Evidence map›Paper›PMID 41059391›Full record

ArticleRadiology advances2024

Deep learning-based liver cyst segmentation in MRI for autosomal dominant polycystic kidney disease.

Mina Chookhachizadeh Moghadam, Mohit Aspal, Xinzi He, Dominick J Romano, Arman Sharbatdaran, Zhongxiu Hu, Kurt Teichman, Hui Yi Ng He, Usama Sattar, Chenglin Zhu and 8 more

Abstract read
In one paragraph

Article in Radiology advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors.

Mina Chookhachizadeh MoghadamDepartment of Radiology, Weill Cornell Medicine, New York, NY 10065, United States.
Mohit AspalDepartment of Radiology, Weill Cornell Medicine, New York, NY 10065, United States.
Xinzi HeDepartment of Radiology, Weill Cornell Medicine, New York, NY 10065, United States.
Dominick J RomanoDepartment of Radiology, Weill Cornell Medicine, New York, NY 10065, United States.ORCID https://orcid.org/0000-0002-8691-406X
Arman SharbatdaranDepartment of Radiology, Weill Cornell Medicine, New York, NY 10065, United States.
Zhongxiu HuDepartment of Radiology, Weill Cornell Medicine, New York, NY 10065, United States.
Kurt TeichmanDepartment of Radiology, Weill Cornell Medicine, New York, NY 10065, United States.ORCID https://orcid.org/0000-0002-5122-7067
Hui Yi Ng HeDepartment of Radiology, Weill Cornell Medicine, New York, NY 10065, United States.
Usama SattarDepartment of Radiology, Weill Cornell Medicine, New York, NY 10065, United States.
Chenglin ZhuDepartment of Radiology, Weill Cornell Medicine, New York, NY 10065, United States.
Hreedi DevDepartment of Radiology, Weill Cornell Medicine, New York, NY 10065, United States.
Daniil ShimonovThe Rogosin Institute, New York, NY 10021, United States.
James M ChevalierThe Rogosin Institute, New York, NY 10021, United States.
Akshay GoelDepartment of Radiology, Weill Cornell Medicine, New York, NY 10065, United States.
George ShihDepartment of Radiology, Weill Cornell Medicine, New York, NY 10065, United States.
Jon D BlumenfeldThe Rogosin Institute, New York, NY 10021, United States.
Mert R SabuncuDepartment of Radiology, Weill Cornell Medicine, New York, NY 10065, United States.
Martin R PrinceDepartment of Radiology, Weill Cornell Medicine, New York, NY 10065, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Autosomal dominant polycystic kidney disease (ADPKD) can lead to polycystic liver disease (PLD), characterized by liver cysts. Although majority of the patients are asymptomatic, massively enlarged liver secondary to PLD can cause discomfort, and compression on adjacent structures requiring cyst aspiration/fenestration, partial liver resection, or liver transplantation. Monitoring PLD by measuring liver volume fails to track the early stages when liver cyst volume is too small to affect liver volume. Purpose: To improve PLD assessment in the early stages by automating detection and segmentation of liver cysts using deep learning (DL) models. Materials and Methods: A self-configured UNet-based platform (nnU-Net) was trained with 40 ADPKD subjects with liver cysts annotated by a radiologist. Internal (n = 7), External (n = 10), and test-retest reproducibility (n = 17) validations included macro- and micro-level performance metrics: patient-level Dice scores (PDice), along with voxel-level true positive rates (VTPR), as well as analysis of time saved in a model-assisted scenario. Additionally, we assessed human-level reliability in liver cyst segmentation and evaluated the model's test-retest reproducibility. We further compared liver volume vs cyst volume for tracking disease in a subject with 16+ years follow-up. Results: The model achieved an 82% ± 11% PDice and a 75% ± 15% VTPR on the internal test sets (n = 7 patients), and 80% ± 12% Dice score and a 91% ± 7% VTPR on the external test sets (n = 10 patients). It excelled particularly in detecting small liver cysts, a challenging task for manual annotation. This efficiency translated to a median of 91% (IQR: 14%) reduction in annotation time compared to manual labeling. Test-retest assessment demonstrated excellent reproducibility, with coefficients of variation of 94% for liver cyst fraction and 92% for cyst count. Conclusion: DL automation of liver cyst segmentations demonstrates potential to improve tracking of liver cyst volume in polycystic liver disease.

Indexed as

ADPKDdeep learningliver cystPLDsegmentation

Identifiers

PMID41059391
PMCPMC12429238

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.