How affected is oxygen metabolism in DWI lesions? A combined acute stroke PET-MR study

被引:73
作者
Guadagno, J. V.
Warburton, E. A.
Jones, P. S.
Day, D. J.
Aigbirhio, F. I.
Fryer, T. D.
Harding, S.
Price, C. J.
Green, H. A.
Barret, O.
Gillard, J. H.
Baron, J. -C.
机构
[1] Univ Cambridge, Addenbrookes Hosp, Dept Neurol, Stroke Unit, Cambridge CB2 2QQ, England
[2] Univ Cambridge, Dept Clin Neurosci, Cambridge CB2 2QQ, England
[3] Univ Cambridge, Sch Clin, Wolfson Brain Imaging Ctr, Cambridge, England
[4] Univ Cambridge, Sch Clin, Dept Med, Cambridge, England
[5] Univ Cambridge, Sch Clin, Dept Radiol, Cambridge, England
基金
英国医学研究理事会;
关键词
APPARENT DIFFUSION-COEFFICIENT; CEREBRAL-BLOOD-FLOW; POSITRON-EMISSION-TOMOGRAPHY; ISCHEMIC PENUMBRA; BRAIN ISCHEMIA; INJURY; O-15; PATHOPHYSIOLOGY; EVOLUTION; PERFUSION;
D O I
10.1212/01.wnl.0000233984.66907.db
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To use back-to-back diffusion-weighted imaging (DWI) and PET to obtain quantitative measures of the cerebral metabolic rate of oxygen (CMRO2) within DWI lesions, and to assess the perfusion-metabolism coupling status by measuring the cerebral blood flow and the oxygen extraction fraction within DWI lesions. Methods: Six prospectively recruited acute carotid-territory stroke patients completed the imaging protocol, which was commenced 7 to 21 hours from onset and combined DWI derived from state-of-the-art diffusion tensor imaging sequencing using a 3-T magnet and fully quantitative O-15-PET. The PET variables were obtained in individual DWI lesions in each patient. Results: Across patients, the CMRO2 was reduced in the DWI lesion relative to mirror (mean reduction 39.5%; p = 0.028). Examining individual DWI lesions, however, revealed considerable variability in the extent of this CMRO2 reduction. The flow-metabolism coupling pattern underlying the DWI lesion was also variable, including ongoing ischemia, mild oligemia, and partial or complete reperfusion. Discussion: Diffusion-weighted imaging (DWI) lesions generally reflect substantial disruption of energy metabolism. However, the degree of metabolic disruption is variable, indicating DWI lesions may not always represent irreversibly damaged tissue. Finally, because DWI lesions can persist despite reperfusion, assessment of perfusion is necessary for interpretation of DWI changes in acute stroke.
引用
收藏
页码:824 / 829
页数:6
相关论文
共 40 条
[1]   Magnetic resonance imaging of acute stroke [J].
Baird, AE ;
Warach, S .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1998, 18 (06) :583-609
[2]   Mapping the ischaemic penumbra with PET: Implications for acute stroke treatment [J].
Baron, JC .
CEREBROVASCULAR DISEASES, 1999, 9 (04) :193-201
[3]   USE OF PET METHODS FOR MEASUREMENT OF CEREBRAL ENERGY-METABOLISM AND HEMODYNAMICS IN CEREBROVASCULAR-DISEASE [J].
BARON, JC ;
FRACKOWIAK, RSJ ;
HERHOLZ, K ;
JONES, T ;
LAMMERTSMA, AA ;
MAZOYER, B ;
WIENHARD, K .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1989, 9 (06) :723-742
[4]   Mapping the ischaemic penumbra with PET: a new approach [J].
Baron, JC .
BRAIN, 2001, 124 :2-4
[5]   PATHOPHYSIOLOGY OF ACUTE CEREBRAL-ISCHEMIA - PET STUDIES IN HUMANS [J].
BARON, JC .
CEREBROVASCULAR DISEASES, 1991, 1 :22-31
[6]   Intersubject variability and reproducibility of 15O PET studies [J].
Coles, JP ;
Fryer, TD ;
Bradley, PG ;
Nortje, J ;
Smielewski, P ;
Rice, K ;
Clark, JC ;
Pickard, JD ;
Menon, DK .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2006, 26 (01) :48-57
[7]   Defining ischemic burden after traumatic brain injury using 15O PET imaging if cerebral physiology [J].
Coles, JP ;
Fryer, TD ;
Smielewski, P ;
Rice, K ;
Clark, JC ;
Pickard, JD ;
Menon, DK .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2004, 24 (02) :191-201
[8]  
DEGRADO TR, 1994, J NUCL MED, V35, P1398
[9]   Diffusion-weighted imaging in acute stroke -: A tool of uncertain value? [J].
Fiehler, J ;
Fiebach, JB ;
Gass, A ;
Hoehn, M ;
Kucinski, T ;
Neumann-Haefelin, T ;
Schellinger, PD ;
Siebler, M ;
Villringer, A ;
Röther, J .
CEREBROVASCULAR DISEASES, 2002, 14 (3-4) :187-196
[10]   Severe ADC decreases do not predict irreversible tissue damage in humans [J].
Fiehler, J ;
Foth, M ;
Kucinski, T ;
Knab, R ;
von Bezold, M ;
Weiller, C ;
Zeumer, H ;
Röther, J .
STROKE, 2002, 33 (01) :79-86