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. 2017 Oct 9;12(10):e0185977. doi: 10.1371/journal.pone.0185977

Table 4. Covariate-adjusted ANA associations with mortality by cause of death, group analyzed, and analysis performed.

Cause of Death Group Analyzed Analysis Performed HR (95% CI) a N/C/C+
All Causes Enrolled at age ≥75 years Primary Analysis 1.27 (0.89, 1.82) 431/249/53
Exclude participants with ENA or a possible autoimmune disease 1.51 (1.03, 2.21) 329/185/38
Enrolled at age ≥75 years, Primary Analysis 1.99 (1.04, 3.80)b 77/54/8
history of cancer Exclude first 2 years of follow-up 2.64 (1.09, 6.38)b 65/43/7
Exclude participants with ENA or a possible autoimmune disease 2.14 (1.07, 4.28)b 60/42/6
Enrolled at age ≥75 years, Primary Analysis 1.16 (0.78, 1.74) 237/115/25
no history of CVD or cancer Exclude participants with ENA or a possible autoimmune disease 1.54 (1.01, 2.36) 189/90/19
CVD Enrolled at age ≥75 years Primary Analysis 1.69 (0.93, 3.07) 424/52/13
Exclude first 2 years of follow-up 1.99 (1.04, 3.78)b 379/34/9
Enrolled at age ≥65 years Redefine age-at-enrollment strata 1.90 (1.05, 3.43) 867/74/18
Cancer Enrolled at age <75 years Primary Analysis 1.62 (0.71, 3.69) 2903/75/18
Enrolled at age <65 years Redefine age-at-enrollment strata 2.70 (1.02, 7.14) 2454/39/11

Abbreviations: ANA = antinuclear antibodies; HR = hazard ratio; CI = confidence interval; N = number of participants analyzed; C = number of participants who died from the cause of interest; C+ = number of ANA-positive participants who died from the cause of interest; CVD = cardiovascular disease; BMI = body mass index.

a Each HR estimate was derived from a Cox model for cause-specific mortality, fitted within a given group of participants and focused on the effect of baseline ANA status on death from the cause of interest. The continuous event time variable for all-cause mortality was age at death from non-accidental causes, the continuous event time variable for cause-specific mortality was age at death from the cause of interest (either CVD or cancer), and baseline ANA status was represented by a dichotomous indicator variable. All analyses adjusted for age at risk (via the baseline hazard function) and included covariates for sex, race/ethnicity, education, and BMI. Analyses that did not stratify on disease history also adjusted for self-reported history of the disease of interest at baseline. Participants with missing values were excluded.

b Interpret cautiously, as these results are based on fewer than 10 events of interest.