Key result
Higher baseline cathepsin S is linked to increased CRP and IL-6 independent of obesity.
Why the study?
Previous data showed an association between circulating cathepsin S and inflammatory markers in the obese, but community-based reports were lacking.
Cohort (n=991)
Effect estimate: regression coefficient 0.13 (95% CI 0.07-0.19)
p-value: p=<0.001
Supports cathepsin S as obesity-independent inflammation marker; leaves open its role in CV risk prediction.
OBJECTIVE: Cathepsin S has been suggested provide a mechanistic link between obesity and atherosclerosis, possibly mediated via adipose tissue-derived inflammation. Previous data have shown an association between circulating cathepsin S and inflammatory markers in the obese, but to date, community-based reports are lacking. Accordingly, we aimed to investigate the association between serum levels of cathepsin S and markers of cytokine-mediated inflammation in a community-based sample, with prespecified subgroup analyses in nonobese participants. METHODS: Serum cathepsin S, C-reactive protein (CRP), and IL-6 were measured in a community-based cohort of elderly men (Uppsala Longitudinal Study of Adult Men; mean age 71 years, n = 991). CRP and IL-6 were also measured at a reexamination after 7 yr. RESULTS: After adjustment for age, body mass index, fasting plasma glucose, diabetes treatment, systolic blood pressure, diastolic blood pressure, hypertension treatment, serum cholesterol, serum high-density lipoprotein cholesterol, prior cardiovascular disease, smoking, and leisure time physical activity, higher cathepsin S was associated with higher CRP (regression coefficient for 1 sd increase, 0.13; 95% confidence interval 0.07-0.19; P < 0.001) and higher serum IL-6 (regression coefficient for 1 sd increase, 0.08; 95% confidence interval 0.01-0.14; P = 0.02). These associations remained similar in normal-weight participants (body mass index <25 kg/m(2), n = 375). In longitudinal analyses, higher cathepsin S at baseline was associated with higher serum CRP and IL-6 after 7 yr. CONCLUSIONS: These results provide additional evidence for the interplay between cathepsin S and inflammatory activity and suggest that this association is present also in normal-weight individuals in the community.
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Jobs et al. (2010) reported a cohort. Serum cathepsin S was evaluated on C-reactive protein (CRP) (regression coefficient 0.13, 95% CI 0.07-0.19, p=<0.001). Higher baseline serum cathepsin S was associated with higher C-reactive protein (regression coefficient per 1 SD increase 0.13; 95% CI 0.07-0.19; P<0.001) and IL-6, independently of obesity.
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