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Noninvasive detection of filaggrin gene mutations using Raman spectroscopy

机译:拉曼光谱法无创检测丝聚蛋白基因突变

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Knowledge of the existence of filaggrin (FLG) gene mutations might be helpful for a subclassification of patients with atopic dermatitis (AD) which can be used to introduce individualized treatments. In this work the filaggrin content in the skin is assessed using Raman spectroscopy and the results are compared to FLG genotyping of Mexican-mestizo patients. Results showed that the 2282del4 and R501X mutations present in the European population but absent in people of Asian or African descent are also present in the Mexican-mestizo population. The results also showed that patients with filaggrin gene mutations presented lower filaggrin concentrations measured using the vector correlation of their skin Raman spectra and a fixed spectrum of pure human recombinant filaggrin, these results indicate that Raman spectroscopy may be used as a noninvasive tool to detect FLG gene mutations.
机译:了解丝蛋白(FLG)基因突变的存在可能有助于特应性皮炎(AD)患者的亚分类,可用于引入个性化治疗。在这项工作中,使用拉曼光谱法评估了皮肤中丝蛋白的含量,并将结果与​​墨西哥间质患者的FLG基因分型进行了比较。结果表明,在墨西哥人群中也存在欧洲人中存在的2282del4和R501X突变,但在亚洲或非洲血统中却不存在。结果还显示,具有丝蛋白基因突变的患者使用皮肤拉曼光谱和固定的纯人类重组丝蛋白光谱的矢量相关性测量,其丝蛋白浓度较低,这些结果表明拉曼光谱法可用作检测FLG的非侵入性工具基因突变。

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