Lundin Sori K, Hu Xinyue, Feng Jingna, Lundin Karl K, Chen Yong, Tao Cui
Department of Biostatistics and Data Science, School of Public Health, The University of Texas Health Science Center at Houston, Houston, TX, USA 77030.
Center for Biomedical Semantics and Data Intelligence (BSDI), University of Texas Health Science Center at Houston, Houston, TX, USA 77030.
Res Sq. 2023 Apr 13:rs.3.rs-2629005. doi: 10.21203/rs.3.rs-2629005/v1.
While hypertension is a modifiable risk factor of Alzheimer's disease and related dementias (ADRD), limited studies have been conducted on the effectiveness of antihypertensive medications (AHMs) in altering the progression from mild cognitive impairment (MCI) to ADRD; similarly, few studies have assessed drug-drug interactions of AHMs with drugs targeted to modify other risk factors of ADRD such as type II diabetes and hypercholesterolemia.
128,683 unique hypertensive patients with MCI on US-based Optum claims data were identified. Diuretics, beta blockers (BBs), calcium channel blockers (CCBs), angiotensin-converting enzyme inhibitors (ACE inhibitors), and angiotensin II receptor antagonists (ARBs) were identified as five major AHM classes. Baseline characteristics were compared. Cox proportional hazards (PH) models were used to study the association between specific AHM exposure and the progression from MCI to ADRD while controlling for demographic variables, comorbidities, and the use of Statins and Metformin. To examine the association of AHM-Statin or AHM-Metformin interaction with ADRD progression, we also investigated models controlling for the aforementioned confounders, as well as drug-drug interactions.
The study included 100,678 patients who were taking at least one class of AHM and 28,005 who were not taking any AHMs during the study period. AHM users had a higher incidence of comorbidities (all ≤0.039) and consumption of Metformin and Statins (both <0.001) compared to non-users. Users of each major AHM class showed significantly lower risk of developing ADRD compared to non-users of that specific drug class (adjusted hazard ratio (aHR): 0.96-0.98; all ≤0.048). Within patients on monotherapy (using only one AHM drug), no specific AHM class had significantly lower risk of ADRD diagnosis compared to other AHM drug classes (aHR: 0.97-1.11; all ≥0.053). Use of Diuretics or CCBs in combination with Metformin consumption (aHR: 0.89, 0.91, respectively) showed lower risk of MCI to ADRD progression than use without Metformin consumption (aHR: 0.97, 0.98, respectively), whereas use of any of the five major AHMs with Statin consumption (aHR: 0.91-0.94) all showed lower risk than without Statin consumption (aHR: 0.98-1.04).
All five major AHM classes showed a protective effect against ADRD progression among hypertensive patients with MCI. Also, certain combinations of AHMs with Metformin or Statins showed a stronger protective effect compared to AHMs alone, and some drug-drug interactions of AHM-Metformin or AHM-Statin also showed protective effects against progression from MCI to ADRD.
虽然高血压是阿尔茨海默病及相关痴呆症(ADRD)的一个可改变的风险因素,但关于抗高血压药物(AHM)改变从轻度认知障碍(MCI)进展为ADRD有效性的研究有限;同样,很少有研究评估AHM与针对ADRD其他风险因素(如2型糖尿病和高胆固醇血症)的药物之间的药物相互作用。
根据美国Optum索赔数据,识别出128,683名患有MCI的独特高血压患者。利尿剂、β受体阻滞剂(BB)、钙通道阻滞剂(CCB)、血管紧张素转换酶抑制剂(ACE抑制剂)和血管紧张素II受体拮抗剂(ARB)被确定为五大类AHM。比较了基线特征。使用Cox比例风险(PH)模型研究特定AHM暴露与从MCI进展为ADRD之间的关联,同时控制人口统计学变量、合并症以及他汀类药物和二甲双胍的使用。为了研究AHM-他汀类药物或AHM-二甲双胍相互作用与ADRD进展的关联,我们还研究了控制上述混杂因素以及药物相互作用的模型。
该研究纳入了100,678名在研究期间至少服用一类AHM的患者和28,005名未服用任何AHM的患者。与未使用者相比,AHM使用者的合并症发生率更高(均≤0.039),二甲双胍和他汀类药物的消耗量也更高(均<0.001)。与特定药物类别的未使用者相比,每类主要AHM的使用者发生ADRD的风险均显著降低(调整后风险比(aHR):0.96 - 0.98;均≤0.048)。在接受单药治疗(仅使用一种AHM药物)的患者中,与其他AHM药物类别相比,没有特定的AHM类别发生ADRD诊断的风险显著更低(aHR:0.97 - 1.11;均≥0.053)。与未服用二甲双胍相比,联合使用利尿剂或CCB与二甲双胍(aHR分别为0.89、0.91)显示从MCI进展为ADRD的风险更低,而与未服用他汀类药物相比,使用五大类AHM中的任何一种与他汀类药物联合使用(aHR:0.91 - 0.94)均显示风险更低(aHR:0.98 - 1.04)。
所有五大类AHM在患有MCI的高血压患者中均显示出对ADRD进展的保护作用。此外,与单独使用AHM相比,AHM与二甲双胍或他汀类药物的某些联合使用显示出更强的保护作用,并且AHM-二甲双胍或AHM-他汀类药物的一些药物相互作用也显示出对从MCI进展为ADRD的保护作用。