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Interleukin-6 May Not Affect Bone Resorption Marker CTX or Bone Formation Marker P1NP in Humans

机译:白细胞介素-6可能不会影响人类中的骨吸收标志物CTX或骨形成标记P1NP

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Context Interleukin 6 (IL-6) contributes to bone remodeling in preclinical studies. Clinical trials investigating the role of IL-6 in bone remodeling are limited. Objective To investigate if IL-6 regulates bone remodeling in humans. Design Plasma concentrations of the bone resorption marker carboxy-terminal type I collagen crosslinks (CTX) and of the bone formation marker procollagen type 1 N-terminal propeptide (P1NP) were measured during a mixed-meal tolerance test (MMTT) in 3 placebo-controlled human studies. Participants Five healthy individuals participated in study 1; 52 obese individuals, in study 2; and 10 healthy individuals, in study 3. Interventions Study 1 was a single-blinded crossover study consisting of a 1-h infusion of saline (placebo) or the IL-6 receptor antibody tocilizumab followed by an exercise bout. Study 2 was a randomized, double-blinded 12-week exercise training intervention study. Participants received infusions of saline or tocilizumab. Study 3 was a randomized, double-blinded, crossover study consisting of 30 min infusion of saline or IL-6. Main outcomes measures Effect of IL-6 on CTX levels. Results CTX was significantly ( P 0.01) decreased during MMTTs in all 3 studies. Treatment with tocilizumab did not affect exercise or meal induced changes in plasma CTX or P1NP concentrations acutely (study 1) or after a 12-week treatment period (study 2). Exogenous IL-6 had no effect on CTX or P1NP plasma concentrations (study 3). Conclusions IL-6 may not regulate bone remodeling in humans.
机译:背景外介素6(IL-6)有助于在临床前研究中重塑。调查IL-6在骨重塑中的作用的临床试验是有限的。目的探讨IL-6是否调节人类的骨质重塑。在3安慰剂中,测量在3安慰剂中的混合膳食耐受试验(MMTT)期间测量骨吸收标记羧酸末端I胶原交联(CTX)和骨形成标记型1N末端肽(P1NP)的骨吸收交联(CTX)和骨形成标记肽(P1NP)。受控人类研究。参与者参加第1研究的五个健康个人; 52个肥胖个体,在研究2;和10个健康的个体,在研究3.干预研究1是一种单一盲目的交叉研究,由盐水(安慰剂)或IL-6受体抗体与巯基因的1小时输注,然后是运动伴侣。研究2是随机的双盲的12周运动培训干预研究。参与者接受了盐水或幼稚的输注。研究3是由30分钟输注盐水或IL-6的随机,双盲的交叉研究。主要成果测量IL-6对CTX水平的影响。结果CTX显着(P <0.01)在所有3项研究中MMTTS期间减少。与甲硅酸化治疗不影响运动或膳食诱导血浆CTX或P1NP浓度的变化(研究1)或在12周治疗期后(研究2)。外源性IL-6对CTX或P1NP血浆浓度没有影响(研究3)。结论IL-6可能无法调节人类的骨质重塑。

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