Authors: Jiyoung Seo, Amrin Kharawala, Pawel Borkowski, Nikita Singh, Harriet Akunor, Sanjana Nagraj, Dimitrios V. Avgerinos, Damianos G. Kokkinidis
Categories: Review, body mass index, obesity, transcatheter aortic valve replacement
Source: Journal of Cardiovascular Development and Disease
Doi: 10.3390/jcdd11060169
Amidst an aging population and escalating obesity prevalence, elucidating the impact of obesity on transcatheter aortic valve replacement (TAVR) outcomes becomes paramount. The so-called “obesity paradox”—a term denoting the counterintuitive association of obesity, typically a risk factor for cardiovascular diseases, with improved survival outcomes in TAVR patients relative to their leaner or normal-weight counterparts—merits rigorous examination. This review comprehensively investigates the complex relationship between obesity and the clinical outcomes associated with TAVR, with a specific focus on mortality and periprocedural complications. This study aims to deepen our understanding of obesity’s role in TAVR and the underlying mechanisms of the obesity paradox, thereby optimizing management strategies for this patient demographic, tailored to their unique physiological and metabolic profiles.
Keywords: obesity, transcatheter aortic valve replacement, body mass index
Aortic stenosis (AS) is among the most prevalent valvular heart diseases in developed countries, with an increasing incidence reflecting the degenerative process in the aging population [1,2]. Since the first transcatheter delivery of an aortic valve prosthesis by Cribier et al. in 2002 [3], transcatheter aortic valve replacement (TAVR) was introduced as a minimally invasive alternative to surgical aortic valve replacement (SAVR) for patients with severe AS who were deemed to be at high or prohibitive surgical risk [4]. Although there are emerging issues such as the durability of transcatheter heart valves and long-term TAVR outcomes, indications for TAVR continue to expand to younger, low-risk patients with longer life expectancies [5,6]. As the utilization of TAVR expands with the annual TAVR volume in the United States, surpassing all forms of SAVR [7], it is imperative to understand the impact of diverse patient characteristics on TAVR outcomes.
The epidemiological association between obesity and an increasing incidence of various cardiovascular diseases (CVDs) such as hypertension, coronary heart disease, heart failure, and atrial fibrillation is well established [8,9,10]. Considering the obesity epidemic [11] and its growing prevalence in TAVR recipients [12], obesity has emerged as a critical factor in prognostication of clinical outcomes of TAVR. Many studies, however, have paradoxically demonstrated good prognosis and survival among obese patients than their leaner counterparts in heart failure [13,14], atrial fibrillation, and coronary heart disease [15,16], despite having established CVDs [8,17]. This phenomenon, so called the “obesity paradox”, is further applicable to the TAVR patient population [7,18,19].
We previously conducted a systematic review and meta-analysis to further explore the relationship between baseline obesity and mortality as well as the periprocedural outcomes after TAVR [20]. Here, we present an updated, comprehensive review that integrates the most recent and pertinent studies on this topic to the best of our knowledge.
Numerous investigations have been carried out to explore the relationship between being overweight or obese and the outcomes following a TAVR procedure. A summary of these studies, particularly focusing on mortality, peri-procedural, and postprocedural results including major bleeding, major vascular complications, cerebrovascular events, myocardial infarction, atrial fibrillation, pacemaker insertion, and acute kidney injury is presented in Table A1.
The analysis of mortality outcomes in patients with overweight and obesity undergoing TAVR reveals a generally favorable trend, although some studies reported insignificant association (Table A1). The Placement of Aortic Transcatheter Valves (PARTNER) trial demonstrated a favorable correlation between a higher body mass index (BMI) and 2-year all-cause post-TAVR mortality (hazard ratio (HR) per BMI unit increase 0.95; 95% confidence interval (CI) 0.91–0.98; p = 0.005) [21,22]. Additionally, a comprehensive cohort study examining the Transcatheter Valve Therapy (TVT) registry indicated improved 1-year all-cause mortality rates in overweight (BMI, 25.0–29.9 kg/m^2^), class I (BMI, 30.0–34.9 kg/m^2^) and class II (BMI, 35.0–39.9 kg/m^2^) obesity compared to normal-weight patients (HR 0.88, 95%CI 0.81–0.95; HR 0.8, 95%CI 0.72–0.90; HR 0.84, 95%CI 0.72–0.98, respectively) [23]. This observation led to the hypothesis that a lower BMI might be indicative of greater frailty, thereby yielding a poorer prognosis compared to counterparts with a higher BMI. Notably, De Palma et al. [18] expanded this understanding by assessing not just the absolute weight at the time of TAVR but also considering the trajectory of weight change before the procedure as a crucial determinant of patient outcomes. In this study, patients with BMI > 25 kg/m^2^ at the time of TAVR manifested a lower 3-year all-cause mortality compared to their counterparts with BMI < 25 kg/m^2^ (HR 0.68, 95%CI 0.5–0.93, p = 0.02), consistent with the obesity paradox. However, this paradigm shifts for patients in the overweight (BMI 25.1–30 kg/m^2^) and obese (BMI 30.1–35 kg/m^2^) categories who had experienced significant weight loss leading to a change in BMI classification, with poorer 1-year mortality outcomes compared to those with stable weight trajectories (HR 1.64, 95%CI 1.06–2.3, p = 0.025). Interestingly, the BMI < 25 kg/m^2^ group had better 3-year mortality outcome when compared to the severe obesity group (BMI > 35 kg/m^2^) (HR 1.64, 95%CI 1.06–2.3, p = 0.025), and those who gained weight pre-TAVR had a higher 1-year mortality risk than those without weight change, although it was statistically insignificant (HR 2.1, 95%CI 0.96–4.0, p = 0.062). This represents intricate interplay between obesity and TAVR outcomes that necessitates further research to better understand their complex interaction.
Obesity has been identified as an independent risk factor for vascular complications in patients undergoing TAVR [24,25,26]. The existing literature indicates that the incidence of vascular complications in this demographic ranges from 10% to 16% [27,28,29]. Our prior research corroborates this, revealing higher odds of major vascular complications (OR: 1.33; 95%CI: 1.05–1.68) in patients with obesity [20]. While the transfemoral (TF) approach is predominantly utilized in TAVR procedures due to its minimally invasive nature, the management of femoral vascular access and hemostasis in patients with obesity is challenging due to their unique anatomical characteristics. The common femoral artery in such individuals can be up to 10 cm beneath the skin surface [30,31], complicating its access. This complexity is compounded by the challenges in determining the appropriate gauge angulation and securing optimal manual compression proximal to the puncture site, thereby escalating the likelihood of vascular complications [26]. Consequently, vigilance monitoring is essential when attempting vascular access in obese patients to mitigate these increased risks [26,32]. Alternative vascular access routes, such as transcarotid or trans-subclavian approaches, are being explored in this context [26,33,34].
Transcarotid (TC) access for TAVR offers several advantages, particularly in obese patients, being superficial, closer to the skin, and of a shorter distance to the aortic annulus, ultimately facilitating procedural maneuvers [26]. Compared to more invasive transapical and transaortic approaches, studies have shown that the safety and efficacy outcomes of TC-TAVR can parallel those of TF-TAVR in real-world populations [35,36,37]. TC access has been linked to a low rate of vascular and bleeding complications, which is beneficial for TAVR candidates with significant obesity [26,37]. Though there are concerns about cerebrovascular complications, recent studies report stroke rates comparable to the TF approach [37,38,39], although there remains a lack of definitive evidence on the superiority of any non-TF access sites [33].
The trans-subclavian (TS) approach is another emerging alternative to the transfemoral approach, which has yielded similar early mortality, stroke, and major complication rates to the TC access in a general TAVR population [26,34]. Compared to transapical and transaortic TAVR, which require chest entry and have demonstrated worse outcomes, these new methods are considered less invasive and potentially more suitable for specific patient cohorts with severe femoral atherosclerosis, body habitus issues precluding femoral access, or lung diseases, which are common in morbidly obese individuals [40,41,42,43]. However, specific data regarding obese TAVR recipients are limited, and further validation through large-scale registries and randomized trials are essential to confirm these findings, particularly in the obese population who are ineligible for traditional approaches.
Pacemaker (PPM) implantation due to conduction abnormalities post-TAVR is a significant complication, with its incidence rate reported to range from 5% to 33% [44,45,46,47,48,49]. The data from the PARTNER trial identified chronic pacing as an independent factor predicting 1-year mortality post-TAVR [50,51]. Furthermore, PPM implantation is associated with increased overall healthcare costs and prolonged hospitalization [50,51,52,53,54]. The etiology of an atrioventricular (AV) conduction block following TAVR is hypothesized to be related to direct injury to the bundle of His, owing to its proximity to the membranous septum and native aortic valve [52,55]. Other factors, including a pre-existing right bundle branch block (RBBB), the implantation depth, the use of a self-expanding valve, prosthesis-to-left-ventricular-outflow-tract-diameter ratio, male gender, a prolonged partial response interval, and a left anterior hemiblock, have also been identified as predictors of a PPM implantation [45,50,52,56,57,58]. The association between BMI and the necessity for a PPM implantation post-TAVR, however, has not been extensively explored. A retrospective study of 449 patients undergoing TAVR found a significant association between increased BMI (>30 kg/m^2^) and the need for PPM implantation (p = 0.037), though potential independent confounders related to BMI were acknowledged [52]. A meta-analysis involving 981,168 post-TAVR patients across 239 studies identified BMI over 25 kg/m^2^ as a weak predictor for PPM implantation (risk ratio 1.08; p = 0.05) [45]. Obesity may contribute to metaplastic and infiltrative changes in the sinus node, AV node, right bundle branch, and myocardium adjacent to the AV ring, leading to cardiac conduction anomalies [52,59,60]. However, the extent to which these alterations predispose obese patients to post-TAVR PPM implantation remains unclear, underscoring the need for further investigation in this area.
The Valve Academic Research Consortium (VARC) recognizes renal impairment as a major outcome parameter following TAVR [61]. Factors contributing to acute kidney injury (AKI) post-TAVR include periprocedural hypotension [62], blood loss [63], concurrent medication use, the administered volume of contrast agent [64], and severe inflammatory response syndrome following intervention [65,66]. Nevertheless, the existing literature on the incidence of AKI post-TAVR is not definitive, and the association between obesity and post-TAVR AKI remains varied. The research conducted by Schnabel et al. [65] identified BMI as a significant predictor of postprocedural renal function deterioration (β = −1.2; p < 0.0001). Additionally, a study by Ogami et al. [67] of 3883 patients with end-stage renal disease (ESRD) undergoing TAVR found that patients with a BMI below 25 kg/m2 had higher risks of 1-year (HR: 1.2; 95%CI: 1.07–1.36; p = 0.003) and 5-year mortality (HR: 1.18; 95%CI: 1.08–1.29; p < 0.001) compared to those with a BMI above 25 kg/m^2^. While these findings might suggest a protective effect of a higher BMI on renal function post-TAVR, in line with the ‘obesity paradox’, the underlying mechanism remains uncertain. Conversely, other studies report no significant or even adverse associations between a high BMI and renal outcomes following TAVR. A study from the PARTNER 1 trial, comparing groups based on changes in estimated glomerular filtration rate (eGFR) post-TAVR—improved, worsened, or unchanged—found no significant differences in the BMI among these cohorts [68]. Additionally, Koifman et al. [69] identified an association between a higher BMI and an increased incidence of AKI in TAVR patients, as determined using Risk Injury Failure Loss End-Stage (RIFLE) criteria (OR 1.12; p = 0.01). It is crucial to note that the eGFR equation does not incorporate any measure of body size and is subject to inherent biases in different patient groups, particularly in relation to age, gender, and BMI [70]. Furthermore, factors such as fluid status changes may more significantly influence eGFR than serum creatinine levels [69,70]. Consequently, there is a pressing need for further research in this field to elucidate these complex relationships and refine diagnostic and prognostic criteria for renal function assessment post-TAVR.
The association between obesity and other post-TAVR complications, including cerebrovascular events, new-onset atrial fibrillation, and myocardial infarction has received limited research attention.
The counterintuitive impact of BMI on clinical outcomes may be attributed to several potential mechanisms. One such mechanism is the increase in total blood volume and cardiac output in individuals with obesity, primarily due to the increased metabolic demands associated with excess body weight [59,60,71]. This elevation in cardiac output and stroke volume may provide an enhanced hemodynamic reserve, enabling these patients to better tolerate procedural stress. Furthermore, adipose tissue is found to synthesize tumor necrosis factor-alpha (TNF-α) receptors [27,72]. Therefore, individuals with overweight and obesity might have a protective adaptation against the harmful effects of elevated TNF-α levels through increased receptor production [27]. Additionally, various studies indicate that individuals with obesity often present at a younger age, are more prone to pursue medical care promptly, and are more likely to undergo aggressive medical and interventional treatments at earlier stages [7,18,27,28,73,74,75].
The obesity paradox is primarily pronounced in older individuals who typically exhibit more symptoms, poorer ventricular function, and a higher burden of comorbidities. The pathophysiology of this phenomenon has been extensively studied in geriatric medicine and patients with heart failure. A potential mechanism is the association of undernutrition, sarcopenia, and cardiac cachexia which is commonly associated with frailty [76,77,78,79,80]. The current guidelines, American College of Cardiology (ACC) and European Society of Cardiology/European Association for Cardio-Thoracic Surgery (ESC/EACTS), recommend incorporating frailty assessments in patient selection for TAVR, as it is associated with adverse outcomes [80,81,82]. Frailty refers to a state of impaired homeostatic reserve and reduced resilience to stressors which, in turn, increases susceptibility to adverse health outcomes [83,84,85]. While there are numerous methods to assess frailty, the VARC characterizes frailty through multifactorial aspects like slowness, weakness, wasting, malnutrition, poor endurance, inactivity, and reduced independence [86].
Understanding the obesity paradox in the TAVR population requires a multidisciplinary approach, integrating insights from diverse fields such as cardiology, endocrinology, bariatric surgery, geriatrics, and nutrition science. This comprehensive strategy is essential for precisely delineating the primary etiology of the patient’s symptoms, particularly in instances where exertional dyspnea may be multifactorial, and providing individualized interventions aimed at optimizing patient TAVR outcomes.
The incidence of obesity in the United States has escalated to near-epidemic levels, with the data from 2017 to 2018 indicating that 42% of U.S. adults meet the criteria for class I obesity (BMI ≥ 30 kg/m^2^) and 9% are classified as having severe, morbid, class III obesity (BMI ≥ 40 kg/m^2^) [87]. Morbid obesity (MO) is recognized not only as a significant cardiovascular risk [10], but also as a determinant of high surgical risk [88]. This cohort of patients, although frequently encountered in real-world clinical practice, tends to be underrepresented in clinical trials. Although the ‘obesity paradox’ is noted in patients undergoing TAVR, the precise mechanism and the extent to which it applies, especially in instances of extreme obesity, remain unclear. Hence, studies to determine the safety profile and risk factors associated with the MO population are imperative. The prevailing hypothesis suggests a J-shaped correlation between BMI and TAVR outcomes, wherein favorable results are associated with overweight and mild obesity, while underweight or morbid obesity are associated with adverse outcomes [23,89,90].
Sharma et al. [23] investigated the relationship between BMI and both short- and long-term outcomes following TAVR in a substantial cohort of 31,929 patients undergoing TAVR. Utilizing BMI as a continuous variable, their analysis revealed that for BMIs of 30 kg/m^2^ or less, each 1 kg/m^2^ increment was associated with a 2% and 4% reduction in 30-day and 1-year mortality risks, respectively. However, for BMIs over 30 kg/m^2^, each 1 kg/m^2^ increment corresponded to a 3% increased risk of 30-day mortality but not to 1-year mortality. This study supports the J-shape hypothesis with the nadir of BMI at 30 kg/m^2^ and suggests an optimal BMI for post-TAVR outcomes within the range of overweight to mild obesity.
Another study conducted by McInerney et al. [91] compared propensity matched cohorts of 770 patients with MO with equal number of nonobese patients. The study found significantly higher incidence rates of post-TAVR major vascular complications (6.6% vs. 4.3%; p = 0.043) and lower rates of device success (84.4% vs. 88.1%; p = 0.038) in the MO group. However, this did not translate into increased all-cause and cardiovascular mortality at 2 years, which remained comparable between the two groups. Similarly, Ferreiro et al. [92] found no significant difference in the in-hospital, 30-day, and 1-year (12.5% in MO vs. 15.3% in non-MO; p = 0.76) post-TAVR mortality when comparing 25 patients with BMI ≥ 40 kg/m^2^ vs. A total of 493 patients had a BMI < 40 kg/m^2^. In fact, no significant differences were seen even in 1-year cardiovascular mortality rate (12.5% in MO vs. 10.8% in non-MO; p = 0.827) and heart failure (HF) hospitalization rate (14.3% in MO vs. 16.5% in non-MO; p = 0.825). Interestingly, however, they also found higher trends of major vascular complications and vascular closure device failure, corroborating with the findings of our meta-analysis (20) which indicated increased vascular complications in obese cohorts, likely attributed to the challenges in transfemoral access. Of particular interest, a comparison of propensity-matched cohorts of MO patients undergoing TAVR vs. SAVR across 15 centers [93], revealed similar overall outcomes in terms of all-cause mortality, CV mortality and readmissions rates, despite differing predictors of the two-year all-cause mortality. On the contrary, the PARTNER 2A trial [94,95] yielded evidence demonstrating that among intermediate surgical risk patients (predicted 30-day surgical mortality of 4% to 8% determined by the STS mortality risk model [96]) afflicted with severe AS and BMI ≥ 35 kg/m^2^, those undergoing TAVR exhibited a statistically significant reduction in cardiovascular mortality when compared to their counterparts undergoing SAVR. Though the question remains on how MO patients fare in comparison to the overweight/mild obesity groups, the overall safety of TAVR in MO patients has been established.
These studies, however, are not without limitations. It was noted that the MO cohort in Ferreiro et al. [92] consisted of younger patients, more women, a significantly lower rate of coronary artery disease, and a lower risk profile, which could explain the lack of worse mortality outcomes. Moreover, the follow-up duration of 1–2 years in these studies might not comprehensively assess mortality outcomes. Another consideration is the definition of morbid obesity based on BMI, where factors beyond mere ‘weight’ could influence mortality outcomes and adverse effects. Several studies [10,91,97,98] utilizing imaging modalities to characterize visceral adiposity, including ectopic fat, have identified the composition and distribution of fat as an independent indicator of poor cardiovascular outcomes, irrespective of weight or BMI. Hence, further studies exploring other obesity metrics beyond BMI is imperative to effectively risk-stratify individuals with obesity undergoing TAVR [28].
BMI is the ratio of body mass in kilograms (kg) to the square of height in meters (m^2^). The World Health Organization (WHO) stratifies BMI into various underweight (BMI < 18.5 kg/m^2^), normal (BMI 18.5–24.9 kg/m^2^), overweight (BMI 25–29.9 kg/m^2^), and three classes of obesity (Class I: BMI 30–34.9 kg/m^2^, Class II: BMI 35.0–39.9 kg/m^2^, Class III: BMI ≥ 40 kg/m^2^) [99]. Historically, BMI has been a widely accepted measure of obesity. It is favored due to its simplicity in calculation, standardization, and established association with comorbid conditions such as hypertension, diabetes, and coronary artery disease, which can significantly impact TAVR outcomes. Using BMI allows clinicians to identify patients who may be at a higher risk for specific post-TAVR complications. However, BMI carries considerable limitations. It may not accurately reflect health risks across different ages, genders, and ethnicities, and it also fails to reflect health behaviors [100,101]. Furthermore, despite its association with abdominal adiposity, BMI does not differentiate between adipose and lean body mass, nor does it account for the distribution pattern of body fat (visceral adipose tissue [VAT] vs. subcutaneous adipose tissue [SAT]). This renders BMI a less precise indicator of obesity and obscures the understanding of which component of BMI influences clinical outcomes in TAVR [100,102]. The distribution of adipose tissue is of critical relevance in TAVR, affecting procedural technicalities, vascular access, device deployment, postoperative recuperation, and overall suitability for the intervention [91,103]. In the majority of previous studies investigating the ‘obesity paradox’ in the TAVR population, BMI has been the predominant obesity metrics. However, considering the intrinsic limitations of BMI, research endeavors aimed at discerning alternative adiposity metrics that may prognosticate TAVR outcomes with enhanced accuracy are necessary. Table 1 presents a summary of the obesity metrics employed in the evaluation of TAVR outcomes.
BSA is deduced via a formula that incorporates both an individual’s weight (kg) and height (cm). BSA may represent a more refined index for adiposity than BMI, attributable to its capacity to more precisely reflect the disparate densities of muscle and adipose tissue [104,105,106]. There are limited studies, however, evaluating BSA as a prognostic tool for TAVR outcomes, leaving their association unclear. Watanabe et al. [107] conducted a retrospective analysis of 424 individuals undergoing TAVR and compared outcomes between groups categorized by low BSA (<1.75 m^2^) and high BSA (>1.75 m^2^). The study reported a higher incidence of vascular complications in the low BSA group (13% vs. 4.3%, p < 0.01), but no significant difference in mid-term survival rates (p = 0.64). Furthermore, a prospective observational study carried out by Arsalan et al. [105], encompassing 917 TAVR patients, sought to assess the impact of both BMI and BSA on post-TAVR outcomes. Notably, this study revealed that the “obesity paradox” phenomenon emerged only when patients were assessed using BMI with significant association with 1-year survival rates (p = 0.01). However, no statistically significant correlation was observed between increased survival and elevated BSA (p = 0.13). These findings underscore the need for continued research into BSA as a potentially valuable metrics in TAVR, offering insights distinct from BMI in the evaluation of TAVR outcomes linked to obesity.
As BMI is a relatively crude obesity marker failing to differentiate between adipose and muscle mass, there has been growing interest in identifying obesity phenotypes, beyond mere BMI [93,108]. Numerous previous studies have underscored the significance of adipose tissue’s anatomical localization in relation to the predisposition to various diseases, and abdominal obesity is recognized as one of the critical risk factors [100,109]. Particularly, abdominal visceral adipose tissue (VAT) and subcutaneous adipose tissue (SAT) exhibit a robust correlation with the risk of CVDs and metabolic disorders [100,110,111]. The direct visualization and quantification of VAT vs. SAT using CT scans can be instrumental in assessing an individuals’ obesity phenotype and the distribution of adipose tissue components. The regular use of CT scans can expose patients to radiation which can pose a limitation for its wide-scale application. Pre-procedural CT, however, is crucial in the procedural planning of TAVR, which makes SFA and VFA easily measurable and usable as a valuable prognostic marker in TAVR candidates [102,112]. Okuno et al. [102] investigated the association between abdominal total fat area (TFA), VAT, or SAT, and TAVR outcomes in 100 individuals undergoing TAVR with a median follow-up of 665 days. The patients with higher SAT exhibited a significantly reduced incidence of the composite outcome and all-cause mortality compared to those with lower SAT (15.0% vs. 37.7%, p = 0.025; and 8.9% vs. 23.7%, p = 0.047, respectively). In contrast, the individuals with higher TFA or VAT did not demonstrate a significant reduction in the incidence of the composite outcome or all-cause mortality. Furthermore, McInerney et al. [91] identified those with a VAT:SAT ratio ≥ 1 as an adverse obesity phenotype in morbid obesity cohort, with significantly increased risks for 2-year all-cause mortality (HR: 3.06; 95%CI: 1.20–7.77; p = 0.019) and cardiovascular mortality (HR: 4.11; 95%CI: 1.06–15.90; p = 0.041). This continued to remain a strong predictor of 2-year mortality even on multivariable analysis. Visceral adipose tissue, characterized as a metabolically active ectopic fat deposit, is linked with dysregulation of lipid metabolism and insulin resistance [113]. In contrast, subcutaneous adipose tissue has been found to have cardiovascular advantages, primarily due to the secretion of adiponectin, which manifests anti-inflammatory properties, enhances insulin sensitivity, and mitigates atherogenesis [102,114]. Hence, there is a compelling need to promote future investigations that utilize visceral adiposity or adipose tissue distribution as biomarkers for discerning adverse obesity phenotypes to enhance the precision of risk stratification for obese individuals undergoing TAVR.
EAT is a visceral fat located between the myocardium and the visceral pericardium [77,115]. It shares an embryological origin with the epicardial layer of the myocardium and visceral adipose tissue, distinct from subcutaneous adipose tissue [116]. EAT is a metabolically active tissue that has localized endocrine effects [115] and secretes pro- and anti-inflammatory mediators, including adiponectin, interleukin-6, and TNF-α [77,117,118]. Its association with CVDs, such as coronary artery disease [119,120,121], atrial fibrillation [122], and major cardiovascular events [91,110,115,123,124], has been extensively established. While various imaging modalities are capable of assessing EAT, CT is acknowledged as the most precise method for its quantification, attributed to its superior spatial resolution and comprehensive coverage of the heart [77,115]. Several research initiatives have probed the impact of EAT volume on TAVR outcomes. Eberhard et al. [77], in a study involving 503 TAVR patients, observed that a higher EAT volume was associated with increased 1-, 2-, and 3-year all-cause post-TAVR mortality (HR: 1.94, 95%CI: 1.15–3.26, p = 0.002; HR: 1.70, 95%CI: 1.06–2.68, p = 0.001; HR: 1.69, 95%CI: 1.10–2.60, p = 0.001, when using 100 mm^3^, 125 mm^3^, and 130 mm^3^ as cutoff values, respectively). Similarly, McInerney et al. [91] reported that each 10 cm^3^/m^2^ increment in indexed EAT was associated with an increased risk of all-cause mortality at 2 years (HR, 1.16; 95%CI, 1.03–1.30; p = 0.011). Notably, Eberhard’s study cohort exhibited a weak correlation between EAT volume and both BMI (BMI; r = 0.24; p < 0.001) and BSA (r = 0.26; p < 0.001), aligning with previous findings that associate EAT with coronary artery disease independent of BMI [119]. This observation prompts a question into whether the EAT volume should be linked with general obesity in the context of the ‘obesity paradox’, despite its common embryological origin with VAT. Continued exploration into the intricate influence of EAT on TAVR outcomes and its association with obesity is crucial in discerning high-risk profiles among TAVR candidates.
Alternative measures, such as the visceral adiposity index, body adiposity index, or body composition analysis (e.g., dual-energy X-ray absorptiometry and bioelectrical impedance analysis), may offer a more holistic assessment of obesity [100]. Nevertheless, their prognostic efficacy concerning TAVR outcomes warrants further research.
In conclusion, our comprehensive review underscores the complexity in this field, highlighting the heterogeneity in TAVR outcomes observed across varying degrees of obesity and employing different obesity metrics. The nuanced influence of obesity on TAVR outcomes necessitates deeper exploration, particularly considering the unique physiological and metabolic profiles inherent to individuals with obesity. Additionally, the question of whether TAVR outcomes can be modified by weight management interventions, including bariatric surgery, warrants further investigation. As the domain of TAVR continues to evolve, understanding the adipose tissue dynamics on cardiovascular health and the development of sophisticated obesity metrics will be crucial for a more refined risk stratification and for optimizing the management of individuals with obesity undergoing TAVR.
Conceptualization, D.G.K. and J.S.; writing—original draft preparation, J.S., A.K., P.B., N.S. and H.A.; writing—review and editing, J.S., S.N., D.V.A. and D.G.K. All authors have read and agreed to the published version of the manuscript.
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The authors declare no conflicts of interest.
This research received no external funding.
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