• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

解决全球阿片类药物危机:将遗传成瘾风险评估与个性化多巴胺能稳态疗法及意识整合疗法相结合。

Solving the Global Opioid Crisis: Incorporating Genetic Addiction Risk Assessment with Personalized Dopaminergic Homeostatic Therapy and Awareness Integration Therapy.

作者信息

Zeine Foojan, Jafari Nicole, Baron David, Bowirrat Abdalla, Pinhasov Albert, Norling Brian, Martinez Kathleen Carter, Nami Mohammad, Manavi Nima, Sunder Keerthy, Rabin David M, Bagchi Debasis, Khalsa Jag, Gold Mark S, Sipple Daniel, Barzegar Mojtaba, Bodhanapati Jothsna, Khader Waseem, Carney Paul, Dennen Catherine A, Gupta Ashim, Elman Igor, Badgaiyan Rajendra D, Modestino Edward J, Thanos Panayotis K, Hanna Colin, McLaughlin Thomas, Cadet Jean Lud, Soni Diwanshu, Braverman Eric R, Barh Debmalya, Giordano John, Edwards Drew, Ashford J Wesson, Gondre-Lewis Marjorie C, Gilley Elizebeth, Murphy Kevin T, Lewandrowski Kai-Uwe, Sharafshah Alireza, Makale Milan, Fuehrlein Brian, Blum Kenneth

机构信息

Awareness Integration Institute, San Clemente, USA.

Department of Health Science, California State University, Long Beach, USA.

出版信息

J Addict Psychiatry. 2024;8(1):50-95. Epub 2024 Jun 20.

PMID:39635461
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11615735/
Abstract

OBJECTIVES

The opioid crisis in the last few decades has mounted to a global level, impacting all areas of socioeconomic, demographic, geographic, and cultural boundaries. Traditional treatments have not been deemed to show the degree of efficacy necessary to address the crisis. The authors of this review paper have set forth an unprecedented and in-depth look into multi-factorial determinants that have contributed to the opioid crisis becoming global and multi-faceted.

METHODS

For this narrative review/opinion article, we searched PsychINFO, PubMed, Google Scholar, and Web of Science databases to identify relevant articles on topics including the "opioid crisis," "opioid mechanisms," "genetics and epigenetics," "neuropharmacology," and "clinical aspects of opioid treatment and prevention." Since this was not a systematic review the articles selected could represent unitential bias.

RESULTS

Despite some success achieved through Opioid Substitution Therapy (OST) in harm reduction, the annual mortality toll in the US alone surpasses 106,699 individuals, a figure expected to climb to 165,000 by 2025. Data from the Substance Abuse and Mental Health Services Administration's (SAMHSA) National Survey on Drug Abuse and Health (NSDUH) reveals that approximately 21.4% of individuals in the US engaged in illicit drug use in 2020, with 40.3 million individuals aged 12 or older experiencing a Substance Use Disorder (SUD). Provisional figures from the Centers for Disease Control and Prevention (CDC) indicate a troubling 15% increase in overdose deaths in 2021, rising from 93,655 in 2020 to 107,622, with opioids accounting for roughly 80,816 of these deaths.

CONCLUSIONS

We advocate reevaluating the "standard of care" and shifting towards inducing dopamine homeostasis by manipulating key neurotransmitter systems within the brain's reward cascade. We propose a paradigm shift towards a novel "standard of care" that begins with incorporating Genetic Addiction Risk Severity (GARS) testing to assess pre-addiction risk and vulnerability to opioid-induced addiction; emphasis should be placed on inducing dopamine homeostasis through safe and non-addictive alternatives like KB220, and comprehensive treatment approaches that address psychological, spiritual, and societal aspects of addiction through Awareness Integration Therapy (AIT).

摘要

目标

在过去几十年里,阿片类药物危机已上升到全球层面,影响着社会经济、人口、地理和文化边界的各个领域。传统治疗方法被认为未显示出应对该危机所需的疗效程度。这篇综述论文的作者对导致阿片类药物危机变得全球化和多面化的多因素决定因素进行了前所未有的深入研究。

方法

对于这篇叙述性综述/观点文章,我们检索了PsychINFO、PubMed、谷歌学术和科学网数据库,以识别有关“阿片类药物危机”、“阿片类药物机制”、“遗传学和表观遗传学”、“神经药理学”以及“阿片类药物治疗与预防的临床方面”等主题的相关文章。由于这不是一项系统综述,所选文章可能存在无意的偏差。

结果

尽管阿片类药物替代疗法(OST)在减少危害方面取得了一些成功,但仅在美国,每年的死亡人数就超过106,699人,预计到2025年这一数字将攀升至165,000人。物质滥用和精神健康服务管理局(SAMHSA)的全国药物滥用和健康调查(NSDUH)数据显示,2020年美国约21.4%的人使用非法药物,4030万12岁及以上的人患有物质使用障碍(SUD)。疾病控制与预防中心(CDC)的初步数据表明,2021年过量用药死亡人数令人不安地增加了15%,从2020年的93,655人增至107,622人,其中阿片类药物导致的死亡约为80,816人。

结论

我们主张重新评估“护理标准”,并通过操纵大脑奖赏级联中的关键神经递质系统来诱导多巴胺稳态。我们提议向一种新的“护理标准”范式转变,首先纳入遗传成瘾风险严重程度(GARS)测试,以评估成瘾前风险和对阿片类药物诱导成瘾的易感性;应强调通过安全且无成瘾性的替代品(如KB220)诱导多巴胺稳态,以及通过意识整合疗法(AIT)解决成瘾的心理、精神和社会方面问题的综合治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15e3/11615735/16f9bb6f1863/nihms-2013809-f0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15e3/11615735/585bda417287/nihms-2013809-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15e3/11615735/ea6bd44b6c3e/nihms-2013809-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15e3/11615735/4db64a404712/nihms-2013809-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15e3/11615735/a5ae3e5be24b/nihms-2013809-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15e3/11615735/30620756d760/nihms-2013809-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15e3/11615735/0ab9fdff1808/nihms-2013809-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15e3/11615735/2819271b8916/nihms-2013809-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15e3/11615735/9f9eee17830a/nihms-2013809-f0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15e3/11615735/babd6f7e8cdb/nihms-2013809-f0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15e3/11615735/16f9bb6f1863/nihms-2013809-f0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15e3/11615735/585bda417287/nihms-2013809-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15e3/11615735/ea6bd44b6c3e/nihms-2013809-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15e3/11615735/4db64a404712/nihms-2013809-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15e3/11615735/a5ae3e5be24b/nihms-2013809-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15e3/11615735/30620756d760/nihms-2013809-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15e3/11615735/0ab9fdff1808/nihms-2013809-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15e3/11615735/2819271b8916/nihms-2013809-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15e3/11615735/9f9eee17830a/nihms-2013809-f0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15e3/11615735/babd6f7e8cdb/nihms-2013809-f0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15e3/11615735/16f9bb6f1863/nihms-2013809-f0010.jpg

相似文献

1
Solving the Global Opioid Crisis: Incorporating Genetic Addiction Risk Assessment with Personalized Dopaminergic Homeostatic Therapy and Awareness Integration Therapy.解决全球阿片类药物危机:将遗传成瘾风险评估与个性化多巴胺能稳态疗法及意识整合疗法相结合。
J Addict Psychiatry. 2024;8(1):50-95. Epub 2024 Jun 20.
2
Beyond Mor: Can Induction of Dopamine Homeostasis Along with Electrotherapy Attenuate the Opioid Crisis?超越美沙酮:多巴胺稳态诱导联合电疗法能否缓解阿片类药物危机?
Clin Exp Psychol. 2023 Mar 2;9(2):1-3.
3
Fourth Wave of Opioid (Illicit Drug) Overdose Deaths and Diminishing Access to Prescription Opioids and Interventional Techniques: Cause and Effect.阿片类药物(非法药物)过量死亡的第四波高峰以及处方阿片类药物和介入技术可及性的下降:因果关系
Pain Physician. 2022 Mar;25(2):97-124.
4
Folic acid supplementation and malaria susceptibility and severity among people taking antifolate antimalarial drugs in endemic areas.在流行地区,服用抗叶酸抗疟药物的人群中,叶酸补充剂与疟疾易感性和严重程度的关系。
Cochrane Database Syst Rev. 2022 Feb 1;2(2022):CD014217. doi: 10.1002/14651858.CD014217.
5
A Review of DNA Risk Alleles to Determine Epigenetic Repair of mRNA Expression to Prove Therapeutic Effectiveness in Reward Deficiency Syndrome (RDS): Embracing "Precision Behavioral Management".关于DNA风险等位基因的综述,以确定mRNA表达的表观遗传修复,从而证明在奖赏缺乏综合征(RDS)中的治疗效果:采用“精准行为管理”
Psychol Res Behav Manag. 2021 Dec 17;14:2115-2134. doi: 10.2147/PRBM.S292958. eCollection 2021.
6
A Comprehensive 4-Layered In Silico Pharmacogenomics Analysis of the Genetic Addiction Risk Severity (GARS) Test: Strong Genetic Evidence Supporting GARS as a Novel Personalized Pre-Addiction Assessment Tool in the Opioid Crisis Era.遗传成瘾风险严重程度(GARS)测试的全面四层计算机模拟药物基因组学分析:有力的遗传学证据支持GARS作为阿片类药物危机时代新型个性化成瘾前评估工具。
Curr Pharm Biotechnol. 2025 Apr 16. doi: 10.2174/0113892010353450250408114725.
7
Dopaminergic dysfunction: Role for genetic & epigenetic testing in the new psychiatry.多巴胺能功能障碍:基因与表观遗传检测在新型精神病学中的作用
J Neurol Sci. 2023 Oct 15;453:120809. doi: 10.1016/j.jns.2023.120809. Epub 2023 Sep 23.
8
Future Newborns with Opioid-Induced Neonatal Abstinence Syndrome (NAS) Could Be Assessed with the Genetic Addiction Risk Severity (GARS) Test and Potentially Treated Using Precision Amino-Acid Enkephalinase Inhibition Therapy (KB220) as a Frontline Modality Instead of Potent Opioids.未来患有阿片类药物所致新生儿戒断综合征(NAS)的新生儿可通过遗传成瘾风险严重程度(GARS)测试进行评估,并有可能采用精准氨基酸脑啡肽酶抑制疗法(KB220)作为一线治疗方式,而非强效阿片类药物进行治疗。
J Pers Med. 2022 Dec 6;12(12):2015. doi: 10.3390/jpm12122015.
9
Pro-Dopamine Regulator - (KB220) to Balance Brain Reward Circuitry in Reward Deficiency Syndrome (RDS).促多巴胺调节剂 - (KB220)用于平衡奖赏缺乏综合征(RDS)中的大脑奖赏回路。
J Reward Defic Syndr Addict Sci. 2017;3(1):3-13. Epub 2017 Apr 28.
10
How to Combat the Global Opioid Crisis.如何应对全球阿片类药物危机。
CPQ Neurol Psychol. 2023;5(4). Epub 2023 Jan 23.

引用本文的文献

1
Response to the SAMHSA Clinical Advisory: Considerations for Genetic Testing in the Assessment of Substance Use Disorder Risk.对美国药物滥用和精神健康服务管理局临床咨询的回应:物质使用障碍风险评估中基因检测的考量
Subst Abuse Rehabil. 2025 Jan 26;16:23-26. doi: 10.2147/SAR.S514931. eCollection 2025.

本文引用的文献

1
Summary Document Research on RDS Anti-addiction Modeling: Annotated Bibliography.RDS抗成瘾建模研究总结文档:注释书目
J Addict Psychiatry. 2024 Apr 5;8(1):1-33.
2
Trauma and Resilience in Adolescents and Young Adults With Opioid Use and Eating Disorders.青少年和青年中阿片类药物使用和饮食失调的创伤与韧性
Clin Pediatr (Phila). 2023 Sep;62(8):856-861. doi: 10.1177/00099228231181742. Epub 2023 Jun 16.
3
Community member perspectives on adapting the cascade of care for opioid use disorder for a tribal nation in the United States.
社区成员对美国一个部落国家适应阿片类药物使用障碍级联护理的看法。
Addiction. 2023 Aug;118(8):1540-1548. doi: 10.1111/add.16184. Epub 2023 Apr 1.
4
Reward Deficiency Syndrome Solution System (RDSSS) A Genetically Driven Putative Inducer of "Dopamine Homeostasis" as a Futuristic Alternative to Enhance Rehabilitation Instead of Incarceration.奖励缺乏综合征解决方案系统(RDSSS):一种由基因驱动的“多巴胺稳态”推定诱导剂,作为增强康复而非监禁的未来替代方案。
Asian J Complement Altern Med. 2023;11(1):11-14. doi: 10.53043/2347-3894.acam11003. Epub 2023 Jan 11.
5
Stigma Communication Surrounding Nonmedical Opioid Use Among Affected Family Members.受影响家庭成员中围绕非医疗性阿片类药物使用的污名化交流
Health Commun. 2024 Mar;39(3):429-438. doi: 10.1080/10410236.2023.2167588. Epub 2023 Jan 18.
6
Future Newborns with Opioid-Induced Neonatal Abstinence Syndrome (NAS) Could Be Assessed with the Genetic Addiction Risk Severity (GARS) Test and Potentially Treated Using Precision Amino-Acid Enkephalinase Inhibition Therapy (KB220) as a Frontline Modality Instead of Potent Opioids.未来患有阿片类药物所致新生儿戒断综合征(NAS)的新生儿可通过遗传成瘾风险严重程度(GARS)测试进行评估,并有可能采用精准氨基酸脑啡肽酶抑制疗法(KB220)作为一线治疗方式,而非强效阿片类药物进行治疗。
J Pers Med. 2022 Dec 6;12(12):2015. doi: 10.3390/jpm12122015.
7
Theorizing the Role of Dopaminergic Polymorphic Risk Alleles with Intermittent Explosive Disorder (IED), Violent/Aggressive Behavior and Addiction: Justification of Genetic Addiction Risk Severity (GARS) Testing.探讨多巴胺能多态性风险等位基因在间歇性爆发性障碍(IED)、暴力/攻击行为和成瘾中的作用:基因成瘾风险严重程度(GARS)检测的合理性。
J Pers Med. 2022 Nov 23;12(12):1946. doi: 10.3390/jpm12121946.
8
The Genetically Informed Neurobiology of Addiction (GINA) model.成瘾的遗传神经生物学(GINA)模型。
Nat Rev Neurosci. 2023 Jan;24(1):40-57. doi: 10.1038/s41583-022-00656-8. Epub 2022 Nov 29.
9
Should Reward Deficiency Syndrome (RDS) Be Considered an Umbrella Disorder for Mental Illness and Associated Genetic and Epigenetic Induced Dysregulation of Brain Reward Circuitry?奖励缺陷综合征(RDS)是否应被视为精神疾病以及相关基因和表观遗传诱导的脑奖励回路失调的一种综合性病症?
J Pers Med. 2022 Oct 14;12(10):1719. doi: 10.3390/jpm12101719.
10
Statistical Validation of Risk Alleles in Genetic Addiction Risk Severity (GARS) Test: Early Identification of Risk for Alcohol Use Disorder (AUD) in 74,566 Case-Control Subjects.遗传成瘾风险严重程度(GARS)测试中风险等位基因的统计验证:对74566例病例对照受试者酒精使用障碍(AUD)风险的早期识别
J Pers Med. 2022 Aug 26;12(9):1385. doi: 10.3390/jpm12091385.