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T2 quantitation of human articular cartilage in a clinical setting at 1.5 T: implementation and testing of four multiecho pulse sequence designs for validity.

作者信息

Mendlik Thomas, Faber Sonja Christine, Weber Jürgen, Hohe Jan, Rauch Elisabeth, Reiser Maximilian, Glaser Christian

机构信息

Department of Clinical Radiology, Ludwig-Maximilians-University of Munich, Grosshadern, Marchioninistrasse 15, D-81377 Munich, Germany.

出版信息

Invest Radiol. 2004 May;39(5):288-99. doi: 10.1097/01.rli.0000119196.50924.f3.

DOI:10.1097/01.rli.0000119196.50924.f3
PMID:15087723
Abstract

RATIONALE AND OBJECTIVES

Evaluation of the T2 relaxation time of articular cartilage holds great potential for quantitative assessment of internal changes of the cartilage matrix. The purpose of the present study was to assess the validity of multiecho-based cartilage T2 quantitation in a clinical MRI setting at 1.5 T.

METHODS

Four multisection multiecho sequence variants dedicated for quantitative T2 mapping of human articular cartilage were implemented on a 1.5 T whole-body imager and tested for accuracy in CuSO4-agarose gel phantoms and human patellar cartilage. Sequence design was varied to minimize errors in T2 quantitation due to stimulated echoes.

RESULTS

As compared with single spin-echo experiments, the apparent T2 values calculated from the multiecho sequence variants showed mean deviations ranging from +26% to -32% (phantoms) and from +42% to -18% (cartilage). The patellar cartilage T2 covered a range from about 25 milliseconds to 55 milliseconds, with longer T2 values observed in the more superficial layers. In cartilage, best results were obtained from the sequence design using improved section profiles and a spoiler gradient scheme for suppression of stimulated echoes.

CONCLUSIONS

Our results revealed a clear dependence of apparent T2 relaxation times on the pulse sequence design, emphasizing that the "true" T2 is hard to find. In addition, the effect on the apparent T2 values resulting from the specific modification of any sequence variant varied according to the respective tissue's properties. Therefore, the acquisition technique in conjunction with the specific tissue on which T2 mapping is performed need to be reported in detail and should kept consistent to allow large-scale comparisons and monitoring of treatment strategies, e.g., in osteoarthritis.

摘要

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