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. 2019 Dec 24;51:102520. doi: 10.1016/j.ebiom.2019.10.046

Table 5.

Multimarker associations with longitudinal changes in metabolic risk factors.

Change in metabolic trait Parameter Estimated β* SE P-value R[2]
BMI Baseline BMI −0.08 0.02 1E-04 0.027
Baseline Covariates 0.051
LPC 16:0 −0.56 0.14 <1.0E-04 0.029
Multi-Metabolite Panel 0.029
Glucose Baseline Glucose −0.53 0.04 <1.0E-04 0.221
Baseline Covariates 0.289
SM 36:0 4.05 0.90 <1.0E-04 0.036
DAG 36:2 −4.58 1.23 2.0E-04 0.025
Multi-Metabolite Panel 0.061
HDL-C Baseline HDL-C −0.15 0.04 <1.0E-04 0.032
Baseline Covariates 0.097
SM (d18:2/24:1) 2.67 0.57 <1.0E-04 0.042
LPC 20:3 1.60 0.50 1.6E-03 0.020
PS 36:0 −1.60 0.48 9.0E-04 0.022
Multi-Metabolite Panel 0.084
TAG Baseline TAG −0.57 0.05 <1.0E-04 0.207
Baseline Covariates 0.260
LPC 18:3 −12.75 3.61 4.0E-04 0.023
SM (d18:1/16:0) −21.18 5.05 <1.0E-04 0.032
Cer (d18:1/24:1) 15.91 4.24 2.0E-04 0.026
Multi-Metabolite Panel 0.080

Estimated β coefficients represent the mean differences in longitudinal change (native units) in the stated metabolic trait per one standard deviation difference in lipid measures.

A dynamic p-value threshold for entrance into the model was defined based on FDR < 0.25 [at step i, p < (0.25*i)/154].

Baseline covariates were as follows: age; sex; cohort; batch; and baseline values for total cholesterol, HDL-C, glucose, and BMI.

Abbreviations: LPC = lysophosphatidylcholine; DAG = diacylglycerol; PS = phosphatidylserine; SM = sphingomyelin; Cer = ceramide.

Lipids also significant in individual longitudinal associations are shown in italics.