Correlation between the anatomical morphology of palatal rugae and sex / Correlación entre la morfología anatómica de las rugas palatinas y el sexo

SUMMARY: To investigate the correlation between the anatomical morphology of palatal rugae and sex. The study sample consisted of 120 students studying from Shanxi Medical University, of which 60 were females and 60 were males. The digital model of the palatal rugae was obtained by the 3 Shape TRIOS intraoral scanner. And the shapes of palatal rugae were recorded. Association between palatal rugae shape and sex were tested using Chi-square analysis. And logistic regression analysis (LRA) was carried out to calculate the accuracy of gender prediction using rugae shapes. There was a statistically significant difference between males and females in terms of the distribution of wavy and circular palate rugae. The use of logistic regression analysis obtained a sex predictive value of 65 % when all the rugae shapes were analyzed. Digital images of the palatal rugae morphology contribute to more accurate and convenient for data collection and transformation. It was found that rugae patterns can moderately identify the sex of the specific population when multivariate statistics such as LRA is applied. The palatal rugae morphology can be utilized as an assistant measure for sex identification.

RESUMEN: Investigar la correlación entre la morfología anatómica de las rugas palatinas y el sexo. En la muestra de este estudio se incluyeron 120 estudiantes de la Universidad Médica de Shanxi, (60 mujeres y 60 hombres). El modelo digital de las rugas palatinas se obtuvo mediante escáner intraoral 3 Shape TRIOS, y se registraron las formas de las rugas palatinas. La asociación entre la forma de las rugas palatinas y el sexo se evaluó mediante un análisis de Chi-cuadrado; para calcular la precisión de la predicción de sexo se llevó a cabo un análisis de regresión logística (ARL) Se observó una diferencia estadísticamente significativa entre hombres y mujeres en términos de la distribución de las rugas palatinas onduladas y circulares. El uso de análisis de regresión logística obtuvo un valor predictivo de sexo del 65 % cuando se analizaron todas las formas de las rugas. Las imágenes digitales de la morfología de las rugas palatinas contribuyen a una recopilación de datos más precisa. En este análisis se determinó que los patrones de rugas pueden identificar relativamente el sexo de una población específica, cuando se aplican estadísticas multivariadas como ARL. La morfología de las rugas palatinas se puede utilizar como medida de ayuda para la identificación de sexo.

Identification of sex using SBNO1 gene in the Chinese softshell turtle, Pelodiscus sinensis (Trionychidae)

The Chinese softshell turtle exhibits ZZ/ZW sex determination. To identify the sex of embryos, juvenile and adult individuals, we designed two pairs of polymerase chain reaction primers, SB1-196, which amplifies a fragment of 196 bp in the female and the other, CK1-482, which amplifies the 482-bp fragment in both the sexes. It is validated in 24 adult turtles of known sex, sampled from three different locations. This one-step sexing technique is rapid and easy to perform and is reported for the first time.

Un método molecular rápido, no invasivo y simple para determinar el sexo en pingüinos pigoscélidos / A rapid, non invasive and simple molecular method for sex determination in pygoscelis penguins

En los pingüinos Adélie (Pygoscelis adeliae) y pingüinos gentoo (Pygoscelis papua), no existe un dimorfismo sexual conspicuo y a menudo resulta difícil determinar el sexo en base a la morfología externa. La información sobre el sexo es importante en muchos estudios de ecología y conservación. En este artículo se evaluó el uso de un par de cebadores (2550F/2718R) para identificar el sexo en aves sexualmente monomórficas. Para ambas especies de pingüinos la amplificación produjo dos bandas discretas, CHD1Z y CHD1W, que permitieron la identificación sexual. Se trata de un sistema sencillo, rápido y económico para el sexaje molecular de los pingüinos gentoo y Adélie.

In Adélie penguins (Pygoscelis adeliae) and gentoo penguins (Pygoscelis papua), the conspicuous sexual dimorphism often makes it difficult to determine sex on the basis of external morphology. The information about sex is important in many ecology and conservation studies. In this paper we evaluated the use of an established primer pair (2550F/2718R) to identify sex in sexually monomorphic birds. In both penguin species, it resulted in two distinct CHD1Z and CHD1W PCR bands, allowing sex identification. This is a simple, rapid and cheap system for molecular sexing of gentoo and Adélie penguins.

The prospect of application with H-Y antigen in forensic science / 中国法医学杂志

As is known, H-Y antigens (male specific minor histompatibility antigens) are a group of minor histocompatibility antigens encoded on the Y-chromosome with homologous H-X antigens on the X-chromosome. H-Y antigens were originally discovered as transplant antigens, and they are only expressed in male individuals without specificity for different tissues and organs. A lot of research results show that H-Y antigens play an important role in the sex selection and identification. The paper reviews the above and discusses the application prospect of H-Y antigen in forensic science.

The application of the cloning and expression of SMCY gender-specific fusion antigens with the corresponding polyclonal antibodies / 中国法医学杂志

Objective with the advantages of rapidity in detection protein, We selected the gender-specific amino acid sequence based on human SMCY and SMCX, cloned and expressed SMCY gender-specific fusion antigens. The rabbits were immunized with purified antigens to obtain the polyclonal antibodies. A new method was established for rapidly sex identification of forensic evidence samples by detecting SMCY antigens with the corresponding polyclonal antibodies. Methods We found three differential fragments by analyzing the sequence of human SMCY and SMCX. Then we cloned this three fragments and ligated as a new recombinant.This SMCY gender-specific fusion antigen gene was sub-cloned into pET-28a and expressed in Escherichia coli. The fusion antigen was purified by Ni-NTA column. The rabbits were immunized with purified antigen to produce the specific polyclonal antibodies.The reactivity of the polyclonal antibody was evaluated by ELISA and Western blotting. We developed a colloidal gold test strip for detecting the gender of human samples. Results We successfully selected gender-specific amino acid sequence, the SMCY gender-specific fusion antigen was expressed by prokaryotic expression and the polyclonal antibody was prepared by immunizing rabbit. The results of colloidal gold strip tests showed that there is a significant difference between male and female serums. Conclusion The results showed that the SMCY gender-specific fusion antigen could be recognized by the polyclonal antibody.The colloidal gold strip tests made by SMCY gender-specific fusion antigens and the corresponding polyclonal antibodies could be used for rapidly determining the gender of forensic evidence samples.

Sexual dimorphism using the interstyloid distances and clinical implication for elongated styloid process in Northeastern Thailand / Dimorfismo sexual usando la distancia inter-estiloide y la implicación clínica del proceso estiloides elongado en el Noreste de Tailandia

Skeletal remains are crucial in forensic identification of the sex, especially human skulls including the styloid process, a bony projection from the skull. Hence, the objectives of the present study were undertaken to assess the value of the styloid process for the sex identification of unknown skulls and also to investigate the prevalence of elongated styloid process in 102 human dry skulls from the northeast Thai population. As a result, the interstyloid distances at both base and tip of the styloid processes were found to be significantly different between male and female specimens, although no significant difference was found in the length of the styloid process between males and females. In addition, the occurrence of the elongated styloid process was not associated with the gender, although its prevalent laterality on the left was recognized. It is suggested that the styloid process can be applied to the sex identification by measuring the interstyloid distance at the base or the tip of these processes.

Los restos óseos son cruciales para la identificación forense del sexo, especialmente en los cráneos humanos, incluyendo el proceso estiloides, una proyección ósea del cráneo. Por lo tanto, los objetivos del presente estudio consistieron en evaluar el valor del proceso estiloides en la identificación del sexo de cráneos desconocidos y también para investigar la prevalencia del proceso estiloides elongado en 102 cráneos secos humanos de la población del Noreste de Tailandia. Como resultado, se encontró que las distancias inter-estiloides tanto en la base y la punta de los procesos estiloides eran significativamente diferentes entre las muestras de hombres y mujeres, aunque no se encontró diferencia significativa en la presencia del proceso estiloides entre ambos. Además, la aparición del proceso estiloides elongado no se asoció con el sexo, aún cuando se observó su prevalencia en el lado izquierdo. Sugerimos que el proceso estiloides se puede utilizar en la identificación del sexo mediante la medición de la distancia inter-estiloide en la base o en la punta de estos procesos.

Dental pulp fibroblast and sex determination in controlled burial conditions / Fibroblastos de la pulpa dental y la determinación del sexo en condiciones controladas de enterramiento

The need to identify bodies that are found as a result of disappearances with a diversity of causes, illegal burials and massive disasters, represent a wide percentage of dentistry practice on forensic research. The following study determined the performance of Barr Body Test, in fibroblasts of healthy teeth, under different conditions of burial (in vitro) with variations in pH, humidity and salinity in terms of general accuracy and sensitivity for men and women. Analyzed sample considered 47 dental pulps, taken from teeth under burial conditions during a period of a month. From dental pulps samples, 265 histological cuts valid for this study, were obtained, which were observed with an optical microscope under conventional H/E staining. Results showed a 98.9% of well-diagnosed cases, which correspond to the overall accuracy of the method. Sensitivity for men was 97.5% and 100% for women, over the analyzed sample. In low humidity conditions, 3 samples of badly diagnosed cases in men were observed, with a group accuracy of a 90%, with a sensitivity of 25% for men and 100% for women. The present study establishes that based on these results, the performance of Barr Body Test in fibroblasts, proposed for healthy pulp teeth, is not affected by burial conditions in terms of pH (acid-alkaline), salinity (high-low) and high humidity.

La necesidad de identificar cuerpos que resultan como consecuencia de desapariciones de causas variadas, inhumaciones ilegales y desastres masivos representa un porcentaje amplio en el quehacer odontológico en un escenario de investigación forense. El presente estudio determinó el rendimiento de la prueba diagnóstica de observación del cuerpo de Barr en células de la pulpa de dientes sanos, sometidos a distintas condiciones de enterramiento (in vitro) con variación de pH, humedad y salinidad en términos de exactitud general y sensibilidad para hombres y mujeres. La muestra analizada consideró 47 pulpas dentales, extraídas de dientes sometidos a condiciones de enterramiento durante un mes. De las pulpas dentarias se obtuvieron 265 cortes histológicos válidos para el estudio, los cuales mediante la tinción convencional H/E, fueron observados al microscopio óptico. Los resultados arrojaron un 98,9% de casos bien diagnosticados, que correspondió a la exactitud general del método. La sensibilidad para hombres fue de 97,5% y para mujeres de 100% sobre el total de la muestra analizada. Las condiciones de pH (ácido y alcalino), salinidad (alta y baja) y alta humedad presentaron una exactitud de grupo de 100%, con una sensibilidad para hombres y mujeres de 100%. En la condición de baja humedad se observaron 3 muestras de hombres mal diagnosticadas con una exactitud de grupo de 90% y sensibilidad para hombres de 25% y para mujeres de 100%. A la luz de los resultados, el presente estudio establece que el rendimiento de la prueba diagnóstica de observación del cuerpo de Barr en fibroblastos, propuesto para pulpas de dientes sanos, no se afecta con las condiciones de enterramiento propuestas bajo pH ácido ­ alcalino, salinidad alta ­ baja y humedad alta.

Performance evaluation as a diagnostic test for traditional methods for forensic identification of sex / Evaluación del rendimiento como una prueba diagnóstica de los métodos clásicos para la determinación forense del sexo

This study assesses the quality, as a diagnostic test, of the main indicators of morphological sexual dimorphism through direct anthropometry, biostatistics tools and clinical epidemiology. This study used 284 skulls of adult Brazilians, of which 187 were male and 97 female. A study of the cross-evaluation of the diagnostic test was performed; it was a qualitative approach based on visual examination of 16 traditional indicators of morphological sexual dimorphism, where each indicator determined the level of accuracy, sensitivity, predictive values, likelihood ratios, and odds ratio. All indicators studied had high levels of accuracy (84.75-72.89%). The best indicators were found in traits whose formation is related to the insertion and action of major muscle groups. In 14 of the 16 indicators, intraobserver error was <10%. The best indicators of morphological sexual dimorphism were mastoid process, zygomatic bone, mandible, and roughness of the occipital bone. The authors concluded that morphological dimorphism indicators present an adequate performance as diagnostic tests, however, the values of accuracy and sensitivity must be matched with more robust indicators that are independent of the distribution of the sample, and integrate diagnostic errors such as the likelihood ratios, odds ratios, and positive predictive values.

En el estudio fue evaluada la calidad, como una prueba diagnóstica de los principales indicadores morfológicos de dimorfismo sexual a través de la antropometría, herramientas bioestadísticas y epidemiología clínica. Fueron utilizados 284 cráneos de individuos adultos brasileños, de los cuales 187 eran varones y 97 mujeres. Se realizó un estudio de corte transversal de evaluación de prueba diagnóstica, mediante un enfoque cualitativo en base al examen visual, de 16 indicadores tradicionales morfológicos de dimorfismo sexual, determinándose para cada uno de ellos los niveles de exactitud y de sensibilidad, valores predictivos, coeficientes de probabilidad y Odds ratios. Todos los indicadores estudiados presentaron altos niveles de exactitud (84,75-72,89%). Los mejores indicadores se encontraron en los rasgos cuya formación está relacionada con la inserción y la acción de los grandes grupos musculares. En 14 de los 16 indicadores, el error intraobservador fue <10%. Los mejores indicadores morfológicos de dimorfismo sexual fueron: proceso mastoides, hueso cigomático, mandíbula y rugosidades del hueso occipital. Los autores concluyeron que los indicadores morfológicos de dimorfismo presentan un adecuado rendimiento como pruebas de diagnóstico; sin embargo, los valores de exactitud y sensibilidad deben ser complementados con indicadores más sólidos que sean independientes de la distribución de la muestra, e integren a los errores diagnósticos, tales como los coeficientes de probabilidad, odds ratios y valores predictivos positivos.

Comparison of inclusions in female and male Trichosanthes kirilowii individuals / 中草药

Objective To analyze the different composition and contents of inclusion in female and male Trichosanthes kirilowii individuals and to provide some references for the early sex identification.Methods Physiological and biochemical indices in T.kirilowii leaves were determined and significant analysis of the difference was performed.The difference of chemical composition was analyzed using HPLC.Results The contents of photosynthetic pigments and soluble proteins,the activities of superoxide dismutase(SOD) and peroxidase(POD),and the DNA concentration were higher in male individuals than those in female ones.The difference in photosynthetic pigments content and POD activity reached a significant level.The female individuals possessed higher contents of malondiadehycle(MDA),soluble saccharide,and UV-absorbing compounds than those in male ones,and the difference in UV-absorbing compounds reached a significant level.HPLC Assay revealed obvious differences in the peaking frequency,time,and the peak height.Conclusion There are differences in the composition and contents of inclusions in male and female T.kirilowii individuals,and the UV-absorbing compounds and the characteristic HPLC peak could potentially be as indices of sex identification.

SEX IDENTIFICATION OF AUTOLYSIS TISSUES BY POLYMERASE CHAIN REACTION / 中国法医学杂志

In this paper, the specific male sequeuce in paraffin section of various tissues with autolys is ofdifferent degrees was detected by polymerase chain reaction(PCR).The results shewed that PCR could be used for identifying sex in the tissues with low degrees ofautolysis; its positive rate was lower in high degrees with disappearance of nuclaic member and cell ou-tline,and often gave false negative results when the autolysis degree was high.

THE APPLICATION OF DNA AMPLIFICATION TECHNIQUE IN VITRO IN FORENSIC MEDICNE PRACTICE / 中国法医学杂志

This paper reports the determination of sex of human blood stains in threecriminal cases by the DNA amplification technique.The results fit the cases de-tails and gave the scientific evidence for the justice.The blood stains were dige-sted with proteinase K.The protein was extracted with the phenol-chloroform.The DNA was precipitated with NaCl and ethyl alcohol.Amplification of DNAwas carried out using two pairs of primer Y1.1 Y1.2 and Alu9.1 Alug.2 and heatstable FD polymerase.The amplified products were subjected to agarose gel(con-taining ethidium bromide)electrophoresis.Sex of blood stains was determinedaccording to the amplified products.PCR technique is rapid to perform,sensitiveand simple.No special equipments and isotope labelled probe are required.