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. Author manuscript; available in PMC: 2023 May 1.
Published in final edited form as: Psychoneuroendocrinology. 2022 Feb 12;139:105689. doi: 10.1016/j.psyneuen.2022.105689

Table 4a. Regression models examining the patterning of race, SES, and sex and their pairwise interactions with allostatic load scores in the total sample, using either the simple summary scoring algorithm (versions i and iii) or the MIDUS approach (versions iv and vi).1.

Results from negative binomial regression models where AL was created using primary method of construction (version i)1

AL score (version i)2 Independent associations Pairwise interactions

Model 1 Model 2 Model 3 Model 4 Model 5 Model 6
Intercept 3 0.81 (0.70, 0.91) 1.05 (0.94, 1.16) 0.75 (0.62, 0.88) 0.93 (0.78, 1.06) 0.70 (0.55, 0.85) 0.93 (0.76, 1.10)
non-Black male high SES non-Black male non-Black and high SES male and high SES
Race
(non-Hispanic Black vs. non-Black)
0.42 (0.26, 0.59) - - 0.31 (0.10, 0.53) 0.23 (−0.08, 0.54) -
Sex
(female vs. male)
- −0.17 (−0.34, −0.01) - −0.26 (−0.47, −0.05) - −0.44 (−0.71, −0.17)
Cumulative life course SES3
(low vs. high)
- - 0.36 (0.20, 0.53) 0.21 (0.01, 0.42) 0.21 (−0.01, 0.43)
Race*Sex - - - 0.24 (−0.08, 0.57) - -
Race*SES - - - - 0.17 (−0.20, 0.54) -
Sex*SES - - - - - 0.39 (0.05, 0.73)
1

Associations obtained from a negative binomial regression model; estimated AL scores for a given group can be calculated by summing relevant betas and then exponentiating

2

Version i: simple summary approach, with medication correction and sex- and/or age-specific high-risk quartiles for DHEAS, %BF, and WC

3

Italiscized description under the intercept values identifies the subgroup for which the exponentiated intercept provides an AL score