The Ratio of Triglyceride to High-density Lipoprotein Cholesterol as an Indicator of Risk Stratification for Atherosclerotic Cardiovascular Disease in a Clinical Setting.

Large-scale clinical studies conducted to verify the effects of statins, statins plus concomitant ezetimibe therapy (1), and treatment with a protein convertase subtilisin/kexin type 9 (PCSK9) inhibitor designed to prevent the development of coronary artery disease (CAD) (2) have established the usefulness of low-density lipoprotein cholesterol (LDL-C)-lowering therapy. In addition, countermeasures against residual independent risk factors, such as hypertriglyceridemia (high TG) and low serum levels of high-density lipoprotein cholesterol (HDL-C) (3), are also emphasized. However, the usefulness of reducing serum TG levels with fibrates or increasing serum HDL-C levels using cholesteryl transfer protein (CETP) inhibitors or niacin for preventing CAD (4) has yet to be demonstrated in a large-scale clinical study.

Visceral obesity, a symptom of the disease state of metabolic syndrome, has been seen to lead to a lipid profile characterized by high TG and low HDL-C, the management of which is difficult in clinical settings (3). In addition, it has been reported that the TG/HDL-C ratio is a useful estimator of the LDL particle size, with a higher TG/HDL-C ratio indicating a smaller LDL particle size. In epidemiologic studies, the TG/HDL-C ratio has been recognized as a reliable risk marker of atherosclerotic cardiovascular disease (ASCVD) (5). In demonstrating its usefulness, Moriyama showed that the TG/HDL-C ratio can be easily estimated even in clinical settings using combined serum small-dense LDL (6) and malondialdehyde-modified LDL (7), representing atherogenic LDL subclasses (8). His study also supports the possibility of applying the TG/HDL-C ratio as a new management target for the prevention of ASCVD. (i.e., towards the objective of minimizing any residual risk for ASCVD, in the current scenario), where the validity of control of the serum LDL-C, as one of the strongest risk factors for ASCVD, has become relatively well established.

To investigate the association of the TG/HDL-C ratio with the risk of development of CAD, prospective cohort studies have demonstrated that a higher TG/HDL-C ratio is associated with poorer CAD-related prognosis (9). Regarding the underlying mechanisms, it has been suggested that a higher TG/HDL-C ratio is associated not only with downsizing of LDL particle size and consequent progression of atherosclerosis, but also with worsening insulin resistance and increased visceral fat deposition.

High TG is liable to be complicated by low HDL-C, and although both of these parameters are mutually independent ASCVD risk factors, the most relevant cases are those with concurrent high TG and low HDL-C, which has with a potent atherogenic effect.

Future studies should evaluate the role of other risk factors (i.e., LDL-C, hypertension, diabetes mellitus, chronic kidney disease, and obesity) and establish a concrete numerical value by which the TG/HDL-C ratio may be used as an indicator of the risk of ASCVD.

However, the TG/HDL-C ratio may prove useful for evaluating the results of an intervention study being conducted to verify the effect of a new fibrate agent endowed with more potent TG-lowering and HDL-C-increasing effects designed to suppress cardiovascular events more effectively than conventional fibrate drugs currently in use (10). In order to further reduce the risk of ASCVD, it may be beneficial to focus attention not only on the LDL-C serum level but also on the TG/HDL-C ratio, which is associated with LDL heterogeneity.

The author states that he has no Conflict of Interest (COI).