and an effective therapy in obese diabetic patients, promoting clinically significant weight loss and improved glycaemic control and lipid profile.


Subject(s)
Anti-Obesity Agents/therapeutic use , Diabetes Mellitus, Type 2/drug therapy , Diabetes Mellitus/drug therapy , Lactones/therapeutic use , Obesity , Adolescent , Adult , Aged , Anthropometry , Anti-Obesity Agents/adverse effects , Blood Glucose/metabolism , Blood Pressure/drug effects , Combined Modality Therapy , Diabetes Mellitus/blood , Diabetes Mellitus/diet therapy , Diabetes Mellitus, Type 2/blood , Diabetes Mellitus, Type 2/diet therapy , Diet, Reducing , Double-Blind Method , Enzyme Inhibitors/therapeutic use , Female , Glycated Hemoglobin/metabolism , Humans , Insulin/blood , Lactones/adverse effects , Lipase/antagonists & inhibitors , Lipids/blood , Male , Middle Aged , Orlistat , Risk Factors , Weight Loss/drug effects
13.
Diabetes Care ; 16(1): 90-3, 1993 Jan.
Article in English | MEDLINE | ID: mdl-8422838

ABSTRACT

OBJECTIVE: To determine the prevalence of diabetes and its relationship to age and obesity in an urban community in Colombia. RESEARCH DESIGN AND METHODS: A cluster sample of 670 adults > or = 30 yr of age was selected from the city of Santafé de Bogotá. Classification of diabetes and IGT was according to WHO criteria. RESULTS: Response to the survey, conducted in 1988-1989, was 71% for men and 84% for women. Prevalence of diabetes was 7% in both sexes. Prevalence of IGT was 5% in men and 7% in women. Age-standardized prevalence of diabetes in the 30- to 64-yr age range was comparable with that reported in urban Brazilians and rural Hispanics in the U.S.. Prevalence was higher than in the white population of the U.S. but lower than in several urban U.S. Hispanic communities. Some 40% of men and 30% of women with diabetes were unaware of their condition before the survey, but all those < 50 yr of age were diagnosed previously. Glucose intolerance was associated with high BMI in men and with advancing age in both sexes. CONCLUSIONS: Glucose intolerance is common in this community and will likely increase in frequency in Colombians with further urbanization and population aging.


Subject(s)
Diabetes Mellitus/epidemiology , Glucose Tolerance Test , Hyperglycemia/epidemiology , Urban Population , Adult , Age Factors , Aged , Aged, 80 and over , Analysis of Variance , Blood Glucose/metabolism , Colombia/epidemiology , Diabetes Mellitus/blood , Female , Humans , Male , Middle Aged , Prevalence , Regression Analysis , Sex Characteristics
14.
Diabetes Res Clin Pract ; 18(1): 23-30, 1992 Oct.
Article in English | MEDLINE | ID: mdl-1446575

ABSTRACT

Twenty non-insulin-dependent diabetic patients on insulin therapy for more than 2 months due to secondary failure to oral hypoglycemic agents (OHA) were additionally treated with gliclazide, 80 mg b.i.d., for 1 month and 160 mg b.i.d. for a further 2 months, while reducing insulin dose gradually according to glycemic control. At the end of the first month, fasting blood glucose had decreased from 12.8 +/- 0.7 to 9 +/- 0.8 mM (mean +/- standard error; P < 0.005) and thereafter remained stable. Insulin requirements decreased from 34.2 +/- 2.5 to 18.3 +/- 3.2 U/day (P < 0.001). Three patients were able to cease insulin treatment altogether. A direct correlation was found between final insulin dose and previous duration of infusion monotherapy (r = 0.52; P < 0.05). C-peptide/glucose score (fasting C-peptide/fasting BG x 100) increased from 0.11 +/- 0.03 to 0.21 +/- 0.05 (P < 0.05). We conclude that combined therapy reduces insulin requirement by increasing endogenous secretion, which may mainly affect hepatic glucose production as indicated by greater improvement in fasting vs. post-prandial blood glucose. This therapy could avoid hyperinsulinemia, which has been reported to be involved in macrovascular complications, and the additional haemovascular properties of gliclazide could make it more effective in such a combination.


Subject(s)
Diabetes Mellitus, Type 2/drug therapy , Gliclazide/therapeutic use , Hypoglycemic Agents/therapeutic use , Insulin/therapeutic use , Blood Glucose/metabolism , C-Peptide/blood , Diabetes Mellitus, Type 2/blood , Drug Administration Schedule , Drug Therapy, Combination , Eating , Fasting , Female , Gliclazide/administration & dosage , Humans , Insulin/administration & dosage , Islets of Langerhans/metabolism , Male , Middle Aged , Treatment Failure
15.
Acta méd. colomb ; 8(2): 119-23, 1983.
Article in Spanish | LILACS | ID: lil-16406
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