2018
DOI: 10.1371/journal.pone.0198250
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Rapid high resolution T1 mapping as a marker of brain development: Normative ranges in key regions of interest

Abstract: ObjectivesWe studied in a clinical setting the age dependent T1 relaxation time as a marker of normal late brain maturation and compared it to conventional techniques, namely the apparent diffusion coefficient (ADC).Materials and methodsForty-two healthy subjects ranging from ages 1 year to 20 years were included in our study. T1 brain maps in which the intensity of each pixel corresponded to T1 relaxation times were generated based on MR imaging data acquired using a MP2RAGE sequence. During the same session,… Show more

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Cited by 36 publications
(28 citation statements)
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“…Phase‐based T 2 maps were reconstructed as described in the theory section. T 1 of 915 ms was assumed (midpoint between the T 1 of white matter and the putamen at the age of 20) . The reference T 2 map was reconstructed using least square error fitting to a single‐exponential model.…”
Section: Methodsmentioning
confidence: 99%
“…Phase‐based T 2 maps were reconstructed as described in the theory section. T 1 of 915 ms was assumed (midpoint between the T 1 of white matter and the putamen at the age of 20) . The reference T 2 map was reconstructed using least square error fitting to a single‐exponential model.…”
Section: Methodsmentioning
confidence: 99%
“…Moreover, a comparison with the present data is precluded because no direct T1 values have been reported. Eminian et al [18] measured T1 relaxation times of gray and white matter in 42 children ages 1-20 years using MP2RAGE. Four regions matched those in our study: the nucleus caudatus, putamen, thalamus and frontal white matter.…”
Section: Discussionmentioning
confidence: 99%
“…overlap with pathologies such as inflammation and edema [5]. On the other hand, and despite these limitations, a diagnostic benefit of quantitative T1 mapping of the brain has been convincingly demonstrated for a number of conditions, including hepatic encephalopathy [6], multiple sclerosis [7][8][9], sickle cell anemia [10], epilepsy [11], heavy metal deposition [12], neurofibromatosis [13], brain tumor follow-up [14,15], infantile brain development [16][17][18] and aging [19]. The continuing desire for a viable quantitative MR sequence is also reflected in the multitude of recent faster mapping approaches, such as the MP2RAGE sequence [20], synthetic MRI [21] and MR fingerprinting [22].…”
Section: Introductionmentioning
confidence: 99%
“…The use of quantitative imaging such as T1 mapping in MRI could provide considerable understanding of changing normal and pathologic conditions. MRI has been used to evaluate the development of the human brain, and myelination plays a key role in brain maturation with microarchitectural changes [17]. The T1 relaxation time is affected by myelin, water and iron concentrations in brain tissue, so demyelination increases the T1 value and increased iron accumulation shortens the T1 value [18,19].…”
Section: Discussionmentioning
confidence: 99%