Could the Combination of eGFR and mGPS Facilitate the Differential Diagnosis of Age-Related Renal Decline from Diseases? A Large Study on the Population of Western Sicily

Author:

Carella Miriam1,Porreca Annamaria2ORCID,Piazza Cinzia1,Gervasi Francesco3ORCID,Magro Daniele4,Venezia Marika4,Verso Raffaella Lo1,Vitale Giuseppe1,Agnello Annalisa Giusy1,Scola Letizia4,Aronica Tommaso Silvano1,Balistreri Carmela Rita4ORCID

Affiliation:

1. Complex Operative Unit of Clinical Pathology, ARNAS Civico Di Cristina e Benfratelli Hospitals, 90127 Palermo, Italy

2. Department of Medical, Oral Science and Biotechnology, University “G. d’Annunzio” Chieti-Pescara, 66100 Chieti, Italy

3. Specialized Laboratory of Oncology, ARNAS Civico Di Cristina e Benfratelli Hospitals, 90127 Palermo, Italy

4. Cellular and Molecular Laboratory, Department of Biomedicine, Neuroscience and Advanced Diagnostics (Bi.N.D.), University of Palermo, 90134 Palermo, Italy

Abstract

The assessment of renal function is critical to diagnosing and managing renal age-related decline, disease (KD), and failure, which are prevalent in the elderly population. The glomerular filtration rate (GFR) is widely used as an indicator of kidney function, but its direct measurement is challenging, as are its age and gender caveats. This makes difficult the differential diagnosis between age-related physiological decline and KD and/or failure. Currently, the inflammation-based modified Glasgow prognostic score (mGPS) is emerging as a promising biomarker of several inflammatory acute/chronic diseases. In this study, the large variability of eGFR with age and gender was evaluated as the association of eGFR values with mGPS levels. A population of 57,449 adult participants (age ≥ 18 years) was enrolled. Appropriate circulating biomarkers were measured to detect eGFR and mGPS values. The data obtained demonstrated a significant decrease in eGFR in men vs. women across the four selected age classes (18–40, 40–60, 60–80, 80–100 years); eGFR classes were significantly associated with mGPS (p < 0.001), as were age classes and gender with mGPS categories. Accordingly, the percentage of people having an mGPS score = 2 significantly increased across the eGFR classes: with an 11% in the G1/eGFR class needed to achieve 44% in G5/eGFR. Thus, the combination of mGPS with eGFR could represent the best benchmark risk model for the differential diagnosis of kidney disease from the age-related eGFR reduction.

Funder

Italian Ministerial Institute of Research

Publisher

MDPI AG

Subject

General Medicine

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