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首页> 外文期刊>Romanian Journal of Morphology and Embryology >The prognostic and clinical significance of neuroimagistic and neurobiological vulnerability markers in correlation with the molecular pharmacogenetic testing in psychoses and ultra high-risk categories
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The prognostic and clinical significance of neuroimagistic and neurobiological vulnerability markers in correlation with the molecular pharmacogenetic testing in psychoses and ultra high-risk categories

机译:神经病学和神经生物学易损性标志物与精神病和超高危人群的分子药物遗传学检测相关的预后和临床意义

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摘要

We approach an integrated, multidisciplinary, innovative research-action model in children and adolescents with psychosis and ultra high-risk categories. Our main focus was: to investigate the prognostic and clinical significance of neuroimagistic and neurobiological vulnerability markers in correlation with the molecular pharmacogenetic testing in psychoses and ultra high-risk categories; the dynamic evaluation of the clinical evolution for the studied groups in correlation with specific neurobiological and neuroimagistic variables and markers. Our research was conducted in the period 2009–2015 on 87 patients, children and adolescents with psychosis (42 took treatment after pharmacogenetic testing, 45 without) and 65 children with ultra high-risk (UHR) for psychosis – 32 benefited of pharmacotherapy after pharmacogenetic testing and 33 without. Also, the patients were evaluated through magnetic resonance (MR) spectroscopy at baseline and after pharmacotherapy. The efficacy of the chosen therapy in correlation with the pharmacogenetic testing was evaluated through the mean change in the Positive and Negative Syndrome Scale (PANSS) total scores, in the Clinical Global Impression of Severity and Improvement (CGI-S/I), Children's Global Assessment Scale (CGAS) and through the change registered for the relevant neurobiological markers and MR spectroscopy metabolites, from baseline until endpoint in different timepoints. Our results, showed statistically significant differences of the clinical scores between the studied groups. Our research was a proof, sustaining the use of the pharmacogenetic testing in clinical practice and the value of investigating relevant neurobiological and neuroimagistic markers for a personalized, tailored therapy for psychotic patients and neuro- psychiatric UHR categories, as a fruitful pathway of intervention and care.
机译:我们针对患有精神病和超高风险类别的儿童和青少年采用综合,多学科,创新的研究行动模型。我们的主要重点是:研究与精神病学和超高风险类别的分子药物遗传学检测相关的神经动力学和神经生物学脆弱性标志物的预后和临床意义;与特定的神经生物学和神经生物学变量和标记相关的研究组的临床进展的动态评估。我们的研究是在2009-2015年期间对87例精神病患者,儿童和青少年(42例接受药理遗传学测试后接受治疗,45例未接受药理学治疗)和65例超高危(UHR)精神病患儿进行的– 32例药物遗传学后受益于药物治疗测试和33没有。同样,在基线和药物治疗后通过磁共振波谱(MR)对患者进行评估。通过阳性和阴性综合征量表(PANSS)总分的均值变化,严重程度和改善的临床总体印象(CGI-S / I),儿童的总体评价中所选择的疗法与药物遗传学测试的功效进行评估评估量表(CGAS),并通过注册相关神经生物学标记和MR光谱代谢物的变化,从基线到不同时间点的终点。我们的结果显示了研究组之间临床评分的统计学差异。我们的研究是一个证明,证明了在临床实践中继续使用药物遗传学测试以及研究相关的神经生物学和神经生物学标志物对于为精神病患者和神经精神病学UHR类别量身定制的个性化治疗的价值,作为干预和护理的卓有成效的途径。

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