- 1Health Management Center, The Third Xiangya Hospital, Central South University, Changsha, China
- 2Clinical Research Center, The Third Xiangya Hospital, Central South University, Changsha, China
- 3Department of Metabolic and Bariatric Surgery, The Third Xiangya Hospital, Central South University, Changsha, China
- 4Department of Biochemistry and Molecular Biology, Shenyang Medical College, Shenyang, China
Background: Obstructive sleep apnea (OSA) and atrial fibrillation (AF) are epidemiologically correlated, but the causal relationship between them remains elusive. We aimed to explore the causal relationships between OSA and AF.
Method: Using both the Finnish biobank and publicly available genome-wide association study data (GWAS), we conducted a two-sample Mendelian randomization (MR) analysis to estimate the causal effect of OSA on AF, both in the primary analysis and replicated analysis. The inverse variance weighted MR was selected as the main method. To further test the independent causal effect of OSA on AF, we also performed multivariable MR (MVMR), adjusting for body mass index (BMI), hypertension, and coronary artery disease (CAD), respectively.
Results: In the primary analysis, OSA was significantly associated with the increased risk of AF (OR 1.21, 95% CI 1.11–1.32) and the replicated analysis showed consistent results (OR 1.17, 95% CI 1.05–1.30). Besides, there was no heterogeneity and horizontal pleiotropy observed both in the primary and replicated analysis. Further multivariable MR suggested that the causal relationships between OSA and AF exist independently of BMI and CAD. The MVMR result after the adjustment for hypertension is similar in magnitude and direction to the univariable MR. But it did not support a causal relationship between OSA and AF.
Conclusion: Our study found that genetically driven OSA causally promotes AF. This causal relationship sheds new light on taking effective measures to prevent and treat OSA to reduce the risk of AF.
Introduction
Atrial fibrillation (AF) is the most common type of arrhythmia that causes hemodynamic disorders, thrombotic strokes, heart failure, and increased mortality (1), with an estimated global prevalence of 34 million (2). Prevention of AF is important to improve the societal and personal costs related to the disease. AF is influenced by a number of non-genetic risk factors. In addition to traditional risk factors such as smoking, alcohol, and other lifestyle factors, as well as obesity, diabetes, and hypertension, a growing number of studies are focusing on the impacts of obstructive sleep apnea (OSA) on atrial fibrillation (3–6).
Notably, OSA is characterized by recurrent episodes of airway collapse during sleep, the combined prevalence of OSA in patients with AF has been estimated at 21 to 74% (6, 7). A few large longitudinal cohort studies recruiting a non-aged population reported that those with OSA, also inevitably featured with obesity, had a higher risk of incident AF than those without OSA after a follow-up of several years (8–10). Given that approximately 3–49% of the general population is estimated to be OSA (7), targeting OSA through airway pressure treatment or weight reduction has the potential to lower the incidence of AF if the observed associations between OSA and AF are causal. However, the previous studies are limited in assessing the comorbid confounder of overweight/obesity, a risk factor commonly shared by both OSA and AF (11), so that it is unknown whether OSA and AF have a direct causal relationship, or simply represent comorbidities that cluster in obese subjects. Furthermore, despite guidelines suggesting that OSA treatment might lower AF reoccurrence, the evidence is mainly based on small-sample observational studies or non-randomized clinical trials (12), which are prone to systematic biases and can not support a causal association.
Based on the deficiency of the former studies' design, we considered Mendelian randomization (MR). MR can be used to resolve causal assumptions. It is a genetic instrumental variable analysis that can evaluate the potential relationship between exposure and outcome (13). As MR uses instrumental variable analysis to model the randomization process that underlies causal inference in randomized controlled trials (RCTs), this design is less susceptible to confounding and reverse causality bias (14). In the current study, we aimed to perform two-sample MR analyses to test the hypothesis that there is a potential causality between OSA and AF.
Methods
Study Design Overview
The overview of this study design is presented in Figure 1. Firstly, we extracted five available genetic instrumental variables from the FinnGEN consortium for OSA. Secondly, we obtained the summary data of AF from the genome-wide association study (GWAS). Then, we conducted univariable two-sample MR and several sensitivity analyses to estimate the causal effect. Finally, we carried out a multivariable MR (MVMR) analysis respectively adjusting for body mass index (BMI), hypertension, and coronary artery disease (CAD). In addition to the primary analysis, we constructed another AF dataset from a large meta-analysis to replicate the MR analysis to test our hypothesis.
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Figure 1. Diagram of Mendelian randomization (MR) framework in this study. SNP, single nucleotide polymorphisms; OSA, obstructive sleep apnea; AF, atrial fibrillation; GWAS, genome-wide association study; MR, mendelian randomization; BMI, body mass index; HTN, hypertension; CAD, coronary artery disease.
Data Source for Exposure
Our main exposure genetically determined OSA as an instrumental variable (IV). We extracted exposure data from the FINNGen consortium (https://www.finngen.fi/en), a large study aiming to collect and analyze genome and health data from 500,000 Finnish biobank participants. We identified 5 single nucleotide polymorphisms (SNP) robustly associated with OSA in the FINNGen genome-wide association study that included 217,955 participants (15), nearly all European ancestry (Supplementary Figure S1), with a statistically significant threshold [P < 5 × 10−8; linkage disequilibrium (LD); r2 < 0.001, LD distance > 10,000 kb]. F statistic {calculated as F = [(n-k-1)/k]/[R2/(1-R2)], the explained variance for exposure (R2), sample size (n), and number of SNPs (k)} indicates the strength of the relationship between SNP and OSA. In general, F-statistic >10 indicates a significant association between selected instrumental variables and OSA (16).
Furthermore, we obtained summary data on BMI, hypertension, and CAD from GWAS. The summary-level data for BMI were extracted from a meta-analysis of GWAS including 681,275 individuals of European ancestry (17). Data for hypertension was also obtained from the FinnGen consortium (22,154 cases and 74,345 controls) (https://www.finngen.fi/fi), nearly all of European ancestry. And the summary data on CAD we used was from a large meta-analysis of GWAS which includes 141,217 individuals of European ancestry (18).
Data Source for the Outcome
We constructed two sets of outcome data for two MR analyses to test our hypothesis. For the primary analysis, the summary data for AF were derived from a GWAS meta-analysis involving nearly 1,030,836 European participants, including 60,620 cases and 970,216 controls (19). For the replication analysis, the summary data for AF were extracted from another GWAS meta-analysis, which investigated 537,409 participants of 84.2% European ancestry in up to 55,114 cases and 482,295 controls (20). To our knowledge, there was no sample overlap between the exposure and outcome GWASs.
Statistical Analysis
Two-Sample Mendelian Randomization Analysis
As shown in Supplementary Figure S1, the conventional MR model was used to assess the causal effect of OSA on AF. The ideal instrumental variable must satisfy the following several requirements (Supplementary Figure S1): (i) the instrumental variables have to be closely related to OSA; (ii) there is no association between the instrumental variables and confounders of OSA and AF; (iii) the effect of instrumental variables on AF must be mediated solely by the OSA in the study. In the two-sample MR analysis, we used four different methods [inverse-variance weighted (IVW), weighted median, weight mode, and MR-Egger], to evaluate the causal effects between OSA and AF. And we used the MR-Pleiotropy Residual Sum and Outlier (MR-PRESSO) to address the problem of heterogeneity and pleiotropy effect. The results were shown as odds ratios (OR) and 95% CIs. The inverse-variance weighted method was used as the main analysis in our study. It is the most precise method for estimating causal effects (21). The weighted median estimator pools the median impact of SNPs with more than 50% of the weight coming from valid SNPs (22). The MR-Egger regression was used primarily to account for horizontal pleiotropy. Besides, we used the MR-PRESSO method to identify potential horizontal pleiotropy outliers in the analysis and adjust if necessary (23).
Sensitivity Univariable MR Analyses
To further explain the potential pleiotropy between exposure and outcome, a series of sensitivity analyses were conducted. Cochran's Q test was used to quantify the heterogeneity of instrumental variables, with Ph < 0.05 indicating heterogeneity (24). The Egger intercept in the MR Egger regression analysis was used as an indicator of horizontal pleiotropy (23). Furthermore, we conducted the leave-one-out analysis to remove a single SNP from the analysis in sequence. Both the primary and replicated analysis was conducted in the sensitivity analysis described above.
Multivariable Two-Sample MR Analysis
Previous observational studies have shown that BMI (25), hypertension (26), and CAD (27) were important risk factors for the development of atrial fibrillation, therefore, we further respectively performed an MVMR analysis to estimate the direct causal effect of OSA on the risk of AF. Both the primary and replicated analysis was conducted the MVMR described above.
Mendelian randomized (MR) analysis was performed in R (version 4.0.3; The R Foundation for Statistical Computing, Vienna, Austria, https://www.R-project.org/) with R packages “TwoSampleMR”, and “MVMR”. A two-tailed p-value < 0.05 was considered statistically significant.
Power Calculations
To evaluate the power of our study, a non-centrality parameter-based approach was used, which is a publicly available mRnd web tool (http://cnsgenomics.com/shiny/mRnd/) (28). For binary outcomes (AF), after we inputted the required parameters in mRnd (α = 0.05, R2 = 0.083 in this study), the minimum detectable OR was roughly estimated. The results of the power calculations are shown in Supplementary Table S2.
Results
The Character of SNP and Participants for Analysis
The characteristics of the populations included in the FINNGen and GWAS data of outcomes are shown in Table 1. We selected 5 SNP as instrumental variables for OSA. The F-statistic value >100 suggests that these selected SNPs are significantly associated with OSA in the MR analysis. The details of the available SNPs in the MR analysis are presented in Supplementary Table S1.
Causal Effect of OSA on AF
Univariable Two-Sample MR Analysis Results
The overall results of the univariable MR are shown in Table 2. For the primary analysis, we observed a significant causal effect of OSA on AF (P < 0.05 in the four MR methods, including MR-Egger, IVW, Weighted median, and Weighted mode). OSA was associated with an increased risk of AF (OR 1.21, 95% CI 1.11–1.32). For the replicated analysis, there was still clear evidence to support a causal effect between OSA and AF (P < 0.05 in the IVW, Weighted median, and Weighted mode). The OR and 95%CI of OSA were 1.17 (1.05–1.30) for incident AF risk.
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Table 2. Univariable and multivariable two-sample Mendelian randomization estimations showing the effect of obstructive sleep apnea on the risk of atrial fibrillation.
Sensitivity Analysis Validation
We performed several sensitivity analyses aimed at estimating heterogeneity and horizontal pleiotropy in this MR analysis (Table 2). For the primary analysis, heterogeneity and horizontal pleiotropy were not observed in either Cochran's Q-test or MR Egger regression analysis (Ph = 0.386, Pintercept = 0.236). The results of the replicated analysis were consistent with the primary analysis, with no heterogeneity or horizontal pleiotropy found (Ph = 0.0895, Pintercept = 0.998). Besides, the MR-PRESSO results showed no outlier SNPs. In the leave-one-out analysis, we found that no single SNP was strongly driving the overall effect of OSA on AF in the primary analysis (Figure 2). But in the replicated analysis, we found that the SNP, rs9937053, will impact the overall results when it was removed.
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Figure 2. Scatter plot [primary analysis, (A); replicated analysis, (B)] and leave-one-out test [primary analysis, (C); replicated analysis, (D)] for genetically determined obstructive sleep apnea (OSA) on atrial firbrillation (AF) risk. SNP, single nucleotide polymorphisms; OSA, obstructive sleep apnea; AF, atrial fibrillation; MR, mendelian randomization.
Multivariable MR Analysis Results
In the multivariable MR analysis, for the primary analysis, after adjusting for BMI, the relationship between OSA and risk of AF remains statistically significant (OR 1.10, 95%CI 1.04–1.17). And the adverse effect of OSA on AF existed after adjustment for CAD (OR 1.17, 95% CI 1.02–1.34). However, there was no evidence in favor of an association between OSA and AF after adjustment for hypertension (adjusted P = 0.245). The replicated analysis showed similar results to the primary analysis above (Figure 3).
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Figure 3. The association between genetically determined OSA and the AF risk using univariable and multivariable inverse-variance weighted (IVW) MR adjusted for body mass index (BMI), hypertension (HTN), and coronary artery disease (CAD). UVMR, univariable mendelian randomization; MVMR, multivariable mendelian randomization; SNP, single-nucleotide polymorphism; OR, odds ratio; CI, confidence interval; BMI, body mass index; HTN, hypertension; CAD, coronary artery disease; IVW, inverse-variance weighted; OSA, obstructive sleep apnea; AF, atrial fibrillation.
Discussion
With the MR method, we used genetic and clinical information, and provided the evidence to verify the causal association between the genetic determinants of OSA and the risk of AF, after adjusting for common cardiovascular factors. The major strength of our study is attributed to the large-scale sample, which supports a comprehensive analysis for incident AF and well-powered GWAS to obtain genetic instruments for MR analysis. Since AF remains the leading cardiac arrhythmia and one of the major causes of stroke, heart failure, and subsequent morbidity, our results provide further evidence from epidemiological significance advocating to emphasize the adequate control of OSA to reduce the global burden of AF and its complications.
In line with the current study, OSA was generally reported to be positively associated with the incidence of AF. Two novel pieces of research, using ECG monitoring in middle- or old-aged SA (Sleep Apnea) patients with obesity, found a 3 or 4.8% prevalence of nocturnal AF, higher than that of 0.4–1% in the general population (29, 30). As to longitudinal studies, Cadby (9) reported that the presence of OSA was associated with 1.55-fold of incident AF as measured by AF-related hospitalizations in a cohort of 6,841 middle-aged individuals with an average BMI of 30.7 kg/m2 during a median of 11.9 years of follow-up. Gami's (8) report found a two-fold higher risk of AF in patients with OSA in another large cohort with a similar average anthropometric index, however, a novel result showed that statistical difference lied only in the group of patients less than 65 years old. Conversely, in an age-stratified adjusted analysis, the OSA-AF association was not observed in 843 male cohorts with a mean age of 75 years (31). We speculated that epidemiological effects in the aforementioned studies modified were probably due to selection bias originating from limited sample size and study design. Moreover, despite epidemiological studies demonstrating the potential associations between OSA and AF, this evidence might be subject to residual confounding factors, as both OSA and AF shared several risk factors: at least 70% of OSA patients are obese (32), even MR analysis assessing the causality between genetic predicted BMI and OSA confirmed their strong genetic correlations (14), and a causal relationship was also identified between genetically predicted obesity and risk of AF (33, 34); so that obesity was an extremely important common factor as it was predisposed to result in the co-phenomenon of OSA and AF even in longitudinal studies. Apart from obesity, the habits of smoking (35, 36) and alcohol intake (37, 38) also tended to act as common risks of OSA and AF. With an instrumental variable analysis and a huge sample size, the MR approach can be used to study a cause-and-effect relationship without interferences of bias and confounding that are hard to circumvent in observational design, thus it is more appropriate for our exposure and outcome set. Chen (39) did an MR analysis to investigate the association between OSA and AF. They reported that OSA was related to an increased risk of AF. But they only did univariable analysis rather than multivariable analysis to adjust the potential confoundings such as BMI, CAD, and hypertension. Compared to their study, ours selected two outcome datasets for primary and secondary analysis. Therefore our results may be more robust.
There are several pathophysiologic mechanisms underlying the causal OSA-AF relationship. Apnea directly induces acidosis, hypoxia, hypercarbia, and elevated pulmonary pressure, subsequently resulting in combined sympathovagal activation contributing to hemodynamic and arrhythmogenic electrophysiologic changes, increasing the frequency of premature atrial contractions with the potential to initiate AF in a vulnerable substrate (40–42). Furthermore, long-term exposure to OSA leads to structural remodeling processes. It was observed in animals that intermittent airway obstruction produced connexin dysregulation, atrial fibrosis, atrial abnormal conduction, and increased AF susceptibility/duration (43). Accordingly, human atrial structural changes and conduction abnormalities occur during long-time OSA, forming a substrate for AF vulnerability (44, 45).
To note, some points in the data aroused our consideration. Effect sizes for the presence of OSA on the AF risk in our MR analysis were smaller compared with those obtained using observational data. This might be attributed to several reasons: part of AF is hard to capture when paroxysmal and might remain silent or asymptomatic in clinically stable patients or outpatients. Based on this background, cohort studies with closer follow-up of the participants had more opportunities to document more AF cases than those in our population. Meanwhile, another explanation is related to confounding-derived bias on the association between OSA and AF described above in observational studies. Multivariable MR association persisted after additional adjustment for comorbidities that may either mediate or confound the OSA-AF relationship, effect estimates were similar after BMI and CAD adjustment, but hypertension adjustment abolished the efficacy, suggesting that HTN might substantially mediate the effect of OSA on the risk of AF. It made sense that recognition already suggested that one of the OSA complications was a higher frequency of non-dipping blood pressure (BP) and pattern nocturnal hypertension (46), and genetic BP had a causal impact on AF (47).
Our study has some limitations. First, the limited number of instrumental SNPs in our study may distort MR estimates. But the F statistic of the SNP we used in this study were all >100, suggesting a strong correlation with OSA. Second, it is unlikely to remove all potential horizontal pleiotropy from the study, which may result in the biased estimation of causal inference. However, no pleiotropic effect was detected in the MR-Egger regression. Third, the specific ancestry of the samples also limits the generalizability of our results to other ancestries. Despite relative weaknesses, our study has several noteworthy advantages. First, we used MR method to estimate the causal effect between the OSA and AF, which contributes to the avoidance of measurement errors and residual confusion. In addition, we performed a series of sensitivity analyses to assess heterogeneity and pleiotropy, and we also conducted MVMR to correct for the effects of confounding factors including BMI, hypertension, and CAD.
Conclusion
In summary, the current study provides the first causal evidence of the relationship between genetically predicted OSA and the risk of AF, suggesting that the therapy of OSA might represent an effective strategy to lower the incidence and re-occurrence of AF.
Data Availability Statement
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author/s.
Author Contributions
YLi, YLe, and RM drafted the manuscript. YLi and HT analyzed the data. PM, RM, and HT designed the study. PM and HY obtained the funding. All authors participated in the field survey and data collection, critically revised the manuscript, and gave final approval to the version submitted for publication.
Funding
This work was supported by the National Natural Science Foundation of China (81974054), Liaoning Province's Xingliao talent program in China (No. XLYC1807116), and the Fundamental Research Funds for Central Universities of Central South University (2019zzts106).
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher's Note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fcvm.2022.843681/full#supplementary-material
Supplementary Figure S1. Instrumental variable (IV) assumptions of MR.
Supplementary Table S1. Single-nucleotide polymorphisms associated with OSA.
Supplementary Table S2. Statistical power calculation for MR analyses.
Abbreviations
OSA, obstructive sleep apnea; AF, atrial fibrillation; MR, mendelian randomization; GWAS, genome-wide association study; MVMR, multivariable mendelian randomization; BMI, body mass index; CAD, coronary artery disease; IVW, inverse-variance weighted; MR-PRESSO, MR-pleiotropy residual sum and outlier; OR, odds ratio; IV, instrumental variable; SNP, single-nucleotide polymorphism; LD, linkage disequilibrium; ECG, electrocardiogram; SA, sleep apnea; BP, blood pressure; HTN, hypertension.
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Keywords: obstructive sleep apnea, atrial fibrillation, Mendelian randomization, causal inference, instrumental variable (IV)
Citation: Li Y, Leng Y, Tang H, Deng P, Wang J, Yuan H, Miao R and Mu P (2022) Assessment of the Causal Effects of Obstructive Sleep Apnea on Atrial Fibrillation: A Mendelian Randomization Study. Front. Cardiovasc. Med. 9:843681. doi: 10.3389/fcvm.2022.843681
Received: 26 December 2021; Accepted: 13 January 2022;
Published: 11 February 2022.
Edited by:
Ding-Sheng Jiang, Huazhong University of Science and Technology, ChinaCopyright © 2022 Li, Leng, Tang, Deng, Wang, Yuan, Miao and Mu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Ping Mu, pingmu@symc.edu.cn; Rujia Miao, 454258816@qq.com
†These authors have contributed equally to this work