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. Author manuscript; available in PMC: 2017 Jan 1.
Published in final edited form as: Stroke. 2015 Nov 17;47(1):12–17. doi: 10.1161/STROKEAHA.115.010600

Table 3.

Multivariable associations between vasomotor symptom (VMS) trajectories and IMT

Mean IMT Maximum IMT
β(SE) P β(SE) P
Model 1
VMS trajectory
  Consistently low ------ -----
  Early onset .04(.01) .004 .05(.01) .0006
  Late onset −.01(.01) .50 −.01(.01) .50
  Consistently high .01(.01) .30 .02(.01) .20
Model 2
VMS trajectory
  Consistently low ------ -----
  Early onset .03(.01) .03 .04(.01) .008
  Late onset −.002(.01) .90 −.001(.01) .90
  Consistently high −.001(.01) .90 .002(.01) .90

Model 1 covariates: site, age, ethnicity, education

Model 2 covariates: Adjusted for site, age, ethnicity, education, body mass index, systolic blood pressure, high density lipoproteins; low density lipoproteins, triglycerides, homeostatic model assessment, smoking status, diabetes, anxiety, use of cardiovascular medications

IMT = intima media thickness; VMS=vasomotor symptoms