Early type II fiber atrophy in intensive care unit patients with nonexcitable muscle membrane

被引:62
作者
Bierbrauer, Jeffrey [1 ]
Koch, Susanne [1 ]
Olbricht, Claudio [1 ]
Hamati, Jida
Lodka, Doerte
Schneider, Joanna [3 ]
Luther-Schroeder, Anja [1 ]
Kleber, Christian [2 ]
Faust, Katharina [4 ]
Wiesener, Solveigh [1 ]
Spies, Claudia D. [1 ]
Spranger, Joachim [5 ]
Spuler, Simone [3 ]
Fielitz, Jens
Weber-Carstens, Steffen [1 ]
机构
[1] Campus Virchow Klinikum, Dept Anesthesiol & Operat Intens Care Med, Berlin, Germany
[2] Charite, Campus Virchow Klinikum, Dept Traumatol & Reconstruct Surg, D-13353 Berlin, Germany
[3] Expt & Clin Res Ctr, Muscle Res Unit, Berlin, Germany
[4] Charite, Campus Virchow Klinikum, Dept Neurosurg Pediat Neurosurg, D-13353 Berlin, Germany
[5] Charite, Dept Endocrinol Diabet & Nutr Med, D-13353 Berlin, Germany
关键词
acute critical illness; critical illness myopathy; direct muscle stimulation; ICUAW; ICU-acquired weakness; neuromuscular dysfunction; muscle biopsy; sepsis; CRITICAL ILLNESS MYOPATHY; NEUROPATHY; STRENGTH; WEAKNESS; PARESIS;
D O I
10.1097/CCM.0b013e31823295e6
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objective: Intensive care unit-acquired weakness indicates increased morbidity and mortality. Nonexcitable muscle membrane after direct muscle stimulation develops early and predicts intensive care unit-acquired weakness in sedated, mechanically ventilated patients. A comparison of muscle histology at an early stage in intensive care unit-acquired weakness has not been done. We investigated whether nonexcitable muscle membrane indicates fast-twitch myofiber atrophy during the early course of critical illness. Design: Prospective observational study. Setting: Two intensive care units at Charite University Medicine, Berlin. Patients: Patients at increased risk for development of intensive care unit-acquired weakness, indicated by Sepsis-related Organ Failure Assessment scores >= 8 on 3 of 5 consecutive days within their first week in the intensive care unit. Interventions: None. Measurements and Main Results: Electrophysiological compound muscle action potentials after direct muscle stimulation and muscle biopsies were obtained at median days 7 and 5, respectively. Patients with nonexcitable muscle membranes (n = 15) showed smaller median type II cross-sectional areas (p <. 05), whereas type I muscle fibers did not compared with patients with preserved muscle membrane excitability (compound muscle action potentials after direct muscle stimulation >= 3.0 mV; n = 9). We also observed decreased mRNA transcription levels of myosin heavy chain isoform IIa and a lower densitometric ratio of fast-to-slow myosin heavy chain protein content. Conclusion: We suggest that electrophysiological nonexcitable muscle membrane predicts preferential type II fiber atrophy in intensive care unit patients during early critical illness. (Crit Care Med 2012; 40:647-650)
引用
收藏
页码:647 / 650
页数:4
相关论文
共 16 条
[1]   Acquired weakness, handgrip strength, and mortality in critically ill patients [J].
Ali, Naeem A. ;
O'Brien, James M., Jr. ;
Hoffmann, Stephen P. ;
Phillips, Gary ;
Garland, Allan ;
Finley, James C. W. ;
Almoosa, Khalid ;
Hejal, Rana ;
Wolf, Karen M. ;
Lemeshow, Stanley ;
Connors, Alfred F., Jr. ;
Marsh, Clay B. .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2008, 178 (03) :261-268
[2]   Critical illness polyneuromyopathy: the electrophysiological components of a complex entity [J].
Bednarik, J ;
Lukas, Z ;
Vondracek, P .
INTENSIVE CARE MEDICINE, 2003, 29 (09) :1505-1514
[3]   Paresis acquired in the intensive care unit -: A prospective multicenter study [J].
De Jonghe, B ;
Sharshar, T ;
Lefaucheur, JP ;
Authier, FJ ;
Durand-Zaleski, I ;
Boussarsar, M ;
Cerf, C ;
Renaud, E ;
Mesrati, F ;
Carlet, J ;
Raphaël, JC ;
Outin, H ;
Bastuji-Garin, S .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 288 (22) :2859-2867
[4]  
de Jonghe Bernard, 2009, Crit Care Med, V37, pS309, DOI 10.1097/CCM.0b013e3181b6e64c
[5]   Myosin accumulation and striated muscle myopathy result from the loss of muscle RING finger 1 and 3 [J].
Fielitz, Jens ;
Kim, Mi-Sung ;
Shelton, John M. ;
Latif, Shuaib ;
Spencer, Jeffrey A. ;
Glass, David J. ;
Richardson, James A. ;
Bassel-Duby, Rhonda ;
Olson, Eric N. .
JOURNAL OF CLINICAL INVESTIGATION, 2007, 117 (09) :2486-2495
[6]   Acute type II myofiber atrophy in critical illness [J].
Gutmann, L ;
Blumenthal, D ;
Gutmann, L ;
Schochet, SS .
NEUROLOGY, 1996, 46 (03) :819-821
[7]  
Helliwell TR, 1998, NEUROPATH APPL NEURO, V24, P507
[8]   Functional Disability 5 Years after Acute Respiratory Distress Syndrome [J].
Herridge, Margaret S. ;
Tansey, Catherine M. ;
Matte, Andrea ;
Tomlinson, George ;
Diaz-Granados, Natalia ;
Cooper, Andrew ;
Guest, Cameron B. ;
Mazer, C. David ;
Mehta, Sangeeta ;
Stewart, Thomas E. ;
Kudlow, Paul ;
Cook, Deborah ;
Slutsky, Arthur S. ;
Cheung, Angela M. .
NEW ENGLAND JOURNAL OF MEDICINE, 2011, 364 (14) :1293-1304
[9]   INTEROBSERVER AGREEMENT IN THE ASSESSMENT OF MUSCLE STRENGTH AND FUNCTIONAL ABILITIES IN GUILLAIN-BARRE-SYNDROME [J].
KLEYWEG, RP ;
VANDERMECHE, FGA ;
SCHMITZ, PIM .
MUSCLE & NERVE, 1991, 14 (11) :1103-1109
[10]   Critical illness myopathy is frequent: accompanying neuropathy protracts ICU discharge [J].
Koch, Susanne ;
Spuler, Simone ;
Deja, Maria ;
Bierbrauer, Jeffrey ;
Dimroth, Anna ;
Behse, Friedrich ;
Spies, Claudia D. ;
Wernecke, Klaus-D ;
Weber-Carstens, Steffen .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2011, 82 (03) :287-293