RESUMO
Haplogroup Q originated in Eurasia around 30,000 years ago. It is present in Y-chromosomes from Asia and Europe at rather low frequencies. Since America is undoubtedly one of the continents where this haplogroup is highly represented, it has been defined as one of the founding haplogroups. Its M3 clade has been early described as the most frequent, with pan-American representation. However, it was also possible to find several other haplogroup Q clades at low frequencies. Numerous mutations have been described for haplogroup Q, allowing analysis of its variability and assignment of its geographic origin. We have analyzed 442 samples of unrelated men from Argentina and Paraguay belonging to haplogroup Q; here we report specifically on 27 Q (xM3) lineages. We tested 3 single-nucleotide polymorphisms (SNPs) by amplified product-length polymorphism (APLP) analysis, 3 SNPs for restriction fragment length polymorphism (RFLP) analysis, 15 SNPs by Sanger sequencing, and 17 short tandem repeats (STRs). Our approach allowed us to identify five subhaplogroups. Q-M3 and Q-CTS2730/Z780 are undoubtedly autochthonous lineages and represent the most frequent subhaplogroups, with significant representation in self-defined aboriginal populations, and their autochthonous status has been previously described. The aim of present work was to identify the continental origin of the remaining Q lineages. Thus, we analyzed the STR haplotypes for the samples and compared them with haplotypes described by other authors for the rest of the world. Even when haplogroup Q lineages have been extensively studied in America, some of them could have their origin in post-Columbian human migration from Europe and Middle East.
Assuntos
Cromossomos Humanos Y , Genética Populacional , América , Argentina , Ásia , Cromossomos Humanos Y/genética , Europa (Continente) , Haplótipos/genética , Humanos , Masculino , Repetições de Microssatélites , Oriente Médio , Paraguai , Filogenia , Polimorfismo de Nucleotídeo Único/genéticaRESUMO
Resumen Objetivo: La osteoporosis es una condición de relevancia a nivel epidemiológico en Argentina, así como en el resto del mundo. Si bien actualmente la herramienta diagnóstica más relevante es la densitometría ósea, los análisis radiológicos pueden aportar información, principalmente en lo referente a la calidad ósea. En ese sentido, nos proponemos evaluar la estructura trabecular calcánea de una población local. Métodos: El material para dicho estudio consistió en 91 calcáneos de esqueletos pertenecientes a una muestra esqueletal. Fueron analizados individuos adultos, de ambos sexos, mediante imágenes radiográficas, a fin de clasificar su estructura trabecular de acuerdo al índice propuesto por Jhamaria y col., en una escala de V (normal) a I (osteoporosis severa). Resultados: Las prevalencias estimadas fueron de 23,1% de osteoporosis (fases I y II), 16,5% de borderline (fase III) y 48,4% se clasificó como estructura trabecular normal (fases IV y V). En relación a la edad de los individuos, se encontró una correlación significativa negativa entre ella y la pérdida trabecular (tau-b = -0,524, p = 0,00). No se encontraron diferencias significativas en cuanto a la afección dimórfica de la patología. Discusión: La relación entre envejecimiento y osteoporosis hallada es coincidente con estudios nacionales e internacionales que reconocen una disminución en la densidad mineral ósea (DMO) y una mala calidad ósea en individuos adultos mayores. La ausencia de afección dimórfica podría deberse a la edad promedio de la muestra, sumada a la posible resistencia de la estructura esponjosa del calcáneo a los cambios generados por el déficit estrogénico en las mujeres, característica de la osteoporosis tipo I. Conclusión: Creemos que es necesario revalorizar el análisis óseo por medio de radiografías, puesto que pueden ser de utilidad tanto en la clínica como en la investigación básica, debido a la mayor disponibilidad de equipos y a que posibilitan el análisis de otras propiedades del tejido óseo.
Abstract Objective: Osteoporosis is an important condition in an epidemiologic level in Argentina as in the rest of the world. Even though nowadays the most relevant diagnostic technique is bone densitometry, radiological studies can provide useful information, mainly in relation to bone quality. For this purpose, we aim to evaluate the calcaneus trabecular structure in a contemporary local population. Methods: The sample for this study consisted of 91 calcaneus from skeletons belonging to the skeletal repository. Adult individuals from both sexes were analyzed, to classify their trabecular structure according to the index proposed by Jhamaria et al., on a scale of V (normal) to I (severe osteoporosis). Results: The estimated prevalence were 23,1% of osteoporosis (phase I and II), 16,5% of borderline (phase III) and 48,4% were classified as normal trabecular structure (phase IV and V). In relation to the age of the individuals, a significant negative correlation was found between the first and the trabecular loss (tau-b = -0.524, p = 0.00). No significant differences were found in relation to the sex prevalence of this pathology. Discussion: The association found between aging and osteoporosis matches with the results of national and international studies that recognize that a decrease in Bone Mineral Density (BMD) and a bad bone quality in older adults. Absence of differences between sexes in this condition could be due to age average of the sample, added to the possible resistance of the calcaneus spongy structure to changes generated by estrogen deficit in women, characteristic of osteoporosis type I. Conclusion: We believe that it is necessary to revalue bone analysis by radiographic means, since they can be of use both in clinic and in basic research, due to a greater equipment availability and because they allow the analysis of other properties of bone tissue.
Assuntos
Humanos , Masculino , Feminino , Adolescente , Adulto , Pessoa de Meia-Idade , Idoso , Idoso de 80 Anos ou mais , Adulto Jovem , Osteoporose/diagnóstico por imagem , Calcâneo/diagnóstico por imagem , Osso Esponjoso/diagnóstico por imagem , Osso e Ossos , Radiografia , Densidade Óssea , Estudos TransversaisRESUMO
OBJECTIVE: To compare estimates of underweight, stunting, wasting, overweight and obesity based on three growth charts. DESIGN: Cross-sectional study to estimate weight-for-age, length/height-for-age and weight-for-height comparing the 2006 WHO Child Growth Standards ('the WHO standards'), the 1977 National Center for Health Statistics (NCHS) international growth reference ('the NCHS reference') and the 1987 Argentine Pediatric Society Committee of Growth and Development reference ('the APS reference'). Cut-off points were defined as mean values ±2 s d. Epi-Info software version 6·0 (Centers for Disease Control and Prevention) was used for statistical evaluations (χ 2, P ≤ 0·05). SETTING: Greater La Plata conurbation, Buenos Aires, Argentina. SUBJECTS: A total of 2644 healthy, full-term children from 0 to 5 years of age. RESULTS: Prevalence of underweight was higher with the WHO standards than with the other references up to the first 6 months. For the rest of the ages, prevalence was lower with the WHO standards. Stunting prevalence was higher with the WHO standards at all ages. Prevalence of wasting was higher with the WHO standards compared with the NCHS reference up to the first 6 months and lower at 2-5 years of age. Overweight and obesity prevalences were higher with the WHO standards at all ages. CONCLUSIONS: The new WHO standards appear to be a solid and reliable tool for diagnosis and treatment of nutritional diseases, also being the only one built with infants fed according to WHO recommendations. Therefore, our results support the decision of the National Ministry of Health about the utilization of the new WHO standards to monitor the nutritional status of Argentinean children aged less than 5 years.
Assuntos
Transtornos do Crescimento/epidemiologia , Crescimento , Estado Nutricional , Obesidade/epidemiologia , Magreza/epidemiologia , Síndrome de Emaciação/epidemiologia , Organização Mundial da Saúde , Fatores Etários , Argentina/epidemiologia , Estatura , Peso Corporal , Pré-Escolar , Feminino , Humanos , Lactente , Masculino , National Center for Health Statistics, U.S. , Sobrepeso , Prevalência , Valores de Referência , Sociedades Médicas , Estados UnidosRESUMO
We analyzed 21 paragroup Q* Y chromosomes from South American aboriginal and urban populations. Our aims were to evaluate the phylogenetic status, geographic distribution, and genetic diversity in these groups of chromosomes and compare the degree of genetic variation in relation to Q1a3a haplotypes. All Q* chromosomes from our series and five samples from North American Q* presented the derivate state for M346, that is present upstream to M3, and determined Q1a3* paragroup. We found a restrictive geographic distribution and low frequency of Q1a3* in South America. We assumed that this low frequency could be reflecting extreme drift effects. However, several estimates of gene diversity do not support the existence of a severe bottleneck. The mean haplotype diversity expected was similar to that for South American Q1a3* and Q1a3a (0.478 and 0.501, respectively). The analysis of previous reports from other research groups and this study shows the highest frequencies of Q* for the West Corner and the Grand Chaco regions of South America. At present, there is no information on whether the phylogenetic status of Q* paragoup described in previous reports is similar to that of Q1a3* paragroup though our results support this possibility.
Assuntos
Cromossomos Humanos Y , Variação Genética , Geografia , Indígenas Sul-Americanos/genética , Deriva Genética , Haplótipos , Humanos , Filogenia , América do SulRESUMO
The relationship between protein-energy malnutrition and genetic damage has been studied in human beings and laboratory animals, but results are still conflicting. The aim of the present study was to assess the induction of structural chromosomal aberrations in peripheral blood lymphocytes of children with primary protein-energy malnutrition. A case-control study was performed. Samples were obtained from 25 primary malnourished infants (mean age, 22 months; range, 1-66 months). The control group consisted of 25 eutrophic children from the same population who were matched 1:1 by age and sex. Anthropometric and clinic evaluations were performed to assess nutritional condition. Before blood collection, we interviewed each individual's parent to complete a semi-structural survey specifying age, dietary habits, viral or bacterial diseases; previous exposure to diagnostic x-rays; and use of therapeutic drugs. After 48 hours, 100 cultured lymphocytes were analyzed per patient. Statistical analysis was performed using the Epi Dat 3.0 program (P < or = .05). The chromosomal aberration frequency was nearly 7 times higher in malnourished infants than in controls (14.61% vs 2.2%, respectively). This difference was statistically significant (P < .001) and may be explained by the occurrence of achromatic lesions, breaks, and telomeric associations. DNA damage could be attributed to several factors: severe deficiency of essential nutrients (ie zinc, iron, and vitamin A) required in the synthesis of DNA maintenance factors; deterioration of repair mechanisms allowing the persistence of an unusually high number of structural chromosomal aberrations; and/or the absence of specific factors needed to protect the cell against oxidative DNA damage.
Assuntos
Aberrações Cromossômicas/estatística & dados numéricos , Dano ao DNA , Desnutrição Proteico-Calórica/complicações , Argentina , Estudos de Casos e Controles , Pré-Escolar , Aberrações Cromossômicas/induzido quimicamente , DNA/ultraestrutura , Coleta de Dados , Feminino , Humanos , Lactente , Linfócitos/ultraestrutura , Masculino , Mutagênicos/efeitos adversos , Desnutrição Proteico-Calórica/genéticaRESUMO
La evaluación de la situación nutricional de los niños, depende en gran medida de las curvas de crecimiento utilizadas. El objetivo de esta investigación es comparar las prevalencias de sobrepeso y obesidad estimadas con tres referencias internacionales en una población de niños, a través del Índice de Masa Corporal. Se incluyeron 737 niños/as nacidos de término sanos, de 2 a 5 años (estudio transversal). La Participación fue voluntaria y consentida. Se estableció el Índice de Masa Corporal (kg/m²). Las técnicas de medición se basaron en guías nacionales. Las referencias utilizadas fueron: 1. Centers for Disease Control and Prevention (CDC) (>Pc85: sobrepeso; > Pc95: obesidad); 2. International Obesity Task Force (IOTF) (valores límites sexo-edad específicos) y 3. Organización Mundial de la Salud (OMS) (+2 desvíos estándar: sobrepeso; >+3: obesidad). Los resultados fueron evaluados estadísticamente mediante el programa Epi Info 6.0 (χ², p < 0,05 por ciento). La prevalencia de niños con sobrepeso estimada con la referencia del CDC es 1,1 veces mayor que la de IOTF y 2,33 veces la de OMS y la de IOTF es 2,1 veces la de OMS (p= 0,00001). La prevalencia de niños con obesidad estimada con la referencia del CDC es 5,4 veces la de IOTF y 23,9 veces la de OMS, mientras que la de IOTF es 4,4 veces la de OMS (p= 0,0000001). Las prevalencias de sobrepeso y obesidad, difieren substancialmente de acuerdo a la referencia y valores límite utilizados. No existiendo aún un criterio único, cada una de las referencias debe utilizarse con precaución.
The evaluation of child nutritional status is highly dependent on the growth charts used. The aim of this study was to compare different references assessing overweight and obesity in children population, through the Body Mass Index. A total of 737 healthy children born at term, aged 2-5 years, were included (cross-sectional study). The participation was voluntary and consent. Body Mass Index (kg/m²) was estimated. The measurements techniques were based on national guidelines. We compared three references: (1) Centers for Disease Control and Prevention (CDC) (>Pc85: overweight; >Pc95: obesity; (2) International Obesity Task Force (IOTF) (sex-age-specific body mass index cut-offs); (3) World Health Organization (WHO) (+2 standard deviation: overweight; +3: obesity). The Epi Info 6.0 software was used to the statistical evaluation ((χ2, p≤ , 05 percent). The prevalence of overweight was 1,1 and 2,33 times higher in CDC application respect to the IOTF and the WHO references respectively. The prevalence of overweight was 2,1 times higher in IOTF application respect to the WHO references (p=, 00001). The prevalence of obesity was 5,4 and 23,9 times higher in CDC application respect to the IOTF and the WHO references respectively. The prevalence of obesity was 4,4 times higher in IOTF application respect to the WHO references (p=, 0000001). The prevalence of overweight and obesity, calculated through the BMI, differs substantially according to the reference and cut-off points used. In the absence of even a single criterion, each of the references should be used with care.
Assuntos
Humanos , Masculino , Feminino , Pré-Escolar , Antropometria/métodos , Índice de Massa Corporal , Peso Corporal , Obesidade , Ciências da Nutrição Infantil , PediatriaRESUMO
The evaluation of child nutritional status is highly dependent on the growth charts used. The aim of this study was to compare different references assessing overweight and obesity in children population, through the Body Mass Index. A total of 737 healthy children born at term, aged 2-5 years, were included (cross-sectional study). The participation was voluntary and consent. Body Mass Index (kg/m2) was estimated. The measurements techniques were based on national guidelines. We compared three references: (1) Centers for Disease Control and Prevention (CDC) (> Pc85: overweight; > Pc95: obesity; (2) International Obesity Task Force (IOTF) (sex-age-specific body mass index cut-offs); (3) World Health Organization (WHO) (+2 standard deviation: overweight; +3: obesity). The Epi Info 6.0 software was used to the statistical evaluation (chi2, p < or = .05%). The prevalence of overweight was 1.1 and 2.33 times higher in CDC application respect to the IOTF and the WHO references respectively. The prevalence of overweight was 2.1 times higher in IOTF application respect to the WHO references (p = .00001). The prevalence of obesity was 5.4 and 23.9 times higher in CDC application respect to the IOTF and the WHO references respectively. The prevalence of obesity was 4.4 times higher in IOTF application respect to the WHO references (p = .0000001). The prevalence of overweight and obesity, calculated through the BMI, differs substantially according to the reference and cut-off points used. In the absence of even a single criterion, each of the references should be used with care.
Assuntos
Índice de Massa Corporal , Obesidade/diagnóstico , Obesidade/epidemiologia , Argentina/epidemiologia , Pré-Escolar , Estudos Transversais , Feminino , Humanos , Masculino , Estado Nutricional/fisiologia , Sobrepeso/epidemiologia , Prevalência , Padrões de Referência , Valores de ReferênciaRESUMO
Objetivos: algunos autores encontraron una relación entre la Malnutrición Proteico Energética (MPE) y elaumento de la frecuencia de Aberraciones Cromosómicas Estructurales (ACE) en niños menores de 5 años.El objetivo del siguiente trabajo es analizar la incidencia de ACE en una población de niños del partido de La Plata que presentan MPE. Material y Métodos: se tomó una muestra de 30 niños de 1 a 60 meses de edad cronológica, 15 controles sanos y 15 diagnosticados como MPE primarios a través de una evaluación antropométrica y clínica. Se aplicó una encuesta semiestructurada en la que se tuvieron en cuenta peso al nacimiento, variables antropométricas, alimentación, enfermedades virales, y/o infecciosas y exposición a agentes potencialmente genotóxicos. Se realizaron cultivos de sangre periférica y se analizó la frecuencia de ACE en 100 células por individuo. Los resultados obtenidos fueron sometidos a evaluación estadística utilizando el programa Epi Info 6.0. Resultados: la diferencia en la frecuencia global de ACE entre ambas muestras resultó significativa. Al tratar cada tipo de aberración en forma independiente se encontraron diferencias significativas para gaps y fracturas de mono e isocromátidas, cromosomas dicéntricos, fragmentos y asociaciones telométricas. No se encontraron diferencias significativas respecto a la exposición de los niños a agentes potencialmente genotóxicos tales como medicamentos, radiaciones, pesticidas y desechos industriales. Conclusiones: la MPE es capaz de inducir daño genotóxico, este efecto podria explicarse por la distorsión del ambiente químico interno o bien por la disminución de la acción de los mecanismos de reparación del ADN como consecuencia del déficit proteico
Assuntos
Humanos , Criança , Aberrações Cromossômicas , Desnutrição Proteico-Calórica/classificaçãoRESUMO
Objetivos: algunos autores encontraron una relación entre la Malnutrición Proteico Energética (MPE) y el aumento de frecuencia de Aberraciones Cromosómaticas Estructurales (ACE) en niños menores de 5 años. El objetivo del siguiente trabajo es analizar la incidencia de ACE en una población de niños del partido d La Plata que presentan MPE. Material y Métodos: se tomó una muestra de 30 niños de 1 a 60 meses de edad cronológica, 15 controles sanos y 15 diagnosticados como MPE primarios a través de una evaluación antropométrica y clínica. Se aplicó una encuesta semiestructurada en la que se tuvieron en cuenta peso al nacimiento, variables antropométricas, alimentación, enfermedades virales y/o infecciosas y exposición a agentes potencialmente genotóxico. Se realizaron cultivos de sangre periférica y se analizó la frecuencia de ACE en 100 células por individuo. Los resultados obtenidos fueron sometidos a evaluación estadística utilizando el programa Epi Info 6.0
Assuntos
Aberrações CromossômicasRESUMO
Objetivos: algunos autores encontraron una relación entre la Malnutrición Proteico Energética (MPE) y elaumento de la frecuencia de Aberraciones Cromosómicas Estructurales (ACE) en niños menores de 5 años.El objetivo del siguiente trabajo es analizar la incidencia de ACE en una población de niños del partido de La Plata que presentan MPE. Material y Métodos: se tomó una muestra de 30 niños de 1 a 60 meses de edad cronológica, 15 controles sanos y 15 diagnosticados como MPE primarios a través de una evaluación antropométrica y clínica. Se aplicó una encuesta semiestructurada en la que se tuvieron en cuenta peso al nacimiento, variables antropométricas, alimentación, enfermedades virales, y/o infecciosas y exposición a agentes potencialmente genotóxicos. Se realizaron cultivos de sangre periférica y se analizó la frecuencia de ACE en 100 células por individuo. Los resultados obtenidos fueron sometidos a evaluación estadística utilizando el programa Epi Info 6.0. Resultados: la diferencia en la frecuencia global de ACE entre ambas muestras resultó significativa. Al tratar cada tipo de aberración en forma independiente se encontraron diferencias significativas para gaps y fracturas de mono e isocromátidas, cromosomas dicéntricos, fragmentos y asociaciones telométricas. No se encontraron diferencias significativas respecto a la exposición de los niños a agentes potencialmente genotóxicos tales como medicamentos, radiaciones, pesticidas y desechos industriales. Conclusiones: la MPE es capaz de inducir daño genotóxico, este efecto podria explicarse por la distorsión del ambiente químico interno o bien por la disminución de la acción de los mecanismos de reparación del ADN como consecuencia del déficit proteico