Aims: Improving the composition of circulating fatty acids (FA) leads to a reduction in cardiovascular diseases (CVD) in high-risk individuals. The membrane fluidity of red blood cells (RBC), which reflects circulating FA status, may be a valid biomarker of cardiovascular (CV) risk in type 2 diabetes (T2D). Methods: Red blood cell membrane fluidity, quantified as general polarization (GP), was assessed in 234 subjects with T2D, 86 with prior major CVD. Based on GP distribution, a cut-off of .445 was used to divide the study cohort into two groups: the first with higher GP, called GEL, and the second, defined as lower GP (LGP). Lipidomic analysis was performed to evaluate FA composition of RBC membranes. Results: Although with comparable CV risk factors, the LGP group had a greater percentage of patients with major CVD than the GEL group (40% vs 24%, respectively, p < .05). Moreover, in a logistic regression analysis, a lower GP value was independently associated with the presence of macrovascular complications. Lipidomic analysis showed a clear shift of LGP membranes towards a pro-inflammatory condition due to higher content of arachidonic acid and increased omega 6/omega 3 index. Conclusions: Increased membrane fluidity is associated with a higher CV risk in subjects with T2D. If confirmed in prospective studies, membrane fluidity could be a new biomarker for residual CV risk assessment in T2D.

Erythrocyte membrane fluidity. A novel biomarker of residual cardiovascular risk in type 2 diabetes / Bianchetti, Giada; Cefalo, Chiara Maria Assunta; Ferreri, Carla; Sansone, Anna; Vitale, Marilena; Serantoni, Cassandra; Abeltino, Alessio; Mezza, Teresa; Manuel Ferraro, Pietro; De Spirito, Marco; Riccardi, Gabriele; Giaccari, Andrea; Maulucci, Giuseppe. - In: THE JOURNAL OF CLINICAL INVESTIGATION. - ISSN 1558-8238. - 54:3(2023), pp. 1-12. [10.1111/eci.14121]

Erythrocyte membrane fluidity. A novel biomarker of residual cardiovascular risk in type 2 diabetes

Chiara Maria Assunta Cefalo
Co-primo
;
2023

Abstract

Aims: Improving the composition of circulating fatty acids (FA) leads to a reduction in cardiovascular diseases (CVD) in high-risk individuals. The membrane fluidity of red blood cells (RBC), which reflects circulating FA status, may be a valid biomarker of cardiovascular (CV) risk in type 2 diabetes (T2D). Methods: Red blood cell membrane fluidity, quantified as general polarization (GP), was assessed in 234 subjects with T2D, 86 with prior major CVD. Based on GP distribution, a cut-off of .445 was used to divide the study cohort into two groups: the first with higher GP, called GEL, and the second, defined as lower GP (LGP). Lipidomic analysis was performed to evaluate FA composition of RBC membranes. Results: Although with comparable CV risk factors, the LGP group had a greater percentage of patients with major CVD than the GEL group (40% vs 24%, respectively, p < .05). Moreover, in a logistic regression analysis, a lower GP value was independently associated with the presence of macrovascular complications. Lipidomic analysis showed a clear shift of LGP membranes towards a pro-inflammatory condition due to higher content of arachidonic acid and increased omega 6/omega 3 index. Conclusions: Increased membrane fluidity is associated with a higher CV risk in subjects with T2D. If confirmed in prospective studies, membrane fluidity could be a new biomarker for residual CV risk assessment in T2D.
2023
cardiovascular disease; cardiovascular risk assessment; fatty acids; fluorescence microscopy; machine-learning; membrane fluidity; type 2 diabetes
01 Pubblicazione su rivista::01a Articolo in rivista
Erythrocyte membrane fluidity. A novel biomarker of residual cardiovascular risk in type 2 diabetes / Bianchetti, Giada; Cefalo, Chiara Maria Assunta; Ferreri, Carla; Sansone, Anna; Vitale, Marilena; Serantoni, Cassandra; Abeltino, Alessio; Mezza, Teresa; Manuel Ferraro, Pietro; De Spirito, Marco; Riccardi, Gabriele; Giaccari, Andrea; Maulucci, Giuseppe. - In: THE JOURNAL OF CLINICAL INVESTIGATION. - ISSN 1558-8238. - 54:3(2023), pp. 1-12. [10.1111/eci.14121]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1697687
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