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1.
Arch. endocrinol. metab. (Online) ; 65(6): 695-703, Nov.-Dec. 2021. tab, graf
Article in English | LILACS | ID: biblio-1349995

ABSTRACT

ABSTRACT Objective: Diabetes mellitus (DM) has a high healthcare system cost worldwide. Educational strategies are important to improve self-care and control this disease. This study aimed to evaluate satisfaction and clinical efficacy of a Short Message Service (SMS) educational intervention in self-care and nutrition at a Brazilian university hospital. Materials and methods: We conducted a trial of educational intervention and assigned eligible patients with DM to either receive weekly educational SMS for 6 months (intervention group [IG]) or no SMS at all (control group). A satisfaction questionnaire was applied before and after the intervention in both groups. Laboratory (fasting glucose, hemoglobin [Hb] A1c, total cholesterol, triglycerides, high-density lipoprotein, and low-density lipoprotein) and clinical (blood pressure) data were also collected. Data were analyzed using nonparametric tests with the Statistical Package for the Social Sciences. Results: We included 128 patients (64 in each group). Responses to the satisfaction questionnaire with self-care and healthcare professionals from 112 patients revealed an improvement in the perception of receiving information regarding helpful eating habits and in healthy eating behavior and an improvement in satisfaction with their diabetes care in the IG. In the post-intervention period, improved systolic blood pressure and HbA1c levels were observed in the IG as illustrated by delta % (post-intervention minus pre-intervention data divided by pre-intervention data multiplied by 100) reductions of 2.3% and 3.9%, respectively Conclusion: SMS intervention was useful as an educational tool for improving satisfaction and glycemic and blood pressure control of patients with DM observed at a Brazilian university hospital.


Subject(s)
Humans , Diabetes Mellitus/therapy , Diabetes Mellitus, Type 2 , Text Messaging , Blood Glucose , Glycated Hemoglobin , Hospitals, Public
2.
Arch. endocrinol. metab. (Online) ; 64(4): 412-417, July-Aug. 2020. tab
Article in English | LILACS | ID: biblio-1131101

ABSTRACT

ABSTRACT Objective The consequences of sleep deprivation in type 1 diabetes (T1D) patients are poorly understood. Our aim was to determine how sleep disorders influence lipid profile and insulin sensitivity in T1D patients. Materials and methods This was a cross-sectional study at a public university hospital. Demographic information and medical histories were obtained during regular scheduled visit of T1D patients to the outpatient clinic. Insulin sensitivity was obtained using the estimated glucose disposal rate (eGDR) formula. Sleep quality was assessed using the Pittsburgh Sleep Quality Index, Epworth Sleepiness Scale and Berlin Questionnaire. Results The adult participants (n = 66, 62% women) had a median age of 28.0 years (interquartile range 21.8-33.0). Six patients (9%) had metabolic syndrome according to the International Diabetes Federation criteria. Thirty patients (46%) were considered poor sleepers according to the Pittsburgh Sleep Quality Index. The LDL-c and total cholesterol levels of poor sleepers were higher than those of good sleepers (103 v. 81; p = 0.003 and 178.0 v. 159.5 mg/dL; p = 0.009, respectively). Three patients (4%) were at high risk of obstructive sleep apnea syndrome (OSAS) according to the Berlin Questionnaire. The eGDR was lower in the group of patients with high probability of having OSAS (6.0 v. 9.1 mg.kg-1.min-1;p = .03). Conclusions Poor subjective quality of sleep and higher risk of OSAS were correlated with a worsened lipid profile and decreased insulin sensitivity, respectively. Therefore, T1D patients with sleep disturbances might have an increased cardiovascular risk in the future.


Subject(s)
Humans , Male , Female , Adult , Sleep Wake Disorders , Insulin Resistance , Diabetes Mellitus, Type 1 , Cross-Sectional Studies , Surveys and Questionnaires , Lipids
3.
Arch Endocrinol Metab ; 64(4): 412-417, 2020 Aug.
Article in English | MEDLINE | ID: mdl-32267356

ABSTRACT

Objective The consequences of sleep deprivation in type 1 diabetes (T1D) patients are poorly understood. Our aim was to determine how sleep disorders influence lipid profile and insulin sensitivity in T1D patients. Materials and methods This was a cross-sectional study at a public university hospital. Demographic information and medical histories were obtained during regular scheduled visit of T1D patients to the outpatient clinic. Insulin sensitivity was obtained using the estimated glucose disposal rate (eGDR) formula. Sleep quality was assessed using the Pittsburgh Sleep Quality Index, Epworth Sleepiness Scale and Berlin Questionnaire. Results The adult participants (n = 66, 62% women) had a median age of 28.0 years (interquartile range 21.8-33.0). Six patients (9%) had metabolic syndrome according to the International Diabetes Federation criteria. Thirty patients (46%) were considered poor sleepers according to the Pittsburgh Sleep Quality Index. The LDL-c and total cholesterol levels of poor sleepers were higher than those of good sleepers (103 v. 81; p = 0.003 and 178.0 v. 159.5 mg/dL; p = 0.009, respectively). Three patients (4%) were at high risk of obstructive sleep apnea syndrome (OSAS) according to the Berlin Questionnaire. The eGDR was lower in the group of patients with high probability of having OSAS (6.0 v. 9.1 mg.kg-1.min-1;p = .03). Conclusions Poor subjective quality of sleep and higher risk of OSAS were correlated with a worsened lipid profile and decreased insulin sensitivity, respectively. Therefore, T1D patients with sleep disturbances might have an increased cardiovascular risk in the future.


Subject(s)
Diabetes Mellitus, Type 1 , Insulin Resistance , Sleep Wake Disorders , Adult , Cross-Sectional Studies , Female , Humans , Lipids , Male , Surveys and Questionnaires
4.
J Clin Densitom ; 23(4): 623-629, 2020.
Article in English | MEDLINE | ID: mdl-30545683

ABSTRACT

INTRODUCTION: Human immunodeficiency virus-related lipodystrophy is characterized by a variety of phenotypes and metabolic changes; however, consensus has not yet been reached on its diagnostic criteria. Different cutoff values for fat mass ratio have been proposed for this specific population as an objective diagnostic criterion for lipodystrophy. This study aimed to establish sex-specific reference values for fat mass ratio and to correlate them with anthropometric measurements for the diagnosis of human immunodeficiency virus-related lipodystrophy. METHODOLOGY: A cross-sectional study was performed on 189 human immunodeficiency virus-infected patients under antiretroviral therapy. Anthropometric measurements were evaluated, and body composition was determined using dual-energy X-ray absorptiometry. Fat mass ratio was calculated as the ratio of the percentage of the trunk fat mass and the percentage of the lower limb fat mass. RESULTS: One hundred and thirty-two patients (69%) presented lipodystrophy by objective criteria. In men, the cutoff for the fat mass ratio was 1.55 (area under the receiver operating characteristic curve: 0.73 [95% confidence interval: 0.62-0.83], p = 0.000008), with a sensitivity of 62.5%, a specificity of 70.5%, a positive predictive value of 77.8%, and a negative predictive value of 53.4%. In women, the cutoff for the fat mass ratio was 0.959 (area under the receiver operating characteristic curve: 0.70 [95% confidence interval: 0.56-0.85], p = 0.03), with a sensitivity of 83.60%, a specificity of 61.5%, a positive predictive value of 90.2%, and a negative predictive value of 47.1%. Fat mass ratio was positively correlated with waist circumference (men: r = 0.246, p = 0.019; women: r = 0.302, p = 0.014) and neck circumference (men: r = 0.304, p = 0.004; women: r = 0.366, p = 0.003) in both sexes; and body mass index (r = 0.288, p = 0.006) and waist-hip ratio (r = 0.288, p = 0.006) in men. CONCLUSION: The fat mass ratio evaluated using dual-energy X-ray absorptiometry with the sex-specific cutoffs is an objective tool to define human immunodeficiency virus-related lipodystrophy.


Subject(s)
Adipose Tissue/diagnostic imaging , Anti-HIV Agents/therapeutic use , HIV Infections/drug therapy , HIV-Associated Lipodystrophy Syndrome/diagnosis , Absorptiometry, Photon , Adipose Tissue/pathology , Adult , Anthropometry , Anti-HIV Agents/adverse effects , Body Composition/drug effects , Brazil , Cross-Sectional Studies , Female , HIV-Associated Lipodystrophy Syndrome/diagnostic imaging , HIV-Associated Lipodystrophy Syndrome/pathology , Humans , Male , Middle Aged , Sex Factors
5.
São Paulo med. j ; 134(6): 473-479, Nov.-Dec. 2016. tab, graf
Article in English | LILACS | ID: biblio-846257

ABSTRACT

ABSTRACT: CONTEXT AND OBJECTIVE: The prevalence of vitamin B12 deficiency varies from 5.8% to 30% among patients undergoing long-term treatment with metformin. Because of the paucity of data on Brazilian patients, this study aimed to determine the frequency of B12 deficiency and related factors among Brazilian patients with type 2 diabetes mellitus (T2DM) using metformin. DESIGN AND SETTING: Cross-sectional study at a public university hospital. METHODS: Patients with T2DM and a control group of non-diabetics were included. Serum B12 levels were measured and biochemical B12 deficiency was defined as serum levels < 180 pg/ml. Associations between B12 deficiency and age, duration of T2DM, duration of use and dosage of metformin, and use of proton pump inhibitors (PPIs) or histamine H2 antagonists were determined. RESULTS: 231 T2DM patients using metformin (T2DM-met) and 231 controls were included. No difference in the frequency of PPI or H2-antagonist use was seen between the groups. B12 deficiency was more frequent in the T2DM-met group (22.5% versus 7.4%) and this difference persisted after excluding PPI/H2-antagonist users (17.9% versus 5.6%). The factors that interfered with serum B12 levels were PPI/H2-antagonist use and duration of metformin use ≥ 10 years. Use of PPI/H2-antagonists was associated with B12 deficiency, with an odds ratio of 2.60 (95% confidence interval, 1.34-5.04). CONCLUSIONS: Among T2DM patients, treatment with metformin and concomitant use of PPI/H2-antagonists are associated with a higher chance of developing B12 deficiency than among non-diabetics.


RESUMO: CONTEXTO E OBJETIVO: A prevalência de deficiência de vitamina B12 varia de 5,8% a 30% nos pacientes em tratamento a longo prazo com metformina. Devido à escassez de dados em pacientes brasileiros, este estudo determinou a frequência de deficiência de B12 e fatores relacionados em pacientes brasileiros com diabetes mellitus tipo 2 (DM2) usando metformina. TIPO DE ESTUDO E LOCAL: Estudo transversal em hospital público universitário. MÉTODOS: Pacientes com DM2 e um grupo controle de não diabéticos foram incluídos. Os níveis séricos de vitamina B12 foram dosados e deficiência bioquímica de B12 foi definida como níveis séricos < 180 pg/ml. Foi investigada a associação entre deficiência de B12 e idade, duração do DM2, duração do uso e dose de metformina, uso de inibidores de bomba de prótons (IBP) ou antagonistas dos receptores histamínicos H2 (antagonistas-H2). RESULTADOS: 231 pacientes DM2 usando metformina (DM2-met) e 231 controles foram incluídos. Não houve diferença na frequência de uso de IBP/antagonistas-H2 entre os grupos. Deficiência de B12 foi mais frequente no grupo DM2-met (22,5% versus 7,4%) e essa diferença persistiu após exclusão dos usuários de IBP/antagonistas-H2 (17,9% versus 5,6%). Fatores que interferiram nos níveis séricos de B12 foram: uso de IBP/antagonistas-H2 e duração do uso de metformina ≥ 10 anos. O uso de IBP/antagonistas-H2 associou-se com deficiência de B12, com um risco relativo de 2,60 (95% intervalo de confiança, 1,34-5,04). CONCLUSÕES: Considerando pacientes com DM2, o tratamento com metformina e uso concomitante de IBP/antagonistas-H2 estão associados com maior chance de desenvolver deficiência de B12 quando comparado aos não diabéticos.


Subject(s)
Humans , Male , Female , Middle Aged , Aged , Vitamin B 12 Deficiency/chemically induced , Vitamin B 12 Deficiency/epidemiology , Diabetes Mellitus, Type 2/drug therapy , Hypoglycemic Agents/adverse effects , Metformin/adverse effects , Vitamin B 12/blood , Brazil/epidemiology , Case-Control Studies , Logistic Models , Prevalence , Cross-Sectional Studies , Risk Factors , Statistics, Nonparametric , Proton Pump Inhibitors/adverse effects , Histamine H2 Antagonists/adverse effects , Hospitals, Public
6.
Arq Bras Cardiol ; 102(3): 263-9, 2014 Mar.
Article in English, Portuguese | MEDLINE | ID: mdl-24676226

ABSTRACT

BACKGROUND: Metabolic syndrome (MS) is an aggregation of risk factors that increase the incidence of cardiovascular events and diabetes mellitus (DM). Population aging is accompanied by higher prevalence of MS, which varies depending on the population studied and the diagnostic criteria used. OBJECTIVE: To determine prevalence of MS in the elderly using four diagnostic criteria and agreement between them. METHODS: Cross-sectional study on 243 patients older than 60 years (180 women) in Niterói, RJ. They were evaluated by clinical examination, fasting glucose, fasting insulin, lipid profile and anthropometric measurements - weight, height, waist circumference and waist/hip ratio. Prevalence of MS was estimated by World Health Organization (WHO) modified, National Cholesterol Education Program - Adult Treatment Panel III (NCEP-ATP III), International Diabetes Federation (IDF) and Joint Interim Statement (JIS) criteria. RESULTS: Prevalence was high with the four criteria WHO (51.9%), NCEP-ATPIII (45.2%), IDF (64.1%) and JIS (69.1%), and agreement between criteria by kappa was moderate in almost all comparisons WHO vs. IDF (k = 0.47;95% confidence interval (CI), 0.35 to 0.58); WHO vs. NCEP-ATPIII (k = 0.51; 95% CI, 0.40 to 0.61); WHO vs. JIS (k = 0.45; 95% CI, 0.33 to 0.56); IDF vs. NCEP-ATPIII (k = 0.55; 95% CI, 0.45 to 0.65) and NCEP-ATPIII vs. JIS (k = 0.53; 95% CI, 0.43-0.64), except between IDF vs. JIS (K = 0.89;95% CI, 0.83 to 0.95), which was considered good. CONCLUSION: Prevalence of MS was high with the four diagnostic criteria, mainly by JIS. There was good agreement between JIS and IDF criteria and moderate among the others.


Subject(s)
Metabolic Syndrome/diagnosis , Metabolic Syndrome/epidemiology , Age Distribution , Aged , Analysis of Variance , Blood Glucose/analysis , Body Mass Index , Brazil/epidemiology , Cardiovascular Diseases/etiology , Cardiovascular Diseases/metabolism , Cross-Sectional Studies , Diabetes Mellitus/metabolism , Female , Humans , Male , Middle Aged , Prevalence , Risk Factors , Waist Circumference , Waist-Hip Ratio
7.
Arq. bras. cardiol ; 102(3): 263-269, 03/2014. tab, graf
Article in Portuguese | LILACS | ID: lil-705722

ABSTRACT

Fundamento: A Síndrome Metabólica (SM) é uma agregação de fatores de risco que aumenta a incidência de eventos cardiovasculares e Diabete Melito (DM). O envelhecimento da população vem acompanhado de maior prevalência de SM, que varia dependendo da população estudada e do critério diagnóstico utilizado. Objetivo: Determinar a prevalência de SM em idosos por quatro critérios diagnósticos e a concordância entre esses. Métodos: Estudo transversal realizado em 243 indivíduos acima de 60 anos (180 mulheres) em Niterói (RJ). Foram avaliados através de exame clínico glicemia jejum, insulinemia jejum, perfil lipídico e medidas antropométricas - peso, estatura, circunferência abdominal e relação cintura/quadril. A prevalência de SM foi estimada utilizando critérios diagnósticos da Organização Mundial da Saúde (OMS) modificado, National Cholesterol Education Program - Adult Treatment Panel III (NCEP-ATPIII), International Diabetes Federation (IDF) e Joint Interim Statement (JIS). Resultados: A prevalência foi elevada pelos quatro critérios, OMS (51,9%), NCEP-ATPIII (45,2%), IDF (64,1%) e JIS (69,1%), e a concordância entre os critérios diagnósticos pelo índice kappa foi moderada em quase todas as comparações OMS vs. IDF (k = 0,47; intervalo de confiança (IC) 95%, 0,35 - 0,58); OMS vs. NCEP-ATPIII (k = 0,51; IC 95%, 0,40 - 0,61); OMS vs. JIS (k = 0,45; IC 95%, 0,33 - 0,56); IDF vs. NCEP-ATPIII (k = 0,55, IC 95%, 0,45 - 0,65) e NCEP-ATPIII vs. JIS (k = 0,53; IC 95%, 0,43 - 0,64), exceto entre IDF vs. JIS (K= 0,89; IC 95%, 0,83 - 0,95), considerada boa. Conclusão: A prevalência de SM foi elevada pelos quatro critérios diagnósticos, principalmente pelo JIS. Houve uma boa concordância entre os critérios ...


Background: Metabolic syndrome (MS) is an aggregation of risk factors that increase the incidence of cardiovascular events and diabetes mellitus (DM). Population aging is accompanied by higher prevalence of MS, which varies depending on the population studied and the diagnostic criteria used. Objective: To determine prevalence of MS in the elderly using four diagnostic criteria and agreement between them. Methods: Cross-sectional study on 243 patients older than 60 years (180 women) in Niterói, RJ. They were evaluated by clinical examination, fasting glucose, fasting insulin, lipid profile and anthropometric measurements - weight, height, waist circumference and waist/hip ratio. Prevalence of MS was estimated by World Health Organization (WHO) modified, National Cholesterol Education Program - Adult Treatment Panel III (NCEP-ATP III), International Diabetes Federation (IDF) and Joint Interim Statement (JIS) criteria. Results: Prevalence was high with the four criteria WHO (51.9%), NCEP-ATPIII (45.2%), IDF (64.1%) and JIS (69.1%), and agreement between criteria by kappa was moderate in almost all comparisons WHO vs. IDF (k = 0.47;95% confidence interval (CI), 0.35 to 0.58); WHO vs. NCEP-ATPIII (k = 0.51; 95% CI, 0.40 to 0.61); WHO vs. JIS (k = 0.45; 95% CI, 0.33 to 0.56); IDF vs. NCEP-ATPIII (k = 0.55; 95% CI, 0.45 to 0.65) and NCEP-ATPIII vs. JIS (k = 0.53; 95% CI, 0.43-0.64), except between IDF vs. JIS (K = 0.89;95% CI, 0.83 to 0.95), which was considered good. Conclusion: Prevalence of MS was high with the four diagnostic criteria, mainly by JIS. There was good agreement between JIS and IDF criteria and moderate among the others. .


Subject(s)
Aged , Female , Humans , Male , Middle Aged , Metabolic Syndrome/diagnosis , Metabolic Syndrome/epidemiology , Age Distribution , Analysis of Variance , Body Mass Index , Blood Glucose/analysis , Brazil/epidemiology , Cross-Sectional Studies , Cardiovascular Diseases/etiology , Cardiovascular Diseases/metabolism , Diabetes Mellitus/metabolism , Prevalence , Risk Factors , Waist Circumference , Waist-Hip Ratio
8.
Rev. bras. neurol ; 36(3): 67-9, maio-jun. 2000.
Article in Portuguese | LILACS | ID: lil-277454

ABSTRACT

A síndrome de Down foi descrita inicialmente em 1866 pelo médico John Langdon Down, que observou sinais clínicos comuns tais como: retardo mental, hipotonia muscular, protusäo da língua, pregas na nuca e epicanto. Pela semelhança com o povo da Mongólia, ele os denominou de mongolóides. Este termo foi sempre considerado uma ofensa racial, sendo retirado em 1960 para uso científico, quando passou a ser denominada de síndrome de Down. Em 1930 foi especulada pela primeira vez , uma possível anormalidade cromossômica da síndorme, feita por Bleyer e Waaderberg. Trinta anos mais tarde, Jerome Lejeune e Patrícias Jacobs, em pesquisas independentes, determinaram a trissomia do cromossomo 21 na síndrome. Estudos posteriores documentaram a associaçäo com malformaçöes cardiovasculares, do aparelho respiratório, das vias urinárias, doenças neurológicas, hematológicas, imunológicas, da audiçäo, osteoarticulares e da arcada dentária. As disfunçöes tireoideanas têm uma alta prevalência na síndrome de Down, sendo importante ressaltar a dificulade do diagnóstico em funçäo dos sinais e sintomas näo serem facilmente reconhecidas, Ë importante salientar a possibilidade da doença subclínica ter influência no agravamento da deficiência mental destes pacientes, piorando sua qualidade de vida


Subject(s)
Humans , Endocrine System Diseases/etiology , Down Syndrome/complications
9.
Revista Brasileira de Neurologia ; 3(36): 67-69, maio/jun. 2000.
Article | Index Psychology - journals | ID: psi-15070

ABSTRACT

A sindrome de Down foi descrita inicialmente em 1866 pelo medico John Langdon Down, que observou sinais clinicos comuns tais como: retardo mental, hipotonia muscular, protusao da lingua, pregas na nuca e epicanto. Pela semelhanca com o povo da Mongolia, ele os denominou de mongoloides. Este termo foi sempre considerado uma ofensa racial, sendo retirado em 1960 para uso cientifico, quando passou a ser denominada sindrome de Down. Em 1930 foi especulada pela primeira vez uma possivel anormalidade cronossomica na sindrome, feita por Bleyer e Waaderberg. Trinta anos mais tarde, Jerome Lejeune e Patricias Jacobs, em pesquisas idependentes, determinaram a trissomia do cronossomo 21 na sindrome. Estudos posteriores documentaram a associacao com malformacoes cardiovasculares, do aparelho respiratorio, das vias urinarias, doencas neurologicas, hematologicas, imunologicas, da audicao, osteoarticulares e da arcada dentaria. As disfuncoes tireoideanas tem uma alta prevalencia na sindrome de Down, sendo importante ressaltar a dificuldade do diagnostico em funcao dos sinais e sintomas nao serem facilmente reconhecidos. E importante salientar a possibilidade da doenca subclinica ter influencia no agravamento da deficiencia mental destes pacientes, piorando sua qualidade de vida.


Subject(s)
Down Syndrome , Endocrine System Diseases , History , Down Syndrome , History
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