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We can define subjects' risk preferences based on the value of CRRA, with r < 0 denoting risk loving, r = 0 denoting risk neutral, and r > 0 indicating risk aversion.
Taken together, these results, the mechanistic findings in animal models of atherosclerosis, and our correlative findings between LDL cholesterol and CX3CL1 levels in humans, suggest that CX3CL1 may represent a biomarker of the inflammatory component of atherosclerosis and potentially define subjects at increased risk for atherosclerotic disease events.
The same principle was followed to define subjects with hypertension.
Therefore, we used a combination of criteria to define subjects with PAD.
Second, the thresholds used to define subjects at high risk also varied (30 46%), as shown in Table 1.
The phenotypic classification that we have adopted pools the *1/*1 or *1/*2 or *2/*2 to define subjects with a high activity, those with genotypes *1/*3 or *2/*3 to define subjects with intermediate activity, while genotype *3/*3 defines low activity [ 7].
Similar(48)
At the same time they know certain defined subjects in depth.
We defined subjects with a score in the highest quartile to have a severe sleep disturbance.
We defined subjects as having comorbidity if at least three NHI diagnoses were identified in 1999.
We defined subjects with clinical DSPN as being unaware of their disorder if they had answered this question with "no".
We defined subjects' satisfaction as the level of positive appreciation for each item of the WHOQOL-Bref [ 29].
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