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1.
J Clin Lab Anal ; 34(8): e23337, 2020 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-32410296

RESUMEN

BACKGROUND: Polymorphisms (rs1801133 or C677T; rs1801131 or A1298C) of the MTHFR gene and rs1801394 (A66G) of the MTRR gene are important genetic determinants of folate metabolism. A convenient, sensitive, and reliable method is required to detect polymorphisms for the precise supplementation of folate. METHODS: A rapid detection method based on molecular beacon probes that can detect rs1801133, rs1801131, and rs1801394 simultaneously was developed in this study. Specific primers and probes were designed, and the amplification system and conditions were optimized. We applied our method to a group of 500 unrelated women of gestational age in the Dongguan region of Guangdong Province in China. The clinical performance of this assay was evaluated by testing 94 samples in comparison with Sanger sequencing. RESULTS: The molecular-beacon-based PCR assay we established is extremely sensitive, with a detection limit of 2 ng/µL of genomic DNA, and validated by direct sequencing in a blind study with 100% concordance. CONCLUSION: The results demonstrate that our molecular-beacon-based asymmetric PCR assay is an easy, reliable, high-yield, and cost-effective method for the simultaneous detection of three polymorphisms related to folate metabolism. It could help evaluate the risk of perinatal-neonatal neural tube malformation, pregnancy hypertension, and other diseases and guide the individualized supplementation of folic acid. Data on the spectrum of mutations in the Dongguan District in this study are beneficial for guiding the supplementation of folic acid.


Asunto(s)
Ferredoxina-NADP Reductasa/genética , Ácido Fólico , Metilenotetrahidrofolato Reductasa (NADPH2)/genética , Reacción en Cadena de la Polimerasa/métodos , Polimorfismo Genético/genética , Adulto , Femenino , Ácido Fólico/genética , Ácido Fólico/metabolismo , Genotipo , Humanos , Límite de Detección , Mutación/genética , Reproducibilidad de los Resultados , Análisis de Secuencia de ADN/métodos , Adulto Joven
2.
Sensors (Basel) ; 16(2): 192, 2016 Feb 04.
Artículo en Inglés | MEDLINE | ID: mdl-26861322

RESUMEN

In this study, a numerical simulation method was employed to investigate and analyze superstructure fiber Bragg gratings (SFBGs) with five duty cycles (50%, 33.33%, 14.28%, 12.5%, and 10%). This study focuses on demonstrating the relevance between design period and spectral characteristics of SFBGs (in the form of graphics) for SFBGs of all duty cycles. Compared with complicated and hard-to-learn conventional coupled-mode theory, the result of the present study may assist beginner and expert designers in understanding the basic application aspects, optical characteristics, and design techniques of SFBGs, thereby indirectly lowering the physical concepts and mathematical skills required for entering the design field. To effectively improve the accuracy of overall computational performance and numerical calculations and to shorten the gap between simulation results and actual production, this study integrated a perfectly matched layer (PML), perfectly reflecting boundary (PRB), object meshing method (OMM), and boundary meshing method (BMM) into the finite element method (FEM) and eigenmode expansion method (EEM). The integrated method enables designers to easily and flexibly design optical fiber communication systems that conform to the specific spectral characteristic by using the simulation data in this paper, which includes bandwidth, number of channels, and band gap size.

3.
Sensors (Basel) ; 14(6): 10876-94, 2014 Jun 19.
Artículo en Inglés | MEDLINE | ID: mdl-24949643

RESUMEN

Compared with coupled-mode theory (CMT), which is widely used for studies involving optical fiber Bragg gratings (FBGs), the proposed investigation scheme is visualized, diagrammatic, and simple. This method combines the finite element method (FEM) and eigenmode expansion method (EEM). The function of the FEM is to calculate all guided modes that match the boundary conditions of optical fiber waveguides. Moreover, the FEM is used for implementing power propagation for HE11 in optical fiber devices. How the periodic characteristic of FBG causes this novel scheme to be substantially superior to CMT is explained in detail. Regarding current numerical calculation techniques, the scheme proposed in this paper is the only method capable of the 3D design and analysis of large periodic components. Additionally, unlike CMT, in which deviations exist between the designed wavelength λ(D) and the maximal reflection wavelength λmax, the proposed method performs rapid scans of the periods of optical FBG. Therefore, once the operating wavelength is set for the component design, the maximal reflection wavelength of the final products can be accurately limited to that of the original design, such as λ = 1550 nm. Furthermore, a comparison between the period scan plot and the optical spectra plot for FBG indicated an inverse relationship between the periods and wavelengths. Consequently, this property can be used to predict the final FBG spectra before implementing time-consuming calculations. By employing this novel investigation scheme involving a rigorous design procedure, the graphical and simple calculation method reduces the studying time and professional expertise required for researching and applying optical FBG.

4.
Front Endocrinol (Lausanne) ; 14: 1198984, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-37383400

RESUMEN

In previous studies, adipocytes were found to play an important role in regulating whole-body nutrition and energy balance, and are also important in energy metabolism, hormone secretion, and immune regulation. Different adipocytes have different contributions to the body, with white adipocytes primarily storing energy and brown adipocytes producing heat. Recently discovered beige adipocytes, which have characteristics in between white and brown adipocytes, also have the potential to produce heat. Adipocytes interact with other cells in the microenvironment to promote blood vessel growth and immune and neural network interactions. Adipose tissue plays an important role in obesity, metabolic syndrome, and type 2 diabetes. Dysfunction in adipose tissue endocrine and immune regulation can cause and promote the occurrence and development of related diseases. Adipose tissue can also secrete multiple cytokines, which can interact with organs; however, previous studies have not comprehensively summarized the interaction between adipose tissue and other organs. This article reviews the effect of multi-organ crosstalk on the physiology and pathology of adipose tissue, including interactions between the central nervous system, heart, liver, skeletal muscle, and intestines, as well as the mechanisms of adipose tissue in the development of various diseases and its role in disease treatment. It emphasizes the importance of a deeper understanding of these mechanisms for the prevention and treatment of related diseases. Determining these mechanisms has enormous potential for identifying new targets for treating diabetes, metabolic disorders, and cardiovascular diseases.


Asunto(s)
Diabetes Mellitus Tipo 2 , Humanos , Tejido Adiposo , Fenómenos Fisiológicos Celulares , Estado Nutricional , Adipocitos Marrones
5.
PLoS One ; 10(3): e0120683, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-25775246

RESUMEN

BACKGROUND: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a common enzymatic disorder of the erythrocytes that affects 400 million people worldwide. We developed a PCR-reverse dot blot (RDB) assay to screen twenty genotypes of seventeen Chinese G6PD mutations and investigate the spectrum of G6PD deficiency mutations in Dongguan District, Guangdong Province, in southern China. METHOD: The PCR-RDB assay consists of multiplex PCR amplification of seven fragments in the G6PD target sequence of wild-type and mutant genomic DNA samples followed by hybridization to a test strip containing allele-specific oligonucleotide probes. A total of 16,464 individuals were analyzed by a combination of phenotypic screening and genotypic detection using the PCR-RDB assay and DNA sequence analysis. RESULTS: The PCR-RDB assay had a detection rate of 98.1%, which was validated by direct sequencing in a blind study with 100% concordance. The G6PD deficiency incidence rate in Dongguan District is 4.08%. Thirty-two genotypes from 469 individuals were found. The two most common variants were c.1376G>T and c.1388G>A, followed by c.95A>G, c.871G>A, c.392G>T, and c.1024 C>T. In addition, two rare mutations (c.703C>A and c.406C>T) were detected by DNA sequencing analysis. In our study, 65 cases harbored the C1311T/IVS polymorphism and 67 cases were homozygote. CONCLUSION: The PCR-RDB assay we established is a reliable and effective method for screening G6PD mutations in the Chinese population. Data on the spectrum of mutations in the Dongguan District is beneficial to the clinical diagnosis and prevention of G6PD deficiency.


Asunto(s)
Frecuencia de los Genes , Deficiencia de Glucosafosfato Deshidrogenasa/genética , Polimorfismo de Nucleótido Simple , Adolescente , Adulto , Niño , Preescolar , China , Femenino , Genotipo , Glucosafosfato Deshidrogenasa/genética , Deficiencia de Glucosafosfato Deshidrogenasa/epidemiología , Humanos , Incidencia , Lactante , Recién Nacido , Masculino , Persona de Mediana Edad
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