Colpo Gabriela D, Leffa Daniella D, Köhler Cristiano A, Kapczinski Flávio, Quevedo João, Carvalho André F
Center for Translational Psychiatry, Department of Psychiatry and Behavioral Sciences, The University of Texas Medical School at Houston, Houston, TX, USA.
Laboratório de Neurociências, Programa de Pós-Graduação em Ciências da Saúde, Unidade Acadêmica de Ciências da Saúde, Universidade do Extremo Sul Catarinense, Laboratório de Biologia Celular e Molecular, Criciúma, SC, Brazil.
J Affect Disord. 2015 Nov 1;186:241-8. doi: 10.1016/j.jad.2015.06.034. Epub 2015 Jul 26.
Bipolar disorder (BD) is associated with a reduced life expectancy compared to the general population mainly due to a high prevalence of comorbid somatic illnesses. A model of accelerated aging has been proposed as a potential explanation to these epidemiological findings. Nevertheless, studies measuring telomere length (TL) in patients with BD compared to healthy controls have provided mixed results.
To compare TL between BD patients and healthy controls, and to search for potential modeP<rators for observed differences.
We performed a systematic review and meta-analysis of original studies comparing TL in patients with BD vs. healthy controls published up to February 24th, 2015 in main electronic databases. Heterogeneity was explored through meta-regression and subgroup analysis.
Seven studies met inclusion criteria (N=1115). There was no difference in TL between participants with BD and healthy controls (Hedges's g=-0.012; 95% CI=-0.418 to 0.393, P=0.952). There was no evidence for publication bias. Heterogeneity was high (I(2)=89.65%). In meta-regression analyses, the percentage of females in healthy control samples (P=0.04) and the methodological quality of included studies (P<0.001) emerged as significant moderators, while subgroup analyses suggest that the type of assay employed to measure TL and age- and gender-matching of BD and HC participants may contribute to heterogeneity.
Telomere length does not differ between participants with BD vs. healthy controls; this finding does not support the view of BD as an illness associated with accelerated cellular aging. However, more studies controlling for potential confounders are necessary.
与普通人群相比,双相情感障碍(BD)患者的预期寿命缩短,主要原因是共病躯体疾病的高患病率。有人提出加速衰老模型来解释这些流行病学发现。然而,与健康对照相比,测量BD患者端粒长度(TL)的研究结果不一。
比较BD患者与健康对照的TL,并寻找观察到的差异的潜在调节因素。
我们对截至2015年2月24日在主要电子数据库中发表的比较BD患者与健康对照TL的原始研究进行了系统评价和荟萃分析。通过荟萃回归和亚组分析探讨异质性。
七项研究符合纳入标准(N = 1115)。BD患者与健康对照的TL无差异(Hedges's g = -0.012;95%CI = -0.418至0.393,P = 0.952)。没有证据表明存在发表偏倚。异质性较高(I(2)=89.65%)。在荟萃回归分析中,健康对照样本中的女性百分比(P = 0.04)和纳入研究的方法学质量(P < 0.001)是显著的调节因素,而亚组分析表明,用于测量TL的检测方法类型以及BD和HC参与者的年龄和性别匹配可能导致异质性。
BD患者与健康对照的端粒长度没有差异;这一发现不支持将BD视为与细胞加速衰老相关疾病的观点。然而,需要更多控制潜在混杂因素的研究。