5 -羟色胺和去甲肾上腺素再摄取抑制剂(SNRIs)治疗纤维肌痛:一项全面的临床综述。

Psychopharmacology bulletin Pub Date : 2025-02-03
Aila Malik, Zoe Brown, Alexa Ryder, Vanshika Balayan, Lauren Jameson, Peter Vu, Rana Al-Jumah, Jamal Hasoon
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引用次数: 0

摘要

纤维肌痛是一种复杂的临床症状,其症状范围广泛,包括慢性广泛的肌肉骨骼疼痛、深度疲劳、认知障碍和情绪障碍。目前对疾病发病机制的理解认为神经递质失调和中枢疼痛敏感化在导致疼痛敏感性升高的关键作用。遗传易感性以及内分泌和免疫功能的改变已被牵连。准确的诊断需要全面的评估,需要个性化的治疗方法来解决疾病过程的生物、心理和社会因素。在药物治疗方案中,血清素去甲肾上腺素再摄取抑制剂(SNRIs)除了具有稳定情绪的特性外,还具有镇痛作用。目前,度洛西汀和米那西普兰已被美国食品和药物管理局批准,尽管该药物类别中的其他药物包括文拉法辛和地文拉法辛已被研究用于治疗纤维肌痛。此外,选择性去甲肾上腺素再摄取抑制剂,esreboxetine和reboxetine,以及曲马多(一种具有SNRI活性的弱阿片受体激动剂)已显示出潜在的效用。尽管一些研究已经证明SNRIs对纤维肌痛患者有效且耐受性良好,但个体反应可能有所不同。仍然需要进行大规模的临床试验,以确定这些药物在这一患者群体中的安全性和临床有效性。需要进一步的信息来优化患者选择和给药方案,以及阐明与不良反应相关的临床因素。此外,药物制剂可以与生活方式的改变和非药物治疗相结合,以解决促进疾病发展和症状持续的生物和社会心理因素的复杂相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Serotonin and Norepinephrine Reuptake Inhibitors (SNRIs) for Treatment of Fibromyalgia: A Comprehensive Clinical Review.

Fibromyalgia is a complex clinical entity characterized by a broad range of symptoms including chronic widespread musculoskeletal pain, profound fatigue, impaired cognition, and mood disturbances. Current understanding of disease pathogenesis assumes neurotransmitter dysregulation and central pain sensitization play a key role resulting in heightened pain sensitivity. Genetic predisposition as well as alterations in endocrine and immune function have been implicated. Accurate diagnosis requires a comprehensive evaluation, and a personalized treatment approach is needed to address the biopsychosocial components of the disease process. Among pharmacologic treatment options, serotonin norepinephrine reuptake inhibitors (SNRIs) have demonstrated analgesic effects in addition to mood stabilizing properties. Currently, duloxetine and milnacipran are approved by the Food and Drug Administration although other agents in this drug class including venlafaxine and desvenlafaxine have been studied in the management of fibromyalgia. In addition, selective norepinephrine reuptake inhibitors, esreboxetine and reboxetine, as well as tramadol, a weak opioid mu-receptor agonist with SNRI activity have shown potential utility. Although some studies have demonstrated SNRIs to be effective and well tolerated in patients with fibromyalgia, individual response may vary. There remains a continued need for large scale clinical trials to establish the safety and clinical effectiveness of these agents in this patient population. Further information is needed to optimize patient selection and dosing regimens as well as elucidate the clinical factors associated with poor response. Moreover, pharmacologic agents may be combined with lifestyle changes and non-drug-based treatments to address the complex interactions of biological and psychosocial factors that facilitate disease development and persistence of symptoms.

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