BIOMARCADORES RETINIANOS Y RADIOLÓGICOS DE ENFERMEDAD RENAL CRÓNICA EN DIABETES
Palabras clave:
Retina, Nefropatías diabéticas, Insuficiencia renal crónica, Biomarcadores, Microcirculación, Diabetes mellitusResumen
DOI: https://doi.org/10.46296/yc.v10i18.0900
Resumen
Introducción: La imagen retiniana permite observar la microcirculación humana de forma no invasiva y ha ganado interés como biomarcador de enfermedad renal crónica y de daño microvascular sistémico en personas con diabetes. Objetivo: Sintetizar críticamente la evidencia clínica y traslacional sobre fotografía de fondo de ojo, tomografía de coherencia óptica, angiografía por tomografía de coherencia óptica e inteligencia artificial aplicadas a la predicción, detección o fenotipificación de enfermedad renal en diabetes, y discutir su relación con hallazgos sistémicos en radiología. Metodología de búsqueda: Se realizó una revisión crítica estructurada de literatura publicada entre 2008 y agosto de 2025 en bases biomédicas internacionales, priorizando revisiones sistemáticas, metaanálisis, cohortes longitudinales y estudios con validación externa. Resultados: La asociación más robusta corresponde a la severidad de la retinopatía diabética, que se relaciona con albuminuria, descenso de la filtración glomerular y progresión renal, aunque con precisión diagnóstica insuficiente para sustituir los estándares nefrológicos. Los biomarcadores cuantitativos vasculares aportan señal adicional, pero siguen siendo heterogéneos. La tomografía de coherencia óptica y su angiografía muestran potencial para detectar alteraciones más tempranas, y los modelos de inteligencia artificial son prometedores para tamizaje de enfermedad renal crónica, aunque persisten dudas sobre validez externa y utilidad clínica real. Discusión: La retina funciona mejor como biomarcador complementario de riesgo y fenotipo que como sustituto diagnóstico renal. Conclusiones: La integración de imagen retiniana con laboratorio renal y radiología sistémica representa una vía plausible para medicina de precisión, pero requiere estandarización, validación multicéntrica y estudios de impacto.
Palabras claves: Retina, Nefropatías diabéticas, Insuficiencia renal crónica, Biomarcadores, Microcirculación, Diabetes mellitus.
Abstract
Introduction: Retinal imaging enables noninvasive visualization of the human microcirculation and has emerged as a potential biomarker of chronic kidney disease and systemic microvascular injury in people with diabetes. Objective: To critically synthesize the clinical and translational evidence on fundus photography, optical coherence tomography, optical coherence tomography angiography, and artificial intelligence for the prediction, detection, or phenotyping of kidney disease in diabetes, and to discuss their relationship with systemic imaging findings in radiology. Search methodology: A structured critical review of literature published from 2008 to August 2025 was performed in major biomedical databases, prioritizing systematic reviews, meta-analyses, longitudinal cohorts, and externally validated studies. Results: The strongest signal comes from diabetic retinopathy severity, which is associated with albuminuria, reduced glomerular filtration, and kidney disease progression, but has insufficient diagnostic accuracy to replace nephrology standards. Quantitative retinal vascular biomarkers add biological information, although reproducibility remains heterogeneous. Optical coherence tomography and optical coherence tomography angiography are promising for earlier detection, while artificial intelligence improves scalability but still requires stronger external validation. Discussion: The retina currently performs best as a complementary risk and phenotyping biomarker rather than as a stand-alone renal surrogate. Conclusions: Integrating retinal imaging with renal laboratory markers and systemic radiology may support precision medicine in diabetes, but standardization, multicenter validation, and impact studies are still required.
Keywords: Retina, Diabetic Nephropathies, Renal Insufficiency Chronic, Biomarkers, Microcirculation, Diabetes Mellitus.
Información del manuscrito:
Fecha de recepción: 11 de marzo de 2026.
Fecha de aceptación: 20 de mayo de 2026.
Fecha de publicación: 18 de junio de 2026.
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