Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, NC.
Department of Internal Medicine, Section on Hospital Medicine, Medical College of Wisconsin, Milwaukee, WI.
Am Heart J. 2024 Oct;276:31-38. doi: 10.1016/j.ahj.2024.07.012. Epub 2024 Jul 25.
The association of malignant left ventricular hypertrophy (LVH), a specific subphenotype of LVH characterized by elevated levels of high-sensitivity cardiac troponin (hs-cTnT) or N-terminal pro-B-type natriuretic peptide (NT-proBNP), with cognitive decline remains understudied.
This post-hoc analysis included a total of 8,027 (67.9 ± 9.3 years) SPRINT MIND trial participants who had with at least 1 follow-up cognitive assessment. Participants were classified into 6 groups on the basis of LVH status on electrocardiogram (ECG), and elevations in levels of hs-cTnT ≥14 ng/L or NT-proBNP ≥125 pg/mL at baseline visit. Multivariate Cox proportional hazard models were used to examine the association of LVH/biomarker groups with incident probable dementia, mild cognitive impairment (MCI) and a composite of MCI/probable dementia.
Over a median follow-up period of 5 years, there were 306, 597, and 818 incidents of MCI, probable dementia and a composite of MCI/probable dementia, respectively. Compared with participants without LVH and normal biomarker levels, those with concomitant LVH and elevated levels of both biomarkers were associated with a higher risk of probable dementia (HR, 2.50; 95% CI (1.26-4.95), MCI (HR, 1.78; 95% CI (0.99-3.23) and the composite of MCI/ probable dementia (HR, 1.89; 95% CI, 1.16-3.10).
Among SPRINT participants, malignant LVH is associated with incident probable dementia and mild cognitive impairment. These findings underscore the potential utility of measuring hs-cTnT and NT-proBNP levels when LVH is detected on ECG, aiding in the differentiation of individuals with a favorable risk for cognitive impairment from those with a higher risk.
恶性左心室肥厚(LVH)与认知能力下降有关,LVH 是一种特定的 LVH 亚表型,其特征是高水平的高敏心肌肌钙蛋白(hs-cTnT)或 N 末端 pro-B 型利钠肽前体(NT-proBNP)。然而,这种关联在研究中仍未得到充分探讨。
本事后分析共纳入了 SPRINT MIND 试验的 8027 名参与者(平均年龄 67.9 ± 9.3 岁),这些参与者至少有 1 次随访认知评估。根据心电图(ECG)上的 LVH 状态以及基线时 hs-cTnT≥14ng/L 或 NT-proBNP≥125pg/mL 的升高情况,将参与者分为 6 组。使用多变量 Cox 比例风险模型来检验 LVH/生物标志物组与新发可能痴呆、轻度认知障碍(MCI)和 MCI/可能痴呆的复合终点之间的关联。
在中位随访 5 年期间,分别有 306、597 和 818 例发生 MCI、可能痴呆和 MCI/可能痴呆的复合终点事件。与没有 LVH 和正常生物标志物水平的参与者相比,同时存在 LVH 且两种生物标志物水平升高的参与者,发生可能痴呆的风险更高(HR,2.50;95%CI(1.26-4.95))、MCI(HR,1.78;95%CI(0.99-3.23)和 MCI/可能痴呆的复合终点事件(HR,1.89;95%CI,1.16-3.10)。
在 SPRINT 参与者中,恶性 LVH 与新发可能痴呆和轻度认知障碍相关。这些发现强调了在心电图检测到 LVH 时测量 hs-cTnT 和 NT-proBNP 水平的潜在效用,有助于将认知障碍风险较低的个体与风险较高的个体区分开来。