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Cortical cerebral blood flow in ageing: effects of haematocrit, sex, ethnicity and diabetes

OBJECTIVES: Cerebral blood flow (CBF) estimates from arterial spin labelling (ASL) show unexplained variability in older populations. We studied the impact of variation of haematocrit (Hct) on CBF estimates in a tri-ethnic elderly population. MATERIALS AND METHODS: Approval for the study was obtaine...

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Autores principales: Smith, Lorna A., Melbourne, Andrew, Owen, David, Cardoso, M. Jorge, Sudre, Carole H., Tillin, Therese, Sokolska, Magdalena, Atkinson, David, Chaturvedi, Nish, Ourselin, Sebastien, Hughes, Alun D., Barkhof, Frederik, Jäger, H. R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6719435/
https://www.ncbi.nlm.nih.gov/pubmed/30887200
http://dx.doi.org/10.1007/s00330-019-06096-w
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author Smith, Lorna A.
Melbourne, Andrew
Owen, David
Cardoso, M. Jorge
Sudre, Carole H.
Tillin, Therese
Sokolska, Magdalena
Atkinson, David
Chaturvedi, Nish
Ourselin, Sebastien
Hughes, Alun D.
Barkhof, Frederik
Jäger, H. R.
author_facet Smith, Lorna A.
Melbourne, Andrew
Owen, David
Cardoso, M. Jorge
Sudre, Carole H.
Tillin, Therese
Sokolska, Magdalena
Atkinson, David
Chaturvedi, Nish
Ourselin, Sebastien
Hughes, Alun D.
Barkhof, Frederik
Jäger, H. R.
author_sort Smith, Lorna A.
collection PubMed
description OBJECTIVES: Cerebral blood flow (CBF) estimates from arterial spin labelling (ASL) show unexplained variability in older populations. We studied the impact of variation of haematocrit (Hct) on CBF estimates in a tri-ethnic elderly population. MATERIALS AND METHODS: Approval for the study was obtained from the Fulham Research Ethics Committee and participants gave written informed consent. Pseudo-continuous arterial spin labelling was performed on 493 subjects (age 55–90) from a tri-ethnic community-based cohort recruited in London. CBF was estimated using a simplified Buxton equation, with and without correction for Hct measured from blood samples. Differences in perfusion were compared, stratified by sex, ethnicity and diabetes. Results of Student’s t tests were reported with effect size. RESULTS: Hct adjustment decreased CBF estimates in all categories except white European men. The decrease for women was 2.7 (3.0, 2.4) mL/100 g/min) (mean (95% confidence interval (CI)), p < 0.001 d = 0.38. The effect size differed by ethnicity with estimated mean perfusion in South Asian and African Caribbean women found to be lower by 3.0 (3.6, 2.5) mL/100 g/min, p < 0.001 d = 0.56 and 3.1 (3.6, 2.5) mL/100 g/min), p < 0.001 d = 0.48, respectively. Estimates of perfusion in subjects with diabetes decreased by 1.8 (2.3, 1.4) mL/100 g/min, p < 0.001 d = 0.23) following Hct correction. Correction for individual Hct altered sample frequency distributions of CBF values, especially in women of non-European ethnicity. CONCLUSION: ASL-derived CBF values in women, non-European ethnicities and individuals with diabetes are overestimated if calculations are not appropriately adjusted for individual Hct. KEY POINTS: • CBF quantification from ASL using a fixed Hct of 43.5%, as recommended in the ISMRM white paper, may lead to erroneous CBF estimations particularly in non-European and female subjects. • Individually measured Hct values improve the accuracy of CBF estimation and, if these are not available, an adjusted value according to gender, ethnicity or diabetes status should be considered. • Hct-corrected ASL could be potentially important for CBF threshold decision making in the fields of neurodegenerative disease and neuro-oncology. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00330-019-06096-w) contains supplementary material, which is available to authorized users.
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spelling pubmed-67194352019-09-19 Cortical cerebral blood flow in ageing: effects of haematocrit, sex, ethnicity and diabetes Smith, Lorna A. Melbourne, Andrew Owen, David Cardoso, M. Jorge Sudre, Carole H. Tillin, Therese Sokolska, Magdalena Atkinson, David Chaturvedi, Nish Ourselin, Sebastien Hughes, Alun D. Barkhof, Frederik Jäger, H. R. Eur Radiol Neuro OBJECTIVES: Cerebral blood flow (CBF) estimates from arterial spin labelling (ASL) show unexplained variability in older populations. We studied the impact of variation of haematocrit (Hct) on CBF estimates in a tri-ethnic elderly population. MATERIALS AND METHODS: Approval for the study was obtained from the Fulham Research Ethics Committee and participants gave written informed consent. Pseudo-continuous arterial spin labelling was performed on 493 subjects (age 55–90) from a tri-ethnic community-based cohort recruited in London. CBF was estimated using a simplified Buxton equation, with and without correction for Hct measured from blood samples. Differences in perfusion were compared, stratified by sex, ethnicity and diabetes. Results of Student’s t tests were reported with effect size. RESULTS: Hct adjustment decreased CBF estimates in all categories except white European men. The decrease for women was 2.7 (3.0, 2.4) mL/100 g/min) (mean (95% confidence interval (CI)), p < 0.001 d = 0.38. The effect size differed by ethnicity with estimated mean perfusion in South Asian and African Caribbean women found to be lower by 3.0 (3.6, 2.5) mL/100 g/min, p < 0.001 d = 0.56 and 3.1 (3.6, 2.5) mL/100 g/min), p < 0.001 d = 0.48, respectively. Estimates of perfusion in subjects with diabetes decreased by 1.8 (2.3, 1.4) mL/100 g/min, p < 0.001 d = 0.23) following Hct correction. Correction for individual Hct altered sample frequency distributions of CBF values, especially in women of non-European ethnicity. CONCLUSION: ASL-derived CBF values in women, non-European ethnicities and individuals with diabetes are overestimated if calculations are not appropriately adjusted for individual Hct. KEY POINTS: • CBF quantification from ASL using a fixed Hct of 43.5%, as recommended in the ISMRM white paper, may lead to erroneous CBF estimations particularly in non-European and female subjects. • Individually measured Hct values improve the accuracy of CBF estimation and, if these are not available, an adjusted value according to gender, ethnicity or diabetes status should be considered. • Hct-corrected ASL could be potentially important for CBF threshold decision making in the fields of neurodegenerative disease and neuro-oncology. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00330-019-06096-w) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2019-03-18 2019 /pmc/articles/PMC6719435/ /pubmed/30887200 http://dx.doi.org/10.1007/s00330-019-06096-w Text en © The Author(s) 2019 OpenAccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Neuro
Smith, Lorna A.
Melbourne, Andrew
Owen, David
Cardoso, M. Jorge
Sudre, Carole H.
Tillin, Therese
Sokolska, Magdalena
Atkinson, David
Chaturvedi, Nish
Ourselin, Sebastien
Hughes, Alun D.
Barkhof, Frederik
Jäger, H. R.
Cortical cerebral blood flow in ageing: effects of haematocrit, sex, ethnicity and diabetes
title Cortical cerebral blood flow in ageing: effects of haematocrit, sex, ethnicity and diabetes
title_full Cortical cerebral blood flow in ageing: effects of haematocrit, sex, ethnicity and diabetes
title_fullStr Cortical cerebral blood flow in ageing: effects of haematocrit, sex, ethnicity and diabetes
title_full_unstemmed Cortical cerebral blood flow in ageing: effects of haematocrit, sex, ethnicity and diabetes
title_short Cortical cerebral blood flow in ageing: effects of haematocrit, sex, ethnicity and diabetes
title_sort cortical cerebral blood flow in ageing: effects of haematocrit, sex, ethnicity and diabetes
topic Neuro
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6719435/
https://www.ncbi.nlm.nih.gov/pubmed/30887200
http://dx.doi.org/10.1007/s00330-019-06096-w
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