Aortic Valve Calcification Is Associated with Future Cognitive Impairment.

BACKGROUND: While an association between atherosclerosis and dementia has been identified, few studies have assessed the longitudinal relationship between aortic valve calcification (AVC) and cognitive impairment (CI).
OBJECTIVE: We sought to determine whether AVC derived from lung cancer screening CT (LCSCT) was associated with CI in a moderate-to-high atherosclerotic risk cohort.
METHODS: This was a single site, retrospective analysis of 1401 U.S. veterans (65 years [IQI: 61, 68] years; 97%male) who underwent quantification of AVC from LCSCT indicated for smoking history. The primary outcome was new diagnosis of CI identified by objective testing (Mini-Mental Status Exam or Montreal Cognitive Assessment) or by ICD coding. Time-to-event analysis was carried out using AVC as a continuous variable.
RESULTS: Over 5 years, 110 patients (8%) were diagnosed with CI. AVC was associated with new diagnosis of CI using 3 Models for adjustment: 1) age (HR: 1.104; CI: 1.023-1.191; p = 0.011); 2) Model 1 plus hypertension, hyperlipidemia, diabetes, CKD stage 3 or higher (glomerular filtration rate < 60 mL/min) and CAD (HR: 1.097; CI: 1.014-1.186; p = 0.020); and 3) Model 2 plus CVA (HR: 1.094; CI: 1.011-1.182; p = 0.024). Sensitivity analysis demonstrated that the association between AVC and new diagnosis of CI remained significant upon exclusion of severe AVC (HR: 1.100 [1.013-1.194]; p = 0.023). Subgroup analysis demonstrated that this association remained significant when including education in the multivariate analysis (HR: 1.127 [1.030-1.233]; p = 0.009).
CONCLUSION: This is the first study demonstrating that among mostly male individuals who underwent LCSCT, quantified aortic valve calcification is associated with new diagnosis of CI.

INTRODUCTION

Cognitive impairment (CI) is a growing problem in an increasingly aging population and is expected to affect approximately 13.8 million Americans by 2050 [1]. The classification of CI into mild cognitive impairment versus dementia is dependent on identifying decreased mental abilities and impairment of daily functioning [2]. Early identification of patients at risk for CI may be of value to clinicians as studies have shown that the conversion rate of mild cognitive impairment to dementia can be as much as 30%over 5 years [3]. However, few biomarkers exist that reliably predict disease incidence at early or preclinical stages much less risk of progression [4].

Inflammation and atherosclerotic vasculopathy, including microangiopathy, have been strongly associated with the neurodegenerative changes associated with CI [5, 6]. In addition, onset of CI is strongly influenced by cerebrovascular accident (CVA), and by the number of CVA events, with CI occurring in 10%of patients after an initial CVA and 30%after recurrent CVA [7].

Our group recently found aortic valve calcification (AVC) to be independently associated with increased atherosclerotic events, including all-cause mortality, nonfatal myocardial infarction (MI), and nonfatal CVA, despite a very weak correlation between AVC and coronary calcification [8]. Other groups have demonstrated the presence of AVC to be associated with covert brain infarcts identified on MRI [9]. Moreover, cerebral white matter abnormalities, including those attributable to CVA, have been associated with cognitive decline and dementia [10, 11]

While an association between atherosclerotic vascular disease and CI has been identified, few studies have assessed the longitudinal relationship between AVC and CI [12]. Here we sought to determine the prognostic value of AVC derived from low dose, lung cancer screening computed tomography (LCSCT) for CI in a moderate-to-high atherosclerotic risk cohort.

MATERIALS AND METHODS

This study was approved by the Providence Veteran’s Affairs (VA) Medical Center Institutional Review Board and complies with the Declaration of Helsinki, and all patient data were handled in compliance with the Health Insurance Portability and Accountability Act (HIPAA) regulations. All patient records were de-identified and analyzed anonymously. Through the Providence VA Medical Center and the corresponding office of the Associate Chief of Staff for Research, all data, analytical methods, and study materials are available upon request to other researchers, who meet the Institutional Review Board criteria for access to VA confidential research data, for purposes of reproducing the results or replicating the study.

This was a single-center, retrospective analysis of 1654 U.S. veterans who underwent U.S. Preventive Services Task Force guideline–recommended (i.e., 30-pack-year tobacco smoking history, 55 to 80 years of age, active or quit < 5 years previously) LCSCT between October 1, 2013, and July 31, 2014 [13]. A total of 253 patients were excluded from the study due to diagnosis of lung cancer on the LCSCT, prior aortic valve replacement and prior diagnosis of CI resulting in 1401 patients for all subsequent analyses. Prior aortic valve replacement and CI were defined as occurring prior to the date of the LCSCT.

CT examinations were not electrocardiographically (ECG)-gated and were performed with a 128-slice CT scanner (Siemens Healthcare, Erlangen, Germany); 128×0.6 mm collimation, 0.5-s rotation, pitch of 0.84, 380-mm field of view, 512×512 pixel matrix, tube voltage of 120 kV and tube current of 40 mA, image reconstruction thickness of 1.00–1.25 mm, and a minimum area required to identify calcium was 0.55 mm2. AVC and coronary artery calcification (CAC) scores were quantified using the Agatston method via a semiautomated imaging workstation with readers blinded to patient data [14, 15]. The kappa for interobserver agreement was 0.91 (0.85–0.95) and 0.92 (0.88–0.96) for AVC and CAC, respectively. As described elsewhere, there was a strong Pearson correlation between AVC from non-ECG-gated and ECG-gated CT acquisition protocols [8, 16].

The U.S. Department of Veterans Affairs (VA) electronic medical record (EMR) was searched for patient demographics and cardiovascular risk factors. Coronary artery disease (CAD) was defined as a history of MI, prior revascularization or abnormalities on cardiac testing (exercise treadmill testing, echocardiography, myocardial perfusion, cardiac computed tomography, or coronary angiography). MI was defined as EMR-documented evidence of elevated cardiac troponin values with at least one value above the 99th percentile upper reference limit plus clinical evidence of acute myocardial ischemia, consistent with universal definitions [17]. CVA included non-hemorrhagic, ischemic stroke and transient ischemic attack.

The primary outcome was new diagnosis of CI identified by objective cognitive testing or by ICD coding, using the following diagnosis codes: ICD-9:290, 294.11, 331.0, 331.1, 331.2, 331.82, 331.83, 331.9, 438.0, and 780.93; ICD-10:294.8, 294.9, 437.9, 780.93, F00, F01, F02.81, F03, F03.91, F04, F09, G30, G31, G31.84, I67.9, I69.898, I69.918, R41, R41.81, R41.840, and R41.9 (Supplementary Table 1). The ICD-9 and ICD-10 diagnosis codes for CI have been shown to have a sensitivity of 32.3%and 66.9%and a specificity of 100%and 99.8%, respectively [18]. Objective cognitive testing included patients evaluated by either Mini-Mental Status Exam (MMSE) or Montreal Cognitive Assessment (MoCA). The MMSE and MoCA items have been described in detail elsewhere and the utilized cut-off scores for CI by MMSE and MoCA are less than 26 and less than 24, respectively [19, 20]. Evaluations were conducted by the Mental Health and Behavioral Science Services (MHBSS) at the VA by trained behavioral mental health providers. Scores were not adjusted for age or education. Similar to prior studies, the MHBSS documentation detailed the highest educational attainment in the following categories: 8th grade and below, some High School, High School Diploma or General Education Development (GED), some College or Associate’s Degree, Bachelors and Post-Bachelor degree [21]. The highest educational attainment was recorded as a categorical variable. Adjudicators of clinical outcomes were blinded to AVC and CAC and vice versa.

Results are presented as mean (standard error) for continuous variables with normal distribution, median (interquartile range) for continuous variables without normal distribution, and number (percentage) for categorical data. The Shapiro-Wilk test for normality was used to test for normal distribution of age, body mass index (BMI), hyperlipidemia, atherosclerotic cardiovascular disease (ASCVD), CAC and AVC.

The relationship between AVC as a continuous variable and primary outcomes was determined using Cox regression analysis. AVC was treated as continuous variable, using base-10 log transformation of AVC+1 (log[AVC+1]) to account for a right-skewed distribution. The statistical analysis included 3 separate models: Model 1 adjusting for age; Model 2 adjusting for age, hypertension, hyperlipidemia, diabetes mellitus, chronic kidney disease (CKD) stage 3 or higher (glomerular filtration rate < 60 mL/min) and CAD; and Model 3 adjusting for age, hypertension, hyperlipidemia, diabetes mellitus, CKD stage 3 or higher (glomerular filtration rate < 60 mL/min), CAD and prior CVA. A sensitivity analysis was performed by excluding those patients with severe AVC, as defined by ≥1,274 AU in women and ≥2,065 AU in men [22, 23]. A subgroup analysis was performed on a subset of patients for whom highest education attainment was documented in the VA EMR, allowing for inclusion of highest education attainment as a categorical in the multivariate adjustment.

All statistical analyses were conducted with the use of Stata/SE (version 15.1; StataCorp LLC, College Station, TX) or Prism (version 7; GraphPad Software Inc, La Jolla, CA). For all statistical analyses, a p-value less than 0.05 was considered significant.

RESULTS

We evaluated a total of 1401 patients who underwent clinically indicated low dose lung cancer screening CT at Providence VA Medical between October 1, 2013 and July 31, 2014 (Table 1). Indicative of the northeast U.S. veteran population, the median age of this mostly Caucasian (94%), male (97%) population was 65 years (interquartile interval [IQI]: 61, 68 years). The median ASCVD risk score was 18.6%(IQI: 12.4%, 28.0%). Sixty-one percent of patients had hypertension, 75%had dyslipidemia, 28%had diabetes, 14%had CKD, 6%had prior CVA or TIA, and 23%had CAD. The overall median CAC was 528 AU (IQI: 105, 1,512). The overall median AVC was 60 AU (IQI: 0, 338).

Table 1

Baseline demographics and clinical characteristics of overall population

	Overall Population (n = 1,401)
Age, y, median (IQI)	65 (61, 68)
BMI, median (IQI)	28.7 (25.4, 32.6)
Male, n (%)	1353 (96.6)
Caucasian, n (%)	1321 (94.5)
DM, n (%)	386 (27.6)
Hypertension, n (%)	857 (61.2)
Hyperlipidemia, n (%)	1,047 (74.7)
Total Cholesterol, median (IQI)	177 (154, 204)
HDL Cholesterol, median (IQI)	43 (36, 52)
Statin Use, n (%)	825 (58.9)
Current Smoker, n (%)	756 (54.0)
Family History of Early CAD, n (%)	166 (11.9)
CAD, n (%)	325 (23.2)
Prior MI, n (%)	143 (10.2)
Prior CABG, n (%)	59 (4.2)
Prior CVA, n (%)	80 (5.7)
CKD, n (%)	197 (14.1)
GFR, median (IQI)	79.9 (69.3, 92.4)
ASCVD Risk Score, median (IQI)	18.6 (12.4, 28.0)
CACS, median (IQI)	528 (105, 1512)
AVC, median (IQI)	60 (0, 338)
Diagnosis of CI, n (%)	110 (7.9)

AVC, aortic valve calcium score; ASCVD, atherosclerotic cardiovascular disease; BMI, body mass index; CABG, coronary artery bypass graft surgery; CACS, coronary artery calcium score; CAD, coronary artery disease; CKD, chronic kidney disease; CVA, cerebrovascular accident; DM, diabetes mellitus; HDL, high-density lipoprotein; GFR, glomerular filtration rate; CI, cognitive impairment; MI, myocardial infarction.

Over 5 person-years of follow-up, 110 patients (7.9%) were newly diagnosed with CI. Of these 110 patients, 74 patients were diagnosed by objective testing with MoCA (71 patients) and MMSE (3 patients). Thirty-six additional patients were identified by ICD coding. By Cox regression, AVC was associated with a new diagnosis of CI (HR: 1.151; 95%CI: 1.071–1.236; p < 0.001). In Model 1, the association between AVC and new diagnosis of CI remained significant after adjustment for age (HR: 1.104; CI: 1.023–1.191; p = 0.011; Table 2). In Model 2, the association between AVC and new diagnosis of CI remained significant after adjustment for age, hypertension, hyperlipidemia, diabetes, CKD stage 3 or higher (glomerular filtration rate < 60 mL/min) and CAD (HR: 1.097; CI: 1.014–1.186; p = 0.020; Table 2). In Model 3, the association between AVC and new diagnosis of CI remained significant after multivariate adjustment for age, hypertension, hyperlipidemia, diabetes, CKD stage 3 or higher (glomerular filtration rate < 60 mL/min), CAD and prior CVA (HR: 1.094; CI: 1.011–1.182; p = 0.024; Table 2).

Table 2

Relationship between aortic valve calcification and cognitive impairment

		Cognitive Impairment
Model	HR	(95%CI)	p
1	1.104	1.023–1.191	0.011
2	1.097	1.014–1.186	0.020
3	1.094	1.011–1.182	0.024

Covariate adjustment by model: Model 1 = age. Model 2 = age, hypertension, hyperlipidemia, CKD, diabetes, and CAD. Model 3 = age, hypertension, hyperlipidemia, CKD, diabetes, CAD, and prior CVA.

We next performed a sensitivity analysis excluding 46 patients who met criteria for severe AVC by previously established CT criteria (≥1,274 AU in women and ≥2,065 AU in men) to assess the impact of hemodynamics on the primary outcome [22, 23]. Over 5 person-years of follow-up, 104 patients (7.6%) were newly diagnosed with CI in this nonsevere AVC subset. In this subset analysis, AVC was associated with a new diagnosis of CI by Cox regression (HR: 1.151; 95%CI: 1.067–1.242; p < 0.001). Model 1 demonstrated that the association of AVC and new diagnosis of CI remained significant after adjustment for age (HR: 1.109; CI: 1.024–1.202; p = 0.011; Table 3). Model 2 demonstrated that the association of AVC and new diagnosis of CI remained significant after adjustment for age, hypertension, hyperlipidemia, diabetes, CKD stage 3 or higher (glomerular filtration rate < 60 mL/min) and CAD (HR: 1.102; CI: 1.015–1.197; p = 0.020; Table 3). Model 3 demonstrated that the association of AVC and new diagnosis of CI remained significant after adjustment for age, hypertension, hyperlipidemia, diabetes, CKD stage 3 or higher (glomerular filtration rate < 60 mL/min), CAD and prior CVA (HR: 1.100; CI: 1.013–1.194; p = 0.023; Table 3).

Table 3

Relationship between aortic valve calcification and cognitive impairment in patients with nonsevere AVC

		Cognitive Impairment
Model	HR	(95%CI)	p
1	1.109	1.024–1.202	0.011
2	1.102	1.015–1.197	0.020
3	1.100	1.013–1.194	0.023

Covariate adjustment by model: Model 1 = age. Model 2 = age, hypertension, hyperlipidemia, CKD, diabetes, and CAD. Model 3 = age, hypertension, hyperlipidemia, CKD, diabetes, CAD, and prior CVA.

Of the 1,401 patients, a subset of 803 patients (57.3%) patients had VA EMR documentation of highest education attainment, allowing for inclusion of educational attainment as a categorical variable in the multivariate adjustment. From this subgroup, 707 patients (88.04%) had at least a High School Diploma/GED and 406 patients (50.56%) had some form of postsecondary education: 24 patients (2.99%) 8th grade and below; 72 patients (8.97%) some High School; 301 patients (37.48%) High School Diploma or GED; 273 patients (34.00%) some College or Associate’s Degree, 108 patients (13.45%) Bachelors and 25 patients (3.11%) Post-Bachelor degree. Over 5 person-years of follow-up, 87 patients (10.8%) were newly diagnosed with CI in this education attainment subgroup. In the subgroup analysis, AVC was associated with a new diagnosis of CI by Cox regression (HR: 1.194; 95%CI: 1.099–1.296; p < 0.001). Model 1 demonstrated that the association of AVC and new diagnosis of CI remained significant after adjustment for age (HR: 1.141; CI: 1.046–1.246; p = 0.003; Table 4). Model 2 demonstrated that the association of AVC and new diagnosis of CI remained significant after adjustment for age, hypertension, hyperlipidemia, diabetes, CKD stage 3 or higher (glomerular filtration rate < 60 mL/min), CAD, and education (HR: 1.127; CI: 1.030–1.234; p = 0.009; Table 4). Model 3 demonstrated that the association of AVC and new diagnosis of CI remained significant after adjustment for age, hypertension, hyperlipidemia, diabetes, CKD stage 3 or higher (glomerular filtration rate < 60 mL/min), CAD, prior CVA and education (HR:1.127; CI: 1.030–1.233; p = 0.009; Table 4).

Table 4

Relationship between aortic valve calcification and cognitive impairment in subset patients with known highest education attainment

		Cognitive Impairment
Model	HR	(95%CI)	p
1	1.141	1.046–1.246	0.003
2	1.127	1.030–1.234	0.009
3	1.127	1.030–1.233	0.009

Covariate adjustment by model: Model 1 = age. Model 2 = age, hypertension, hyperlipidemia, CKD, diabetes, CAD, and education. Model 3 = age, hypertension, hyperlipidemia, CKD, diabetes, CAD, education, and prior CVA.

DISCUSSION

Calcific aortic valve disease (CAVD) shares many common risk factors with atherosclerotic coronary artery disease, including tobacco cigarette smoking [24]. Despite these similarities, HMG-CoA reductase inhibitors (statins), which have had tremendous success at reducing atherosclerotic disease events, do not appear to impact the natural progression of CAVD, suggesting some biological differences between CAVD and atherosclerosis [24-27].

Aortic valve calcification may be a prognostic indicator for atherosclerotic processes affecting various vascular beds, including those associated with the central nervous system [8]; however, the one prior study assessing the relationship between AVC and CI did not demonstrate a significant association [12]. Here we identify that AVC, as a continuous variable, is associated with CI in patients with an extensive smoking history. The difference between the previous study and our current findings may largely reflect differences in the study cohorts. Overall, the patient cohort in the prior study was at a lower risk from atherosclerotic cardiovascular disease than our cohort which was at moderate-to-high risk of cardiovascular disease as reflected by the increased vascular calcification and the increased incidence of events [28]. Further comparison demonstrated a higher prevalence of cardiovascular risk factors in our cohort relative to the prior study cohort: hypertension (61.2%versus 40.3%), hyperlipidemia (74.7%versus 24.5%), diabetes (27.6%versus12.6%), and CAD (23.2%versus 8.1%). Moreover, by study design, our cohort had such a significant smoking history as to be eligible for LCSCT, and our patient cohort had a significantly higher percentage of current smokers at 54%(versus 12.6%in the prior study). When examining outcomes, 67%of patients in the prior study had an AVC score of 0 and 33%of patients had a nonzero AVC scores, whereas in our study, 36%patients had an AVC score of 0 and 64%of patients had a nonzero AVC score. This suggests that the prior study may have been somewhat underpowered due to the predominance of patients with AVC score of zero.

This study was limited by selection biases inherent to the study design. This particular population of northeast U.S. veterans consisted mostly of older, white men with significant smoking histories. While ICD-coding can be highly specific, the sensitivity is relatively low, and therefore, number of new diagnoses of CI may be underestimated. Overall, events may also be underestimated because of limitations inherent in extracting data or because care outside the Department of Veterans Affairs was not fully captured. After the multivariate analysis, there was attenuation after adjustment, raising the potential question of residual confounding. Using E-value analysis [29], the observed hazard ratio in Model 3 of 1.094 could be explained away by an unmeasured confounder that was associated with both the treatment and the outcome by a hazard ratio of 1.41-fold each, above and beyond the measured confounders, but weaker confounding could not do so; the confidence interval could be moved to include the null by an unmeasured confounder that was associated with both the treatment and the outcome by a hazard ratio of 1.12-fold each, above and beyond the measured confounders, but weaker confounding could not do so. As a retrospective study, information regarding the brain parenchymal status with regard to pathology or imaging were not available.

Hemodynamic impairment from severe AVC, and hence severe physiologic aortic valve stenosis, may also play a role in driving outcomes; however, sensitivity analyses excluding all patients with severe AVC (≥1,274 AU in women and ≥2,065 AU in men) appeared to have no impact on the association between AVC and new diagnosis of CI, suggesting that the incidence of CI in our study population was less likely to be driven by hemodynamic changes associated with severe valve disease. CI objective testing scores were not adjusted for age or education; however, according to a recent study of the U.S. veteran population, 90.1%of veterans held at least a high school diploma or equivalent and 58.8%had some form of postsecondary education [30]. Our subset analysis demonstrated a comparable highest education attainment with 88.04%of veterans holding at least a high school diploma and 50.56%of veterans with some form of postsecondary education. Moreover, in our subgroup analysis, inclusion of education in the multivariate adjustments did not attenuate the association between AVC and new diagnosis of CI, suggesting that educational status was not the key driver of outcomes in our cohort. To address these limitations more completely, further studies are needed, including larger prospective multicenter studies in a more diverse patient population.

In conclusion, scoring AVC derived from LCSCT may be helpful at identifying risk of future CI in patient populations with CAVD and a high risk of atherosclerotic vascular disease. Previous studies have shown that both CAC and AVC derived from non-ECG-gated CT have strong agreement with CAC and AVC derived from ECG-gated CT [8, 16]. Thus, reporting AVC from LCSCT may help physicians identify patients who would benefit from more aggressive cardiovascular care, including early forms of vascular dementia. Additional prospective studies are required to further assess the mechanistic relationship between atherosclerotic or thrombotic events and CI in patients with high AVC in order to determine whether this population would benefit from more aggressive primary and secondary strategies involving lipid/inflammation-based cardiovascular treatment or even antiplatelet/anticoagulant therapies.

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