Prospective association between major depressive disorder and leukocyte telomere length over two years.
Prospective association between major depressive disorder and leukocyte telomere length over two years.
复制标题
两年内重度抑郁症与白细胞端粒长度之间的前瞻性关联。
DOI:
10.1016/j.psyneuen.2018.02.015
复制
发表时间:
2018
影响因子:
3.7
通讯作者:
deVivo,Imma
中科院分区:
文献类型:
--
作者:
Vance,MaryC;Bui,Eric;Hoeppner,SusanneS;Kovachy,Benjamin;Prescott,Jennifer;Mischoulon,David;Walton,ZandraE;Dong,Melissa;Nadal,MireyaF;Worthington,JohnJ;Hoge,ElizabethA;Cassano,Paolo;Orr,EstherH;Fava,Maurizio;deVivo,Imma
BackgroundReduced leukocyte telomere length (LTL) has been found to be associated with multiple common age-related diseases, including heart disease, diabetes, and cancer. A link has also been suggested between shortened LTL and major depressive disorder (MDD), suggesting that MDD may be a disease of accelerated aging. This prospective, longitudinal study examined the association between depression diagnosis at baseline and change in LTL over two years in a well-characterized sample ofN= 117 adults with or without MDD at baseline, using rigorous entry criteria.MethodsParticipants aged 18–70 were assessed with validated instruments by trained, doctoral-level clinician raters at baseline and at two-year follow-up, and blood samples were obtained at both visits. LTL was assayed under identical methods using quantitative polymerase chain reaction (qPCR). The effect of an MDD diagnosis at baseline on change in LTL over two years was examined via hierarchical mixed models, which included potential confounders.ResultsIndividuals with MDD at baseline had greater LTL shortening over two years than individuals without MDD (p= 0.03), even after controlling for differences in age, sex, and body mass index (BMI). In the sub-sample of individuals with MDD diagnoses at baseline, no significant associations between LTL change and symptom severity or duration were found.ConclusionA baseline diagnosis of MDD prospectively predicted LTL shortening over two years. Our results provide further support for MDD as a disease associated with accelerated aging in a well-characterized sample using validated, clinician-rated measures.