Repeatability analysis of ADC histogram metrics of the uterus.


Journal

Acta radiologica (Stockholm, Sweden : 1987)
ISSN: 1600-0455
Titre abrégé: Acta Radiol
Pays: England
ID NLM: 8706123

Informations de publication

Date de publication:
Apr 2019
Historique:
pubmed: 4 7 2018
medline: 9 4 2019
entrez: 4 7 2018
Statut: ppublish

Résumé

Recently, histogram analysis based on voxel-wise apparent diffusion coefficient (ADC) value distribution has been increasingly performed. However, few studies have been reported regarding its repeatability. To evaluate the repeatability of ADC histogram metrics of the uterus in clinical magnetic resonance imaging (MRI). Thirty-three female patients who underwent pelvic MRI including diffusion-weighted imaging (DWI) were prospectively included after providing informed consent. Two sequential DWI acquisitions with identical parameters and position were obtained. Regions of interest (ROIs) for histologically confirmed uterine lesions (five cervical and three endometrial cancers, and one endometrial hyperplasia) and normal appearing tissues (21 endometrium and 33 myometrium) were assigned on the first DWI dataset and then pasted onto the second DWI dataset. ADC histogram metrics within the ROIs were calculated and repeatability was evaluated by calculating within-subject coefficient of variance (%) (wCV (%)) and Bland-Altman plot (%). ADC 10%, 25%, median, 75%, 90%, maximum, mean, and entropy showed high repeatability (wCV (%) < 7, 95% limit of agreement in Bland-Altman plot (%) < ±20), followed by ADC minimum (wCV (%) = 8.12, 95% limit of agreement in Bland-Altman plot (%) < ±30). However, ADC skewness and kurtosis showed very low repeatability in all evaluations. ADC histogram metrics like ADC 10%, 25%, median, 75%, 90%, maximum, mean, and entropy are robust biomarkers and could be applicable to clinical use. However, ADC skewness and kurtosis lack robustness. Radiologists should keep these characteristics and limitations in mind when interpreting quantitative DWI.

Sections du résumé

BACKGROUND BACKGROUND
Recently, histogram analysis based on voxel-wise apparent diffusion coefficient (ADC) value distribution has been increasingly performed. However, few studies have been reported regarding its repeatability.
PURPOSE OBJECTIVE
To evaluate the repeatability of ADC histogram metrics of the uterus in clinical magnetic resonance imaging (MRI).
MATERIAL AND METHODS METHODS
Thirty-three female patients who underwent pelvic MRI including diffusion-weighted imaging (DWI) were prospectively included after providing informed consent. Two sequential DWI acquisitions with identical parameters and position were obtained. Regions of interest (ROIs) for histologically confirmed uterine lesions (five cervical and three endometrial cancers, and one endometrial hyperplasia) and normal appearing tissues (21 endometrium and 33 myometrium) were assigned on the first DWI dataset and then pasted onto the second DWI dataset. ADC histogram metrics within the ROIs were calculated and repeatability was evaluated by calculating within-subject coefficient of variance (%) (wCV (%)) and Bland-Altman plot (%).
RESULTS RESULTS
ADC 10%, 25%, median, 75%, 90%, maximum, mean, and entropy showed high repeatability (wCV (%) < 7, 95% limit of agreement in Bland-Altman plot (%) < ±20), followed by ADC minimum (wCV (%) = 8.12, 95% limit of agreement in Bland-Altman plot (%) < ±30). However, ADC skewness and kurtosis showed very low repeatability in all evaluations.
CONCLUSION CONCLUSIONS
ADC histogram metrics like ADC 10%, 25%, median, 75%, 90%, maximum, mean, and entropy are robust biomarkers and could be applicable to clinical use. However, ADC skewness and kurtosis lack robustness. Radiologists should keep these characteristics and limitations in mind when interpreting quantitative DWI.

Identifiants

pubmed: 29969050
doi: 10.1177/0284185118786062
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

526-534

Auteurs

Koichi Onodera (K)

1 Department of Diagnostic Radiology, Sapporo Medical University, Sapporo, Japan.

Masamitsu Hatakenaka (M)

1 Department of Diagnostic Radiology, Sapporo Medical University, Sapporo, Japan.

Naoya Yama (N)

1 Department of Diagnostic Radiology, Sapporo Medical University, Sapporo, Japan.

Maki Onodera (M)

1 Department of Diagnostic Radiology, Sapporo Medical University, Sapporo, Japan.

Tsuyoshi Saito (T)

2 Department of Obstetrics and Gynecology, Sapporo Medical University, Sapporo, Japan.

Thomas Christian Kwee (TC)

3 Department of Radiology, Nuclear Medicine and Molecular Imaging, University Medical Center Groningen, Groningen, The Netherlands.

Taro Takahara (T)

4 Department of Biomedical Engineering, School of Engineering, Tokai University, Hiratsuka, Japan.

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