Karim Helmet T, Lee Soyoung, Gerlach Andrew, Stinley Mark, Berta Rachel, Mahbubani Rebecca, Tudorascu Dana L, Butters Meryl A, Gross James J, Andreescu Carmen
Department of Psychiatry, University of Pittsburgh, Pittsburgh, PA, United States; Department of Bioengineering, University of Pittsburgh, Pittsburgh, PA, United States.
Department of Psychiatry, University of Maryland, Baltimore, MD, United States.
Neurobiol Aging. 2024 Sep;141:55-65. doi: 10.1016/j.neurobiolaging.2024.02.017. Epub 2024 May 28.
Studies have confirmed that anxiety, especially worry and rumination, are associated with increased risk for cognitive decline, including Alzheimer's disease and related dementias (ADRD). Hippocampal atrophy is a hallmark of ADRD. We investigated the association between hippocampus and its subfield volumes and late-life global anxiety, worry, and rumination, and emotion regulation strategies. We recruited 110 participants with varying worry severity who underwent magnetic resonance imaging and clinical interviews. We conducted cross-sectional regression analysis between each subfield and anxiety, worry, rumination, reappraisal, and suppression while adjusting for age, sex, race, education, cumulative illness burden, stress, neuroticism, and intracranial volume. We imputed missing data and corrected for multiple comparisons across regions. Greater worry was associated with smaller subiculum volume, whereas greater use of reappraisal was associated with larger subiculum and CA1 volume. Greater worry may be detrimental to the hippocampus and to subfields involved in early ADRD pathology. Use of reappraisal appears protective of hippocampal structure. Worry and reappraisal may be modifiable targets for ADRD prevention.
研究证实,焦虑,尤其是担忧和反复思考,与认知能力下降的风险增加有关,包括阿尔茨海默病和相关痴呆症(ADRD)。海马萎缩是ADRD的一个标志。我们研究了海马及其子区域体积与晚年整体焦虑、担忧、反复思考以及情绪调节策略之间的关联。我们招募了110名担忧严重程度各异的参与者,他们接受了磁共振成像检查和临床访谈。我们在调整年龄、性别、种族、教育程度、累积疾病负担、压力、神经质和颅内体积的同时,对每个子区域与焦虑、担忧、反复思考、重新评价和抑制进行了横断面回归分析。我们对缺失数据进行了插补,并对各区域的多重比较进行了校正。更多的担忧与较小的下托体积相关,而更多地使用重新评价与较大的下托和CA1体积相关。更多的担忧可能对海马以及参与早期ADRD病理过程的子区域有害。使用重新评价似乎对海马结构有保护作用。担忧和重新评价可能是ADRD预防中可改变的目标。