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The association between serum cathepsin L and mortality in older adults
Tobias Feldreich1, Axel C Carlsson2, Ulf Risérus3
1School of Health and Social Studies, Dalarna University, Falun, Sweden; Department of Medical Sciences, Uppsala University Hospital, Uppsala, Sweden.
Insights
Higher serum cathepsin L levels are linked to increased cardiovascular mortality risk. This association appears moderated by kidney function, suggesting cathepsin L
Area of Science:
- Cardiovascular disease research
- Biomarker discovery
- Protease function in disease
Background:
- Atherosclerosis is linked to the protease cathepsin L.
- Limited data exist on cathepsin L as a cardiovascular risk marker.
Purpose of the Study:
- To investigate the association between circulating cathepsin L and cardiovascular mortality.
- To explore cathepsin L's role as a potential risk marker.
Main Methods:
- Utilized two independent community-based cohorts: ULSAM (n=776) and PIVUS (n=993).
- Followed participants for cardiovascular deaths over 9.7 and 10.0 years, respectively.
- Analyzed serum cathepsin L levels in relation to mortality risk.
Main Results:
- Elevated serum cathepsin L was associated with increased cardiovascular mortality risk in both cohorts.
- This association remained independent of inflammatory markers and cardiovascular risk factors.
- The association was not significant when adjusting for kidney function, suggesting its moderating role.
Conclusions:
- Higher serum cathepsin L is associated with increased cardiovascular mortality risk.
- Impaired kidney function may mediate or moderate this association.
- Further research is needed to understand mechanisms and clinical utility of cathepsin L.
Background And Aims:
Research suggests that the protease cathepsin L is causally involved in atherosclerosis. However, data on cathepsin L as a risk marker are lacking. Therefore, we investigated associations between circulating cathepsin L and cardiovascular mortality.
Methods:
Two independent community-based cohorts were used: Uppsala Longitudinal Study of Adult Men (ULSAM); n = 776; mean age 77 years; baseline 1997-2001; 185 cardiovascular deaths during 9.7 years follow-up, and Prospective Investigation of the Vasculature in Uppsala Seniors (PIVUS); n = 993; 50% women; mean age 70 years; baseline 2001-2004; 42 cardiovascular deaths during 10.0 years follow-up.
Results:
Higher serum cathepsin L was associated with an increased risk for cardiovascular mortality in age- and sex-adjusted models in both cohorts (ULSAM: hazard ratio (HR) for 1-standard deviation (SD) increase, 1.17 [95% CI, 1.01-1.34], p = 0.032 PIVUS: HR 1.35 [95% CI, 1.07-1.72], p = 0.013). When merging the cohorts, these associations were independent of inflammatory markers and cardiovascular risk factors, but non-significant adjusting for kidney function. Individuals with a combination of elevated cathepsin L and increased inflammation, kidney dysfunction, or prevalent cardiovascular disease had a markedly increased risk, while no increased risk was associated with elevated cathepsin L, in the absence of these disease states.
Conclusions:
An association between higher serum cathepsin L and increased risk of cardiovascular mortality was found in two independent cohorts. Impaired kidney function appears to be an important moderator or mediator of these associations. Further studies are needed to delineate the underlying mechanisms and to evaluate whether the measurement of cathepsin L might have clinical utility.
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