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Torres, Vicente E.

https://orcid.org/0000-0003-2008-1576

Mayo Clinic

Mayo Clinic

Citations 132

Activation of PIEZO1 Attenuates Kidney Cystogenesis In Vitro and Ex Vivo
Hadla, Mohamad , Peterson, Zack, Nelson, Grace, Ye, Hong , Mardirossian, Jean Marc , Harris, Peter C. , Alper, Seth L. , Fan, Qingfeng, Hadla, Mohamad , Nelson, Grace , Mardirossian, Jean Marc , Harris, Peter C , Alper, Seth L , Beyder, Arthur , Torres, Vicente E , Chebib, Fouad T , Fan, Qingfeng , Wang, Xiaofang , Prakash, Y. S. , Beyder, Arthur , Torres, Vicente E. , Chebib, Fouad T.

Kidney360 | October 2, 2024 | Volume: 5 | Issue: 11 | Pages: 1601-1612

10.34067/kid.0000000598 Get It

Key Points PIEZO1 activation reduces cystogenesis: Yoda1 activates PIEZO1, raising calcium and lowering cAMP, reducing cyst growth in autosomal dominant polycystic kidney disease models. Context-dependent role of PIEZO1: PIEZO1 knockout in mice with or without polycystic kidneys does not affect cyst formation, suggesting redundancy in mechanosensitive pathways. Therapeutic potential: Findings support PIEZO1 activation as a part of combination therapy to slow cyst growth in autosomal dominant polycystic kidney disease, needing more in vivo studies. Background The disruption of calcium signaling associated with polycystin deficiency is a key factor in abnormal epithelial growth in autosomal dominant polycystic kidney disease. Calcium homeostasis can be influenced by mechanotransduction. The mechanosensitive cation channel PIEZO1 has been implicated in sensing intrarenal pressure and regulating urinary osmoregulation, but its role in kidney cystogenesis is unclear. Methods We hypothesized that altered mechanotransduction contributes to cystogenesis in autosomal dominant polycystic kidney disease and that activation of mechanosensitive cation channels could be a therapeutic strategy. Results We demonstrate that Yoda1, a PIEZO1 activator, increases intracellular calcium and reduces forskolin-induced cAMP levels in mouse inner medullary collecting duct (mIMCD3) cells. Notably, knockout of polycystin-2 attenuated the efficacy of Yoda1 in reducing cAMP levels in mIMCD3 cells. Yoda1 also reduced forskolin-induced mIMCD3 cyst surface area in vitro and cystic index in mouse metanephros ex vivo in a dose-dependent manner. However, collecting duct–specific PIEZO1 knockout neither induced cystogenesis in wild-type mice nor altered cystogenesis in the Pkd1 RC/RC mouse model. Conclusions These findings support the potential role of PIEZO1 agonists in mitigating cystogenesis by increasing intracellular calcium and reducing cAMP levels, but the unaltered in vivo cystic phenotype after PIEZO1 knockout in the collecting duct suggests possible redundancy in mechanotransductive pathways.
Treatment of transplant renal artery stenosis: Experience and reassessment of therapeutic options
Miller, Alexander R., Stanson, Anthony W., Sterioff, Sylvester, Marsh, Christopher L. , Torres, Vicente E.

Clinical Transplantation | September 28, 2024 | Volume: 3 | Issue: 2 | Pages: 101-109

10.1111/j.1399-0012.1989.tb00545.x Get It

Management of transplant renal artery stenosis has been a controversial issue. The authors have reviewed their experience with 31 such cases which represent 3.1% of a transplant population of 1015 patients. Evidence of chronic allograft rejection was noted in 14 of these patients. Ten patients were treated medically. The remaining patients were managed by either percutaneous transluminal angioplasty (8 cases) or surgery (13 cases). Three patients initially treated by percutaneous transluminal angioplasty later underwent surgical repair. Operative intervention resulted in a significant decrease in mean arterial pressure and the greatest degree of therapeutic success (defined as normal blood pressure without use of antihypertensive agents). In contrast to other reports, use of percutaneous transluminal angioplasty was not successful in a majority of patients. This divergence may reflect differences in criteria for success which, we believe, should be defined more rigorously. Our data indicate that decisions regarding definitive management strategies should be based on the specific characteristics of the lesion with identification of stenoses that may be amenable to surgical rather than angioplastic treatment.
Long-term effect of increasing water intake on repeated self-assessed health-related quality of life (HRQoL) in autosomal dominant polycystic kidney disease
Rangan, Gopala K. , Allman‐Farinelli, Margaret , Boudville, Neil , Fernando, Mangalee, Haloob, Imad, Harris, David C.H. , Kumar, Karthik, Johnson, David W. , Lee, Vincent , Mai, Jun, Roger, Simon D. , Sagar, Priyanka S. , Sud, Kamal , Vilayur, Eswari, Rangan, Anna , Johnson, David W , Lee, Vincent W , Hawley, Carmel M. , Rangan, Anna , Torres, Vicente E.

Clinical Kidney Journal | June 8, 2024 | Volume: 17 | Issue: 7 | Pages: No page available

10.1093/ckj/sfae159 Get It

ABSTRACT Background The aim of this study was to determine the long-term effect of increasing water intake in patients with autosomal dominant polycystic kidney disease (ADPKD) on longitudinal changes in health-related quality of life (HRQoL) in the setting of a clinical trial. Methods Self-completed HRQoL (using the KDQoL-SF, v.1.3 questionnaire) was assessed annually in participants of a 3-year randomized controlled clinical trial (n = 187), allocated (1:1) either to increase water intake to reduce urine osmolality to ≤270 mosmol/kg (implemented by dietetic coaching, self-monitoring tools, text messaging) or continue usual water intake. Results Overall, 96% and 81.8% of participants (n = 187) completed the questionnaire at the baseline and final study visits, respectively. At baseline, the physical component summary score (PCS) and mental component summary score (MCS) were similar in the two groups (P > 0.05) and the five dimensions with the lowest scores in both groups were: energy and fatigue; general and overall health; sleep; emotional well-being; and pain. Within each group, there were no longitudinal changes over time. At the final visit, the PCS was higher in the increased water intake group (51.3 ± 7.6, mean ± standard deviation) compared to the usual water intake group 48.8 ± 9.3; P = 0.037) whereas the MCS was numerically similar. The improvement in the PCS was due to higher sub-scale values for physical functioning and pain (both P < 0.05). By multivariate analysis, only baseline PCS and height-corrected total kidney volume were associated with the final PCS (P < 0.05). Conclusion HRQoL scores remained stable over a 3 year period, and were not adversely affected by the intervention to increase water intake. Future studies should evaluate the clinical significance of the higher PCS in the increased water intake group.
Population Analyses to Determine Genetic Causes of Kidney Cysts
Yang, Hana , Bublitz, Josh, Elbarougy, Doaa E. , Schauer, R., Elbarougy, Doaa E , Larson, Nicholas B. , Schauer, Rachel S., Torres, Vicente E. , Harris, Peter C.

Journal of the American Society of Nephrology | May 18, 2024 | Volume: 34 | Issue: 11S | Pages: 938-938

10.1681/asn.20233411s1938a Get It

Prognostic Model for Progression of Autosomal Dominant Polycystic Kidney Disease to Kidney Failure
Cohen, Aarón , Landsittel, Douglas , Chapman, Arlene B., Mrug, Michal , Bae, Kyongtae T., Yu, Alan S.L. , Ables, Erin , Torres, Vicente E. , Chebib, Fouad T. , Harris, Peter C. , Rahbari-Oskoui, Frederic F. , Dickinson, Stephanie , Bennett, William M.

Journal of the American Society of Nephrology | May 17, 2024 | Volume: 34 | Issue: 11S | Pages: 209-209

10.1681/asn.20233411s1209c Get It

Therapeutic Blocking of IL-17A Binding to IL-17RA Diminishes PD-L1 Expression Is a Novel Therapeutic Approach for ADPKD
Samarpita, Snigdha , Agborbesong, Ewud , Zhou, Xia , Li, Xiaoyan , Torres, Vicente E. , Li, Xiaogang

Journal of the American Society of Nephrology | May 17, 2024 | Volume: 34 | Issue: 11S | Pages: 205-205

10.1681/asn.20233411s1205b Get It

Multicenter Real-Life Experience With Tolvaptan Treatment in Patients With Autosomal Dominant Polycystic Kidney Disease
Duriseti, Parikshit , Wigerinck, Stijn , Chedid, Maroun , Garg, Arvind , Keddis, Mira T. , Trautman, Christopher L. , Dahlen, Erin , Mcfadden, Jennifer E., Bhat, Samrat, Erickson, Stephen B., Radhakrishnan, Yeshwanter , Mao, Michael A. , Hommos, Musab S. , Zoghby, Ziad , Gay, Melissa K. , Harris, Peter C. , Hogan, Marie C. , Torres, Vicente E. , Chebib, Fouad T.

Journal of the American Society of Nephrology | May 17, 2024 | Volume: 33 | Issue: 11S | Pages: 161-161

10.1681/asn.20223311s1161c Get It

Systemic Inflammation and Kidney Stone Disease in Autosomal Dominant Polycystic Kidney Disease
You, Zhiying , Brosnahan, Godela , Chapman, Arlene B., Chonchol, Michel , Gitomer, Berenice Y , Wang, Wei , Hopp, Katharina , Nowak, Kristen L. , Perrone, Ronald D. , Torres, Vicente E. , Yu, Alan S.L.

Journal of the American Society of Nephrology | May 17, 2024 | Volume: 33 | Issue: 11S | Pages: 159-159

10.1681/asn.20223311s1159b Get It

Antibiotic Use and Kidney Stone Disease in Patients With Autosomal Dominant Polycystic Kidney Disease
You, Zhiying , Brosnahan, Godela , Jovanovich, Anna, Chapman, Arlene B., Chonchol, Michel , Gitomer, Berenice Y , Wang, Wei , Hopp, Katharina , Nowak, Kristen L. , Jovanovich, Anna J. , Perrone, Ronald D. , Torres, Vicente E. , Yu, Alan S.L.

Journal of the American Society of Nephrology | May 17, 2024 | Volume: 33 | Issue: 11S | Pages: 159-159

10.1681/asn.20223311s1159a Get It

Evaluation of Advanced MRI Cystic Biomarkers at Kidney Failure in Patients With Autosomal Dominant Polycystic Kidney Disease
Wigerinck, Stijn , Chedid, Maroun , Gregory, Adriana , Kaidbay, Hasan-Daniel N., Kline, Timothy L. , Hanna, Christian , Senum, Sarah R. , Harris, Peter C. , Torres, Vicente E. , Chebib, Fouad T.

Journal of the American Society of Nephrology | May 17, 2024 | Volume: 33 | Issue: 11S | Pages: 158-158

10.1681/asn.20223311s1158b Get It