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This study suggests that the -3826A/G polymorphism is associated with DR in type 1 DM patients. This is the first report demonstrating UCP1 gene expression in human retinas and indicates that the -3826A/G polymorphism influences its expression. In addition, the -3826G allele was associated with increased MnSOD2 expression; thus, suggesting that this allele could be a marker of oxidative stress.

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RESUMOA retinopatia diabética (RD) acomete cerca de 95% dos pacientes com diabetes melito tipo 1 (DM1) e 60% dos pacientes com diabetes melito tipo 2 (DM2), sendo a principal causa de cegueira legal em adultos. O objetivo desse manuscrito foi revisar os principais fatores de risco para RD. Os fatores de risco ambientais mais importantes são a hiperglicemia sustentada, os valores elevados de pressão arterial e a longa duração de DM. Entretanto, nem todos os pacientes desenvolvem RD, o que sugere a presença de fatores genéticos, em especial para as formas graves de RD. Diferentes estratégias têm sido utilizadas para avaliar o papel da genética na RD. Estudos de famílias demonstraram agregação familiar de RD. Genes candidatos têm sido estudados (RAGE; VEGF; PPAR-δ; ICAM-1; ECA; ENPP 1; eNOS), observando-se associações positivas ou negativas com a RD. Também alguns cromossomos, em populações selecionadas, foram associados à RD. Finalmente, estudos de expressão genética reforçam a associação de genes candidatos, ou determinam a participação de outros, com a presença da RD. A RD é uma complicação freqüente do DM e junto com os fatores não-genéticos ou ambientais, a identificação de genes relacionados à RD poderá resultar tratamentos mais específicos e eficazes para a RD. Diabetic retinopathy (DR) occurs in about 95% of patients with type 1 diabetes mellitus (DM) and in 60% of type 2 DM patients and it is the main cause of legal blindness in adult people. The aim of this manuscript was to review the main risk factors for DR. The major environmental risk factors are hyperglycemia, high blood pressure levels, and long-term duration of DM. However, not all patients will not develop DR, suggesting the presence of a genetic predisposition to DR, especially for severe forms of DR. Special strategies has been used to evaluate the genetic role in DR. Family studies shown that there is a familial aggregation of DR. Candidates genes have been studied (RAGE; VEGF; ECA; ENPP 1; eNOS) and positive or negative associations with DR were demonstrated. Some chromosomes were also associated to DR in selected populations. Finally, genetic expression studies reinforce the association of candidate genes, or participation of others genes, with the presence of DR. DR is a common complication of DM and, along with nongenetic or environmental risk factors, the identification of genes related to DR could result in more specific and efficient DR treatment. (Arq Bras Endocrinol Metab 2008; 52/3:431-441)

For the years 1972-1981, 7 333 isolates of dermatophytes belonging to 14 species were obtained from glabrous skin (32%), feet (28%), groin (19%), scalp (8%), toenails (7%), fingernails (3%) and beard (1%). T. rubrum represented 50% of all the isolates and was the most frequent species on glabrous skin, groin and nails. T. mentagrophytes (24%) was mainly obtained from the feet, E. floccosum (9%) from the groin and T. megninii (4%) from uncovered areas of the skin, fingernail and beard. These 4 species predominated in men. M. canis was the commonest agent on the scalp and in children up to 11 years. T. violaceum, previously the main cause of tinea capitis, and T. tonsurans have been decreasing for the period of this study, just as T. schoenleinii for the years 1962-71. The rising prevalence of T. rubrum was observed since 1962. In the whole it seems stable after 1969, but the analysis of the main sites involved shows that in the glabrous skin this species increased from 1962 to 1974; in the groin it was gone up from 30% during 1962-1965, to 64% in the years 1969-1971; in the feet the evolution was slower and only in 1980 T. rubrum became more frequent than T. mentagrophytes. The increase in certain species, whereas others become rare, lacks a satisfactory explanation.

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SummaryPrevalence of diabetic retinopathy in patients with type 1 diabetes mellitus Objectives. Diabetic retinopathy (DR) is the leading cause of legal blindness in young adults. Scarce data from Brazilian subjects with type 1 diabetes mellitus (DM) are available. Aims: The objectives of this study were to determine the prevalence of DR and its risk factors in type 1 diabetes mellitus (DM) outpatients from a general hospital. MethOds. A cross-sectional study of 437 type 1 DM (50.3% males, 82.4% whites) was conducted. DR was graded as absent, mild and moderate non-proliferative DR (mild/moderate NPDR) or severe non-proliferative and proliferative DR (advanced DR). Presence of clinically significant macular edema (CSME) was also recorded. Results. Any DR was present in 44.4% of subjects. In multivariate analysis, DM duration, systolic blood pressure (SBP) and A1C test were associated with mild/moderate NPDR (P<0.005). Advanced DR, was associated with DM duration, SBP, smoking [odds ratio (OR) 2.75, 95%CI 1.15-6.60] and micro-or macroalbuminuria (OR 8.53,. CSME was present in 21 (9.4%) patients and was associated with smoking (OR 3.19,. Its frequency increased with the severity of DR (16.4% in advanced DR, 9.6% in mild/moderate NPDR, and 4.7% in the group without DR; P = 0.020). cOnclusiOn. Patients with type 1 DM attending an endocrine out-patient clinic at a general hospital had a high prevalence of DR associated with traditional risk-factors and smoking.