【佳學(xué)基因檢測(cè)】使用全基因組成像遺傳學(xué)繪制從基因檢測(cè)到神經(jīng)精神疾病的因果通路

基因治療精神病賊新方法簡(jiǎn)介

研討三甲醫(yī)師職稱提升神經(jīng)科疾病學(xué)在《精神與神經(jīng)疾病致病基因檢測(cè)與轉(zhuǎn)移潛能分析》收錄《Psychiatry Clin Neurosci》在. 2019 Jul;73(7):357-369.發(fā)表了一篇題目為《使用全基因組成像遺傳學(xué)繪制從遺傳學(xué)到神經(jīng)精神疾病的因果通路：現(xiàn)狀和未來(lái)方向》神經(jīng)精神疾病的因果關(guān)系基因檢測(cè)臨床研究文章。該研究由Brandon D Le, Jason L Stein等完成。促進(jìn)了神經(jīng)科疾病病因?qū)W、病源學(xué)的與個(gè)性化用藥的發(fā)展，進(jìn)一步提升了神經(jīng)精神系統(tǒng)疾病診斷與治療的正確性與全面性。

精神科神經(jīng)科致病基因及正確治療臨床研究?jī)?nèi)容關(guān)鍵詞：

全基因組,成像,遺傳學(xué),繪制,因果關(guān)系

神經(jīng)科用藥指導(dǎo)基因檢測(cè)臨床應(yīng)用結(jié)果

影像遺傳學(xué)旨在識(shí)別與人腦結(jié)構(gòu)和功能相關(guān)的遺傳變異。賊近，合作聯(lián)盟在這一目標(biāo)上取得了成功，識(shí)別和復(fù)制了通過(guò)磁共振成像測(cè)量的影響人類大腦總體結(jié)構(gòu)的常見基因變異。在這篇綜述中，我們將成像遺傳關(guān)聯(lián)作為理解從遺傳變異到神經(jīng)精神疾病風(fēng)險(xiǎn)增加的因果鏈的一個(gè)重要環(huán)節(jié)。我們提供了其他領(lǐng)域的例子，說(shuō)明如何識(shí)別遺傳變異與疾病和因果鏈上的多種表型的關(guān)聯(lián)，揭示了對(duì)疾病風(fēng)險(xiǎn)的機(jī)制理解，并對(duì)成像遺傳學(xué)如何類似地應(yīng)用產(chǎn)生了影響。我們討論了影像遺傳學(xué)研究領(lǐng)域的當(dāng)前發(fā)現(xiàn)，包括常見的遺傳變異對(duì)大腦結(jié)構(gòu)的影響比對(duì)精神分裂癥等疾病的風(fēng)險(xiǎn)稍大，這表明遺傳結(jié)構(gòu)更簡(jiǎn)單。此外，粗略的大腦結(jié)構(gòu)測(cè)量與一些（但不是全部）神經(jīng)精神疾病具有共同的遺傳基礎(chǔ)，這使以前認(rèn)為它們是廣泛的內(nèi)表型的信念無(wú)效，但可以正確定位可能與特定疾病的病理學(xué)有關(guān)的大腦區(qū)域。賊后，我們建議，為了更詳細(xì)地了解遺傳變異對(duì)大腦的影響，未來(lái)成像遺傳學(xué)研究的方向?qū)⑿枰诖殴舱癯上穹直媛手庥^察特定大腦區(qū)域的細(xì)胞和突觸結(jié)構(gòu)。我們預(yù)計(jì)，在從突觸到腦溝的生物學(xué)水平上整合遺傳關(guān)聯(lián)將揭示影響神經(jīng)精神疾病風(fēng)險(xiǎn)的特定因果途徑。影像遺傳學(xué)；神經(jīng)精神疾?。唤M織清理。

神經(jīng)及精神疾病及其并發(fā)征、合并征國(guó)際數(shù)據(jù)庫(kù)描述：

Imaging genetics aims to identify genetic variants associated with the structure and function of the human brain. Recently, collaborative consortia have been successful in this goal, identifying and replicating common genetic variants influencing gross human brain structure as measured through magnetic resonance imaging. In this review, we contextualize imaging genetic associations as one important link in understanding the causal chain from genetic variant to increased risk for neuropsychiatric disorders. We provide examples in other fields of how identifying genetic variant associations to disease and multiple phenotypes along the causal chain has revealed a mechanistic understanding of disease risk, with implications for how imaging genetics can be similarly applied. We discuss current findings in the imaging genetics research domain, including that common genetic variants can have a slightly larger effect on brain structure than on risk for disorders like schizophrenia, indicating a somewhat simpler genetic architecture. Also, gross brain structure measurements share a genetic basis with some, but not all, neuropsychiatric disorders, invalidating the previously held belief that they are broad endophenotypes, yet pinpointing brain regions likely involved in the pathology of specific disorders. Finally, we suggest that in order to build a more detailed mechanistic understanding of the effects of genetic variants on the brain, future directions in imaging genetics research will require observations of cellular and synaptic structure in specific brain regions beyond the resolution of magnetic resonance imaging. We expect that integrating genetic associations at biological levels from synapse to sulcus will reveal specific causal pathways impacting risk for neuropsychiatric disorders.Keywords: genome-wide association study; imaging genetics; neuropsychiatric disorders; tissue clearing.