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双相障碍患者的生物年龄是否会加速老化?FACE-BD 队列的探索性研究。

Does BioAge identify accelerated aging in individuals with bipolar disorder? An exploratory study in the FACE-BD cohort.

机构信息

Université Paris Cité, INSERM UMR-S 1144, Optimisation Thérapeutique en Neuropsychopharmacologie OTeN, Paris, France.

Département de Psychiatrie et de Médecine Addictologique, AP-HP, Groupe Hospitalo-Universitaire AP-HP Nord, DMU Neurosciences, Hôpital Fernand Widal, Paris, France.

出版信息

Bipolar Disord. 2024 Sep;26(6):595-603. doi: 10.1111/bdi.13480. Epub 2024 Jul 31.

Abstract

BACKGROUND

Individuals with bipolar disorders (BD) have an estimated loss of life expectancy around 10-15 years. Several laboratory-measured biomarkers of accelerated aging exist (e.g., telomere length), however with a questionable transferability to bedside. There is a need for easily and inexpensively measurable markers of aging, usable in routine practice, such as BioAge.

METHODS

We calculated BioAge that estimates biological age based on routine blood tests and a physical exam, in a sample of 2220 outpatients with BD. We investigated associations between BioAge Acceleration (BioAgeAccel), which is an indicator of accelerated aging, and sociodemographic variables, clinical variables, and current psychotropic medication use.

RESULTS

Mean chronological age was 40.2 (±12.9). Mean BioAge was 39.1 (±12.4). Mean BioAgeAccel was 0.08 (±1.8). A minority of individuals (15%) had a BioAgeAccel above 2 years. Multivariable analyses suggested strong associations between a higher BioAgeAccel and younger age, male sex, overweight and sleep disturbances. Regarding current psychotropic medication use, discrepancies between univariate and multivariate analyses were observed.

CONCLUSIONS

A minority of individuals with BD had an accelerated aging as measured by BioAge. We identified associations with potentially modifiable factors, such as higher body mass index and sleep disturbances, that are however nonspecific to BD. These results require replications in independent samples of individuals with BD, and comparisons with a control group matched for age and gender. Longitudinal studies are also required to test whether any change in metabolic health, or sleep might decrease BioAgeAccel.

摘要

背景

双相情感障碍(BD)患者的预期寿命估计缩短了 10-15 年。存在一些实验室测量的加速衰老的生物标志物(例如端粒长度),但在床边应用的可转移性存在疑问。需要一种易于测量且经济实惠的衰老标志物,可在常规实践中使用,例如 BioAge。

方法

我们根据常规血液检查和身体检查,在 2220 名 BD 门诊患者的样本中计算了 BioAge,该值估计了生物年龄。我们研究了 BioAgeAccel(加速衰老的指标)与社会人口统计学变量、临床变量和当前精神药物使用之间的关联。

结果

平均年龄为 40.2(±12.9)岁。平均 BioAge 为 39.1(±12.4)岁。平均 BioAgeAccel 为 0.08(±1.8)岁。少数患者(15%)的 BioAgeAccel 超过 2 年。多变量分析表明,较高的 BioAgeAccel 与年龄较小、男性、超重和睡眠障碍之间存在很强的关联。关于当前精神药物的使用,单变量和多变量分析之间存在差异。

结论

少数 BD 患者的生物年龄通过 BioAge 加速。我们发现与潜在可调节因素的关联,例如较高的体重指数和睡眠障碍,但这些因素与 BD 并不特异。这些结果需要在独立的 BD 患者样本中进行复制,并与年龄和性别匹配的对照组进行比较。还需要进行纵向研究,以测试代谢健康或睡眠的任何变化是否会降低 BioAgeAccel。

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