Maes M, Libbrecht I, Van Hunsel F, Lin A H, Bonaccorso S, Goossens F, De Meester I, De Clerck L, Biondi M, Scharpe S, Janca A
Department of Medical Biochemistry, University of Antwerp, Belgium.
Psychol Med. 1998 Jul;28(4):957-65. doi: 10.1017/s0033291798006801.
The aims of the present study were to examine serum activities of peptidases, i.e. prolyl endopeptidase (PEP) and dipeptidyl peptidase IV (DPP IV), in patients with fibromyalgia and to examine the effects of subchronic treatment with sertraline on these variables.
Serum PEP and DPP IV activity were measured in 28 normal volunteers and 21 fibromyalgia patients, classified according to the American College of Rheumatology criteria. Tenderness at tender points was evaluated by means of dolorimetry. Fibromyalgia patients had repeated measurements of serum PEP and DPP IV both before and after repeated administration of sertraline or placebo for 12 weeks.
Patients with fibromyalgia had significantly lower serum PEP activity than normal volunteers. There were significantly negative correlations between serum PEP activity and severity of pressure hyperalgesia and the non-somatic, cognitive symptoms of the Hamilton Depression Rating Scale. Fibromyalgia patients with severe pressure hyperalgesia had significantly lower PEP activity than normal controls and fibromyalgia patients with less severe hyperalgesia. Fibromyalgia patients with severe non-somatic depressive symptoms had significantly lower serum PEP activity than normal volunteers. There were no significant changes in serum DPP IV activity in fibromyalgia. There were no significant effects of repeated administration of sertraline on serum PEP and DPP IV activity in patients with fibromyalgia.
The results show that fibromyalgia, and aberrant pain perception and depressive symptoms in fibromyalgia are related to lower serum PEP activity. It is hypothesized that lower serum PEP activity may play a role in the biophysiology of fibromyalgia through diminished inactivation of algesic and depression-related peptides.
本研究旨在检测纤维肌痛患者体内肽酶(即脯氨酰内肽酶[PEP]和二肽基肽酶IV[DPP IV])的血清活性,并研究舍曲林亚慢性治疗对这些指标的影响。
根据美国风湿病学会标准,对28名正常志愿者和21名纤维肌痛患者进行血清PEP和DPP IV活性检测。通过痛觉测量法评估压痛点的压痛情况。纤维肌痛患者在重复服用舍曲林或安慰剂12周前后,均重复检测血清PEP和DPP IV。
纤维肌痛患者的血清PEP活性显著低于正常志愿者。血清PEP活性与压力性痛觉过敏的严重程度以及汉密尔顿抑郁量表的非躯体性认知症状之间存在显著负相关。重度压力性痛觉过敏的纤维肌痛患者的PEP活性显著低于正常对照组和痛觉过敏较轻的纤维肌痛患者。伴有严重非躯体性抑郁症状的纤维肌痛患者的血清PEP活性显著低于正常志愿者。纤维肌痛患者的血清DPP IV活性无显著变化。舍曲林重复给药对纤维肌痛患者的血清PEP和DPP IV活性无显著影响。
结果表明,纤维肌痛以及纤维肌痛中异常的疼痛感知和抑郁症状与血清PEP活性降低有关。据推测,血清PEP活性降低可能通过减少痛觉相关肽和抑郁相关肽的失活,在纤维肌痛的生物生理学中发挥作用。