Dynamic cerebral autoregulation in acute lacunar and middle cerebral artery territory ischemic stroke

被引:167
作者
Immink, RV
van Montfrans, GA
Stam, J
Karemaker, JM
Diamant, M
van Lieshout, JJ
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Internal Med, Medium Care Unit, NL-1100 DE Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Cardiovasc Res Inst Amsterdam, Amsterdam, Netherlands
[3] Univ Amsterdam, Acad Med Ctr, Dept Physiol, Amsterdam, Netherlands
[4] Univ Amsterdam, Acad Med Ctr, Dept Anesthesiol, Amsterdam, Netherlands
[5] Univ Amsterdam, Acad Med Ctr, Dept Neurol, Amsterdam, Netherlands
[6] Free Univ Amsterdam, Med Ctr, Dept Endocrinol, Ctr Diabet, Amsterdam, Netherlands
关键词
cerebral circulation; spectral analysis; ultrasonography;
D O I
10.1161/01.STR.0000189624.06836.03
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose - We addressed whether dynamic cerebral autoregulation (dCA) is affected in middle cerebral artery (MCA) territory (MCAS) and lacunar ischemic stroke (LS). Methods - Blood pressure (MAP) and MCA velocity (V) were measured in 10 patients with large MCAS (National Institutes of Health Stroke score, 17 +/- 2; mean +/- SEM), in 10 with LS (score, 9 +/- 1), and in 10 reference subjects. dCA was evaluated in time (delay of the MCA V-mean counter-regulation during changes in MAP) and frequency domains (cross-spectral MCA V-mean-to-MAP phase lead). Results - In reference subjects, latencies for MAP increments (5.3 +/- 0.5 seconds) and decrements (5.6 +/- 0.5 seconds) were comparable, and low frequency MCA V-mean-to-MAP phase lead was 56 +/- 5 and 59 +/- 5 degrees (left and right hemisphere). In MCAS, these latencies were 4.6 +/- 0.7 and 5.6 +/- 0.5 seconds in the nonischemic hemisphere and not detectable in the ischemic hemisphere. In the unaffected hemisphere, phase lead was 61 +/- 6 degrees versus 26 +/- 6 degrees on the ischemic side (P < 0.05). In LS, no latency and smaller phase lead bilaterally (32 +/- 6 and 33 +/- 5 degrees) conformed to globally impaired dCA. Conclusions - In large MCAS infarcts, dynamic cerebral autoregulation was impaired in the affected hemisphere. In LS, dynamic cerebral autoregulation was impaired bilaterally, a finding consistent with the hypothesis of bilateral small vessel disease in patients with lacunar infarcts.
引用
收藏
页码:2595 / 2600
页数:6
相关论文
共 25 条
[1]   AUTOREGULATION OF CEREBRAL BLOOD FLOW - STUDIES DURING DRUG-INDUCED HYPERTENSION IN NORMAL SUBJECTS AND IN PATIENTS WITH CEREBRAL VASCULAR DISEASES [J].
AGNOLI, A ;
FIESCHI, C ;
BOZZAO, L ;
BATTISTINI, N ;
PRENCIPE, M .
CIRCULATION, 1968, 38 (04) :800-+
[2]   Yield of transcranial Doppler in acute cerebral ischemia [J].
Alexandrov, AV ;
Demchuk, AM ;
Wein, TH ;
Grotta, JC .
STROKE, 1999, 30 (08) :1604-1609
[3]   Non-invasive pulsatile arterial pressure and stroke volume changes from the human finger [J].
Bogert, LWJ ;
van Lieshout, JJ .
EXPERIMENTAL PHYSIOLOGY, 2005, 90 (04) :437-446
[4]   Relationship of Xe-133 cerebral blood flow to middle cerebral arterial flow velocity in men at rest [J].
Clark, JM ;
Skolnick, BE ;
Gelfand, R ;
Farber, RE ;
Stierheim, M ;
Stevens, WC ;
Beck, G ;
Lambertsen, CJ .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1996, 16 (06) :1255-1262
[5]   Dynamic but not static cerebral autoregulation is impaired in acute ischaemic stroke [J].
Dawson, SL ;
Blake, MJ ;
Panerai, RB ;
Potter, JF .
CEREBROVASCULAR DISEASES, 2000, 10 (02) :126-132
[6]   Serial changes in static and dynamic cerebral autoregulation after acute ischaemic stroke [J].
Dawson, SL ;
Panerai, RB ;
Potter, JF .
CEREBROVASCULAR DISEASES, 2003, 16 (01) :69-75
[7]   PHASE RELATIONSHIP BETWEEN CEREBRAL BLOOD-FLOW VELOCITY AND BLOOD-PRESSURE - A CLINICAL-TEST OF AUTOREGULATION [J].
DIEHL, RR ;
LINDEN, D ;
LUCKE, D ;
BERLIT, P .
STROKE, 1995, 26 (10) :1801-1804
[8]  
Eames PJ, 2002, J NEUROL NEUROSUR PS, V72, P467
[9]   LACUNES - SMALL DEEP CEREBRAL INFARCTS [J].
FISHER, CM .
NEUROLOGY, 1965, 15 (08) :774-&
[10]   Testing the validity of the lacunar hypothesis: The northern Manhattan stroke study experience [J].
Gan, R ;
Sacco, RL ;
Kargman, DE ;
Roberts, JK ;
BodenAlbala, B ;
Gu, Q .
NEUROLOGY, 1997, 48 (05) :1204-1211