Lei Carina, Park Su Hyoun, Evington Edna J, Rosser Morgan A, Martucci Katherine T
Human Affect and Pain Neuroscience Laboratory, Department of Anesthesiology, Duke University Medical Center, Durham, NC, USA; Center for Translational Pain Medicine, Duke University Medical Center, Durham, NC, USA.
Human Affect and Pain Neuroscience Laboratory, Department of Anesthesiology, Duke University Medical Center, Durham, NC, USA; Center for Translational Pain Medicine, Duke University Medical Center, Durham, NC, USA; BK21 FOUR R&E Center for Psychology, Korea University, Seoul, South Korea.
J Pain. 2025 Aug;33:105455. doi: 10.1016/j.jpain.2025.105455. Epub 2025 Jun 3.
While opioid medications are potent analgesics, their usage in chronic pain conditions can paradoxically result in opioid-induced hyperalgesia (i.e., enhanced pain sensitivity). However, among individuals with chronic pain, minimal research has examined the effects of long-term opioid medication on pain sensitivity. To better understand how long-term opioid use impacts pain sensitivity, we measured pressure pain threshold (PPT) of the bilateral trapezius among three cohorts: pain-free controls, individuals with fibromyalgia who were not taking opioids (FMN), and individuals with fibromyalgia who were taking opioids long-term (FMO) (NCT05905419). Across these 3 groups, we also measured depression (BSI-18) and fatigue (PROMIS) to examine their relationships with pain sensitivity. Compared to the control group, dominant-side PPT was significantly reduced in both FMN (p = 0.015) and FMO groups (p = 0.004). However, PPT did not significantly differ between FMO versus FMN groups (p = 0.500). Across the fibromyalgia groups, depression and fatigue were not significantly correlated with PPT. From a co-variate analysis and its associated sensitivity analysis, the results did not change when controlling for age, self-identified race, self-identified ethnicity, and BMI. From an exploratory analysis of the FMO group, individuals who took their last opioid medication dose more recently prior to PPT assessment had higher PPTs (i.e., lower pain sensitivity, p < 0.001). In summary, reduced PPT appears to occur similarly across individuals with fibromyalgia regardless of long-term opioid use status; meanwhile, short-term (i.e., more acute) opioid dose timing- related effects on PPT may occur in individuals with fibromyalgia taking opioids long-term. PERSPECTIVE: Compared to pain-free controls, we identified significantly lower pressure pain threshold (PPT) in individuals with fibromyalgia. When comparing individuals taking opioids versus not, PPT was similar across groups regardless of opioid use status. Among the opioid-taking individuals, we identified potential opioid-related effects of PPT increase with more recent opioid dose.
虽然阿片类药物是强效镇痛药,但它们在慢性疼痛病症中的使用却可能反常地导致阿片类药物诱导的痛觉过敏(即疼痛敏感性增强)。然而,在慢性疼痛患者中,极少有研究探讨长期使用阿片类药物对疼痛敏感性的影响。为了更好地理解长期使用阿片类药物如何影响疼痛敏感性,我们测量了三组人群双侧斜方肌的压力疼痛阈值(PPT):无痛对照组、未服用阿片类药物的纤维肌痛患者(FMN)以及长期服用阿片类药物的纤维肌痛患者(FMO)(临床试验编号:NCT05905419)。在这三组人群中,我们还测量了抑郁(BSI - 18)和疲劳(PROMIS)情况,以研究它们与疼痛敏感性的关系。与对照组相比,FMN组(p = 0.015)和FMO组(p = 0.004)优势侧的PPT均显著降低。然而,FMO组与FMN组之间的PPT没有显著差异(p = 0.500)。在纤维肌痛组中,抑郁和疲劳与PPT没有显著相关性。从协变量分析及其相关敏感性分析来看,在控制年龄、自我认定的种族、自我认定的民族和体重指数后,结果没有变化。在对FMO组的探索性分析中,在PPT评估前更近时间服用最后一剂阿片类药物的个体具有更高的PPT(即更低的疼痛敏感性,p < 0.001)。总之,无论长期阿片类药物使用状况如何,纤维肌痛患者的PPT降低情况似乎相似;同时,但长期服用阿片类药物的纤维肌痛患者可能会出现短期(即更急性)阿片类药物剂量时间相关的PPT影响。观点:与无痛对照组相比,我们发现纤维肌痛患者的压力疼痛阈值(PPT)显著更低。在比较服用阿片类药物与未服用阿片类药物的个体时,无论阿片类药物使用状况如何,各组之间的PPT相似。在服用阿片类药物的个体中,我们发现随着更近一次阿片类药物剂量的增加,PPT存在潜在的阿片类药物相关影响。