Growth differentiation factor-15 is associated with muscle mass in chronic obstructive pulmonary disease and promotes muscle wasting in vivo

被引:112
作者
Patel, Mehul S. [1 ,2 ]
Lee, Jen [3 ]
Baz, Manuel [1 ,2 ]
Wells, Claire E. [4 ]
Bloch, Susannah [1 ,2 ]
Lewis, Amy [3 ]
Donaldson, Anna V. [1 ,2 ]
Garfield, Benjamin E. [1 ,2 ]
Hopkinson, Nicholas S. [1 ,2 ]
Natanek, Amanda [1 ,2 ]
Man, William D-C [1 ,2 ]
Wells, Dominic J. [5 ]
Baker, Emma H. [4 ]
Polkey, Michael I. [1 ,2 ]
Kemp, Paul R. [3 ]
机构
[1] Royal Brompton & Harefield NHS Fdn Trust, NIHR Resp Biomed Res Unit, London, England
[2] Imperial Coll, London, England
[3] Imperial Coll London, Sect Mol Med, Natl Heart & Lung Inst, SAF Bldg South Kensington Campus, London SW7 2AZ, England
[4] St Georges Univ London, Inst Infect & Immun, London, England
[5] Royal Vet Coll, Comparat Biomed Sci, London, England
关键词
Atrophy; GDF-15; Muscle mass; COPD; Electroporation; MACROPHAGE INHIBITORY CYTOKINE-1; INDEPENDENT PREDICTOR; SKELETAL-MUSCLE; ALL-CAUSE; COPD; QUADRICEPS; MORTALITY; EXPRESSION; LUNG; HYPERTENSION;
D O I
10.1002/jcsm.12096
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
030301 [社会学]; 100201 [内科学];
摘要
BackgroundLoss of muscle mass is a co-morbidity common to a range of chronic diseases including chronic obstructive pulmonary disease (COPD). Several systemic features of COPD including increased inflammatory signalling, oxidative stress, and hypoxia are known to increase the expression of growth differentiation factor-15 (GDF-15), a protein associated with muscle wasting in other diseases. We therefore hypothesized that GDF-15 may contribute to muscle wasting in COPD. MethodsWe determined the expression of GDF-15 in the serum and muscle of patients with COPD and analysed the association of GDF-15 expression with muscle mass and exercise performance. To determine whether GDF-15 had a direct effect on muscle, we also determined the effect of increased GDF-15 expression on the tibialis anterior of mice by electroporation. ResultsGrowth differentiation factor-15 was increased in the circulation and muscle of COPD patients compared with controls. Circulating GDF-15 was inversely correlated with rectus femoris cross-sectional area (P<0.001) and exercise capacity (P<0.001) in two separate cohorts of patients but was not associated with body mass index. GDF-15 levels were associated with 8-oxo-dG in the circulation of patients consistent with a role for oxidative stress in the production of this protein. Local over-expression of GDF-15 in mice caused wasting of the tibialis anterior muscle that expressed it but not in the contralateral muscle suggesting a direct effect of GDF-15 on muscle mass (P<0.001). ConclusionsTogether, the data suggest that GDF-15 contributes to the loss of muscle mass in COPD.
引用
收藏
页码:436 / 448
页数:13
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