Abstract
Diffusion-weighted imaging lesions in intracerebral hemorrhage are related to a higher risk of recurrent intracerebral hemorrhage, cognitive damage, and mortality. However, it has been reported that the relationship between the risk of diffusion-weighted imaging lesions and intracerebral hemorrhage subtype or the possible risk factors for diffusion-weighted imaging lesions is variable. This meta-analysis was performed to evaluate this relationship. A systematic literature search up-to August 2020 was performed and 12 studies included 2815 subjects at the baseline with intracerebral hemorrhage. Odds ratio (OR) or mean difference (MD) with 95% confidence intervals (CIs) was calculated to evaluate the prognostic role of diffusion-weighted imaging lesions and intracerebral hemorrhage subtype and investigated the possible risk factors for diffusion-weighted imaging lesions using the dichotomous and continuous methods with a random or fixed-effect model. Lobar intracerebral hemorrhage was not significantly related to a higher rate of diffusion-weighted imaging lesions (OR, 1.01; 95% CI, 0.75–1.36, p = 0.94) compared to the non-lobar intracerebral hemorrhage. Also, history of diabetes mellitus (OR, 1.15; 95% CI, 0.83–1.60, p = 0.39); history of smoking (OR, 0.95; 95% CI, 0.68–1.33, p = 0.76); history of hypercholesterolemia (OR, 1.04; 95% CI, 0.73–1.48, p = 0.83); and history of ischemic stroke (OR, 1.63; 95% CI, 0.57–4.66, p = 0.36) were not significantly related to higher rate of diffusion-weighted imaging lesions compared to no history of those factors. However, the history of hypertension was significantly related to a higher rate of diffusion-weighted imaging lesions (OR, 1.33; 95% CI, 1.04–1.70, p = 0.02) compared to no history of hypertension. Also, Subjects with diffusion-weighted imaging lesions had a greater decrease in systolic pressure in the acute phase of the intracerebral hemorrhage (MD, 10.23; 95% CI, 7.41–13.06, p < 0.001) compared to without diffusion-weighted imaging lesions. Based on this meta-analysis, the history of hypertension may have an independent risk relationship with a higher rate of diffusion-weighted imaging lesions. Also, subjects with diffusion-weighted imaging lesions had a greater decrease in systolic pressure in the acute phase of the intracerebral hemorrhage compared to those without diffusion-weighted imaging lesions. This relationship forces us to recommend that identification of diffusion-weighted imaging lesions might add appreciated evidence to evaluate the progression of the underlying micro-angiopathy especially in subjects with a history of hypertension. Though further studies are needed to define the mechanisms by which these lesions may lead to cognitive damage and stroke reappearance.
Similar content being viewed by others
Data availability
The datasets analyzed during the current study are available from the corresponding author on reasonable request.
References
Kimberly W et al (2009) Silent ischemic infarcts are associated with hemorrhage burden in cerebral amyloid angiopathy. Neurology 72(14):1230–1235
van Veluw SJ et al (2017) Evolution of DWI lesions in cerebral amyloid angiopathy: evidence for ischemia. Neurology 89(21):2136–2142
Auriel E et al (2014) Microinfarct disruption of white matter structure: a longitudinal diffusion tensor analysis. Neurology 83(2):182–188
Feigin VL et al (2009) Worldwide stroke incidence and early case fatality reported in 56 population-based studies: a systematic review. Lancet Neurol 8(4):355–369
Counsell C et al (1995) Primary intracerebral haemorrhage in the Oxfordshire community stroke project. Cerebrovasc Dis 5(1):26–34
Flaherty M et al (2006) Long-term mortality after intracerebral hemorrhage. Neurology 66(8):1182–1186
Prabhakaran S et al (2010) Acute brain infarcts after spontaneous intracerebral hemorrhage: a diffusion-weighted imaging study. Stroke 41(1):89–94
Anderson CS et al (2008) Intensive blood pressure reduction in acute cerebral haemorrhage trial (INTERACT): a randomised pilot trial. Lancet Neurol 7(5):391–399
Diringer MN et al (2010) Thromboembolic events with recombinant activated factor VII in spontaneous intracerebral hemorrhage: results from the Factor Seven for Acute Hemorrhagic Stroke (FAST) trial. Stroke 41(1):48–53
Kumar MA et al (2009) Anemia and hematoma volume in acute intracerebral hemorrhage. Critical care medicine 37(4):1442–1447
Sheth KN et al (2011) Packed red blood cell transfusion and decreased mortality in intracerebral hemorrhage. Neurosurgery 68(5):1286–1292
Naidech AM et al (2007) Higher hemoglobin is associated with improved outcome after subarachnoid hemorrhage. Crit Care Med 35(10):2383–2389
Stroup DF et al (2000) Meta-analysis of observational studies in epidemiology: a proposal for reporting. Jama 283(15):2008–2012
Gupta A et al (2018) Obesity is independently associated with increased risk of hepatocellular cancer–related mortality. Am J Clin Oncol 41(9):874–881
Hayden JA et al (2013) Assessing bias in studies of prognostic factors. Ann Intern Med 158(4):280–286
Higgins JP et al (2003) Measuring inconsistency in meta-analyses. Bmj 327(7414):557–560
Tsai Y-H et al (2014) Fate of diffusion restricted lesions in acute intracerebral hemorrhage. PLoS One 9(8):e105970
Xu Xh et al (2019) Association between remote diffusion-weighted imaging lesions and cerebral small vessel disease in primary intracerebral hemorrhage. Eur J Neurol 26(7):961–968
Gregoire SM et al (2011) Acute ischaemic brain lesions in intracerebral haemorrhage: multicentre cross-sectional magnetic resonance imaging study. Brain 134(8):2376–2386
Auriel E et al (2012) Characteristic distributions of intracerebral hemorrhage–associated diffusion-weighted lesions. Neurology 79(24):2335–2341
Arsava EM et al (2013) Elevated admission blood pressure and acute ischemic lesions in spontaneous intracerebral hemorrhage. J Stroke Cerebrovasc Dis 22(3):250–254
Wu B et al (2015) Enlarged perivascular spaces and small diffusion-weighted lesions in intracerebral hemorrhage. Neurology 85(23):2045–2052
Menon RS et al (2012) Predictors of highly prevalent brain ischemia in intracerebral hemorrhage. Ann Neurol 71(2):199–205
Kidwell CS et al (2017) Ischemic lesions, blood pressure dysregulation, and poor outcomes in intracerebral hemorrhage. Neurology 88(8):782–788
Kang D-W et al (2012) New ischemic lesions coexisting with acute intracerebral hemorrhage. Neurology 79(9):848–855
Gioia LC et al (2015) Ischemia in intracerebral hemorrhage is associated with leukoaraiosis and hematoma volume, not blood pressure reduction. Stroke 46(6):1541–1547
Garg RK et al (2012) Blood pressure reduction, decreased diffusion on MRI, and outcomes after intracerebral hemorrhage. Stroke 43(1):67–71
Terborg C et al (2000) Reduced vasomotor reactivity in cerebral microangiopathy: a study with near-infrared spectroscopy and transcranial Doppler sonography. Stroke 31(4):924–929
Ali AMA, Abdelrahim MEA (2014) Modeling and optimization of terbutaline emitted from a dry powder inhaler and influence on systemic bioavailability using data mining technology. J Pharm Innov 9(1):38–47
Abdelrahim ME, Assi KH, Chrystyn H (2011) Relative bioavailability of terbutaline to the lung following inhalation, using urinary excretion. Br J Clin Pharmacol 71(4):608–610
Abdelrahim M, Assi KH, Chrystyn H (2013) Dose emission and aerodynamic characterization of the terbutaline sulphate dose emitted from a Turbuhaler at low inhalation flow. Pharm Dev Technol 18(4):944–949
De Reuck J et al (2011) The impact of cerebral amyloid angiopathy on the occurrence of cerebrovascular lesions in demented patients with Alzheimer features: a neuropathological study. Eur J Neurol 18(6):913–918
Viswanathan A et al (2006) Cortical neuronal apoptosis in CADASIL. Stroke 37(11):2690–2695
Smith EE et al (2012) Cerebral microinfarcts: the invisible lesions. Lancet Neurol 11(3):272–282
Auriel E et al (2015) Estimating total cerebral microinfarct burden from diffusion-weighted imaging. Stroke 46(8):2129–2135
Manno EM et al (2005) Emerging medical and surgical management strategies in the evaluation and treatment of intracerebral hemorrhage. In: Mayo clinic proceedings. Elsevier, Amsterdam
Fredriksson K, Norrving B, Strömblad L (1992) Emergency reversal of anticoagulation after intracerebral hemorrhage. Stroke 23(7):972–977
Levy JH et al (2010) Multidisciplinary approach to the challenge of hemostasis. Anesthesia Analgesia 110(2):354–364
Acknowledgements
Not applicable.
Funding
There was no external funding for this study itself. All authors had full access to all of the data in this study and take complete responsibility for the integrity of the data and accuracy of the data analysis.
Author information
Authors and Affiliations
Contributions
Conception and design: ML. Administrative support: All authors. Provision of study materials or subjects: All authors. Collection and assembly of data: XL, BZ. Data analysis and interpretation: All authors. Manuscript writing: All authors. Final approval of manuscript: All authors. All authors have read and approved the manuscript.
Corresponding author
Ethics declarations
Conflict of interest
Xiang Li declares that he has no conflict of interest. Bei Zhang declares that he/she has no conflict of interest, Mingwu Lou declares that he/she has no conflict of interest.
Additional information
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
About this article
Cite this article
Li, X., Zhang, B. & Lou, M. The relation between acute intracerebral hemorrhage and diffusion-weighted imaging lesions: a meta-analysis. J Thromb Thrombolysis 52, 962–970 (2021). https://doi.org/10.1007/s11239-021-02430-6
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11239-021-02430-6