{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,22]],"date-time":"2026-10-22T10:36:27Z","timestamp":1792665387047,"version":"4.5.0"},"reference-count":28,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"10","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Kidney360"],"published-print":{"date-parts":[[2020,10]]},"abstract":"<jats:p>\n                    Polycystic kidney disease (PKD) is an inherited disorder characterized by renal cyst formation and enlargement of the kidney. PKD severity can be staged noninvasively by measuring total kidney volume (TKV), a promising biomarker that has recently received regulatory qualification. In preclinical mouse models, where the disease is studied and potential therapeutics are evaluated, the most popular noninvasive method of measuring TKV is magnetic resonance imaging (MRI). Although MRI provides excellent 3D resolution and contrast, these systems are expensive to operate, have long acquisition times, and, consequently, are not heavily used in preclinical PKD research. In this study, a new imaging instrument, based on robotic ultrasound (US), was evaluated as a complementary approach for assessing PKD in rodent models. The objective was to determine the extent to which TKV measurements on the robotic US scanner correlated with both\n                    <jats:italic toggle=\"yes\">in vivo<\/jats:italic>\n                    and\n                    <jats:italic toggle=\"yes\">ex vivo<\/jats:italic>\n                    reference standards (MRI and Vernier calipers, respectively). A cross-sectional study design was implemented that included both PKD-affected mice and healthy wild types, spanning sex and age for a wide range of kidney volumes. It was found that US-derived TKV measurements and kidney lengths were strongly associated with both\n                    <jats:italic toggle=\"yes\">in vivo<\/jats:italic>\n                    MRI and\n                    <jats:italic toggle=\"yes\">ex vivo<\/jats:italic>\n                    Vernier caliper measurements (\n                    <jats:italic toggle=\"yes\">R<\/jats:italic>\n                    <jats:sup>2<\/jats:sup>\n                    =0.94 and 0.90, respectively). In addition to measuring TKV, renal vascular density was assessed using acoustic angiography (AA), a novel contrast-enhanced US methodology. AA image intensity, indicative of volumetric vascularity, was seen to have a strong negative correlation with TKV (\n                    <jats:italic toggle=\"yes\">R<\/jats:italic>\n                    <jats:sup>2<\/jats:sup>\n                    =0.82), suggesting impaired renal vascular function in mice with larger kidneys. These studies demonstrate that robotic US can provide a rapid and accurate approach for noninvasively evaluating PKD in rodent models.\n                  <\/jats:p>","DOI":"10.34067\/kid.0003912020","type":"journal-article","created":{"date-parts":[[2020,8,18]],"date-time":"2020-08-18T17:55:15Z","timestamp":1597773315000},"page":"1128-1136","source":"Crossref","is-referenced-by-count":4,"title":["Assessing Polycystic Kidney Disease in Rodents: Comparison of Robotic 3D Ultrasound and Magnetic Resonance Imaging"],"prefix":"10.34067","volume":"1","author":[{"given":"Nathan J.","family":"Beaumont","sequence":"first","affiliation":[{"name":"SonoVol, Inc., Durham, North Carolina"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Heather L.","family":"Holmes","sequence":"additional","affiliation":[{"name":"Department of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, Minnesota"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Adriana V.","family":"Gregory","sequence":"additional","affiliation":[{"name":"Nephrology and Hypertension, Mayo Clinic, Rochester, Minnesota"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Marie E.","family":"Edwards","sequence":"additional","affiliation":[{"name":"Radiology, Mayo Clinic, Rochester, Minnesota"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Juan D.","family":"Rojas","sequence":"additional","affiliation":[{"name":"SonoVol, Inc., Durham, North Carolina"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ryan C.","family":"Gessner","sequence":"additional","affiliation":[{"name":"SonoVol, Inc., Durham, North Carolina"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Paul A.","family":"Dayton","sequence":"additional","affiliation":[{"name":"Joint Department of Biomedical Engineering, The University of North Carolina and North Carolina State University, Chapel Hill, North Carolina"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Timothy L.","family":"Kline","sequence":"additional","affiliation":[{"name":"Nephrology and Hypertension, Mayo Clinic, Rochester, Minnesota"},{"name":"Radiology, Mayo Clinic, Rochester, Minnesota"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Michael F.","family":"Romero","sequence":"additional","affiliation":[{"name":"Department of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, Minnesota"},{"name":"Nephrology and Hypertension, Mayo Clinic, Rochester, Minnesota"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-5493-4058","authenticated-orcid":false,"given":"Tomasz J.","family":"Czernuszewicz","sequence":"additional","affiliation":[{"name":"SonoVol, Inc., Durham, North Carolina"},{"name":"Joint Department of Biomedical Engineering, The University of North Carolina and North Carolina State University, Chapel Hill, North Carolina"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","published-online":{"date-parts":[[2020,10,29]]},"reference":[{"key":"B1-20230821","doi-asserted-by":"crossref","first-page":"925","DOI":"10.1046\/j.1523-1755.2000.00250.x","article-title":"Estimating prevalence in single-gene kidney diseases progressing to renal failure","volume":"58","author":"Levy","year":"2000","journal-title":"Kidney Int"},{"key":"B3-20230821","doi-asserted-by":"crossref","first-page":"1371","DOI":"10.1681\/ASN.2007030299","article-title":"Polycystic kidney disease","volume":"18","author":"Igarashi","year":"2007","journal-title":"J Am Soc Nephrol"},{"key":"B4-20230821","doi-asserted-by":"crossref","first-page":"41","DOI":"10.2147\/IJNRD.S125942","article-title":"Tolvaptan in the treatment of autosomal dominant polycystic kidney disease: Patient selection and special considerations","volume":"11","author":"Sans-Atxer","year":"2018","journal-title":"Int J Nephrol Renovasc 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