Prevalence of skin diseases in children 1 to 6 years old in the city of Bogota, Colombia.

BACKGROUND: Skin diseases represent an important part of the morbidity among children and are possibly influenced by geographic, racial, social, cultural, and economic factors. Despite being so frequent around the world, skin diseases have not been important in developing strategies in public health. AIM: The purpose of this study was to evaluate the prevalence of skin diseases among the student population between 1 and 6 years of age in Bogotá, Colombia between March 2009 and June 2011. MATERIALS AND METHODS: This cross-sectional study was performed across a probabilistic, stratified, randomized sampling by proportional assignment (based on locality and type of institution) and was developed in schools in Bogotá, Colombia. RESULTS: A total of 2437 children between 1 and 6 years of age were examined, and 42.8% (1035) presented a dermatologic disease. Papular urticaria was the most frequent (62.9%) (IC: 58.4%; 67.1%), followed by dermatitis/eczema (13.0%) (IC: 10.8%; 15.4%), and infectious diseases (12.3%) (IC: 9.7%; 15.3%). CONCLUSION: The research demonstrates a high prevalence of papular urticaria as a result of flea and mosquito bites and infectious diseases of the skin in the studied population. The dermatologic diseases found are easy to diagnose, respond to the proper treatment, and are preventable. However, the fact that many of the examined children likely had not visited the doctor for the detected pathology could indicate the lack of access to health services affecting this population.

Prevalence of papular urticaria caused by flea bites and associated factors in children 1-6 years of age in Bogotá, D.C.

BACKGROUND: Papular urticaria is a chronic inflammatory disease caused by exposure to arthropod bites. The disease has been reported in children attending medical centers, but the causes as the risk factors associated with the disease have not been established. The objective of this study was to determine the prevalence of papular urticaria caused by flea bite and identify the risk factors in children between 1 to 6 years of age in Bogotá D.C, between March 2009 and June 2011. METHODS: A cross-sectional, two-stage, clustered study using random probability sampling and stratified with proportional allocation was carried out in children (1-6 years of age) in educational institutions in Bogotá D.C. to determine the prevalence of the disease. Children underwent a dermatological examination by general practitioners with a previous training. Furthermore, digital photographs of skin lesions were taken for further confirmation of the diagnosis by dermatologists. A structured survey was completed by the parents or caregivers, and it was evaluated using an unconditional logistic regression to identify factors associated with the disease. RESULTS: A total of 2437 children were included in the study. The prevalence of papular urticaria caused by flea bite in this population was 20.3% (CI 95%: 18.2 to 22.5%). The major risk factors associated with the disease were the presence of fleas in households (OR 1.74, CI 95%: 1.35 to 2.25), using mattresses without springs (OR 1.73, CI 95%: 1.20 to 2.50), the use of daily public transportation to carry the children to the educational institutions (OR 1.76, CI 95%: 1.07 to 2.89), having a soil/earth floor in the main bedroom (OR 6.81, CI 95%:1.16-39.96), and having siblings with a history of atopic dermatitis (OR 1.76 CI 95%: 1.07-2.89). CONCLUSIONS: A high prevalence of papular urticaria caused by flea bite was found in Bogotá D.C. The main factors associated with the disease might be modified with the implementation of prevention, control strategies in housing, educational institutions, and public transportation.

Differences in IgE mediated basophil degranulation induced by proteic fractions from whole flea body extract in patients with papular urticaria by flea bite and healthy controls.

BACKGROUND: Papular urticaria by flea bite (PUFB) is a chronic inflammatory disease in children. The aim of this study was to assess the functional activity of IgE to protein fractions from flea body extract, through basophil degranulation in PUFB patients and controls. METHODS: Basophil degranulation, measured by overexpression of CD63 surface molecules, was evaluated by flow cytometry in samples from patients and controls. Cell stimulation was performed with three fractions with different molecular weight from flea body extract using a Basotest® modified protocol. Mann-Whitney U-test was used for comparisons. RESULTS: Specific IgE from PUFB patients and healthy controls induced basophil degranulation to flea body extract with no significant differences between them (16.2 ± 3.1% vs 13.6 ± 2.8% p = 0.77). However, when flea extract was analyzed in fractions with proteins ranging different molecular weights, significant differences were observed on the response from patients compared with controls to <50 kD (14.9 ± 5.1% vs 9.7 ± 2.1% p = 0.0058) and 50-100 kD proteic fractions (8.3 ± 3.2% vs 2.8 ± 1.6% p = 0.0021). CONCLUSION: In this study, was established that the differential response by IgE, in PUFB, depends from the molecular weight of the antigens contained in the flea extract. These antigens may be related to 30-35 kD proteins previously described as major allergens.

Differences in systemic and skin migrating-specific CD4 T cells in papular urticaria by flea bite.

BACKGROUND: Papular urticaria by flea bite is a chronic allergic condition in which clinical improvement may occur at the age of 7 years, thus representing a natural model of acquired immunologic tolerance in humans. The aim of this study was to characterize regulatory cells and specific responses to flea antigens of CD4(+) T lymphocytes expressing cutaneous migration markers in patients with papular urticaria caused by flea bite and with different disease evolution times. METHODS: Cell populations were characterized by flow cytometry in samples from patients and healthy controls. Specific cell stimulation was performed with a complete flea body extract. The Mann-Whitney U test was used for comparisons. RESULTS: Total dendritic cells were lower in patients than in healthy controls. No quantitative differences were found in CD4 regulatory T cells. CD4(+) T cells from patients produced more IL-4, lL-10, IL-17, and IFN-γ. Patients who experienced the onset of symptoms within the first 5 years of age showed a greater percentage of local (cutaneous lymphocyte antigen +) IL-4- and IL-17-producing cells, while patients who experienced the onset of symptoms after the age of 5 years had a higher percentage of systemic (cutaneous lymphocyte antigen -) IL-10-producing cells. CONCLUSION: Analysis of the cellular immune response against whole flea antigen in patients with papular urticaria by flea bites suggests a possible participation of inflammatory cytokines in the skin reaction (Th17) and a systemic control mechanism (IL-10). This pattern of cytokine production in patients could be a consequence of an impaired dendritic cell population.

Expresión de IL-10, IL-4 e IFN- γ en lesiones activas de piel en niños con urticaria papular por picadura de pulga / Expression of IL-10, IL-4 and IFN-γ in active skin lesions of children with papular urticaria

Introducción. La urticaria papular por picadura de pulga se conoce como una enfermedad alérgica. Sin embargo, las investigaciones no muestran una clara relación con las enfermedades alérgicas. Objetivo. Estudiar la expresión de IL-10, IL-4 e IFN-γ, como marcadores de la respuesta efectora de células T en lesiones de piel de pacientes con urticaria papular por picadura de pulga. Materiales y métodos. Se incluyeron 14 biopsias de lesiones de piel de niños con diagnóstico de urticaria papular por picadura de pulga y 5 biopsias de piel sana obtenidas de niños sometidos a cirugía por enfermedades no inflamatorias. Todas las muestras se obtuvieron de niños menores de 12 años. Se extrajo ARN con trizol y se cuantificaron los niveles de expresión de las citocinas con la técnica de reacción en cadena de la polimerasa en tiempo real. Resultados. En los pacientes con urticaria papular por picadura de pulga, se encontró amplia diversidad en los niveles de expresión de IFN-γ e IL-10, y valores bajos constantes para IL-4. Se observaron tres perfiles que no corresponden a un patrón común en los pacientes. Las muestras obtenidas de tejidos sanos no presentaron expresión de las citocinas. Conclusiones. Los datos corresponden a la primera descripción de citocinas que median la respuesta inmunitaria en el sitio de la lesión cutánea en niños con con urticaria papular por picadura de pulga, lo cual indica que la respuesta local es mixta ya que no se encuentra predominio de un fenotipo específico en ninguno de los pacientes.

Introduction: Papular urticaria caused by the bites of fleas traditionally has been defined as a chronic allergic disease. However, currently no clear relationship has been described between this pathology and common allergic diseases. Objective: The expression of IL-10, IL-4 and IFN-γ as markers of effector T cell responses was examined in skin lesions of patients with papular urticaria by flea bite. Materials and methods: Fourteen skin lesion biopsies were sampled from children with a clinical diagnosis of papular urticaria by flea bite and were compared with 5 healthy skin biopsies of children with no history of the disease. All children were under 12 years old. RNA was extracted with trizol and the expression levels of cytokines were analyzed by real time PCR technique. Results: A wide range in the expression levels of IFN-γ and IL-10 was noted as well as constant low values of IL-4. Three distinct profiles were observed, but which did not correspond to a recognizable pattern among the patients. The samples obtained from healthy tissues showed no expression of any of the cytokines. Conclusions: This is the first characterization of cytokines that mediate the immune response at the site of the skin lesion in children with papular urticaria by flea bite. The data indicated that the local response was mixed and that a single phenotype is not predominant among the patients.

[Expression of IL-10, IL-4 and IFN-γ in active skin lesions of children with papular urticaria]. / Expresión de IL-10, IL-4 e IFN- γ en lesiones activas de piel en niños con urticaria papular por picadura de pulga.

INTRODUCTION: Papular urticaria caused by the bites of fleas traditionally has been defined as a chronic allergic disease. However, currently no clear relationship has been described between this pathology and common allergic diseases. OBJECTIVE: The expression of IL-10, IL-4 and IFN-γ as markers of effector T cell responses was examined in skin lesions of patients with papular urticaria by flea bite. MATERIALS AND METHODS: Fourteen skin lesion biopsies were sampled from children with a clinical diagnosis of papular urticaria by flea bite and were compared with 5 healthy skin biopsies of children with no history of the disease. All children were under 12 years old. RNA was extracted with trizol and the expression levels of cytokines were analyzed by real time PCR technique. RESULTS: A wide range in the expression levels of IFN-γ and IL-10 was noted as well as constant low values of IL-4. Three distinct profiles were observed, but which did not correspond to a recognizable pattern among the patients. The samples obtained from healthy tissues showed no expression of any of the cytokines. CONCLUSIONS: This is the first characterization of cytokines that mediate the immune response at the site of the skin lesion in children with papular urticaria by flea bite. The data indicated that the local response was mixed and that a single phenotype is not predominant among the patients.

Asociación de polimorfismos de la región promotora del gen de la interleucina 10 con la urticaria papular por picadura de pulga / Association of Interleukin 10 (IL-10) gene promoter region polymorphisms with flea bite papular urticaria

Objetivos. Establecer si los polimorfismos en la región promotora del gen de la IL-10 localizados en las posiciones -819 y -592 están asociados con la urticaria papular causada por la picadura de pulga, en pacientes pediátricos que asistieron a consulta de alergia o de dermatología a la Fundación Santa Fe de Bogotá, Colombia. Métodos. La frecuencia de estos dos polimorfismos en el ADN fue analizada en 25 niños con urticaria papular y 22 controles por medio de PCR (Polymerase Chain Reaction) y RFLP (Restriction Fragment Length Polymorphisms). Resultados. No hubo diferencias significativas entre las frecuencias alélicas y genotípicas de cada polimorfismo individual o SNP (-819 o -592) entre pacientes y controles (p=0,21, OR=1,87, IC95% 0,79-4,40) cuando fueron calculados por la prueba exacta de Fisher. Conclusiones. Aunque en este trabajo preliminar no se encontró asociación de los polimorfismos reportados en otras poblaciones con la enfermedad alérgica, hay una tendencia en nuestros experimentos a encontrar un mayor número de haplotipos AT en pacientes que en controles Los resultados publicados por nuestro grupo de investigación, en cuanto a que la secreción de IL-10 in vitro se encuentra disminuida en pacientes con urticaria papular y no en controles sanos, indicar ían que la expresión genética de esta citocina estaría alterada en pacientes y, por consiguiente, esta condición estaría exacerbando la enfermedad. Los niveles disminuidos de esta citocina reguladora permitirían el desarrollo de condiciones hiperinmunes, como la alergia y la autoinmunidad...

Objectives: In this study we aimed to establish whether IL-10 promoter region genetic polymorphisms in positions -819 and -592 were associated with papular urticaria caused by flea bite in pediatric patients from the Fundación Santa Fe de Bogotá, Colombia.Methods: The frequency of these DNA polymorphisms was analyzed in 25 infants suffering papular urticaria and 22 healthy controls, after amplification of their corresponding DNA through polymerase chain reaction (PCR) and further analysis of resulting restriction fragment length polymorphisms (RFLP). Results: We found no significant differences in allelic and genotypic frequencies of either -819 or -592 SNPs between patients and healthy controls (p=0.21, OR=1.87, 95% IC=0.79-4.40). Conclusions: Although we did not find in this preliminary study a genetic association between papular urticaria and previously reported allergyassociated SNPs such as -819 and -592, we found higher numbers of allergy-associated AT haplotypes in patients than in controls. Previously published results from our group showed in vitro a diminished IL-10 secretion in patients and not in healthy controls. This finding, together with our present results, would indicate that the genetic expression of this cytokine could be altered in patients and that this condition could determine the exacerbation of papular urticaria. Low levels of this cytokine would allow for the development of hyperimmune conditions such as allergy and autoimmunity...

Functional dysregulation of dendritic cells in patients with papular urticaria caused by fleabite.

BACKGROUND: Papular urticaria is a chronic allergic disease caused by fleabite. The presence of eosinophils, predominance of CD4-positive T cells in lesions, and IgE response suggest a Th2 immune response to flea proteins in patients with papular urticaria caused by fleabite (PUFB). Although PUFB is defined as an allergic reaction, the immunological mechanisms and the role of dendritic cells (DCs) have not been established. OBSERVATIONS: Flea body extract did not induce the maturation of monocyte-derived DCs in 10 patients with PUFB and in 10 healthy children. Simultaneous exposure of DCs to flea extract and lipopolysaccharide induced increased expression of CD83 (P < .01), CD86 (P < .01), and HLA-DR (P < .05), which was statistically significantly greater in patients' cells. Dendritic cells from patients stimulated with lipopolysaccharide secreted less interleukin 6 (IL-6) and IL-10 than DCs from control subjects. CONCLUSIONS: Results of this study indicate that the involvement of DCs in an immune response produced in the disease is mediated through the altered expression of membrane molecules. This may be related to constitutive impairment in the production of regulatory cytokines such as IL-6 and IL-10 in these patients.

Immune and histopathologic examination of flea bite-induced papular urticaria.

BACKGROUND: Papular urticaria caused by flea bite presents clinical symptoms of hypersensitive reaction accompanied by skin lesions. Diagnostic and therapeutic approaches to the disease often go unrewarded, partly because of our incomplete understanding of the underlying immunopathogenesis. OBJECTIVE: To characterize the immune response to the flea bite in patients with papular urticaria. METHODS: This study included 45 randomly selected patients and 17 controls. Cutaneous allergy tests were performed. The histopathologic and immunohistochemical characteristics of cellular infiltrate in skin lesions were established. Immunoblot analysis was used to describe the specific characteristics of flea proteins recognized by IgE and IgG in patients' serum samples. RESULTS: Cutaneous allergy test results were negative in 87% to 98% of patients and in 88% to 100% of controls. Histopathologic and immunohistochemical studies revealed a predominance of eosinophils and CD4+ T lymphocytes. Immunoblotting did not show significant differences in IgG response between patients and controls. IgE recognition of flea proteins appears to decrease as the disease progresses. CONCLUSIONS: Our results suggest that the clinical manifestations of papular urticaria are mediated by a complex immune response involving more than one mechanism, with evidence forboth an IgE response and a cell-mediated type IV response.

Manifestaciones cutáneas en el recién nacido

Se ha informado que hasta un 90 por ciento de los neonatos presentan alguna alteración de su piel. En su mayoría, tales alteraciones son de carácter transitorio, obedecen a procesos fisiológicos normales y, por tanto, no requieren ningún tipo de tratamiento. Tanto su alta frecuencia como la necesidad de diferenciar los procesos normales de los relamente patológicos hacen necesario el conocimiento de las manifestaciones cutáneas del recién nacido por parte del personal médico y paramédico especializado y no especializado. Se presenta a continuación una síntesis de las manifestaciones cutáneas fisiológicas y en el próximo número de esta revista se revisarán las principales alteraciones patológicas de la piel de los neonatos.