Premium
Simultaneous quantification of PCr, Cr, and pH in muscle CEST ‐ MRI
Author(s) -
Wang Yi,
Yan Caiwen,
Feng Xinhong,
Gao Nan,
Gao JiaHong,
Song Xiaolei
Publication year - 2025
Publication title -
magnetic resonance in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.696
H-Index - 225
eISSN - 1522-2594
pISSN - 0740-3194
DOI - 10.1002/mrm.30508
Subject(s) - in vivo , chemistry , skeletal muscle , imaging phantom , proton , analytical chemistry (journal) , nuclear magnetic resonance , chromatography , nuclear medicine , physics , anatomy , biology , medicine , microbiology and biotechnology , quantum mechanics
Abstract Purpose CEST‐MRI allows sensitive in vivo detection of PCr and Cr in muscle. However, the accurate quantification is difficult due to overlapped “peaks” from multiple solutes and mixed contributions from fractional concentration (f b $$ {f}_{\mathrm{b}} $$ ) and exchange rate (k b $$ {k}_{\mathrm{b}} $$ ). This study aims to achieve simultaneous and accurate mapping of PCr, Cr, and pH in muscle. Methods A two‐step quantification method was proposed, by considering the co‐existence of PCr and Cr in muscle and their dynamic transition. Firstly, exchangeable protons resonating at +2.6 ppm (PCr 2.6 $$ {\mathrm{PCr}}_{2.6} $$ ) were quantified using our previous gQUCESOP. In the second gQUCESOP for resolving parameters at +1.9 ppm, we included both Cr's and another exchangeable guanidino proton of PCr resonating at +1.9 ppm (PCr 1.9 $$ {\mathrm{PCr}}_{1.9} $$ ), withf b $$ {f}_{\mathrm{b}} $$ andk b $$ {k}_{\mathrm{b}} $$ forPCr 1.9 $$ {\mathrm{PCr}}_{1.9} $$ estimated fromPCr 2.6 $$ {\mathrm{PCr}}_{2.6} $$ estimation in the first step. The method was validated by simulation and phantom study. In vivo rat experiments were performed at 9.4T, with pH measured also by 31 P‐MRS. Results Simulation suggested an over‐estimatedf b $$ {f}_{\mathrm{b}} $$ and an under‐estimatedk b $$ {k}_{\mathrm{b}} $$ of Cr if including a non‐neglectable content of PCr. For a phantom with mixed PCr and Cr, the proposed method allowed accurate calculation of both concentrations and pH. For in vivo rat scans performed before and right after euthanasia, our methods achieved coincidedf b $$ {f}_{\mathrm{b}} $$ andk b $$ {k}_{\mathrm{b}} $$ with literatures. Furthermore, the pH values from 31 P‐MRS,k b $$ {k}_{\mathrm{b}} $$ ofPCr 2.6 $$ {\mathrm{PCr}}_{2.6} $$ , andk b $$ {k}_{\mathrm{b}} $$ of Cr could verify each other. Conclusion The proposed method is promising for quantifying thef b $$ {f}_{\mathrm{b}} $$ andk b $$ {k}_{\mathrm{b}} $$ for both PCr and Cr in skeletal muscular tissue.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom