Epidemiological data and interventional studies with hormone replacement therapy suggest that women, at least until menopause, are at decreased cardiovascular risk compared to men. Still the molecular mechanisms beyond this difference are debated and the investigation in experimental models of atherosclerosis has been pivotal to prove that the activation of the estrogen receptor is atheroprotective, despite not enough to explain the differences reported in cardiovascular disease between male and female. This casts also for investigating the importance of the sex chromosome complement (genetic sex) beyond the contribution of sex hormones (gonadal sex) on atherosclerosis. Aim of this review is to present the dualism between gonadal sex and genetic sex with a focus on the data available from experimental models. The molecular mechanisms driving changes in lipid metabolism, immuno-inflammatory reactivity and vascular response in males and females that affect atherosclerosis progression will be discussed.

Gonadal sex vs genetic sex in experimental atherosclerosis / J. Nour, F. Bonacina, G.D. Norata. - In: ATHEROSCLEROSIS. - ISSN 1879-1484. - 384:(2023 Nov), pp. 117277.1-117277.10. [10.1016/j.atherosclerosis.2023.117277]

Gonadal sex vs genetic sex in experimental atherosclerosis

J. Nour
Primo
;
F. Bonacina;G.D. Norata
Ultimo
2023

Abstract

Epidemiological data and interventional studies with hormone replacement therapy suggest that women, at least until menopause, are at decreased cardiovascular risk compared to men. Still the molecular mechanisms beyond this difference are debated and the investigation in experimental models of atherosclerosis has been pivotal to prove that the activation of the estrogen receptor is atheroprotective, despite not enough to explain the differences reported in cardiovascular disease between male and female. This casts also for investigating the importance of the sex chromosome complement (genetic sex) beyond the contribution of sex hormones (gonadal sex) on atherosclerosis. Aim of this review is to present the dualism between gonadal sex and genetic sex with a focus on the data available from experimental models. The molecular mechanisms driving changes in lipid metabolism, immuno-inflammatory reactivity and vascular response in males and females that affect atherosclerosis progression will be discussed.
No
English
Experimental atherosclerosis; Inflammation; Lipids; Sexual chromosomes; Sexual hormones;
Settore BIO/14 - Farmacologia
Review essay
Esperti anonimi
Pubblicazione scientifica
Goal 3: Good health and well-being
   Integrating metabolism and immunity: cellular and molecular pathways leading to metabolic dysregulation and autoimmunity
   MINISTERO DELL'ISTRUZIONE E DEL MERITO
   2017K55HLC_003

   MUSA - Multilayered Urban Sustainability Actiona
   MUSA
   MINISTERO DELL'UNIVERSITA' E DELLA RICERCA

   Molecular mechanisms of T regulatory impairment in Familial Hypercholesterolemia: exploring cellular metabolic reprogramming as a tool to restore theirsuppressive function
   FONDAZIONE CARIPLO
   2019-1560
nov-2023
Elsevier
384
117277
1
10
10
Pubblicato
Periodico con rilevanza internazionale
pubmed
scopus
crossref
Aderisco
info:eu-repo/semantics/article
Gonadal sex vs genetic sex in experimental atherosclerosis / J. Nour, F. Bonacina, G.D. Norata. - In: ATHEROSCLEROSIS. - ISSN 1879-1484. - 384:(2023 Nov), pp. 117277.1-117277.10. [10.1016/j.atherosclerosis.2023.117277]
open
Prodotti della ricerca::01 - Articolo su periodico
3
262
Article (author)
Periodico con Impact Factor
J. Nour, F. Bonacina, G.D. Norata
File in questo prodotto:
File Dimensione Formato  
Gonadal sex vs genetic sex in experimental atherosclerosis..pdf

accesso aperto

Tipologia: Publisher's version/PDF
Dimensione 4.23 MB
Formato Adobe PDF
4.23 MB Adobe PDF Visualizza/Apri
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1026881
Citazioni
  • ???jsp.display-item.citation.pmc??? 0
  • Scopus 7
  • ???jsp.display-item.citation.isi??? 0
social impact