RÉSUMÉ
Most studies on chronic chikungunya virus (CHIKV) arthritis include patients treated with disease-modifying antirheumatic drugs (DMARDs), likely altering the expression of clinical manifestations and outcome. Therefore, we sought to evaluate the clinical features and correlates in DMARD-naive patients with chronic CHIKV arthritis. We conducted a case-control study in adult patients with serologically confirmed CHIKV infection in Puerto Rico. Demographic features, clinical manifestations, comorbidities, disease activity (per Clinical Disease Activity Index [CDAI]), functional status (per Health Assessment Questionnaire Disability Index [HAQ-DI]), and pharmacologic treatment were ascertained. Patients with and without chronic CHIKV arthritis were compared. Furthermore, a sub-analysis was performed among patients with chronic CHIKV who presented with mild disease activity versus moderate-to-high disease activity at study visit. In total, 61 patients were studied; 33 patients had chronic arthritis and 28 had resolved arthritis. Patients with chronic arthritis had significantly more diabetes mellitus, chronic back pain, and fever, tiredness, and myalgias on the acute phase. The mean (SD) HAQ score was 0.95 (0.56), and 57.6% had moderate-to-high disease activity. Patients with moderate-to-high disease activity had higher scores in overall HAQ-DI and HAQ-DI categories (dressing and grooming, arising, hygiene, reaching, and activities) than in those with mild activity. In conclusion, in this group of DMARD-naive patients with chronic CHIKV arthritis, nearly 58% had moderate-to-high disease activity and had substantial functional disability. Diabetes mellitus, chronic back pain, and some manifestations on acute infection were associated with chronic CHIKV arthritis.
Sujet(s)
Antirhumatismaux/usage thérapeutique , Arthrite infectieuse/traitement médicamenteux , Dorsalgie/traitement médicamenteux , Fièvre chikungunya/traitement médicamenteux , Complications du diabète/traitement médicamenteux , Diabète/traitement médicamenteux , Activités de la vie quotidienne , Adulte , Arthrite infectieuse/complications , Arthrite infectieuse/physiopathologie , Arthrite infectieuse/virologie , Dorsalgie/complications , Dorsalgie/physiopathologie , Dorsalgie/virologie , Études cas-témoins , Fièvre chikungunya/complications , Fièvre chikungunya/physiopathologie , Fièvre chikungunya/virologie , Virus du chikungunya , Maladie chronique , Complications du diabète/physiopathologie , Complications du diabète/virologie , Diabète/physiopathologie , Diabète/virologie , Fatigue/complications , Fatigue/traitement médicamenteux , Fatigue/physiopathologie , Fatigue/virologie , Femelle , Fièvre/complications , Fièvre/traitement médicamenteux , Fièvre/physiopathologie , Fièvre/virologie , Humains , Mâle , Adulte d'âge moyen , Porto Rico , Indice de gravité de la maladie , Résultat thérapeutiqueRÉSUMÉ
BACKGROUND: Solanum lycocarpum is a medicinal plant used in Brazil with hypoglycemic activity by its fruits use. However, the fruits production is restricted in some periods of the year, differently of leaves. OBJECTIVE: To evaluate the effects of hydroalcoholic extracts of S. lycocarpum leaves in alloxan-induced diabetic mice. METHODS: Hydroalcoholic extract of S. lycocarpum was characterized by phytochemical and GCMS analysis. The Antidiabetic activity was assessed following treatment for 22 days with S. lycocarpum extract at 125, 250, and 500 mg/kg. Bodyweight, water, and food intake, glycemia, biochemical parameters, anatomy-histopathology of the pancreas, liver and kidney, and expression of target genes were analyzed. In addition, oral acute toxicity was evaluated. RESULTS: Animals treated showed a significant reduction (p < 0.05) in glycemia following a dose of 125 mg/kg. Food intake remained similar for all groups. Decreased polydipsia symptoms were observed after treatment with 250 (p < 0.001) and 500 mg/kg (p < 0.01) compared with diabetic control, although normal rates were observed when 125 mg/kg was administered. A protective effect was also observed in the pancreas, liver, and kidneys, through the regeneration of the islets. Hypoglycemic activity can be attributed to myo-inositol, which stimulates insulin secretion, associated with α-tocopherol, which prevents damage from oxidative stress and apoptosis of ß-pancreatic cells by an increased Catalase (CAT) and Glutathione peroxidase 4 (GPX4) mRNA expression. The toxicological test demonstrated safe oral use of the extract under the present conditions. CONCLUSION: Hydroalcoholic extract of S. lycocarpum promotes the regulation of diabetes in the case of moderate glycemic levels, by decreasing glycemia and exerting protective effects on the islets.
Sujet(s)
Complications du diabète/traitement médicamenteux , Diabète expérimental/traitement médicamenteux , Hypoglycémiants/pharmacologie , Extraits de plantes/pharmacologie , Solanum/composition chimique , Alanine transaminase/métabolisme , Phosphatase alcaline/métabolisme , Alloxane/administration et posologie , Animaux , Aspartate aminotransferases/métabolisme , Glycémie/métabolisme , Poids/effets des médicaments et des substances chimiques , Catalase/métabolisme , Complications du diabète/métabolisme , Complications du diabète/anatomopathologie , Diabète expérimental/induit chimiquement , Diabète expérimental/métabolisme , Diabète expérimental/anatomopathologie , Consommation de boisson/effets des médicaments et des substances chimiques , Consommation alimentaire/effets des médicaments et des substances chimiques , Hypoglycémiants/composition chimique , Inositol/pharmacologie , Rein/effets des médicaments et des substances chimiques , Rein/métabolisme , Rein/anatomopathologie , Foie/effets des médicaments et des substances chimiques , Foie/métabolisme , Foie/anatomopathologie , Mâle , Souris , Pancréas/effets des médicaments et des substances chimiques , Pancréas/métabolisme , Pancréas/anatomopathologie , Phospholipid hydroperoxide glutathione peroxidase/métabolisme , Extraits de plantes/composition chimique , Feuilles de plante/composition chimique , alpha-Tocophérol/pharmacologieRÉSUMÉ
Diabetes mellitus (DM) leads to complications, the majority of which are nephropathy, retinopathy, and neuropathy. Redox imbalance and inflammation are important components of the pathophysiology of these complications. Many studies have been conducted to find a specific treatment for these neural complications, and some of them have investigated the therapeutic potential of melatonin (MEL), an anti-inflammatory agent and powerful antioxidant. In the present article, we review studies published over the past 21 years on the therapeutic efficacy of MEL in the treatment of DM-induced neural complications. Reports suggest that there is a real prospect of using MEL as an adjuvant treatment for hypoglycemic agents. However, analysis shows that there is a wide range of approaches regarding the doses used, duration of treatment, and treatment times in relation to the temporal course of DM. This wide range hinders an objective analysis of advances and prospective vision of the paths to be followed for the unequivocal establishment of parameters to be used in an eventual therapeutic validation of MEL in neural complications of DM.
Sujet(s)
Complications du diabète/traitement médicamenteux , Neuropathies diabétiques/traitement médicamenteux , Rétinopathie diabétique/traitement médicamenteux , Mélatonine/pharmacologie , Animaux , Diabète/anatomopathologie , HumainsRÉSUMÉ
SHORT syndrome is a rare developmental disorder frequently associated with growth failure and insulin resistant diabetes mellitus (IRDM). Since GH has a diabetogenic effect, GH therapy has been regarded as a contraindication. We observed a Brazilian girl with SHORT syndrome who received GH therapy from 4 6/12 years of age for SGA short stature. GH dosage was increased from 0.23 to 0.36 mg/kg/week, but statural response to GH therapy remained poor. Her blood HbA1c level, though it remained 5.5-6.0% in childhood, began to elevate with puberty and increased to 9.2% at 10 6/12 years of age, despite the discontinuation of GH therapy at 9 11/12 years of age. Laboratory studies indicated antibody-negative IRDM. She was treated with metformin and canagliflozin (a sodium glucose co-transporter 2 (SGLT2) inhibitor), which ameliorated overt diurnal hyperglycemia and mild nocturnal hypoglycemia and reduced her blood HbA1c around 7%. Whole exome sequencing revealed a de novo heterozygous pathogenic variant (c.1945C>T:p.(Arg649Trp)) in PIK3R1 known as the sole causative gene for SHORT syndrome. Subsequent literature review for patients with molecularly confirmed SHORT syndrome revealed the development of IRDM in 10 of 15 GH-untreated patients aged ≥12 years but in none of three GH-treated and six GH-untreated patients aged ≤10 years. These findings imply a critical role of pubertal development and/or advanced age rather than GH therapy in the development of IRDM, and a usefulness of SGLT2 inhibitor in the treatment of IRDM.
Sujet(s)
Diabète/diagnostic , Troubles de la croissance/complications , Hypercalcémie/complications , Insulinorésistance/physiologie , Maladies métaboliques/complications , Néphrocalcinose/complications , Brésil , Canagliflozine/administration et posologie , Enfant , Complications du diabète/diagnostic , Complications du diabète/traitement médicamenteux , Diabète/traitement médicamenteux , Diabète/métabolisme , Association de médicaments , Femelle , Troubles de la croissance/diagnostic , Troubles de la croissance/traitement médicamenteux , Troubles de la croissance/métabolisme , Hormone de croissance humaine/administration et posologie , Humains , Hypercalcémie/diagnostic , Hypercalcémie/traitement médicamenteux , Hypercalcémie/métabolisme , Maladies métaboliques/diagnostic , Maladies métaboliques/traitement médicamenteux , Maladies métaboliques/métabolisme , Metformine/administration et posologie , Néphrocalcinose/diagnostic , Néphrocalcinose/traitement médicamenteux , Néphrocalcinose/métabolisme , Puberté/effets des médicaments et des substances chimiques , Puberté/métabolisme , Inhibiteurs du cotransporteur sodium-glucose de type 2/administration et posologieRÉSUMÉ
Diabetes and its complications represent a major cause of morbidity and mortality in diabetes patients. This review is aimed to find the potential of gold nanoparticles (AuNPs) to act as therapeutic agents for diabetes and its complications. Here, we outline the literature related to the self-therapeutic effects of AuNPs. The first goal of this review is to highlight and summarize some of the existing studies (10 years ago) in terms of several parameters such as the size of AuNPs, dose, administration route, experimental model, experimental analysis, and findings. The second goal is to describe the self-therapeutic effects of AuNPs against the pathogenesis determinants of diabetic complications. AuNPs have been found to have inhibitory effects on transforming growth factor-ß, antiglycation, antiangiogenic, anti-hyperglycemic, anti-inflammatory, and antioxidant effects. AuNPs treatment effectively disrupts multiple pathogenesis determinants in an animal model of diabetes and diabetic complications. The present review provides insight into the potential applications of AuNPs, which may help reduce the incidence of diabetes and its complications
Sujet(s)
Utilisations thérapeutiques , Complications du diabète/traitement médicamenteux , Nanoparticules/métabolisme , Or/classification , Organisation et administration , Patients , Modèles animaux , Modèles théoriques , Antioxydants/pharmacologieRÉSUMÉ
BACKGROUND: The most common aetiological agents of mucormycosis are Rhizopus, Mucor, Apophysomyces and Lichtheimia. Apophysomyces is comparatively rare, as it has been reported in less than 3% of mucormycosis cases. The genus Apophysomyces includes six species, and only A. elegans, A. mexicanus, A. variabilis and A. ossiformis have been reported to cause infections in both immunocompetent and immunocompromised patients. CASE PRESENTATION: We present a case of a 46-year-old male patient with bilateral blepharoedema, corneal opacity in the left eye and poorly controlled diabetes mellitus. The patient was subjected to total maxillectomy, exenteration of the left orbit and treatment with liposomal amphotericin B. Direct mycological analysis with KOH 10% revealed hyaline, coenocytic, long and wide hyphae. Apophysomyces ossiformis was identified from maxillary biopsy using 18S-ITS1-5.8S-ITS2-28S rRNA gene amplification and sequencing. The patient requested to be transferred to another hospital to continue treatment, where he died on the ninth day after admittance. CONCLUSION: To the best of our knowledge, this is the first case of rhino-orbital mucormycosis due to A. ossiformis with a fatal outcome. This case reveals the need to identify the fungus causing mucormycosis with molecular methods to identify adequate treatment therapies for patients with this infection.
Sujet(s)
Complications du diabète/microbiologie , Mucorales/génétique , Mucormycose/complications , Maladies de l'orbite/complications , Rhinite/complications , Amphotéricine B/usage thérapeutique , Antifongiques/usage thérapeutique , Biopsie , Complications du diabète/traitement médicamenteux , Complications du diabète/chirurgie , Issue fatale , Humains , Sujet immunodéprimé , Mâle , Maxillaire/microbiologie , Maxillaire/anatomopathologie , Maxillaire/chirurgie , Adulte d'âge moyen , Mucormycose/traitement médicamenteux , Mucormycose/microbiologie , Mucormycose/chirurgie , Maladies de l'orbite/traitement médicamenteux , Maladies de l'orbite/microbiologie , Maladies de l'orbite/chirurgie , ARN ribosomique 28S/génétique , Rhinite/traitement médicamenteux , Rhinite/microbiologie , Rhinite/chirurgieRÉSUMÉ
OBJECTIVES: The number of bariatric procedures has significantly increased in Brazil, especially in the public Unified Health System. The present study describes health outcomes and medication use in obese patients treated in a major hospital that performs publicly funded surgery in Brazil. METHODS: A retrospective, single center study was conducted to collect real-world evidence of health outcomes and medication use in 247 obese patients (female, 82.2%) who underwent open Roux-en-Y gastric bypass. Changes in weight and body mass index (BMI), presence of apnea, hypertension, and type 2 diabetes (T2D), and medication use (hypertension, diabetes, and dyslipidemia) were assessed preoperatively and up to 24 months postoperatively. The mean cost of medications was calculated for the 12-month preoperative and 24-month postoperative periods. RESULTS: During the surgery, the mean age of patients was 43.42 years (standard deviation [SD], 10.9 years), and mean BMI was 46.7 kg/m2 (SD, 6.7 kg/m2). At 24 months, significant declines were noted in weight (mean, -37.6 kg), BMI (mean, -14.3 kg/m2); presence of T2D, hypertension, and apnea (-29.6%, -50.6%, and -20.9%, respectively); and number of patients using medications (-66.67% for diabetes, -41.86% for hypertension, and -55.26% for dyslipidemia). The mean cost of medications (total costs for all medications) decreased by >50% in 12-24 postoperative months compared to that in 12 preoperative months. CONCLUSION: Roux-en-Y gastric bypass successfully reduced weight, BMI, and comorbidities and medication use and cost at 24 months in Brazilian patients treated in the public Unified Health System.
Sujet(s)
Chirurgie bariatrique , Ordonnances médicamenteuses/statistiques et données numériques , Dérivation gastrique/méthodes , Laparoscopie , Obésité morbide/chirurgie , Adulte , Indice de masse corporelle , Brésil , Complications du diabète/traitement médicamenteux , Diabète de type 2/complications , Diabète de type 2/traitement médicamenteux , Dyslipidémies/complications , Dyslipidémies/traitement médicamenteux , Femelle , Reflux gastro-oesophagien/complications , Reflux gastro-oesophagien/traitement médicamenteux , Humains , Hypertension artérielle/complications , Hypertension artérielle/traitement médicamenteux , Obésité morbide/complications , 29918 , Études rétrospectives , Résultat thérapeutique , Perte de poidsRÉSUMÉ
OBJECTIVES: The number of bariatric procedures has significantly increased in Brazil, especially in the public Unified Health System. The present study describes health outcomes and medication use in obese patients treated in a major hospital that performs publicly funded surgery in Brazil. METHODS: A retrospective, single center study was conducted to collect real-world evidence of health outcomes and medication use in 247 obese patients (female, 82.2%) who underwent open Roux-en-Y gastric bypass. Changes in weight and body mass index (BMI), presence of apnea, hypertension, and type 2 diabetes (T2D), and medication use (hypertension, diabetes, and dyslipidemia) were assessed preoperatively and up to 24 months postoperatively. The mean cost of medications was calculated for the 12-month preoperative and 24-month postoperative periods. RESULTS: During the surgery, the mean age of patients was 43.42 years (standard deviation [SD], 10.9 years), and mean BMI was 46.7 kg/m2 (SD, 6.7 kg/m2). At 24 months, significant declines were noted in weight (mean, -37.6 kg), BMI (mean, -14.3 kg/m2); presence of T2D, hypertension, and apnea (-29.6%, -50.6%, and -20.9%, respectively); and number of patients using medications (-66.67% for diabetes, -41.86% for hypertension, and -55.26% for dyslipidemia). The mean cost of medications (total costs for all medications) decreased by >50% in 12-24 postoperative months compared to that in 12 preoperative months. CONCLUSION: Roux-en-Y gastric bypass successfully reduced weight, BMI, and comorbidities and medication use and cost at 24 months in Brazilian patients treated in the public Unified Health System.
Sujet(s)
Humains , Femelle , Adulte , Ordonnances médicamenteuses/statistiques et données numériques , Obésité morbide/chirurgie , Dérivation gastrique/méthodes , Laparoscopie , Chirurgie bariatrique , Obésité morbide/complications , Brésil , Perte de poids , Reflux gastro-oesophagien/complications , Reflux gastro-oesophagien/traitement médicamenteux , Indice de masse corporelle , Études rétrospectives , Résultat thérapeutique , 29918 , Complications du diabète/traitement médicamenteux , Diabète de type 2/complications , Diabète de type 2/traitement médicamenteux , Dyslipidémies/complications , Dyslipidémies/traitement médicamenteux , Hypertension artérielle/complications , Hypertension artérielle/traitement médicamenteuxRÉSUMÉ
Autoimmune pancreatitis is uncommon, responds to steroids and is usually associated with diabetes mellitus. We report a 73 year-old male who, two months after a diagnosis of diabetes mellitus, presented with obstructive jaundice and weight loss. Abdominal magnetic resonance imaging was suggestive of an autoimmune pancreatitis and serum IgG4 was 339 mg/dl (normal range 3-201). The patient was treated with prednisone 40 mg/day with a good clinical and laboratory response. During outpatient care, the dose of prednisone was tapered.
Sujet(s)
Pancréatite auto-immune/complications , Pancréatite auto-immune/traitement médicamenteux , Complications du diabète , Diabète , Glucocorticoïdes/usage thérapeutique , Prednisone/usage thérapeutique , Sujet âgé , Pancréatite auto-immune/imagerie diagnostique , Complications du diabète/complications , Complications du diabète/traitement médicamenteux , Diabète/traitement médicamenteux , Humains , Hypoglycémiants/usage thérapeutique , Immunoglobuline G/sang , Insuline/usage thérapeutique , Imagerie par résonance magnétique , Mâle , Résultat thérapeutiqueRÉSUMÉ
OBJECTIVE: Guidelines for hypertension treatment in patients with diabetes diverge regarding the systolic blood pressure (SBP) threshold at which treatment should be initiated and treatment goal. We examined associations of early SBP treatment with atherosclerotic cardiovascular disease (ASCVD) events in U.S. adults with diabetes. RESEARCH DESIGN AND METHODS: We studied 43,986 patients with diabetes who newly initiated antihypertensive therapy between 2002 and 2007. Patients were classified into categories based on SBP at treatment initiation (130-139 or ≥140 mmHg) and after 2 years of treatment (100-119, 120-129, 130-139, 140-159, and ≥160 mmHg). The primary outcome was composite ASCVD events (fatal and nonfatal myocardial infarction and stroke), estimated using inverse probability of treatment-weighted Poisson regression and multivariable Cox proportional hazards regression. RESULTS: Relative to individuals who initiated treatment when SBP was 130-139 mmHg, those with pretreatment SBP ≥140 mmHg had higher ASCVD risk (hazard ratio 1.10 [95% CI 1.02, 1.19]). Relative to those with pretreatment SBP of 130-139 mmHg and on-treatment SBP of 120-129 mmHg (reference group), ASCVD incidence was higher in those with pretreatment SBP ≥140 mmHg and on-treatment SBP 120-129 mmHg (adjusted incidence rate difference [IRD] 1.0 [-0.2 to 2.1] events/1,000 person-years) and in those who achieved on-treatment SBP 130-139 mmHg (IRD 1.9 [0.6, 3.2] and 1.1 [0.04, 2.2] events/1,000 person-years for those with pretreatment SBP 130-139 mmHg and ≥140 mmHg, respectively). CONCLUSIONS: In this observational study, patients with diabetes initiating antihypertensive therapy when SBP was 130-139 mmHg and those achieving on-treatment SBP <130 mmHg had better outcomes than those with higher SBP levels when initiating or after 2 years on treatment.
Sujet(s)
Antihypertenseurs/usage thérapeutique , Maladies cardiovasculaires/épidémiologie , Diabète/traitement médicamenteux , Intervention médicale précoce , Hypertension artérielle/traitement médicamenteux , Anciens combattants , Adulte , Sujet âgé , Athérosclérose/complications , Athérosclérose/traitement médicamenteux , Athérosclérose/épidémiologie , Athérosclérose/physiopathologie , Pression sanguine/effets des médicaments et des substances chimiques , Maladies cardiovasculaires/complications , Complications du diabète/traitement médicamenteux , Complications du diabète/épidémiologie , Complications du diabète/physiopathologie , Diabète/physiopathologie , Intervention médicale précoce/méthodes , Femelle , Humains , Hypertension artérielle/complications , Hypertension artérielle/épidémiologie , Incidence , Mâle , Adulte d'âge moyen , Études rétrospectives , Accident vasculaire cérébral/épidémiologie , Anciens combattants/statistiques et données numériquesRÉSUMÉ
Autoimmune pancreatitis is uncommon, responds to steroids and is usually associated with diabetes mellitus. We report a 73 year-old male who, two months after a diagnosis of diabetes mellitus, presented with obstructive jaundice and weight loss. Abdominal magnetic resonance imaging was suggestive of an autoimmune pancreatitis and serum IgG4 was 339 mg/dl (normal range 3-201). The patient was treated with prednisone 40 mg/day with a good clinical and laboratory response. During outpatient care, the dose of prednisone was tapered.
Sujet(s)
Humains , Mâle , Sujet âgé , Prednisone/usage thérapeutique , Complications du diabète/complications , Complications du diabète/traitement médicamenteux , Diabète/traitement médicamenteux , Pancréatite auto-immune/complications , Pancréatite auto-immune/traitement médicamenteux , Glucocorticoïdes/usage thérapeutique , Immunoglobuline G/sang , Imagerie par résonance magnétique , Résultat thérapeutique , Pancréatite auto-immune/imagerie diagnostique , Hypoglycémiants/usage thérapeutique , Insuline/usage thérapeutiqueRÉSUMÉ
OBJECTIVE: To understand the feelings and behaviors of people being treated for Systemic Hypertension (SH) and Diabetes Mellitus (DM). METHOD: A qualitative study based on Grounded Theory and Symbolic Interactionism, with 27 participants in treatment for SH and DM followed up by the Family Health Strategy team. Open, axial and selective coding was performed, giving rise to three theoretical categories and the central category. RESULTS: The daily life is explicit in the (lack of)care of the self with the chronic disease and feelings of sadness and anxiety are expressed as reasons for the lack of control of the disease. It points out that people take care of themselves because of fear of complications, reinforced the need for guidance on the use of medication and the empowerment of the chronic patient for self-care and care for the other. FINAL CONSIDERATIONS: Knowing behaviors and feelings of people with SH and/or DM allows a professional performance beyond the chronic condition.
Sujet(s)
Diabète/psychologie , Hypertension artérielle/psychologie , Adhésion au traitement médicamenteux/psychologie , Adulte , Brésil , Complications du diabète/traitement médicamenteux , Complications du diabète/psychologie , Diabète/traitement médicamenteux , Prise en charge de la maladie , Femelle , Théorie ancrée , Humains , Hypertension artérielle/complications , Hypertension artérielle/traitement médicamenteux , Mâle , Recherche qualitative , Gestion de soi/psychologieRÉSUMÉ
ABSTRACT Objective: To understand the feelings and behaviors of people being treated for Systemic Hypertension (SH) and Diabetes Mellitus (DM). Method: A qualitative study based on Grounded Theory and Symbolic Interactionism, with 27 participants in treatment for SH and DM followed up by the Family Health Strategy team. Open, axial and selective coding was performed, giving rise to three theoretical categories and the central category. Results: The daily life is explicit in the (lack of)care of the self with the chronic disease and feelings of sadness and anxiety are expressed as reasons for the lack of control of the disease. It points out that people take care of themselves because of fear of complications, reinforced the need for guidance on the use of medication and the empowerment of the chronic patient for self-care and care for the other. Final considerations: Knowing behaviors and feelings of people with SH and/or DM allows a professional performance beyond the chronic condition.
RESUMEN Objetivo: Comprender los sentimientos y comportamientos de personas en tratamiento de la hipertensión arterial sistémica (HAS) y la diabetes mellitus (DM). Método: Estudio cualitativo basado en la Teoría Fundamentada en los Datos y en el Interaccionismo Simbólico, con 27 participantes en tratamiento de la HAS y DM, y acompañados por el equipo Estrategia Salud de la Familia. Se procedió a la codificación abierta, axial y selectiva que originó las tres categorías teóricas y la categoría central. Resultados: El cotidiano de la vida está explícito en el (des) cuidado de sí con una enfermedad crónica. Los sentimientos de tristeza y ansiedad se expresan como motivos condicionantes para el descontrol de la enfermedad. Se señala que las personas se cuidan movidas por el miedo a las complicaciones. Se reforzó la necesidad de orientación sobre el uso de la medicación y del empoderamiento del paciente crónico para el autocuidado y cuidado del otro. Consideraciones finales: Conocer los comportamientos y sentimientos de las personas con HAS y/o DM permite una actuación profesional más allá de la condición crónica.
RESUMO Objetivo: Compreender os sentimentos e comportamentos de pessoas em tratamento para a Hipertensão Arterial Sistêmica (HAS) e Diabetes Mellitus (DM). Método: Estudo qualitativo embasado na Teoria Fundamentada nos Dados e no Interacionismo Simbólico, com 27 participantes em tratamento para HAS e DM acompanhados pela equipe Estratégia Saúde da Família. Procedeu-se a codificação aberta, axial e seletiva que originaram três categorias teóricas e a categoria central. Resultados: O cotidiano de vida está explícito no (des)cuidado de si com a doença crônica e sentimentos de tristeza e ansiedade são expressos como motivos condicionantes para o descontrole da doença. Aponta que as pessoas se cuidam movidas pelo medo das complicações, reforçou a necessidade de orientação sobre o uso da medicação e do empoderamento do doente crônico para o autocuidado e cuidado do outro. Considerações finais: Conhecer comportamentos e sentimentos das pessoas com HAS e/ou DM permite uma atuação profissional além da condição crônica.
Sujet(s)
Humains , Mâle , Femelle , Adulte , Diabète/psychologie , Adhésion au traitement médicamenteux/psychologie , Hypertension artérielle/psychologie , Brésil , Prise en charge de la maladie , Recherche qualitative , Complications du diabète/psychologie , Complications du diabète/traitement médicamenteux , Diabète/traitement médicamenteux , Théorie ancrée , Gestion de soi/psychologie , Hypertension artérielle/complications , Hypertension artérielle/traitement médicamenteuxRÉSUMÉ
Abstract Background: Trimetazidine (TMZ) is an anti-ischemic drug. In spite of its protective effects on cardiovascular system, there is no scientific study on the usefulness of TMZ treatment for prolonged QT interval and cardiac hypertrophy induced by diabetes. Objectives: To evaluate the effects of TMZ on QT interval prolongation and cardiac hypertrophy in the diabetic rats. Methods: Twenty-four male Sprague-Dawley rats (200-250 g) were randomly assigned into three groups (n = 8) by simple random sampling method. Control (C), diabetic (D), and diabetic administrated with TMZ at 10 mg/kg (T10). TMZ was administrated for 8 weeks. The echocardiogram was recorded before isolating the hearts and transfer to a Langendorff apparatus. Hemodynamic parameters, QT and corrected QT interval (QTc) intervals, heart rate and antioxidant enzymes were measured. The hypertrophy index was calculated. The results were evaluated by one-way ANOVA and paired t-test using SPSS (version 16) and p < 0.05 was regarded as significant. Results: The diabetic rats significantly indicated increased hypertrophy, QT and QTc intervals and decreased Left ventricular systolic pressure (LVSP), Left ventricular developed pressure (LVDP), rate pressure product (RPP), Max dp/dt, and min dp/dt (±dp/dt max), heart rate, superoxide dismutase (SOD), glutathione peroxidase (GPx) and catalase in the heart. Treatment with TMZ in the diabetic animals was significantly improved these parameters in comparison to the untreated diabetic group. Conclusions: TMZ improves QTc interval prolongation and cardiac hypertrophy in diabetes.
Resumo Fundamento: A trimetazidina (TMZ) é uma droga anti-isquêmica. Apesar de seus efeitos protetores sobre o sistema cardiovascular, não há estudos científicos sobre a utilidade do tratamento com TMZ para o intervalo QT prolongado e a hipertrofia cardíaca induzida pelo diabetes. Objetivo: Avaliar os efeitos da TMZ no prolongamento do intervalo QT e na hipertrofia cardíaca em ratos diabéticos. Métodos: Vinte e quatro ratos machos Sprague-Dawley (200-250 g) foram distribuídos aleatoriamente em três grupos (n = 8) pelo método de amostragem aleatória simples. Controle (C), diabético (D) e diabético administrado com TMZ a 10 mg/kg (T10). A TMZ foi administrada por 8 semanas. O ecocardiograma foi registrado antes de isolar os corações e transferir para um aparelho de Langendorff. Foram medidos os parâmetros hemodinâmicos, intervalo QT e intervalo QT corrigido (QTc), frequência cardíaca e enzimas antioxidantes. O índice de hipertrofia foi calculado. Os resultados foram avaliados pelo one-way ANOVA e pelo teste t pareado pelo SPSS (versão 16) e p < 0,05 foi considerado significativo. Resultados: Os ratos diabéticos indicaram hipertrofia aumentada, intervalos QT e QTc e diminuição da pressão sistólica no ventrículo esquerdo (PSVE), pressão desenvolvida no ventrículo esquerdo (PDVE), duplo produto (DP), Max dp/dt e min dp/dt (± dp/dt max), frequência cardíaca, superóxido dismutase (SOD), glutationa peroxidase (GPx) e catalase no coração. O tratamento com TMZ nos animais diabéticos melhorou significativamente esses parâmetros em comparação com o grupo diabético não tratado. Conclusões: A TMZ melhora o prolongamento do intervalo QTc e a hipertrofia cardíaca no diabetes.
Sujet(s)
Animaux , Mâle , Trimétazidine/pharmacologie , Syndrome du QT long/traitement médicamenteux , Cardiomégalie/traitement médicamenteux , Agents protecteurs/pharmacologie , Complications du diabète/traitement médicamenteux , Superoxide dismutase/analyse , Facteurs temps , Syndrome du QT long/enzymologie , Syndrome du QT long/physiopathologie , Échocardiographie , Catalase/analyse , Répartition aléatoire , Reproductibilité des résultats , Rat Sprague-Dawley , Cardiomégalie/enzymologie , Cardiomégalie/étiologie , Cardiomégalie/physiopathologie , Complications du diabète/enzymologie , Complications du diabète/physiopathologie , Diabète expérimental/complications , Diabète expérimental/physiopathologie , Glutathione peroxidase/analyse , Hémodynamique/effets des médicaments et des substances chimiquesRÉSUMÉ
BACKGROUND: Trimetazidine (TMZ) is an anti-ischemic drug. In spite of its protective effects on cardiovascular system, there is no scientific study on the usefulness of TMZ treatment for prolonged QT interval and cardiac hypertrophy induced by diabetes. OBJECTIVES: To evaluate the effects of TMZ on QT interval prolongation and cardiac hypertrophy in the diabetic rats. METHODS: Twenty-four male Sprague-Dawley rats (200-250 g) were randomly assigned into three groups (n = 8) by simple random sampling method. Control (C), diabetic (D), and diabetic administrated with TMZ at 10 mg/kg (T10). TMZ was administrated for 8 weeks. The echocardiogram was recorded before isolating the hearts and transfer to a Langendorff apparatus. Hemodynamic parameters, QT and corrected QT interval (QTc) intervals, heart rate and antioxidant enzymes were measured. The hypertrophy index was calculated. The results were evaluated by one-way ANOVA and paired t-test using SPSS (version 16) and p < 0.05 was regarded as significant. RESULTS: The diabetic rats significantly indicated increased hypertrophy, QT and QTc intervals and decreased Left ventricular systolic pressure (LVSP), Left ventricular developed pressure (LVDP), rate pressure product (RPP), Max dp/dt, and min dp/dt (±dp/dt max), heart rate, superoxide dismutase (SOD), glutathione peroxidase (GPx) and catalase in the heart. Treatment with TMZ in the diabetic animals was significantly improved these parameters in comparison to the untreated diabetic group. CONCLUSIONS: TMZ improves QTc interval prolongation and cardiac hypertrophy in diabetes.
Sujet(s)
Cardiomégalie/traitement médicamenteux , Complications du diabète/traitement médicamenteux , Syndrome du QT long/traitement médicamenteux , Agents protecteurs/pharmacologie , Trimétazidine/pharmacologie , Animaux , Cardiomégalie/enzymologie , Cardiomégalie/étiologie , Cardiomégalie/physiopathologie , Catalase/analyse , Complications du diabète/enzymologie , Complications du diabète/physiopathologie , Diabète expérimental/complications , Diabète expérimental/physiopathologie , Échocardiographie , Glutathione peroxidase/analyse , Hémodynamique/effets des médicaments et des substances chimiques , Syndrome du QT long/enzymologie , Syndrome du QT long/physiopathologie , Mâle , Répartition aléatoire , Rat Sprague-Dawley , Reproductibilité des résultats , Superoxide dismutase/analyse , Facteurs tempsRÉSUMÉ
AIM: Sol-gel is a suitable and advantageous method to synthesize mixed oxide nanomaterials with unique physicochemical and biological properties. MATERIALS & METHODS: In this work, TiO2-SiO2 nanopowders cogeled with platinum acetylacetonate were developed and studied in the perspective of nanomedicine. The physicochemical properties of the Pt/TiO2-SiO2 nanopowders, named NanoRa2-Pt, were evaluated in detail by means of complementary spectroscopic and microscopic tools. The nanopowder's biocatalytic efficiency in wound healing was evaluated in a Type I diabetes animal model. RESULTS: These are TiO2-SiO2 submicron mesoporous particles with variable size and shape containing ultra-small platinum nanoparticles with catalytic properties. CONCLUSION: The use of NanoRa2-Pt catalyzes the natural healing processes with a faster remodeling stage. These sols, which we call nanobiocatalysts, belong to an emerging and very promising research field known as catalytic nanomedicine.
Sujet(s)
Nanoparticules/composition chimique , Platine/composition chimique , Silice/composition chimique , Titane/composition chimique , Cicatrisation de plaie/effets des médicaments et des substances chimiques , Animaux , Catalyse , Complications du diabète/traitement médicamenteux , Complications du diabète/physiopathologie , Diabète de type 1/complications , Diabète de type 1/traitement médicamenteux , Humains , Mâle , Nanoparticules métalliques/composition chimique , Nanomédecine , Porosité , Rats , Rat Wistar , Propriétés de surfaceSujet(s)
Humains , Mâle , Femelle , Adulte , Adulte d'âge moyen , Sujet âgé , Sujet âgé de 80 ans ou plus , Jeune adulte , Maladies cardiovasculaires/traitement médicamenteux , Acide acétylsalicylique/usage thérapeutique , Complications du diabète/traitement médicamenteux , Maladies cardiovasculaires/prévention et contrôle , Essais contrôlés randomisés comme sujet , Facteurs de risque , Études de suivi , Études multicentriques comme sujetRÉSUMÉ
Purpose: To investigate the specific molecular mechanisms and effects of curcumin derivative J147 on diabetic peripheral neuropathy (DPN). Methods: We constructed streptozotocin (STZ)-induced DPN rat models to detected mechanical withdrawal threshold (MWT) in vivo using Von Frey filaments. In vitro, we measured cell viability and apoptosis, adenosine 5-monophosphate-activated protein kinase (AMPK) and transient receptor potential A1 (TRPA1) expression using MTT, flow cytometry, qRT-PCR and western blot. Then, TRPA1 expression level and calcium reaction level were assessed in agonist AICAR treated RSC96cells. Results: The results showed that J147reduced MWT in vivo, increased the mRNA and protein level of AMPK, reduced TRPA1 expression and calcium reaction level in AITCR treated RSC96 cells, and had no obvious effect on cell viability and apoptosis. Besides, AMPK negative regulated TRPA1 expression in RSC96 cells. Conclusions: J147 could ameliorate DPN via negative regulation AMPK on TRPA1 in vivo and in vitro. A curcumin derivative J147might be a new therapeutic potential for the treatment of DPN.(AU)
Sujet(s)
Animaux , Mâle , Adulte , Rats , Curcumine/analogues et dérivés , Curcumine/pharmacologie , Curcumine/usage thérapeutique , Neuropathies périphériques/traitement médicamenteux , Protein kinases , Canaux cationiques TRP , Complications du diabète/induit chimiquement , Complications du diabète/traitement médicamenteuxRÉSUMÉ
INTRODUCTION: DM spending in the world is high, and Brazilian studies of public spending caused by DM are scarce. OBJECTIVE: To estimate the annual direct cost for the municipal health sphere, related to DM2 treatment, in patients with and without glycemic control. METHOD: A cross-sectional study carried out in a city in the interior of Minas Gerais state, with patients with DM2, being municipal PHS users. Data were collected from the computerized system of the municipality and patient records, and analyzed using the IBM SPSS v.19 statistical package. The response variable was categorized into controlled A1c (≤7%) and uncontrolled A1c (>7%). RESULTS: Glycemic control in 56.6% of the patients was unsatisfactory; the mean cost of pharmacotherapy for DM2 was US$ 3.14 per year for patients in the control group and US$ 45.54 per year for uncontrolled patients. CONCLUSION: Patients with unsatisfactory glycemic control are more expensive for the municipal health system.
Sujet(s)
Complications du diabète/économie , Diabète de type 2/économie , Services de santé/économie , Hyperglycémie/économie , Hypoglycémie/économie , Hypoglycémiants/économie , Évaluation des résultats et des processus en soins de santé/économie , Brésil/épidémiologie , Coûts indirects de la maladie , Études transversales , Complications du diabète/traitement médicamenteux , Complications du diabète/épidémiologie , Diabète de type 2/traitement médicamenteux , Diabète de type 2/épidémiologie , Femelle , Études de suivi , Humains , Hyperglycémie/prévention et contrôle , Hypoglycémie/prévention et contrôle , Hypoglycémiants/usage thérapeutique , Mâle , Adulte d'âge moyen , PronosticRÉSUMÉ
Chronic hyperglycemia increases production of reactive oxygen species, which favors carcinogenesis. The association between diabetes and prostate cancer is controversial. Melatonin has antioxidant, anti-inflammatory, and antiproliferative properties. We investigated whether low doses of melatonin prevent the tissue alterations caused by diabetes and alter prostate histology of healthy rats. We also investigated whether experimental diabetes promoted the development of pathological lesions in the ventral prostate of rats. Melatonin was provided in drinking water (10 µg/kg/day) from age 5 weeks until the end of experiment. Diabetes was induced at 13 weeks by administration of streptozotocin (40 mg/kg, ip). Rats were euthanized at 14 or 21 weeks. Histological and stereological analyses were carried out and the incidence and density of malignant and pre-malignant lesions were assessed. Immunohistochemical assays of α-actin, cell proliferation (PCNA), Bcl-2, glutathione S-transferase (GSTPI), and DNA methylation (5-methylcytidine) were performed. Melatonin did not elicit conspicuous changes in the prostate of healthy animals; in diabetic animals there was a higher incidence of atrophy (93%), microinvasive carcinoma (10%), proliferative inflammatory atrophy, PIA (13%), prostatitis (26%), and prostate intraepithelial neoplasia, PIN (20%) associated with an increase of 40% in global DNA methylation. Melatonin attenuated epithelial and smooth muscle cell (smc) atrophy, especially at short-term diabetes-and normalized incidence of PIN (11%), inflammatory cells infiltrates, prostatitis (0%) and PIA (0%) at long-term diabetes. MLT was effective in preventing inflammatory disorders and PIN under diabetic condition. Although MLT has antioxidant action, it did not influence DNA methylation and not avoid carcinogenesis at low doses.