A Conversation with Joshua A. Gordon.

{"title":"A Conversation with Joshua A. Gordon.","authors":"","doi":"10.1101/sqb.2018.83.037291","DOIUrl":null,"url":null,"abstract":"Dr. Gordon: I spoke generally about what I perceive as the challenges and opportunities in psychiatric neuroscience. In particular, we in psychiatry—in trying to understand our disorders and help our patients—have significant challenges that we face around the burden of our disease, around challenges in terms of diagnoses and whether they correspond to the real entities that are causing people’s suffering. In terms of what we call biomarkers, tests that we can do in people to help diagnose them or guide treatment decisions, we have none. And our treatments, although they generally do work for many people, don’t work well enough for many and don’t work for a significant chunk of the patients who need help. You put those together and we face considerable challenges in terms of trying to help people who are suffering from mental illnesses. The opportunities, though, are equally impressive. We now have, in the area of genetics, knowledge of 200+ places in the genome that predispose to various psychiatric illnesses, included schizophrenia, bipolar disorder, and depression. Each one of those places in the genome that’s associated with psychiatric disorder represents a clue as to the biology underlying the disorders, and those clues are then opportunities for us to understand and potentially develop treatments for these illnesses. We also face tremendous opportunity in a specific area of neuroscience that’s really blossomed in the last 10 years, circuit neuroscience, wherewe’ve gained—at least in mice —the ability to monitor and modulate neural activity in very precise parts of the brain. Not just anatomical parts, but neuron-specific cells in the nervous system, specific projections, specific wires within the nervous system that have allowed us to dissect the elements of the brain that control behavior. The hope is that, in understanding those elements, we can develop knowledge or treatments for psychiatric illness. The third area that presents a unique opportunity for psychiatry are computational and theoretical approaches. We have “big data” approaches, machine learning approaches, but also modeling approaches and theoretical approaches that allow us to ask questions about how the brain produces behavior and how that might go awry in psychiatric illness with greater sophistication and greater precision. So I think if we are able to exploit genetics, neural circuits, and computational approaches, we can make progress more rapidly than we’ve been able to do in the past.","PeriodicalId":72635,"journal":{"name":"Cold Spring Harbor symposia on quantitative biology","volume":"83 ","pages":"255-257"},"PeriodicalIF":0.0000,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1101/sqb.2018.83.037291","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cold Spring Harbor symposia on quantitative biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/sqb.2018.83.037291","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2019/1/14 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Dr. Gordon: I spoke generally about what I perceive as the challenges and opportunities in psychiatric neuroscience. In particular, we in psychiatry—in trying to understand our disorders and help our patients—have significant challenges that we face around the burden of our disease, around challenges in terms of diagnoses and whether they correspond to the real entities that are causing people’s suffering. In terms of what we call biomarkers, tests that we can do in people to help diagnose them or guide treatment decisions, we have none. And our treatments, although they generally do work for many people, don’t work well enough for many and don’t work for a significant chunk of the patients who need help. You put those together and we face considerable challenges in terms of trying to help people who are suffering from mental illnesses. The opportunities, though, are equally impressive. We now have, in the area of genetics, knowledge of 200+ places in the genome that predispose to various psychiatric illnesses, included schizophrenia, bipolar disorder, and depression. Each one of those places in the genome that’s associated with psychiatric disorder represents a clue as to the biology underlying the disorders, and those clues are then opportunities for us to understand and potentially develop treatments for these illnesses. We also face tremendous opportunity in a specific area of neuroscience that’s really blossomed in the last 10 years, circuit neuroscience, wherewe’ve gained—at least in mice —the ability to monitor and modulate neural activity in very precise parts of the brain. Not just anatomical parts, but neuron-specific cells in the nervous system, specific projections, specific wires within the nervous system that have allowed us to dissect the elements of the brain that control behavior. The hope is that, in understanding those elements, we can develop knowledge or treatments for psychiatric illness. The third area that presents a unique opportunity for psychiatry are computational and theoretical approaches. We have “big data” approaches, machine learning approaches, but also modeling approaches and theoretical approaches that allow us to ask questions about how the brain produces behavior and how that might go awry in psychiatric illness with greater sophistication and greater precision. So I think if we are able to exploit genetics, neural circuits, and computational approaches, we can make progress more rapidly than we’ve been able to do in the past.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
专访约书亚·A·戈登。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Erratum: Attenuation of Eukaryotic Protein-Coding Gene Expression via Premature Transcription Termination. Corrigendum: Adolescence and "Late Blooming" Synapses of the Prefrontal Cortex. A Conversation with Alberto Kornblihtt. A Conversation with David Bartel. A Conversation with Ling-Ling Chen.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1