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Arterial Spin-Labeling Perfusion MR Imaging Demonstrates Regional CBF Decrease in Idiopathic Normal Pressure Hydrocephalus - AJNR News Digest
July-August 2018
ADULT BRAIN

Arterial Spin-Labeling Perfusion MR Imaging Demonstrates Regional CBF Decrease in Idiopathic Normal Pressure Hydrocephalus

Johan Virhammar

Epidemiologic studies indicate that idiopathic normal pressure hydrocephalus (iNPH) is a much more common disease in the elderly population than previously believed.1 Even though iNPH is increasingly recognized, the number of shunt implantations performed is far lower than the occurrence of the disease. For decades, reliable tests that can aid in the diagnosis of iNPH and predict outcome after shunt surgery have been sought. The most common tests used in the clinical work-up of patients with iNPH are invasive and time-consuming. With hopes of finding a reliable, noninvasive, and fast diagnostic and predictive test, our research group started investigating patients with iNPH using pseudocontinuous arterial spin-labeling (ASL) around 2013.

Previous perfusion studies in iNPH have reported reduced perfusion in the frontal cortex, periventricular white matter, basal ganglia, thalamus, and cerebellum in patients with iNPH.2–5 These studies used methods that require the administration of a radioactive tracer or a contrast agent, and often methods that expose the patient to ionizing radiation. Compared with these methods, ASL seems appealing, as the sequence is rapid, noninvasive, and without ionizing radiation.

In our study, we were able to replicate the findings of previous perfusion studies using pseudocontinuous ASL. Cerebral perfusion was decreased in the periventricular white matter, basal ganglia, and thalamus in patients with iNPH compared with age- and sex-matched healthy controls. However, even if there were significant differences at a group level, it is still uncertain

whether the differences are large enough in individual patients to aid in clinical routine.

Using ASL in elderly patients, who are not always able to lie still in the scanner and have a disease that causes extended arterial transit times, was a challenge, especially because of special interest in iNPH are the periventricular white matter regions, and the white matter perfusion signal can suffer from a low signal-to-noise ratio when using ASL. Despite these problems, test-retest data between 2 baseline scans were good in our study. In summary, we believe that ASL is an ideal method for perfusion studies in iNPH and, with further research, possibly will have a place in future clinical routine.

We will present longitudinal ASL perfusion data before and after shunt surgery at the ISHCSF Hydrocephalus meeting in Bologna, Italy in October of this year. Also, a new prospective study using ASL is underway at our center, with the goal of investigating perfusion changes after shunt surgery as well as volumetric changes of periventricular hyperintensities.

References

  1. Jaraj D, Rabiei K, Marlow T, et al. Prevalence of idiopathic normal-pressure hydrocephalusNeurology 2014;82:1449–54, 10.1212/WNL.0000000000000342.
  2. Owler BK, Momjian S, Czosnyka Z, et al. Normal pressure hydrocephalus and cerebral blood flow: a PET study of baseline valuesJ Cereb Blood Flow Metab 2004;24:17–23,10.1097/01.WCB.0000093326.88757.49.
  3. Sasaki H, Ishii K, Kono AK, et al. Cerebral perfusion pattern of idiopathic normal pressure hydrocephalus studied by SPECT and statistical brain mappingAnn Nucl Med 2007;21:39–45, 10.1007/BF03033998.
  4. Ziegelitz D, Starck G, Kristiansen D, et al. Cerebral perfusion measured by dynamic susceptibility contrast MRI is reduced in patients with idiopathic normal pressure hydrocephalusJ Magn Reson Imaging 2014;39:1533–42,10.1002/jmri.24292.
  5. Corkill RG, Garnett MR, Blamire AM, et al. Multi-modal MRI in normal pressure hydrocephalus identifies pre-operative haemodynamic and diffusion coefficient changes in normal appearing white matter correlating with surgical outcomeClin Neurol Neurosurg 2003;105:193-202, 10.1016/S0303-8467(03)00010-6.

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