AI Article Synopsis

  • * Out of 847 patients, those who achieved optimal LDL-C levels (below 1.4 mmol/L and a reduction of at least 50% from baseline) showed a significantly lower rate of NTL plaque progression compared to those in the non-optimal group.
  • * Both univariate and multivariate logistic regression analyses identified achieving the recommended LDL-C levels as an independent protective factor against NTL plaque progression, suggesting that managing LDL-C effectively may reduce future cardiac events.

Article Abstract

The progression of NTLs after PCI accounts for a significant portion of future adverse cardiac events. The reduction in LDL-C reduces cardiovascular events. This has, however, not yet been shown in a real-world setting. We aimed to investigate the association between LDL-C changes with progression in NTLs. A total of 847 patients with successful PCI were enrolled. Patients with follow-up LDL-C ≥ 1.4 mmol/L or percent reduction <50% compared to baseline were Non-optimal group ( = 793); patients with follow-up LDL-C < 1.4 mmol/L and percent reduction ≥50% compared to baseline were Optimal group ( = 54). Compared to Non-optimal group, Optimal group presented a lower rate of NTL plaque progression (11.11% vs. 23.96%; = 0.007) and a lower follow-up TC (2.77 ± 0.59 vs. 3.66 ± 0.97; < 0.001) and LDL-C (1.09 ± 0.26 vs. 2.03 ± 0.71; < 0.001). The univariate logistic regression analysis revealed that follow-up LDL-C < 1.4 mmol/L and a percent reduction ≥50% from baseline was a protective factor for NTL plaque progression (OR: 0.397; 95%CI: 0.167-0.941; = 0.036). The multivariate logistic regression model revealed that follow-up LDL-C < 1.4 mmol/L and percent reduction ≥50% was indeed an independent factor associated with a lower rate of plaque progression of NTLs (OR: 0.398; 95% CI: 0.167-0.945; = 0.037). Therefore, achieving guideline-recommended LDL-C level was associated with a significantly reduced risk of NTL plaque progression.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9917377PMC
http://dx.doi.org/10.3390/jcm12030785DOI Listing

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