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Lamacchia, O.* ; Menzaghi, C.* ; Copetti, M.* ; Mastroianno, M.* ; Corsano, C.* ; Prehn, C. ; Adamski, J. ; Fontana, A.* ; Trischitta, V.* ; De Cosmo, S.*

GFR decline predicts total mortality and mediates the effect of tryptophan metabolism on death risk in type 2 diabetes.

J. Clin. Endocrinol. Metab. 110, e1451-e1457 (2024)
Postprint DOI PMC
Open Access Green
CONTEXT: The independent role of glomerular filtration rate (GFR) decline in shaping the risk of mortality in people with type 2 diabetes has only been partially addressed. OBJECTIVE: The objective of the study was twofold: i) to investigate the association between all-cause mortality and eGFR changes over time; ii) to understand whether renal dysfunction mediates the effect of tryptophan metabolism on death risk. DESIGN: Prospective study with an average follow-up of 14.8 years. SETTING: Research Hospital. PATIENTS: The aggregate Gargano Mortality Study included 962 patients with type 2 diabetes who had at least three eGFR recordings and at least 1.5 years of follow-up. INTERVENTIONS: This was an observational study, with no intervention. MAIN OUTCOME MEASURES: Rate of all-cause mortality. RESULTS: Age and sex adjusted annual incident rate of mortality was 2.75 events per 100 person-years. The median annual rate of decline of eGFR was 1.3 ml/min per 1.73 m2 per year (range -3.7; 7.8). The decline of kidney function was strongly and independently associated with the risk of death. Serum kynurenine-to-tryptophan ratio (KTR) was associated with both eGFR decline and all-cause mortality. Causal mediation analysis showed that 24.3% of the association between KTR and mortality was mediated by eGFR decline. CONCLUSIONS: In patients with type 2 diabetes, eGFR decline is independently associated with the risk of all-cause mortality and mediates a significant proportion of the association between tryptophan metabolism and death.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Albuminuria ; Causal Mediation ; Death ; Kidney Function ; Tryptophan Metabolism; Kidney-function Decline; Cardiovascular-disease; Glucose
Sprache englisch
Veröffentlichungsjahr 2024
HGF-Berichtsjahr 2024
ISSN (print) / ISBN 0021-972X
e-ISSN 1945-7197
Quellenangaben Band: 110, Heft: 5, Seiten: e1451-e1457 Artikelnummer: , Supplement: ,
Verlag Endocrine Society
Verlagsort Bethesda, Md.
Begutachtungsstatus Peer reviewed
POF Topic(s) 30505 - New Technologies for Biomedical Discoveries
30201 - Metabolic Health
Forschungsfeld(er) Enabling and Novel Technologies
Genetics and Epidemiology
PSP-Element(e) A-630710-001
G-500600-001
Förderungen European Union
Innovative Medicines Initiative 2 Joint Undertaking (JU)
European Health Data & Evidence Network (EHDEN) project
Ricerca corrente
PNRR M4C2I1.3 Heal Italia project
Scopus ID 105003470736
PubMed ID 39136240
Erfassungsdatum 2024-09-03