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This research is just one of the very first to examine the partnership from lean muscle mass in order to vasomotor symptoms longitudinally
Characteristics of the sample were described by means (standard deviation) and frequency (%). At baseline, two VMS groups – any or none – were compared for group differences in, and associations among, demographics (age, race/ethnicity, education), quality of life (SF-36 score), and clinical characteristics (weight, hip and waist circumference, menopausal status, fat mass, fat free mass, skeletal mass), and VMS was estimated using chi square test (x 2 ) for categorical variables, and Kruskal-Wallis test for continuous variables. A scatter plot matrix was used to examine linear correlations among variables. For the purposes of modelling, LBM is represented by the SMI variable. Additionally, to account for the nonindependence of longitudinal observations derived from the same woman and data in which the number of observations may differ across women, longitudinal modeling using SAS PROC MIXED incorporated a random intercept term to account for the correlated errors among repeated measures of the same woman. Missing values of time-varying variables were interpolated based on prior and subsequent values for gaps of one to two visits as in previous SWAN analyses . To assess H1, incident VMS was modeled as a function of concurrent LBM using logistic regression analysis. To address H2 regarding long term change in LBM, the model was expanded to add within-woman percent change in LBM since baseline and to address H3, regarding recent change in LBM, the model was expanded to add within-woman percent change in LBM since prior visit (approximately 1 year earlier). The overall association between LBM and VMS was estimated in binary logistic regression models. Statistical analyses were one-tailed with an alpha level of 0.05 and conducted using SAS University Edition (© 2012–2018, SAS Institute Inc., Cary, NC).