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Chemical Shift-Encoded MRI of Bone Metabolic Markers in Ankylosing Spondylitis
OBJECTIVE: To investigate the feasibility and correlation of sacroiliac joint (SIJ) fat fraction (FF) and R2(∗) as markers of bone metabolism in patients with ankylosing spondylitis (AS). METHODS: 75 AS patients were classified into an early active group (EA), late active group (LA), and inactive gr...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9584712/ https://www.ncbi.nlm.nih.gov/pubmed/36277974 http://dx.doi.org/10.1155/2022/1846667 |
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author | Ma, Li-ping Sheng, Cui-yun Qian, Long Zeng, Zhi-bin Li, Gen |
author_facet | Ma, Li-ping Sheng, Cui-yun Qian, Long Zeng, Zhi-bin Li, Gen |
author_sort | Ma, Li-ping |
collection | PubMed |
description | OBJECTIVE: To investigate the feasibility and correlation of sacroiliac joint (SIJ) fat fraction (FF) and R2(∗) as markers of bone metabolism in patients with ankylosing spondylitis (AS). METHODS: 75 AS patients were classified into an early active group (EA), late active group (LA), and inactive group (IA). Additionally, 54 matched healthy individuals were selected to be part of the normal control group (NC). All participants underwent chemical shift encoded based MRI (IDEAL-IQ) and routine clinical SIJ MRI at 3.0 T. FF and R2(∗) were measured in subchondral bone, bone marrow edema (BME), and fat metaplasia (FM). Out of the participants, 39 with BME lesions (15 from EA, 16 from LA, 8 from IA) and 39 with FM lesions (9 from EA, 17 from LA, 13 from IA) were included. Differences in FF, R2(∗) value for subchondral bone of all participants and for BME, FM lesions were evaluated. Subsequently, different stages of BME and FM in patient groups were compared, and the relationship between FF and R2(∗) was analyzed. RESULTS: A significant difference in FF was demonstrated among the BME, FM and the normal bone marrow (p < 0.001), meanwhile, the difference of R2(∗) value in FM was significantly lower (p = 0.034, 0.012) than that of BME and that of normal bone marrow. At lever of different lesions, only the FF for BME was significantly different among 3 patient groups (p = 0.001), while there was no significantly different FF for FM among 3 patient groups. Unlike in BME lesions, the FF in FM lesions had a negative correlation with R2(∗) (p < 0.001, r = −0.488). CONCLUSION: FF and R2(∗) measurements help to quantitatively analyze the bone marrow fat composition and bony trabecular microstructure changes in AS, providing a noninvasive and accurate assessment basis for AS bone metabolism abnormalities. |
format | Online Article Text |
id | pubmed-9584712 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-95847122022-10-21 Chemical Shift-Encoded MRI of Bone Metabolic Markers in Ankylosing Spondylitis Ma, Li-ping Sheng, Cui-yun Qian, Long Zeng, Zhi-bin Li, Gen Dis Markers Research Article OBJECTIVE: To investigate the feasibility and correlation of sacroiliac joint (SIJ) fat fraction (FF) and R2(∗) as markers of bone metabolism in patients with ankylosing spondylitis (AS). METHODS: 75 AS patients were classified into an early active group (EA), late active group (LA), and inactive group (IA). Additionally, 54 matched healthy individuals were selected to be part of the normal control group (NC). All participants underwent chemical shift encoded based MRI (IDEAL-IQ) and routine clinical SIJ MRI at 3.0 T. FF and R2(∗) were measured in subchondral bone, bone marrow edema (BME), and fat metaplasia (FM). Out of the participants, 39 with BME lesions (15 from EA, 16 from LA, 8 from IA) and 39 with FM lesions (9 from EA, 17 from LA, 13 from IA) were included. Differences in FF, R2(∗) value for subchondral bone of all participants and for BME, FM lesions were evaluated. Subsequently, different stages of BME and FM in patient groups were compared, and the relationship between FF and R2(∗) was analyzed. RESULTS: A significant difference in FF was demonstrated among the BME, FM and the normal bone marrow (p < 0.001), meanwhile, the difference of R2(∗) value in FM was significantly lower (p = 0.034, 0.012) than that of BME and that of normal bone marrow. At lever of different lesions, only the FF for BME was significantly different among 3 patient groups (p = 0.001), while there was no significantly different FF for FM among 3 patient groups. Unlike in BME lesions, the FF in FM lesions had a negative correlation with R2(∗) (p < 0.001, r = −0.488). CONCLUSION: FF and R2(∗) measurements help to quantitatively analyze the bone marrow fat composition and bony trabecular microstructure changes in AS, providing a noninvasive and accurate assessment basis for AS bone metabolism abnormalities. Hindawi 2022-10-13 /pmc/articles/PMC9584712/ /pubmed/36277974 http://dx.doi.org/10.1155/2022/1846667 Text en Copyright © 2022 Li-ping Ma et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Ma, Li-ping Sheng, Cui-yun Qian, Long Zeng, Zhi-bin Li, Gen Chemical Shift-Encoded MRI of Bone Metabolic Markers in Ankylosing Spondylitis |
title | Chemical Shift-Encoded MRI of Bone Metabolic Markers in Ankylosing Spondylitis |
title_full | Chemical Shift-Encoded MRI of Bone Metabolic Markers in Ankylosing Spondylitis |
title_fullStr | Chemical Shift-Encoded MRI of Bone Metabolic Markers in Ankylosing Spondylitis |
title_full_unstemmed | Chemical Shift-Encoded MRI of Bone Metabolic Markers in Ankylosing Spondylitis |
title_short | Chemical Shift-Encoded MRI of Bone Metabolic Markers in Ankylosing Spondylitis |
title_sort | chemical shift-encoded mri of bone metabolic markers in ankylosing spondylitis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9584712/ https://www.ncbi.nlm.nih.gov/pubmed/36277974 http://dx.doi.org/10.1155/2022/1846667 |
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