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Chin Med J (Engl). 2018 Mar 5;131(5):608-614. doi: 10.4103/0366-6999.226066.

Research Progress on the Relationship between Coronary Artery Calcification and Chronic Renal Failure.

Author information

1
Department of Cardiology, Zhujiang Hospital, Southern Medical University, Guangzhou, Guangdong 510280, China.

Abstract

in English, Chinese

Objective:

Coronary artery calcification (CAC) is thought to be a controlled metabolic process that is very similar to the formation of new bone. In patients with chronic renal failure (CRF), CAC is very common, and CAC severity correlates with the deterioration of renal function. We summarized the current understanding and emerging findings of the relationship between CAC and CRF.

Data Sources:

All studies were identified by systematically searching PubMed, Embase, and CNKI databases for the terms "coronary calcification", "chronic renal failure", "vascular smooth muscle cell", and their synonyms until September 2017.

Study Selection:

We examined the titles and abstracts of all studies that met our search strategy thoroughly. The full text of relevant studies was evaluated. Reference lists of retrieved articles were also scrutinized for the additional relevant studies.

Results:

CRF can accelerate CAC progression. CRF increases the expression of pro-inflammatory factors, electrolyte imbalance (e.g., of calcium, phosphorus), parathyroid hormone, and uremic toxins and their ability to promote calcification. These factors, through the relevant signaling pathways, trigger vascular smooth muscle cells to transform into osteoblast-like cells while inhibiting the reduction of vascular calcification factors, thus inducing further CAC.

Conclusions:

Coronary heart disease in patients with CRF is due to multiple factors. Understanding the mechanism of CAC can help interventionists to protect the myocardium and reduce the prevalence of coronary heart disease and mortality.

KEYWORDS:

Chronic Renal Failure; Coronary Calcification; Vascular Smooth Muscle Cell

PMID:
29483398
PMCID:
PMC5850680
DOI:
10.4103/0366-6999.226066
[Indexed for MEDLINE]
Free PMC Article

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