Suppr超能文献

阿片类激动剂药物辅助治疗患者的代谢和成瘾指标:丁丙诺啡与美沙酮的比较。

Metabolic and Addiction Indices in Patients on Opioid Agonist Medication-Assisted Treatment: A Comparison of Buprenorphine and Methadone.

机构信息

Center for Pain and the Brain, Department of Anesthesia, Critical Care and Pain Medicine, Boston Children's Hospital, Boston, MA, USA.

Rhode Island Department of Behavioral Healthcare, Cranston, RI, USA.

出版信息

Sci Rep. 2020 Mar 27;10(1):5617. doi: 10.1038/s41598-020-62556-0.

Abstract

Metabolic hormones stabilize brain reward and motivational circuits, whereas excessive opioid consumption counteracts this effect and may impair metabolic function. Here we addressed the role of metabolic processes in the course of the agonist medication-assisted treatment for opioid use disorder (OUD) with buprenorphine or methadone. Plasma lipids, hemoglobin A1C, body composition, the oral glucose tolerance test (oGTT) and the Sweet Taste Test (STT) were measured in buprenorphine- (n = 26) or methadone (n = 32)- treated subjects with OUD. On the whole, the subjects in both groups were overweight or obese and insulin resistant; they displayed similar oGTT and STT performance. As compared to methadone-treated subjects, those on buprenorphine had significantly lower rates of metabolic syndrome (MetS) along with better values of the high-density lipoproteins (HDL). Subjects with- vs. without MetS tended to have greater addiction severity. Correlative analyses revealed that more buprenorphine exposure duration was associated with better HDL and opioid craving values. In contrast, more methadone exposure duration was associated with worse triglycerides-, HDL-, blood pressure-, fasting glucose- and hemoglobin A1C values. Buprenorphine appears to produce beneficial HDL- and craving effects and, contrary to methadone, its role in the metabolic derangements is not obvious. Our data call for further research aimed at understanding the distinctive features of buprenorphine metabolic effects vis-à-vis those of methadone and their potential role in these drugs' unique therapeutic profiles.

摘要

代谢激素稳定大脑奖赏和动机回路,而过量的阿片类药物消耗则会抵消这种作用,并可能损害代谢功能。在这里,我们研究了代谢过程在阿片类药物使用障碍(OUD)的激动剂药物辅助治疗中(用丁丙诺啡或美沙酮)的作用。我们测量了接受丁丙诺啡(n=26)或美沙酮(n=32)治疗的 OUD 患者的血浆脂质、糖化血红蛋白 A1C、身体成分、口服葡萄糖耐量试验(oGTT)和甜味测试(STT)。总的来说,两组受试者均超重或肥胖且胰岛素抵抗;他们的 oGTT 和 STT 表现相似。与美沙酮治疗的受试者相比,丁丙诺啡治疗的受试者具有显著更低的代谢综合征(MetS)发生率,以及更好的高密度脂蛋白(HDL)值。与没有 MetS 的受试者相比,有 MetS 的受试者的成瘾严重程度更高。相关分析显示,丁丙诺啡的暴露时间越长,HDL 和阿片类药物渴求值越好。相比之下,美沙酮的暴露时间越长,甘油三酯、HDL、血压、空腹血糖和糖化血红蛋白值越差。丁丙诺啡似乎产生有益的 HDL 和渴求效应,与美沙酮相反,其在代谢紊乱中的作用并不明显。我们的数据呼吁进一步研究,旨在了解丁丙诺啡代谢效应与美沙酮代谢效应的区别及其在这些药物独特治疗特征中的潜在作用。

相似文献

2
Use of naltrexone in treating opioid use disorder in pregnancy.
Am J Obstet Gynecol. 2020 Jan;222(1):83.e1-83.e8. doi: 10.1016/j.ajog.2019.07.037. Epub 2019 Jul 31.
3
Comparison of neonatal outcomes in pregnant women undergoing medication-assisted treatment of opioid use disorder with methadone or buprenorphine/naloxone.
J Matern Fetal Neonatal Med. 2022 Dec;35(26):10481-10486. doi: 10.1080/14767058.2022.2130238. Epub 2022 Oct 6.
4
Medication-assisted treatment for opioid addiction: methadone and buprenorphine.
J Food Drug Anal. 2013 Dec;21(4):S69-S72. doi: 10.1016/j.jfda.2013.09.037.
6
Medication Treatment of Opioid Use Disorder.
Biol Psychiatry. 2020 Jan 1;87(1):82-88. doi: 10.1016/j.biopsych.2019.06.020. Epub 2019 Jul 2.
8
Delivery dose of methadone, but not buprenorphine, is associated with the risk and severity of neonatal opiate withdrawal syndrome.
Am J Obstet Gynecol MFM. 2020 Feb;2(1):100075. doi: 10.1016/j.ajogmf.2019.100075. Epub 2019 Dec 10.
10
Counselor training and attitudes toward pharmacotherapies for opioid use disorder.
Subst Abus. 2016;37(1):47-53. doi: 10.1080/08897077.2015.1062457. Epub 2015 Jul 13.

引用本文的文献

1
The Relevance of Pharmacokinetic Biomarkers in Response to Methadone Treatment: A Systematic Review.
Pharmaceuticals (Basel). 2025 Apr 25;18(5):623. doi: 10.3390/ph18050623.
2
High BMI is a specific risk factor for drug-related mortality in patients receiving methadone: A case control study.
Addiction. 2025 Jul;120(7):1460-1465. doi: 10.1111/add.70015. Epub 2025 Feb 13.
6
Validity of mental and physical stress models.
Neurosci Biobehav Rev. 2024 Mar;158:105566. doi: 10.1016/j.neubiorev.2024.105566. Epub 2024 Feb 1.
7
Metabolic profiles associated with opioid use and opioid use disorder: a narrative review of the literature.
Curr Addict Rep. 2023 Sep;10(3):581-593. doi: 10.1007/s40429-023-00493-4. Epub 2023 May 19.
8
Association between body mass index and treatment completion in extended-release naltrexone-treated patients with opioid dependence.
Front Psychiatry. 2023 Aug 2;14:1247961. doi: 10.3389/fpsyt.2023.1247961. eCollection 2023.
9
Weight change among patients engaged in medication treatment for opioid use disorder: a scoping review.
Am J Drug Alcohol Abuse. 2023 Sep 3;49(5):551-565. doi: 10.1080/00952990.2023.2207720. Epub 2023 May 18.
10
Ketogenic diet enhances the effects of oxycodone in mice.
Sci Rep. 2023 May 9;13(1):7507. doi: 10.1038/s41598-023-33458-8.

本文引用的文献

1
Craving in Opioid Use Disorder: From Neurobiology to Clinical Practice.
Front Psychiatry. 2019 Aug 30;10:592. doi: 10.3389/fpsyt.2019.00592. eCollection 2019.
2
The role of orexin-1 receptor signaling in demand for the opioid fentanyl.
Neuropsychopharmacology. 2019 Sep;44(10):1690-1697. doi: 10.1038/s41386-019-0420-x. Epub 2019 May 21.
3
Progress in agonist therapy for substance use disorders: Lessons learned from methadone and buprenorphine.
Neuropharmacology. 2019 Nov 1;158:107609. doi: 10.1016/j.neuropharm.2019.04.015. Epub 2019 Apr 19.
4
Management of opioid use disorder in the USA: present status and future directions.
Lancet. 2019 Apr 27;393(10182):1760-1772. doi: 10.1016/S0140-6736(18)33078-2. Epub 2019 Mar 14.
5
The effects of buprenorphine/naloxone maintenance treatment on sexual dysfunction, sleep and weight in opioid use disorder patients.
Psychiatry Res. 2019 Feb;272:450-453. doi: 10.1016/j.psychres.2018.12.153. Epub 2018 Dec 29.
6
Insulin in the ventral tegmental area reduces cocaine-evoked dopamine in the nucleus accumbens in vivo.
Eur J Neurosci. 2019 Aug;50(3):2146-2155. doi: 10.1111/ejn.14291. Epub 2018 Dec 11.
8
Daily opioid analgesic use reduces blood insulin levels.
J Opioid Manag. 2018 May/Jun;14(3):165-170. doi: 10.5055/jom.2018.0446.
9
Programming of central and peripheral insulin resistance by low birthweight and postnatal catch-up growth in male mice.
Diabetologia. 2018 Oct;61(10):2225-2234. doi: 10.1007/s00125-018-4694-z. Epub 2018 Jul 24.
10
Neuroscience of Addiction: Relevance to Prevention and Treatment.
Am J Psychiatry. 2018 Aug 1;175(8):729-740. doi: 10.1176/appi.ajp.2018.17101174. Epub 2018 Apr 25.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验