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病例报告:哌甲酯和文拉法辛改善了一名患有注意力缺陷多动障碍、自闭症谱系障碍和共病重度抑郁症的成年患者的腹部伤害性感受性疼痛。

Case Report: Methylphenidate and venlafaxine improved abdominal nociplastic pain in an adult patient with attention deficit hyperactivity disorder, autism spectrum disorder, and comorbid major depression.

作者信息

Kasahara Satoshi, Takahashi Miwako, Takahashi Kaori, Morita Taito, Matsudaira Ko, Sato Naoko, Momose Toshimitsu, Niwa Shin-Ichi, Uchida Kanji

机构信息

Department of Anesthesiology and Pain Relief Center, The University of Tokyo Hospital, Tokyo, Japan.

Department of Pain Medicine, Fukushima Medical University School of Medicine, Fukushima, Japan.

出版信息

Front Pain Res (Lausanne). 2024 Aug 21;5:1394131. doi: 10.3389/fpain.2024.1394131. eCollection 2024.

DOI:10.3389/fpain.2024.1394131
PMID:39234404
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11371746/
Abstract

INTRODUCTION

Nociplastic pain (NP), classified as a third type of pain alongside nociceptive and neuropathic pain, is chronic pain arising from the amplification of nociceptive stimuli through central sensitization, despite the absence of tissue damage, sensory nerve damage, or disease. An important clinical feature of NP is that it is not only associated with pain but also with sensory hypersensitivity to sound and light and cognitive dysfunction, including mood and attention disorders. Recent studies have suggested that depression and developmental disorders, such as attention deficit hyperactivity disorder (ADHD) and autism spectrum disorder (ASD), coexist with NP at high frequency. Additionally, cognitive impairment in individuals with NP may be associated with these psychiatric comorbidities. However, to our knowledge, there are no reports on (1) multidimensional evaluation and diagnostic details of abdominal NP in adults with ADHD/ASD; (2) how ADHD drugs and antidepressants are administered when ADHD and depression coexist with NP; and (3) how central sensitization, brain function, and family relationship problems underlying NP are altered by treatments of ADHD and depression.

CASE PRESENTATION

Herein, we present the case of a 51-year-old woman with abdominal NP. She developed severe right lower abdominal pain and underwent a thorough medical examination; however, the physical, medical cause remained unknown, making treatment challenging. Additionally, she took time off work as she began to complain of insomnia and anxiety. She was referred to our pain center, where a diagnosis of depression, ADHD, and ASD was confirmed, and treatment with ADHD medication was initiated. While ADHD medications alone did not yield sufficient improvement, a combination of methylphenidate and the antidepressant venlafaxine eventually led to improvements in abdominal NP, depression, ADHD symptoms, central sensitization, and family relationship issues. During treatment, cerebral blood flow in the anterior cingulate, prefrontal, and parietal cortices also improved.

CONCLUSION

The treatment of comorbid depression is important while treating NP, and venlafaxine may be effective, especially in cases of comorbid ADHD/ASD. Screening for developmental disorders and depression is required in patients with abdominal NP.

摘要

引言

伤害感受性疼痛(NP)被归类为与伤害感受性疼痛和神经性疼痛并列的第三种疼痛类型,是尽管没有组织损伤、感觉神经损伤或疾病,但通过中枢敏化使伤害性刺激放大而产生的慢性疼痛。NP的一个重要临床特征是,它不仅与疼痛有关,还与对声音和光线的感觉超敏以及认知功能障碍有关,包括情绪和注意力障碍。最近的研究表明,抑郁症和发育障碍,如注意力缺陷多动障碍(ADHD)和自闭症谱系障碍(ASD),与NP高频共存。此外,NP患者的认知障碍可能与这些精神共病有关。然而,据我们所知,尚无关于(1)ADHD/ASD成年患者腹部NP的多维度评估和诊断细节;(2)当ADHD和抑郁症与NP共存时如何使用ADHD药物和抗抑郁药;以及(3)ADHD和抑郁症的治疗如何改变NP潜在的中枢敏化、脑功能和家庭关系问题的报道。

病例介绍

在此,我们介绍一名患有腹部NP的51岁女性病例。她出现严重的右下腹痛并接受了全面的医学检查;然而,身体上的医学病因仍不明确,这使得治疗具有挑战性。此外,她开始抱怨失眠和焦虑,于是请假。她被转诊至我们的疼痛中心,在那里确诊为抑郁症、ADHD和ASD,并开始使用ADHD药物治疗。虽然单独使用ADHD药物没有产生足够的改善,但哌甲酯和抗抑郁药文拉法辛联合使用最终使腹部NP、抑郁症、ADHD症状、中枢敏化和家庭关系问题得到改善。在治疗期间,前扣带回、前额叶和顶叶皮质的脑血流量也有所改善。

结论

在治疗NP时,合并抑郁症的治疗很重要,文拉法辛可能有效,尤其是在合并ADHD/ASD的情况下。腹部NP患者需要筛查发育障碍和抑郁症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/541a/11371746/db30e1f72b90/fpain-05-1394131-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/541a/11371746/d700b32ca8e2/fpain-05-1394131-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/541a/11371746/d1e5c94340a5/fpain-05-1394131-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/541a/11371746/90fba1877ac7/fpain-05-1394131-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/541a/11371746/db30e1f72b90/fpain-05-1394131-g004.jpg

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