Volume 53, Issue 2 pp. 564-576
Original Research

Hemorrhagic Cysts and Other MR Biomarkers for Predicting Renal Dysfunction Progression in Autosomal Dominant Polycystic Kidney Disease

Sadjad Riyahi MD

Sadjad Riyahi MD

Department of Radiology, Weill Cornell Medicine, New York, New York, USA

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Hreedi Dev

Hreedi Dev

Department of Radiology, Weill Cornell Medicine, New York, New York, USA

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Jon D. Blumenfeld MD

Jon D. Blumenfeld MD

The Rogosin Institute, New York, New York, USA

Department of Medicine, Weill Cornell Medicine, New York, New York, USA

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Hanna Rennert PhD

Hanna Rennert PhD

Department of Pathology, Weill Cornell Medicine, New York, New York, USA

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Xiaorui Yin MD

Xiaorui Yin MD

Department of Radiology, Weill Cornell Medicine, New York, New York, USA

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Hanieh Attari MD

Hanieh Attari MD

Department of Radiology, Weill Cornell Medicine, New York, New York, USA

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Irina Barash MD

Irina Barash MD

The Rogosin Institute, New York, New York, USA

Department of Medicine, Weill Cornell Medicine, New York, New York, USA

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Ines Chicos MS

Ines Chicos MS

The Rogosin Institute, New York, New York, USA

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Warren Bobb NP

Warren Bobb NP

The Rogosin Institute, New York, New York, USA

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Stephanie Donahue NP

Stephanie Donahue NP

The Rogosin Institute, New York, New York, USA

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Martin R. Prince MD, PhD

Corresponding Author

Martin R. Prince MD, PhD

Department of Radiology, Weill Cornell Medicine, New York, New York, USA

Columbia College of Physicians and Surgeons, New York, New York, USA

Address reprint requests to: M.R.P., 416 East 55th Street, New York, NY 10022, USA. E-mail: [email protected]

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First published: 23 September 2020
Citations: 5

Contract grant sponsor: National Institutes of Health: National Center for Advancing Translational Sciences (NCATS).

Abstract

Background

Screening for rapidly progressing autosomal dominant polycystic kidney disease (ADPKD) is necessary for assigning and monitoring therapies. Height-adjusted total kidney volume (ht-TKV) is an accepted biomarker for clinical prognostication, but represents only a small fraction of information on abdominal MRI.

Purpose

To investigate the utility of other MR features of ADPKD to predict progression.

Study Type

Single-center retrospective.

Population

Longitudinal data from 186 ADPKD subjects with baseline serum creatinine, PKD gene testing, abdominal MRI measurements, and ≥2 follow-up serum creatinine were reviewed.

Field Strength/Sequence

1.5T, T2-weighted single-shot fast spin echo, T1-weighted 3D spoiled gradient echo (liver accelerated volume acquisition) and 2D cine velocity encoded gradient echo (phase contrast MRA).

Assessment

Ht-TKV, renal blood flow (RBF), number and fraction of renal and hepatic cysts, bright T1 hemorrhagic renal cysts, and liver and spleen volumes were independently assessed by three observers blinded to estimated glomerular filtration rate (eGFR) data.

Statistical Tests

Linear mixed-effect models were applied to predict eGFR over time using MRI features at baseline adjusted for confounders. Validation was performed in 158 patients who had follow-up MRI using receiver operator characteristic, sensitivity, and specificity.

Results

Hemorrhagic cysts, fraction of renal and hepatic cysts, height-adjusted liver and spleen volumes were significant independent predictors of future eGFR (final prediction model R2 = 0.88 P < 0.05). The number of hemorrhagic cysts significantly improved the prediction compared to ht-TKV in predicting future eGFR (area under the curve [AUC] = 0.94, 95% confidence interval [CI]: 0.9–0.94 vs. R2 = 0.9, 95% CI: 0.85–0.9, P = 0.045). For baseline eGFR ≥60 ml/min/1.73m2, sensitivity for predicting eGFR<45 ml/min/1.73m2 by ht-TKV alone was 29%. Sensitivity increased to 72% with all MRI variables in the model (P < 0.05 = 0.019), whereas specificity was unchanged, 100% vs. 99%.

Data Conclusion

Combining multiple MR features including hemorrhagic renal cysts, renal cyst fraction, liver and spleen volume, hepatic cyst fraction, and renal blood flow enhanced sensitivity for predicting eGFR decline in ADPKD compared to the standard model including only ht-TKV.

Level of Evidence 2

Technical Efficacy Stage 2

J. MAGN. RESON. IMAGING 2021;53:564–576.

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