M Magdalena Perez-Cardelo

Dr. M Magdalena Perez-Cardelo

Lipids and Atherosclerosis Research Unit, Internal Medicine Unit, Reina Sofia University Hospital, Cordoba, 14004, Spain.
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Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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25 April 2024 in Nature Metabolism
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Journal Article
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JSJonathan Sun
Jonathan Sun
EEEnric Esplugues
Enric Esplugues
ABAlicia Carmen Bueno
Alicia Carmen Bueno
MPM Magdalena Perez-Cardelo
M Magdalena Perez-Cardelo
IRInmaculada Ruz-Maldonado
Inmaculada Ruz-Maldonado
CFCarlos Fernández
Carlos Fernández

6 January 2022 in Clinical Nutrition
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Journal Article
Open access
APAlicia Podadera-Herreros
Alicia Podadera-Herreros
JAJuan F. Alcala-Diaz
Juan F. Alcala-Diaz
FGFrancisco Miguel Gutierrez-Mariscal
Francisco Miguel Gutierrez-Mariscal
JJJose Jimenez-Torres
Jose Jimenez-Torres
SASilvia de la Cruz Ares
Silvia de la Cruz Ares
EYElena Yubero-Serrano
Elena Yubero-Serrano
Lifestyle and dietary habits influence kidney function, playing an important role in the prevention and development of chronic kidney disease (CKD). The effectiveness of the Mediterranean diet in preserving kidney function has been seen in primary prevention. However, no scientific evidence is currently available to determine which dietary pattern is more effective in the management of CKD in secondary cardiovascular disease prevention. Thus, our aim was to evaluate the efficacy of the long-term consumption of two healthy dietary patterns (a Mediterranean diet rich in extra-virgin olive oil (EVOO) compared to a low-fat diet rich in complex carbohydrates) in preserving kidney function in coronary heart disease (CHD) patients. CHD patients (n = 1002) from the CORDIOPREV study were randomized to follow a Mediterranean diet (35% fat, 22% MUFA, 55% carbohydrates). Kidney function was assessed by the determination of serum creatinine-based estimated glomerular filtration rate (eGFR) at baseline and after 5-years of dietary intervention. Patients were classified according to their type 2 diabetes (T2DM) status, using baseline eGFR (normal eGFR: ≥ 90 mL/min/1.73 m2; mildly-impaired eGFR: 60 to <90 mL/min/1.73 m2, severely-impaired eGFR: <60 mL/min/1.73 m2) to evaluate its influence on the progression of kidney function. Multiple linear regression analysis were performed to determine the contribution of different clinical and anthropometric parameters to changes in eGFR. Although eGFR declined after both dietary interventions compared to baseline (all p < 0.001), the Mediterranean diet produced a lower decline of eGFR compared to the low-fat diet in patients with T2DM (p = 0.040). This effect was also observed when the overall population was considered (p = 0.033). No significant differences were observed in eGFR between the two diets in non-T2DM patients. In addition, this differential effect of the Mediterranean diet was mainly observed in patients with mildly-impaired eGFR in which this diet slowed eGFR progression (p = 0.002). The long-term consumption of a Mediterranean diet rich in EVOO, when compared to a low-fat diet, may preserve kidney function, as shown by a reduced decline in eGFR in CHD patients with T2DM. Patients with mildly-impaired eGFR may benefit more from the beneficial effect of the consumption of the Mediterranean diet in preserving kidney function. These findings reinforce the clinical benefits of the Mediterranean diet in the context of secondary cardiovascular disease prevention. URL, http://www.cordioprev.es/index.php/en. Clinicaltrials.gov number, NCT00924937.

16 January 2020 in Nutrients
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SASilvia de la Cruz Ares
Silvia de la Cruz Ares
MPM Magdalena Perez-Cardelo
M Magdalena Perez-Cardelo
FGFrancisco Miguel Gutierrez-Mariscal
Francisco Miguel Gutierrez-Mariscal
JTJose David Torres-Peña
Jose David Torres-Peña
ARAntonio Garcia Rios
Antonio Garcia Rios
EYElena Yubero-Serrano
Elena Yubero-Serrano
Endothelial dysfunction and intima-media thickness of common carotid arteries (IMT-CC) are considered subclinical markers of atherosclerotic cardiovascular disease (ASCVD). Advanced glycation end products (AGEs) are increased in type 2 diabetes mellitus (T2DM) patients, compared with non-diabetics, being implicated in micro- and macrovascular complications. Our aim was to compare serum AGEs levels and subclinical atherosclerotic markers between patients with established and newly diagnosed T2DM. Among 540 patients with T2DM and coronary heart disease from the CORDIOPREV study, 350 patients had established T2DM and 190 patients had newly diagnosed T2DM. Serum levels of AGEs (methylglyoxal (MG) and N-carboxymethyl lysine (CML)) and subclinical atherosclerotic markers (brachial flow-mediated vasodilation (FMD) and IMT-CC) were measured. AGEs levels (all p < 0.001) and IMT-CC (p = 0.025) were higher in patients with established vs. newly diagnosed T2DM, whereas FMD did not differ between the two groups. Patients with established T2DM and severe endothelial dysfunction (i.e., FMD < 2%) had higher serum MG levels, IMT-CC, HOMA-IR and fasting insulin levels than those with newly diagnosed T2DM and non-severe endothelial dysfunction (i.e., FMD ≥ 2%) (all p < 0.05). Serum CML levels were greater in patients with established vs. newly diagnosed T2DM, regardless of endothelial dysfunction severity. Serum AGEs levels and IMT-CC were significantly higher in patients with established vs. newly diagnosed T2DM, highlighting the progressively increased risk of ASCVD in the course of T2DM. Establishing therapeutic strategies to reduce AGEs production and delay the onset of cardiovascular complications in newly diagnosed T2DM patients or minimize ASCVD risk in established T2DM patients is needed.

11 June 2020 in Molecular Nutrition & Food Research
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FGFrancisco M. Gutierrez‐Mariscal
Francisco M. Gutierrez‐Mariscal
MPM Magdalena Perez-Cardelo
M Magdalena Perez-Cardelo
SCSilvia de la Cruz
Silvia de la Cruz
JAJuan F. Alcala-Diaz
Juan F. Alcala-Diaz
IRIrene Roncero‐Ramos
Irene Roncero‐Ramos
JLJosé López-Miranda
José López-Miranda

14 November 2016 in Food & Function
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Sergio Montserrat-De La PazSergio Montserrat-De La Paz
Sergio Montserrat-De La Paz
BBBeatriz Bermudez
Beatriz Bermudez
MPM Magdalena Perez-Cardelo
M Magdalena Perez-Cardelo
SLSergio Lopez
Sergio Lopez
RARocio Abia
Rocio Abia
FMFrancisco J. G. Muriana
Francisco J. G. Muriana
Olive oil is the primary source of fat in the Mediterranean diet, which is associated with a significant improvement in health status, as measured by reduced mortality from several chronic diseases.

27 August 2024 in JCI Insight
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Pablo Fernandez-TussyPablo Fernandez-Tussy
Pablo Fernandez-Tussy
MPM Magdalena Perez-Cardelo
M Magdalena Perez-Cardelo
HZHanming Zhang
Hanming Zhang
JSJonathan Sun
Jonathan Sun
NPNathan L. Price
Nathan L. Price
CFCarlos Fernández
Carlos Fernández
The complexity of the mechanisms underlying metabolic dysfunction–associated steatotic liver disease (MASLD) progression remains a significant challenge for the development of effective therapeutics. miRNAs have shown great promise as regulators of biological processes and as therapeutic targets for complex diseases. Here, we study the role of hepatic miR-33, an important regulator of lipid metabolism, during the progression of MASLD and the development of hepatocellular carcinoma (HCC). We report that miR-33 was elevated in the livers of humans and mice with MASLD and that its deletion in hepatocytes (miR-33 HKO ) improved multiple aspects of the disease, including steatosis and inflammation, limiting the progression to metabolic dysfunction–associated steatotic hepatitis (MASH), fibrosis, and HCC. Mechanistically, hepatic miR-33 deletion reduced lipid synthesis and promoted mitochondrial fatty acid oxidation, reducing lipid burden. Additionally, absence of miR-33 altered the expression of several known miR-33 target genes involved in metabolism and resulted in improved mitochondrial function and reduced oxidative stress. The reduction in lipid accumulation and liver injury resulted in decreased YAP/TAZ pathway activation, which may be involved in the reduced HCC progression in HKO livers. Together, these results suggest suppressing hepatic miR-33 may be an effective therapeutic approach to temper the development of MASLD, MASH, and HCC in obesity.