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. 2019 Jun 4;9(1):157.
doi: 10.1038/s41398-019-0489-3.

Methylation age acceleration does not predict mortality in schizophrenia

Affiliations

Methylation age acceleration does not predict mortality in schizophrenia

Kaarina Kowalec et al. Transl Psychiatry. .

Abstract

Schizophrenia (SCZ) is associated with high mortality. DNA methylation levels vary over the life course, and pre-selected combinations of methylation array probes can be used to estimate "methylation age" (mAge). mAge correlates highly with chronological age but when it differs, termed mAge acceleration, it has been previously associated with all-cause mortality. We tested the association between mAge acceleration and mortality in SCZ and controls. We selected 190 SCZ cases and 190 controls from the Sweden Schizophrenia Study. Cases were identified from the Swedish Hospital Discharge Register with ≥5 specialist treatment contacts and ≥5 antipsychotic prescriptions. Controls had no psychotic disorder or antipsychotics. Subjects were selected if they had died or survived during follow-up (2:1 oversampling). Extracted DNA was assayed on the Illumina MethylationEPIC array. mAge was regressed on age at sampling to obtain mAge acceleration. Using Cox proportional hazards regression, the association between mAge acceleration and mortality was tested. After quality control, the following were available: n = 126 SCZ died, 63 SCZ alive, 127 controls died, 62 controls alive. In the primary analyses, we did not find a significant association between mAge acceleration and SCZ mortality (adjusted p > 0.005). Sensitivity analyses excluding SCZ cases with pre-existing cancer demonstrated a significant association between the Hannum mAge acceleration and mortality (hazard ratio = 1.13, 95% confidence interval = 1.04-1.22, p = 0.005). Per our pre-specified criteria, we did not confirm our primary hypothesis that mAge acceleration would predict subsequent mortality in people with SCZ, but we cannot rule out smaller effects or effects in patient subsets.

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Conflict of interest statement

P.F.S. reports the following potentially competing financial interests: Current: Lundbeck (advisory committee, grant recipient); Past 3 years: Pfizer (scientific advisory board), Element Genomics (consultation fee), and Roche (speaker reimbursement). The remaining authors declare that they have no conflict of interest.

Figures

Fig. 1
Fig. 1. Plot of predicted Hannum methylation age (mAge) against age at sampling, by status: a SCZ-died, b SCZ-alive, c Control-died, d Control-alive.
Correlation between age at sampling and Hannum mAge across all samples was 0.85. r = Pearson correlation coefficient, black line = linear model, gray region = 95% confidence intervals

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