Skip to content
DraconiticResearch
Search Sources API
203,234 studies31 sourcesUpdated 3 min ago
Peer-reviewedCC BYClinics and practice

Antiproteinuric Response to Finerenone in Diabetic Kidney Disease: Responder and Non-Responder Subgroup Analysis of the FINDKDLATAM Study.

12 more authors
26 affiliations
  1. 1Latin American Society of Nephrology and Hypertension (SLANH), Panamá City 0801, Panama.
  2. 2Colombian Association of Nephrology and Arterial Hypertension, Bogota 110221, Colombia.
  3. 3Department of Nephrology, Faculty of Medicine, Simón Bolívar University of Barranquilla, Barranquilla 080001, Colombia.
  4. 4Department of Nephrology, Hospital Central de la Defensa Gómez Ulla, 28047 Madrid, Spain.
  5. 5Department of Medicine and Medical Specialties, Faculty of Medicine, Alcala University, 28805 Madrid, Spain.
  6. 6Faculty of Medicine, Department of Nephrology, University of San Carlos of Guatemala (USAC), Guatemala City 01011, Guatemala.
  7. 7Department of Epidemiology, El Rosario University, Bogota 111221, Colombia.
  8. 8Medical and Surgical Research, GIBACUS Research Group, Sinú University EBZ, Cartagena Campus, Cartagena 130010, Colombia.
  9. 9Faculty of Nursing, Health Services Administration Program, University of Cartagena, Cartagena 130005, Colombia.
  10. 10Department of Nephrology, Del Valle Hospital, Catholic University of Honduras, San Pedro Sula 21102, Honduras.
  11. 11Department of Nephrology, Dr. Abel Gilbert Pontón Hospital of Guayaquil, Ministry of Public Health, O'Connors, Guayaquil 090104, Ecuador.
  12. 12Department of Nephrology, Honduran Institute of Social Security, North Region, San Pedro Sula 21102, Honduras.
  13. 13Department of Nephrology, Bendaña Hospital, San Pedro Sula 21102, Honduras.
  14. 14Internal Medicine, Mario Catarino Rivas Hospital, San Pedro Sula 21102, Honduras.
  15. 15Department of Nephrology, Rafael Rodríguez Zambrano Hospital, Manta 130206, Ecuador.
  16. 16Department of Internal Medicine East, Faculty of Medicine, University of Chile, Providencia, Santiago 8320000, Chile.
  17. 17Department of Nephrology, Metropolitan Hospital of Santiago, Santiago de los Caballeros 51000, Dominican Republic.
  18. 18Department of Engineering, Faculty of Science and Engineering, Peruana Cayetano Heredia University, Lima 15012, Peru.
  19. 19Department of Nephrology, San Jose Maicao ESE Hospital, Maicao 442001, Colombia.
  20. 20Department of Internal Medicine, Faculty of Medicine, University of Cartagena, Cartagena 130005, Colombia.
  21. 21Department of Nephrology, Armed Forces Specialty Hospital Number 1, Quito City 170403, Ecuador.
  22. 22Department of Internal Medicine, University of Valle, Cali 760042, Colombia.
  23. 23Department of Nephrology, Davita Kidney Care, Barranquilla 080020, Colombia.
  24. 24Department of Nephrology, Hospital General de Fuerteventura, 35600 Puerto del Rosario, Spain.
  25. 25Department of Nephrology, Hospital Señora de Sonsoles, 05004 Avila, Spain.
  26. 26Surgery Department, Faculty of Medicine, University of Salamanca, 37007 Salamanca, Spain.

Abstract

Background/Objectives: Albuminuria is an early marker of kidney damage and an independent predictor of adverse outcomes, making its reduction a key therapeutic goal. Finerenone, a selective nonsteroidal mineralocorticoid receptor antagonist, has demonstrated renal and cardiovascular benefits in patients with diabetic kidney disease (DKD), although the magnitude of the antiproteinuric response may vary in clinical practice. This post hoc analysis aimed to characterize the six-month antiproteinuric response to finerenone and to descriptively explore baseline clinical and treatment characteristics across response categories in the FINDKDLATAM cohort. Methods: A subgroup analysis was performed on a real-world, multicenter, retrospective, observational study that included patients from the FINDKDLATAM study who had urinary albumin-to-creatinine ratio (UACR) measurements taken at baseline and six months. Patients were classified as absolute responders (≥50% reduction in UACR), partial responders (30-49% reduction), and non-responders (<30% reduction or no reduction in UACR) at six months of follow-up. Sociodemographic, clinical, biochemical, therapeutic, and safety variables were analyzed. Results: Of the 347 patients included in the original cohort, 334 had complete UACR data at six months and were included in the analysis. Of these, 80.2% (n = 268) were absolute responders, 11.7% (n = 39) partial responders, and 8.1% (n = 27) non-responders. Median UACR decreased from 350.7 to 67.0 mg/g among absolute responders and from 240.5 to 143.0 mg/g among partial responders (both p < 0.0001), whereas no significant change was observed among non-responders. No baseline clinical characteristic consistently distinguished responders from non-responders. Serum potassium increased during follow-up, particularly among non-responders. Conclusions: In this retrospective Latin American cohort, most patients experienced a reduction in UACR after six months of finerenone treatment. However, the uncontrolled observational design, concomitant therapies, UACR variability, and regression to the mean preclude attributing these changes exclusively to finerenone. These exploratory findings do not support selecting patients according to a particular responder phenotype but rather support prescribing finerenone according to currently approved clinical criteria. Prospective studies with adjusted analyses are needed to identify independent predictors of response.

Related

  1. Association of Finerenone Dose and Estimated Glomerular Filtration Rate (eGFR) Slope Changes in Patients With Diabetic Kidney Disease: A Real-World Retrospective Study.
    Hazuki Otani, Soichi Kurioka
    CureusPeer-reviewedCC BYFull textGeneral medicineEurope PMC
  2. Association of finerenone plus tripterygium glycosides with proteinuria reduction in patients with diabetic kidney disease: a retrospective cohort study
    Qi Gao, Yuan Cai, Yuanbo Zhang +5
    Frontiers in PharmacologyPeer-reviewedCC BY 4.0Full textPharmacology & toxicologyFrontiersCrossrefDOAJ
  3. Longitudinal kidney outcomes and safety after finerenone initiation in patients with non-diabetic chronic kidney disease: a single-center retrospective cohort study
    Xuejuan Sun, Juan Pei, Xing Chen +6
    Frontiers in medicinePeer-reviewedCC BYFull textGeneral medicineEurope PMCPMCEurope PMC
  4. Short-term superiority in proteinuria control with exploratory longitudinal trajectories: finerenone-dapagliflozin combination in non-diabetic kidney disease
    Mali Zhu, Yingyi Deng, Lijun Su +3
    Frontiers in PharmacologyPeer-reviewedCC BY 4.0Full textPharmacology & toxicologyCrossrefEurope PMCPMC
  5. Baseline gut microbiota and short-term response to acupressure combined with thermal stimulation in maintenance hemodialysis patients with functional constipation: an exploratory responder analysis.
    Saiping Chen, Mengqi Wu, Min Huang +12
    Frontiers in cellular and infection microbiologyPeer-reviewedCC BYFull textGeneral medicineEurope PMCPMC
BibTeX
@article{fontalvo2026antiproteinuric,
  title = {{Antiproteinuric Response to Finerenone in Diabetic Kidney Disease: Responder and Non-Responder Subgroup Analysis of the FINDKDLATAM Study.}},
  author = {Jorge Rico Fontalvo and María Raad Sarabia and José C De La Flor and Vicente Sánchez Polo and Jenniffer Benavides Garcia and Enrique Ramos Clason and Daniel Domínguez and Giovanny Mera Rebutti and Carlos Madrid Mancia and Rene Tabora López and Manuel Rocha Meza and Dany Tabora López and James J Muñoz Zambrano and Eduardo Lorca Herrera and Eliana Dina-Batlle and Michael Cieza Terrones and Alvaro Pedroza Pallares and Tomas Rodríguez Yánez and Washington Osorio and Alyi Arellano Cabeza and Juan Felipe Gutiérrez and Avinash Chandu Nanwani and Celia Rodríguez Tudero and Rodrigo Daza Arnedo},
  journal = {Clinics and practice},
  year = {2026},
  month = sep,
  doi = {10.3390/clinpract16100174},
  url = {https://europepmc.org/article/MED/42930360},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Antiproteinuric Response to Finerenone in Diabetic Kidney Disease: Responder and Non-Responder Subgroup Analysis of the FINDKDLATAM Study.
AU  - Jorge Rico Fontalvo
AU  - María Raad Sarabia
AU  - José C De La Flor
AU  - Vicente Sánchez Polo
AU  - Jenniffer Benavides Garcia
AU  - Enrique Ramos Clason
AU  - Daniel Domínguez
AU  - Giovanny Mera Rebutti
AU  - Carlos Madrid Mancia
AU  - Rene Tabora López
AU  - Manuel Rocha Meza
AU  - Dany Tabora López
AU  - James J Muñoz Zambrano
AU  - Eduardo Lorca Herrera
AU  - Eliana Dina-Batlle
AU  - Michael Cieza Terrones
AU  - Alvaro Pedroza Pallares
AU  - Tomas Rodríguez Yánez
AU  - Washington Osorio
AU  - Alyi Arellano Cabeza
AU  - Juan Felipe Gutiérrez
AU  - Avinash Chandu Nanwani
AU  - Celia Rodríguez Tudero
AU  - Rodrigo Daza Arnedo
PY  - 2026
DA  - 2026/09/22
JO  - Clinics and practice
DO  - 10.3390/clinpract16100174
UR  - https://europepmc.org/article/MED/42930360
AB  - Background/Objectives: Albuminuria is an early marker of kidney damage and an independent predictor of adverse outcomes, making its reduction a key therapeutic goal. Finerenone, a selective nonsteroidal mineralocorticoid receptor antagonist, has demonstrated renal and cardiovascular benefits in patients with diabetic kidney disease (DKD), although the magnitude of the antiproteinuric response may vary in clinical practice. This post hoc analysis aimed to characterize the six-month antiproteinuric response to finerenone and to descriptively explore baseline clinical and treatment characteristics across response categories in the FINDKDLATAM cohort. Methods: A subgroup analysis was performed on a real-world, multicenter, retrospective, observational study that included patients from the FINDKDLATAM study who had urinary albumin-to-creatinine ratio (UACR) measurements taken at baseline and six months. Patients were classified as absolute responders (≥50% reduction in UACR), partial responders (30-49% reduction), and non-responders (<30% reduction or no reduction in UACR) at six months of follow-up. Sociodemographic, clinical, biochemical, therapeutic, and safety variables were analyzed. Results: Of the 347 patients included in the original cohort, 334 had complete UACR data at six months and were included in the analysis. Of these, 80.2% (n = 268) were absolute responders, 11.7% (n = 39) partial responders, and 8.1% (n = 27) non-responders. Median UACR decreased from 350.7 to 67.0 mg/g among absolute responders and from 240.5 to 143.0 mg/g among partial responders (both p < 0.0001), whereas no significant change was observed among non-responders. No baseline clinical characteristic consistently distinguished responders from non-responders. Serum potassium increased during follow-up, particularly among non-responders. Conclusions: In this retrospective Latin American cohort, most patients experienced a reduction in UACR after six months of finerenone treatment. However, the uncontrolled observational design, concomitant therapies, UACR variability, and regression to the mean preclude attributing these changes exclusively to finerenone. These exploratory findings do not support selecting patients according to a particular responder phenotype but rather support prescribing finerenone according to currently approved clinical criteria. Prospective studies with adjusted analyses are needed to identify independent predictors of response.
SN  - 2039-7275
SN  - 2039-7283
ER  -