White Matter Hyperintensities Quantification in Healthy Adults: A Systematic Review and Meta‐Analysis
Background Although white matter hyperintensities (WMH) volumetric assessment is now customary in research studies, inconsistent WMH measures among homogenous populations may prevent the clinical usability of this biomarker. Purpose To determine whether a point estimate and reference standard for WM...
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Published in: | Journal of magnetic resonance imaging Vol. 53; no. 6; pp. 1732 - 1743 |
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Hoboken, USA
John Wiley & Sons, Inc
01-06-2021
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Abstract | Background
Although white matter hyperintensities (WMH) volumetric assessment is now customary in research studies, inconsistent WMH measures among homogenous populations may prevent the clinical usability of this biomarker.
Purpose
To determine whether a point estimate and reference standard for WMH volume in the healthy aging population could be determined.
Study Type
Systematic review and meta‐analysis.
Population
In all, 9716 adult subjects from 38 studies reporting WMH volume were retrieved following a systematic search on EMBASE.
Field Strength/Sequence
1.0T, 1.5T, or 3.0T/fluid‐attenuated inversion recovery (FLAIR) and/or proton density/T2‐weighted fast spin echo sequences or gradient echo T1‐weighted sequences.
Assessment
After a literature search, sample size, demographics, magnetic field strength, MRI sequences, level of automation in WMH assessment, study population, and WMH volume were extracted.
Statistical Tests
The pooled WMH volume with 95% confidence interval (CI) was calculated using the random‐effect model. The I2 statistic was calculated as a measure of heterogeneity across studies. Meta‐regression analysis of WMH volume on age was performed.
Results
Of the 38 studies analyzed, 17 reported WMH volume as the mean and standard deviation (SD) and were included in the meta‐analysis. Mean and SD of age was 66.11 ± 10.92 years (percentage of men 50.45% ± 21.48%). Heterogeneity was very high (I2 = 99%). The pooled WMH volume was 4.70 cm3 (95% CI: 3.88–5.53 cm3). At meta‐regression analysis, WMH volume was positively associated with subjects' age (β = 0.358 cm3 per year, P < 0.05, R2 = 0.27).
Data Conclusion
The lack of standardization in the definition of WMH together with the high technical variability in assessment may explain a large component of the observed heterogeneity. Currently, volumes of WMH in healthy subjects are not comparable between studies and an estimate and reference interval could not be determined.
Level of Evidence
1
Technical Efficacy Stage
1 |
---|---|
AbstractList | Although white matter hyperintensities (WMH) volumetric assessment is now customary in research studies, inconsistent WMH measures among homogenous populations may prevent the clinical usability of this biomarker.
To determine whether a point estimate and reference standard for WMH volume in the healthy aging population could be determined.
Systematic review and meta-analysis.
In all, 9716 adult subjects from 38 studies reporting WMH volume were retrieved following a systematic search on EMBASE.
1.0T, 1.5T, or 3.0T/fluid-attenuated inversion recovery (FLAIR) and/or proton density/T
-weighted fast spin echo sequences or gradient echo T
-weighted sequences.
After a literature search, sample size, demographics, magnetic field strength, MRI sequences, level of automation in WMH assessment, study population, and WMH volume were extracted.
The pooled WMH volume with 95% confidence interval (CI) was calculated using the random-effect model. The I
statistic was calculated as a measure of heterogeneity across studies. Meta-regression analysis of WMH volume on age was performed.
Of the 38 studies analyzed, 17 reported WMH volume as the mean and standard deviation (SD) and were included in the meta-analysis. Mean and SD of age was 66.11 ± 10.92 years (percentage of men 50.45% ± 21.48%). Heterogeneity was very high (I
= 99%). The pooled WMH volume was 4.70 cm
(95% CI: 3.88-5.53 cm
). At meta-regression analysis, WMH volume was positively associated with subjects' age (β = 0.358 cm
per year, P < 0.05, R
= 0.27).
The lack of standardization in the definition of WMH together with the high technical variability in assessment may explain a large component of the observed heterogeneity. Currently, volumes of WMH in healthy subjects are not comparable between studies and an estimate and reference interval could not be determined.
1 TECHNICAL EFFICACY STAGE: 1. BackgroundAlthough white matter hyperintensities (WMH) volumetric assessment is now customary in research studies, inconsistent WMH measures among homogenous populations may prevent the clinical usability of this biomarker.PurposeTo determine whether a point estimate and reference standard for WMH volume in the healthy aging population could be determined.Study TypeSystematic review and meta‐analysis.PopulationIn all, 9716 adult subjects from 38 studies reporting WMH volume were retrieved following a systematic search on EMBASE.Field Strength/Sequence1.0T, 1.5T, or 3.0T/fluid‐attenuated inversion recovery (FLAIR) and/or proton density/T2‐weighted fast spin echo sequences or gradient echo T1‐weighted sequences.AssessmentAfter a literature search, sample size, demographics, magnetic field strength, MRI sequences, level of automation in WMH assessment, study population, and WMH volume were extracted.Statistical TestsThe pooled WMH volume with 95% confidence interval (CI) was calculated using the random‐effect model. The I2 statistic was calculated as a measure of heterogeneity across studies. Meta‐regression analysis of WMH volume on age was performed.ResultsOf the 38 studies analyzed, 17 reported WMH volume as the mean and standard deviation (SD) and were included in the meta‐analysis. Mean and SD of age was 66.11 ± 10.92 years (percentage of men 50.45% ± 21.48%). Heterogeneity was very high (I2 = 99%). The pooled WMH volume was 4.70 cm3 (95% CI: 3.88–5.53 cm3). At meta‐regression analysis, WMH volume was positively associated with subjects' age (β = 0.358 cm3 per year, P < 0.05, R2 = 0.27).Data ConclusionThe lack of standardization in the definition of WMH together with the high technical variability in assessment may explain a large component of the observed heterogeneity. Currently, volumes of WMH in healthy subjects are not comparable between studies and an estimate and reference interval could not be determined.Level of Evidence1Technical Efficacy Stage1 Background Although white matter hyperintensities (WMH) volumetric assessment is now customary in research studies, inconsistent WMH measures among homogenous populations may prevent the clinical usability of this biomarker. Purpose To determine whether a point estimate and reference standard for WMH volume in the healthy aging population could be determined. Study Type Systematic review and meta‐analysis. Population In all, 9716 adult subjects from 38 studies reporting WMH volume were retrieved following a systematic search on EMBASE. Field Strength/Sequence 1.0T, 1.5T, or 3.0T/fluid‐attenuated inversion recovery (FLAIR) and/or proton density/T2‐weighted fast spin echo sequences or gradient echo T1‐weighted sequences. Assessment After a literature search, sample size, demographics, magnetic field strength, MRI sequences, level of automation in WMH assessment, study population, and WMH volume were extracted. Statistical Tests The pooled WMH volume with 95% confidence interval (CI) was calculated using the random‐effect model. The I2 statistic was calculated as a measure of heterogeneity across studies. Meta‐regression analysis of WMH volume on age was performed. Results Of the 38 studies analyzed, 17 reported WMH volume as the mean and standard deviation (SD) and were included in the meta‐analysis. Mean and SD of age was 66.11 ± 10.92 years (percentage of men 50.45% ± 21.48%). Heterogeneity was very high (I2 = 99%). The pooled WMH volume was 4.70 cm3 (95% CI: 3.88–5.53 cm3). At meta‐regression analysis, WMH volume was positively associated with subjects' age (β = 0.358 cm3 per year, P < 0.05, R2 = 0.27). Data Conclusion The lack of standardization in the definition of WMH together with the high technical variability in assessment may explain a large component of the observed heterogeneity. Currently, volumes of WMH in healthy subjects are not comparable between studies and an estimate and reference interval could not be determined. Level of Evidence 1 Technical Efficacy Stage 1 BACKGROUNDAlthough white matter hyperintensities (WMH) volumetric assessment is now customary in research studies, inconsistent WMH measures among homogenous populations may prevent the clinical usability of this biomarker. PURPOSETo determine whether a point estimate and reference standard for WMH volume in the healthy aging population could be determined. STUDY TYPESystematic review and meta-analysis. POPULATIONIn all, 9716 adult subjects from 38 studies reporting WMH volume were retrieved following a systematic search on EMBASE. FIELD STRENGTH/SEQUENCE1.0T, 1.5T, or 3.0T/fluid-attenuated inversion recovery (FLAIR) and/or proton density/T2 -weighted fast spin echo sequences or gradient echo T1 -weighted sequences. ASSESSMENTAfter a literature search, sample size, demographics, magnetic field strength, MRI sequences, level of automation in WMH assessment, study population, and WMH volume were extracted. STATISTICAL TESTSThe pooled WMH volume with 95% confidence interval (CI) was calculated using the random-effect model. The I2 statistic was calculated as a measure of heterogeneity across studies. Meta-regression analysis of WMH volume on age was performed. RESULTSOf the 38 studies analyzed, 17 reported WMH volume as the mean and standard deviation (SD) and were included in the meta-analysis. Mean and SD of age was 66.11 ± 10.92 years (percentage of men 50.45% ± 21.48%). Heterogeneity was very high (I2 = 99%). The pooled WMH volume was 4.70 cm3 (95% CI: 3.88-5.53 cm3 ). At meta-regression analysis, WMH volume was positively associated with subjects' age (β = 0.358 cm3 per year, P < 0.05, R2 = 0.27). DATA CONCLUSIONThe lack of standardization in the definition of WMH together with the high technical variability in assessment may explain a large component of the observed heterogeneity. Currently, volumes of WMH in healthy subjects are not comparable between studies and an estimate and reference interval could not be determined. LEVEL OF EVIDENCE1 TECHNICAL EFFICACY STAGE: 1. |
Author | Di Leo, Giovanni Griffanti, Ludovica Melazzini, Luca Vitali, Paolo Zanardo, Moreno Olivieri, Emanuele Codari, Marina Savoldi, Filippo Sardanelli, Francesco Baselli, Giuseppe Bolchini, Marco |
Author_xml | – sequence: 1 givenname: Luca orcidid: 0000-0002-2287-2163 surname: Melazzini fullname: Melazzini, Luca organization: Università degli Studi di Milano – sequence: 2 givenname: Paolo surname: Vitali fullname: Vitali, Paolo organization: IRCCS Policlinico San Donato – sequence: 3 givenname: Emanuele surname: Olivieri fullname: Olivieri, Emanuele organization: Università degli Studi di Milano – sequence: 4 givenname: Marco surname: Bolchini fullname: Bolchini, Marco organization: Università degli Studi di Brescia – sequence: 5 givenname: Moreno surname: Zanardo fullname: Zanardo, Moreno organization: IRCCS Policlinico San Donato – sequence: 6 givenname: Filippo surname: Savoldi fullname: Savoldi, Filippo organization: Università degli Studi di Milano – sequence: 7 givenname: Giovanni surname: Di Leo fullname: Di Leo, Giovanni organization: IRCCS Policlinico San Donato – sequence: 8 givenname: Ludovica surname: Griffanti fullname: Griffanti, Ludovica organization: University of Oxford – sequence: 9 givenname: Giuseppe surname: Baselli fullname: Baselli, Giuseppe organization: Politecnico di Milano – sequence: 10 givenname: Francesco surname: Sardanelli fullname: Sardanelli, Francesco email: francesco.sardanelli@unimi.it organization: IRCCS Policlinico San Donato – sequence: 11 givenname: Marina surname: Codari fullname: Codari, Marina organization: Stanford University School of Medicine |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/33345393$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_6009_jjrt_2023_1359 crossref_primary_10_1007_s11682_022_00629_6 crossref_primary_10_3389_fnagi_2023_1096808 crossref_primary_10_3389_fnhum_2023_1068216 crossref_primary_10_1097_WAD_0000000000000620 crossref_primary_10_3389_fnagi_2023_1165324 crossref_primary_10_1007_s11357_024_01238_5 crossref_primary_10_3389_fpsyt_2023_1149663 crossref_primary_10_2147_CIA_S438782 crossref_primary_10_18632_aging_203843 crossref_primary_10_1093_braincomms_fcae077 crossref_primary_10_21307_ane_2021_029 crossref_primary_10_3389_fneur_2022_843260 crossref_primary_10_1093_sleep_zsae030 |
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Keywords | image processing small vessel disease segmentation white matter hyperintensities |
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Snippet | Background
Although white matter hyperintensities (WMH) volumetric assessment is now customary in research studies, inconsistent WMH measures among homogenous... Although white matter hyperintensities (WMH) volumetric assessment is now customary in research studies, inconsistent WMH measures among homogenous populations... BackgroundAlthough white matter hyperintensities (WMH) volumetric assessment is now customary in research studies, inconsistent WMH measures among homogenous... BACKGROUNDAlthough white matter hyperintensities (WMH) volumetric assessment is now customary in research studies, inconsistent WMH measures among homogenous... |
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SubjectTerms | Age Aging Automation Biomarkers Confidence intervals Demographics Demography Field strength Heterogeneity image processing Magnetic fields Magnetic resonance imaging Mean Meta-analysis Population (statistical) Population studies Proton density (concentration) Regression analysis segmentation small vessel disease Standardization Statistical analysis Statistical tests Substantia alba Systematic review white matter hyperintensities |
Title | White Matter Hyperintensities Quantification in Healthy Adults: A Systematic Review and Meta‐Analysis |
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