米氮平治疗患有肠易激综合征的老年人的胃肠道症状和神经心理学症状。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-10-24 eCollection Date: 2024-01-01 DOI:10.1177/17562848241278125
Ayesha Khan, Raakhi Menon, Brooke Corning, Steven Cohn, Cecil Kumfa, Mukaila Raji
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引用次数: 0

摘要

肠易激综合征(IBS)是一种常见的、可能导致过度残疾、发病率和生活质量低下的疾病。治疗肠易激综合征的药物临床试验主要针对年轻人。然而,越来越多 65 岁及以上的成年人患有肠易激综合征。目前还没有数据可以指导临床医生安全有效地使用药物(如抗胆碱能药、抗痉挛药和三环类抗抑郁药 (TCA))治疗老年人肠易激综合征。这些药物,尤其是抗胆碱能药和 TCAs,在老年人中发生不良反应(ADE)的风险很高,因为老年人的药物代谢会随着年龄的增长而下降,而且多种慢性疾病的发病率也很高。治疗肠易激综合征的常见精神和内科合并症经常使用五种或更多种药物(多药联用):焦虑、抑郁、失眠、偏头痛、腹泻、恶心、食欲不振、皮肤瘙痒/过敏和纤维肌痛。这些神经和精神并发症反映了共同的致病机制,以及高度炎症、肠道微生物群改变、多种胃肠道和中枢神经系统活性神经递质(如血清素、神经肽)失调的双向串联。目前,治疗这些肠易激综合征相关病症需要使用多种药物,这增加了药物之间发生不良相互作用的风险。减少治疗肠易激综合征相关病症药物数量的一种方法是使用一种可治疗多种或所有这些病症的药物--米氮平。在这篇透视文章中,我们从基础科学、系列病例、观察性研究和流行病学研究、临床研究和临床试验等方面提出证据,支持米氮平这种去甲肾上腺素能和特异性血清素能受体拮抗剂(具有 5- 羟色胺-2 和 3 拮抗作用)作为一种潜在的药物治疗干预措施,用于治疗肠易激综合征相关的各种症状和病症。具体而言,我们发现了米氮平在治疗腹泻、失眠、偏头痛、恶心和食欲不振方面发挥作用的证据。我们建议开展一项大型随机对照试验,将米氮平作为治疗多种肠易激综合征症状的潜在一站式疗法进行研究,以减少多药治疗和 ADE,尤其是在老年人群中。
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Mirtazapine for gastrointestinal and neuropsychological symptoms in older adults with irritable bowel syndrome.

Irritable bowel syndrome (IBS) is a common and potentially modifiable contributor to excess disability, morbidity, and poor quality of life. Clinical trials of medications for IBS have largely been in younger adults. Yet, a growing number of adults aged 65 and older are living with IBS. No data exist to guide clinicians in the safe and effective use of medications (e.g., anticholinergics, anti-spasmodics, and tricyclic antidepressants (TCA)) for IBS in the geriatric population. These medications-especially anticholinergics and TCAs-carry a high risk of adverse effects (ADE) in older adults because of age-associated decline in drug metabolism and the high prevalence of multiple chronic conditions. Five or more medications (polypharmacy) are frequently used to treat common psychiatric and medical comorbidities of IBS: anxiety, depression, insomnia, migraine headache, diarrhea, nausea, poor appetite, pruritus/skin atopy, and fibromyalgia. These neurological and psychiatric comorbidities reflect shared pathogenic mechanisms and bidirectional crosstalk of high inflammation, alteration of gut microbiota, and dysregulation of multiple gastrointestinal and central nervous system-active neurotransmitters (e.g., serotonin, neuropeptides). Currently, these IBS-associated conditions are treated with multiple medications-which increase the risk of adverse drug-drug interactions. One way to reduce the number of medications used for IBS-associated conditions is the use of one medication that treats many or all of these conditions-Mirtazapine. In this perspective article, we present evidence from basic science, case series, observational and epidemiological studies, clinical studies, and clinical trials supporting mirtazapine, a noradrenergic and specific serotonergic receptor antagonist-with 5-hydroxytryptamine-2 and 3 antagonism, as a potential pharmacotherapeutic intervention for the myriad symptoms and conditions associated with IBS. Specifically, we found evidence of mirtazapine's role in treating diarrhea, insomnia, migraine headache, nausea, and poor appetite. We propose a large randomized controlled trial to study mirtazapine as a potential one-stop treatment for multiple IBS symptoms, with the potential to reduce polypharmacy and ADEs, especially in the geriatric population.

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