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In the complete sample, adjusted for age, sex, educational level (both as a continuous and categorical variable) and race/ethnicity, sarcopenia (without obesity) was significantly associated with increased HOMA-IR and pre-diabetes, but not with dysglycemia or diabetes outcomes, and in particular there was a marginally significant association with decreased risk of DM (Table 2).
aMayo Clinic sample adjusted for age and region of residence (Minnesota, Iowa, Wisconsin, Illinois, North Dakota and South Dakota); SEARCH sample adjusted for age; pooled Mayo Clinic + SEARCH sample adjusted for age and study.
aMayo sample adjusted for age and region of residence (Minnesota, Iowa, Wisconsin, Illinois, North Dakota and South Dakota); SEARCH sample adjusted for age; pooled Mayo + SEARCH sample adjusted for age and study.
It may be interpreted directly as the proportion of discriminations made in the sample, adjusted for the length of the scale.
Table 2 presents an overview of the socioeconomic distribution of health care utilization in the sample, adjusted for age, gender, self-reported health and municipality size.
The sample (adjusted for stratification) was compared with data from all parents of 4-year-olds in Trondheim in the years 2007 and 2008 using register information from Statistics Norway.
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BAF and LRR thresholds are calculated both globally and locally for each sample, adjusting for quality-related variation between samples and chromosomes.
Associations with GDM across pyrosequenced loci were modeled using linear mixed models with a random intercept for sample, adjusting for maternal age, pre-pregnancy BMI, infant sex, maternal smoking, and self-reported ethnicity.
Positive values indicate an increase in methylation with GDM bChange in methylation associated with GDM across pyrosequenced loci modeled using linear mixed models with a random intercept for sample, adjusting for the same covariates.
Second, externalising problems may cause more burden in families and therefore parents may underreport their children's positive attributes; however, in our sample, adjusting for parental burden did not change the pattern of the results.
Table 5 gives ORs for seroconversion and unit changes in IgG values between samples, adjusted for parity and, for parous women, with additional adjustment for age at first birth.
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