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. Author manuscript; available in PMC: 2022 Apr 1.
Published in final edited form as: Chronobiol Int. 2021 Jan 13;38(4):543–556. doi: 10.1080/07420528.2020.1868490

Table 3.

Associations between Rest-Activity Rhythms and Cardiometabolic Biomarkers after adjustment for BMI

Rest-Activity Rhythm Parameter Cardiometabolic Biomarker Model 4
β (95% CI)
Interdaily Stability Systolic BP, mmHg −0.67 (−2.63, 1.30)
Diastolic BP, mmHg −0.25 (−2.17, 1.66)
Total-C, mg/dL −9.92 (−17.05, −2.79)
LDL-C, mg/dL −6.51 (−12.74, −0.27)*
HDL-C, mg/dL −2.10 (−5.78, 1.57)
Non-HDL-C, mg/dL −7.82 (−14.46, −1.17)*
Triglycerides, mg/dL −10.10 (−18.41, −1.79)*
Glucose, mg/dL −0.51 (−2.42, 1.39)
CRP, mg/L −0.21 (−0.45, 0.04)
Intradaily Variability Systolic BP, mmHg −0.11 (−2.10, 1.88)
Diastolic BP, mmHg −0.03 (−1.96, 1.90)
Total-C, mg/dL 7.75 (−0.94, 16.39)
LDL-C, mg/dL 4.00 (−2.50, 10.50)
HDL-C, mg/dL 2.02 (−1.71, 5.75)
Non-HDL-C, mg/dL 5.15 (−1.81, 12.11)
Triglycerides, mg/dL 7.18 (−0.34, 14.69)
Glucose, mg/dL 0.43 (−1.51, 2.36)
CRP, mg/L 0.30 (0.06, 0.55)*
Relative Amplitude Systolic BP, mmHg −1.19 (−3.17, 0.81)
Diastolic BP, mmHg −0.36 (−2.33, −1.61)
Total-C, mg/dL −6.28 (−15.11, 2.55)
LDL-C, mg/dL −5.39 (−11.87, 1.09)
HDL-C, mg/dL 0.43 (−3.38, 4.24)
Non-HDL-C, mg/dL −6.17 (−13.13, 0.78)
Triglycerides, mg/dL −5.74 (−13.43, 1.95)
Glucose, mg/dL 0.20 (−1.75, 2.15)
CRP, mg/L −0.09 (−0.33, 0.14)
Autocorrelation at 24h Systolic BP, mmHg −0.53 (−2.48, 1.41)
Diastolic BP, mmHg −0.72 (−2.61, 1.16)
Total-C, mg/dL −8.24 (−15.44, −1.04)*
LDL-C, mg/dL −5.47 (−11.70, 0.76)
HDL-C, mg/dL −1.68 (−5.33, 1.96)
Non-HDL-C, mg/dL −6.56 (−13.22, 0.10)
Triglycerides, mg/dL −7.62 (−16.03, 0.78)
Glucose, mg/dL −0.19 (−2.07, 1.70)
CRP, mg/L −0.24 (−0.48, −0.01)*

Results are presented as unstandardized β values and 95% confidence intervals (CI) for every 1-SD increase in each rest-activity rhythm parameter. Model 4 also adjusts for sex.

*

p≤0.05

p≤0.01. BP, blood pressure; C, cholesterol; LDL, low-density lipoprotein; HDL, high-density lipoprotein; CRP, C-reactive protein