ISSN : 1301-5680
e-ISSN : 2149-8156
Turkish Journal of Thoracic and Cardiovascular Surgery     
Atrial fibrillation after cardiac surgery and preoperative vitamin D levels: A systematic review and meta-analysis
Selen Öztürk1, İbrahim Öztürk2
1Department of Cardiovascular Surgery, Dr. Siyami Ersek Thoracic and Cardiovascular Surgery Training and Research Hospital, Istanbul, Turkey
2Department of Anesthesiology and Reanimation, Göztepe Training and Research Hospital, Istanbul, Turkey
DOI : 10.5606/tgkdc.dergisi.2020.18387

Abstract

Background: In this meta-analysis, we aimed to investigate the possible relationship between atrial fibrillation development after cardiac surgery and preoperative vitamin D levels.

Methods: Literature review was carried out in the PubMed, ScienceDirect and Ovid electronic databases without any limitation of time frame. Published studies which recorded the preoperative levels of vitamin D and atrial fibrillation after cardiac surgery in the English language were included. The results of the studies were evaluated based on either random or fixed effect model according to the presence of heterogeneity (I2>25%).

Results: A total of 1,865 articles were screened. After the article titles and abstracts were analyzed, six articles involving 769 patients which met the inclusion criteria were included. The results indicated that there was a relationship between preoperative vitamin D levels and postoperative atrial fibrillation (SMD: -0.46, 95% CI: -0.79 to -0.12; p<0.007). Heterogeneity was observed for studies conducted (I2 =76.1%).

Conclusion: We concluded that low preoperative vitamin D levels were associated with the development of atrial fibrillation after cardiac surgery. However, there is a need for large-scale, randomized-controlled trials for preventing the heterogeneity of the results.

Atrial fibrillation (AF) following cardiac surgery occurs in 20 to 50% of patients.[1] Increased age is the most well-known risk factor for POAF.[2] The increasing number of elderly patients for cardiac surgery also increases the possibility of postoperative AF (POAF) development. Postoperative AF is associated with increased mortality, cost, and stroke.[3-5] In the pathogenesis of POAF, several factors such as local/systemic inflammation and oxidative stress or electrolyte imbalance have been proposed to play a role.[6] There are also several risk factors which contribute to POAF such as age, heart failure, coronary artery disease, prior history of AF, other arrhythmias, hypertension, male gender, chronic obstructive pulmonary disease, kidney disease, diabetes, and obesity.[6]

Vitamin D is a fat-soluble vitamin.[7] It is produced under the skin on exposure to ultraviolet sunlight and metabolized in liver and kidney.[8] Rickets, osteomalacia, osteoporosis, and skin diseases are associated with the low levels of vitamin D. [7] Although vitamin D is associated with calcium metabolism and bone health, vitamin D receptors have been found in cells throughout the body, such as cardiomyocytes, suggesting that it has additional functions.[9] In addition, studies have demonstrated that vitamin D is associated with cardiovascular diseases such as coronary artery disease, myocardial infarction, cardiomyopathy, and heart failure.[10-13] Vitamin D can regulate the renin-angiotensin-aldosterone system activity and inflammatory processes.[14] These processes which implicate in the pathophysiology of AF, suggest a potential role of vitamin D in the etiology of AF.

In previous prospective cohort studies, no significant relationship between AF and vitamin D deficiency has been established.[15,16] However, two case-control studies demonstrated that there was a link between low vitamin D levels and non-valvular AF.[17,18] In recent years, the number of studies regarding vitamin D levels and AF has been on a rise. In this systematic review and meta-analysis, we aimed to investigate the possible relationship between AF after cardiac surgery and preoperative vitamin D levels in the light of literature data.

Methods

Database search
We carried out our database search in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA®) statement which was specifically developed for meta-analyses to improve the reporting of reviews by Moher et al.[19] in 2015. An electronic database search in the English language was conducted to identify whether preoperative vitamin D levels might be associated with POAF. The database was screened until the date of March 9, 2019. No time frame limitation was applied. The PubMed, ScienceDirect, and Ovid were utilized as the electronic databases. No searches were conducted other than the electronic database. However, articles found in the references section of articles which may be of interest were analyzed.

The following English keywords or a combination of them were used: "atrial fibrillation", "cardiac surgery", "heart surgery", "valve surgery", "coronary artery bypass grafting", and "vitamin D". Only articles published in English were screened, and those in other languages were excluded.

Selection of studies
All retrospective and prospective studies were included, irrespective of the sample size. Inclusion criteria were as follows: (i) clinical study, (ii) adult patient population, and (iii) articles in English language. Exclusion criteria were as follows: (i) experimental studies, (ii) case studies or case series, (iii) articles in languages other than English, and (iv) utilizing non-cardiac surgical interventions. Studies which were relevant to our subject of study, but that did not investigate preoperative vitamin D levels were not included. In addition, articles in which relevant data were presented as figures or graphs were also excluded.

Data collection
Researchers recorded the data in the relevant articles (name of the first author, date of publication, sample number, and research design) independently from each other. Disagreements between the data and articles were resolved on the basis of consensus. Data were entered using the meta-analysis software and expressed in mean and standard deviation (SD), or number and frequency. Data presented in median (minmax) were calculated in mean and SD values according to the formula by Hozo et al.[20]

Statistical analysis
For the statistical analysis, Open Meta-Analyst® software (Brown University, Rhode Island, USA) was used. For funnel plot, we performed analysis with MetaLight® v1.2.0 s oftware (University College London, London, United Kingdom). Data were expressed in standard mean differences (SMD) and 95% confidence interval (CI). Heterogeneity was evaluated by I2 statistics. If I2 ?25%, heterogeneity was accepted as significant, and analysis of moderators was undertaken to identify the cause of heterogeneity. Meta-analysis was carried out using fixed or random models. In the presence of heterogeneity (I2>25%), random effects model was used, while in its absence (I2<25%), fixed effect model was used. Publication bias was evaluated with the Begg's test. File drawer analysis was performed using the Jamovi® v0.9 software (retrieved from https://www.jamovi.org). A p value of <0.05 was considered statistically significant.

Results

The flow chart of literature search is shown in Figure 1.

Figure 1: Flow chart of database search.
CABG: Coronary artery bypass grafting

A total of 1,865 articles were identified in the electronic databases. After the repeating articles were excluded, 436 articles were left. Upon reviewing the abstracts and titles of the articles, 351 articles which were not relevant with the subject were eliminated. Of the remaining 85 articles, the entire texts of 78 which were analyzed for compliance with the metaanalysis were excluded (review article: 7, editorial: 4, case report: 14, not in English language: 9, letter to editor: 8, non-coronary artery bypass grafting [CABG] or valve surgery population: 24, and experimental trial: 12). Seven of them were evaluated in the qualitative synthesis and finally, a total of six research studies involving 769 patients were included in the quantitative synthesis.[21-26] Demographic data and characteristics of the articles are summarized in Table 1. The overall POAF development rate was 34.98% (269/769).

Table 1: Properties of trials included the analysis

As a result of analysis of the articles, heterogeneity was observed (Q: 20.92, df(5), p<0.001, I2: 76.1%). Therefore, the random effects model was used for the final analysis. Accordingly, there was a statistically significant relationship between the preoperative levels of vitamin D and AF after cardiac surgery (SMD: -0.46, 95% CI: -0.79 to -0.12; p=0.007). The results are given in Figure 2 and Table 2.

Figure 2:Forest plot of overall analysis.
CI: Confidence interval;

Table 2: Results of analysis

When we analyzed heterogeneity among the studies, we reviewed the randomization as a moderator. We also found the main reason of heterogeneity to be non-randomization (I2>25%). Subgroup analysis for moderator is shown in Figure 3 and Table 2. However, we were unable to perform the designs of studies according to time process such as prospective or retrospective, as there was only one retrospective study.[23] The results of the heterogeneity analysis are summarized in Table 2.

Figure 3: Forest plot of subgroup analysis according to randomization.
CI: Confidence interval.

Model fitting weights were between 19.79% (Emren et al.[25]) and 13.83% (Gode et al.[22]).

According to the Begg"s test, there was no significant publication bias among the studies (tau 2 >0.05). However, due to its asymmetrical nature, this was not completely corrected based on visual analysis with funnel plot. Funnel plot is shown in Figure 4. The number of fail-safe studies according to the file drawer analysis was 7. However, we thought that this figure was not realistic, as only three databases were able to be screened in detail. Furthermore, we were unable to perform meta-regression, due to the small number (<10) of studies included in the meta-analysis.

Figure 4: Funnel plot for publication bias.

Discussion

In this meta-analysis, we found that there was a significant relationship between the preoperative levels of vitamin D and AF after cardiac surgery (p<0.05). However, there was heterogeneity among the studies and non-randomization was the main reason for heterogeneity.

Ruiz-Núñez et al.[27] reviewed 55 patients undergoing CABG and found that dietary vitamin D intake was below the recommendations. The percentage was 13%, while the recommended dose was 10 to 20 ?g/dL. A recent study also demonstrated that preoperative vitamin D supplementation had a preventive effect for POAF in vitamin D deficiency (serum levels of vitamin D <20 ng/mL).[28]

In the literature, Rienstra et al.[15] and Qayyum et al.[29] found no significant correlation between AF development and 25(OH)D, while more recent studies[9,10] demonstrated that low 25(OH)D was related to non-valvular AF. In addition, hypertension, coronary artery disease, and stroke have been shown to be linked with vitamin D deficiency.[30] On the other hand, the relationship with vitamin D and AF is still controversial. In recent two meta-analyses, this topic was examined.[31,32] Zhang et al.[31] concluded that vitamin D deficiency modestly increased the risk for AF and found that there was a need for further studies to determine the direct causal relationship. In the second and more recent meta-analysis, Huang et al.[32] was unable to show that vitamin D levels might play a major role in the development of new-onset AF. Of note, Zhang et al.[31] did not include the cardiac surgery patients, while Huang et al.[32] i ncluded either surgical or non-surgical patients in their study. In our analysis, cardiac surgery population was included.

In an experimental study, Xiang et al.[33] reported that vitamin D regulated cardiac functions through systemic and cardiac renin-angiotensin-aldosterone system. Due to the activation of tissue renin-angiotensinaldosterone system, vitamin D may lead to new-onset AF.[34] Therefore, the mechanism between v itamin D and AF is associated with apoptosis of cardiomyocytes and changes in the atrial structure due to reninangiotensin- aldosterone system induction.[35] Also, vitamin D was found to be related with endothelial dysfunction and subclinical atherosclerosis.[36] In the in vitro experiments, Canning et al.[37] showed that vitamin D regulated inflammation and up-regulated expression of cytokines (interleukin 10 and 6).

Among the studies included in this meta-analysis, only Shadvar et al.[24] was unable to find a statistically significant difference between the groups. The other studies[21-23,25,26] demonstrated that preoperative vitamin D levels were independent predictors of POAF as assessed by univariate regression analysis. Also, Özsin et al.,[21] Emren et al.,[25] and Gode et al.[22] found vitamin D to be an independent predictor according to the multivariate analysis.

Among the studies, all patients had isolated CABG surgery, except for Skuladottir et al."s population.[26] They studied both CABG and valve surgery patients, although the type of surgery was not a risk factor for POAF according to the multivariate analysis. In the literature, the incidence of POAF ranges between 25 and 40% for CABG, while it is 62% for combined CABG and valve surgery.[21,38]

Our analysis showed that the main reason for heterogeneity was non-randomized trials. Only two studies were prospective and randomized.[21,24] Among these two studies, only Özsin et al.'s study[21] supported the results of our analysis. The aforementioned authors found the levels of vitamin D as a predictor after univariate and multivariate regression analysis,[21] while Shadvar et al.[24] failed.

There are several limitations of this meta-analysis. First, our analysis includes a small number of studies. Therefore, we were unable to perform meta-regression. Second, studies included have different designs which resulted in heterogeneity. The randomized controlled trials, particularly large-scale trials, may be helpful to eliminate the heterogeneity by standardization of the possible risk factors between the groups. Finally, only articles in the English language were selected, which may have resulted in some useful sources of evidence being missed.

In conclusion, low preoperative vitamin D levels are associated with the development of atrial fibrillation after cardiac surgery. However, there is still a need for large-scale, randomized-controlled trials to prevent the heterogeneity of results and to conduct a metaregression analysis.

Declaration of conflicting interests
The authors declared no conflicts of interest with respect to the authorship and/or publication of this article.

Funding
The authors received no financial support for the research and/or authorship of this article.

References

1) January CT, Wann LS, Alpert JS, Calkins H, Cigarroa JE, Cleveland JC Jr, et al. 2014 AHA/ACC/HRS guideline for the management of patients with atrial fibrillation: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines and the Heart Rhythm Society. J Am Coll Cardiol 2014;64:e1-76.

2) Echahidi N, Pibarot P, O'Hara G, Mathieu P. Mechanisms, prevention, and treatment of atrial fibrillation after cardiac surgery. J Am Coll Cardiol 2008;51:793-801.

3) Almassi GH, Schowalter T, Nicolosi AC, Aggarwal A, Moritz TE, Henderson WG, et al. Atrial fibrillation after cardiac surgery: a major morbid event? Ann Surg 1997;226:501-11.

4) Aranki SF, Shaw DP, Adams DH, Rizzo RJ, Couper GS, VanderVliet M, et al. Predictors of atrial fibrillation after coronary artery surgery. Current trends and impact on hospital resources. Circulation 1996;94:390-7.

5) Mathew JP, Parks R, Savino JS, Friedman AS, Koch C, Mangano DT, et al. Atrial fibrillation following coronary artery bypass graft surgery: predictors, outcomes, and resource utilization. MultiCenter Study of Perioperative Ischemia Research Group. JAMA 1996;276:300-6.

6) Greenberg JW, Lancaster TS, Schuessler RB, Melby SJ. Postoperative atrial fibrillation following cardiac surgery: a persistent complication. Eur J Cardiothorac Surg 2017;52:665-72.

7) Rai V, Agrawal DK. Role of Vitamin D in Cardiovascular Diseases. Endocrinol Metab Clin North Am 2017;46:1039-59.

8) Holick MF. Vitamin D deficiency. N Engl J Med 2007;357:266-81.

9) DeLuca HF. Overview of general physiologic features and functions of vitamin D. Am J Clin Nutr 2004;80:1689S-96S.

10) Chen S, Swier VJ, Boosani CS, Radwan MM, Agrawal DK. Vitamin D deficiency accelerates coronary artery disease progression in swine. Arterioscler Thromb Vasc Biol 2016;36:1651-9.

11) Aleksova A, Belfiore R, Carriere C, Kassem S, La Carrubba S, Barbati G, et al. Vitamin D Deficiency in Patients with Acute Myocardial Infarction: An Italian Single-Center Study. Int J Vitam Nutr Res 2015;85:23-30.

12) Yilmaz O, Olgun H, Ciftel M, Kilic O, Kartal I, Iskenderoglu NY, et al. Dilated cardiomyopathy secondary to ricketsrelated hypocalcaemia: eight case reports and a review of the literature. Cardiol Young 2015;25:261-6.

13) Gullestad L, Ueland T, Vinge LE, Finsen A, Yndestad A, Aukrust P. Inflammatory cytokines in heart failure: mediators and markers. Cardiology 2012;122:23-35.

14) Vitezova A, Cartolano NS, Heeringa J, Zillikens MC, Hofman A, Franco OH, et al. Vitamin D and the risk of atrial fibrillation--the Rotterdam Study. PLoS One 2015;10:e0125161.

15) Rienstra M, Cheng S, Larson MG, McCabe EL, Booth SL, Jacques PF, et al. Vitamin D status is not related to development of atrial fibrillation in the community. Am Heart J 2011;162:538-41. 16 Smith MB, May HT, Blair TL, Anderson JL, Muhlestein JB, Horne BD, et al. Vitamin D excess is significantly associated with risk of atrial fibrillation. Circulation 2011;124:A14699.

17) Demir M, Uyan U, Melek M. The effects of vitamin D deficiency on atrial fibrillation. Clin Appl Thromb Hemost 2014;20:98-103.

18) Chen WR, Liu ZY, Shi Y, Yin DW, Wang H, Sha Y, et al. Relation of low vitamin D to nonvalvular persistent atrial fibrillation in Chinese patients. Ann Noninvasive Electrocardiol 2014;19:166-73.

19) Moher D, Shamseer L, Clarke M, Ghersi D, Liberati A, Petticrew M, et al. Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015 statement. Syst Rev 2015;4:1.

20) Hozo SP, Djulbegovic B, Hozo I. Estimating the mean and variance from the median, range, and the size of a sample. BMC Med Res Methodol 2005;5:13.

21) Özsin KK, Sanrı US, Toktaş F, Kahraman N, Yavuz Ş. Effect of plasma level of vitamin D on postoperative atrial fibrillation in patients undergoing isolated coronary artery bypass grafting. Braz J Cardiovasc Surg 2018;33:217-23.

22) Gode S, Aksu T, Demirel A, Sunbul M, Gul M, Bakır I, et al. Effect of vitamin D deficiency on the development of postoperative atrial fibrillation in coronary artery bypass patients. J Cardiovasc Thorac Res 2016;8:140-6.

23) Cerit L, Kemal H, Gulsen K, Ozcem B, Cerit Z, Duygu H. Relationship between Vitamin D and the development of atrial fibrillation after on-pump coronary artery bypass graft surgery. Cardiovasc J Afr 2017;28:104-7.

24) Shadvar K, Ramezani F, Sanaie S, Maleki TE, Arbat BK, Nagipour B. Relationship between plasma level of vitamin D and post operative atrial fibrillation in patients undergoing CABG. Pak J Med Sci 2016;32:900-4.

25) Emren SV, Aldemir M, Ada F. Does deficiency of vitamin D increase new onset atrial fibrillation after coronary artery bypass grafting surgery? Heart Surg Forum 2016;19:E180-4.

26) Skuladottir GV, Cohen A, Arnar DO, Hougaard DM, Torfason B, Palsson R, et al. Plasma 25-hydroxyvitamin D2 and D3 levels and incidence of postoperative atrial fibrillation. J Nutr Sci 2016;5:e10.

27) Ruiz-Núñez B, van den Hurk GH, de Vries JH, Mariani MA, de Jongste MJ, Dijck-Brouwer DA, et al. Patients undergoing elective coronary artery bypass grafting exhibit poor preoperative intakes of fruit, vegetables, dietary fibre, fish and vitamin D. Br J Nutr 2015;113:1466-76.

28) Cerit L, Özcem B, Cerit Z, Duygu H. Preventive effect of preoperative vitamin D supplementation on postoperative atrial fibrillation. Braz J Cardiovasc Surg 2018;33:347-52.

29) Qayyum F, Landex NL, Agner BR, Rasmussen M, Jøns C, Dixen U. Vitamin D deficiency is unrelated to type of atrial fibrillation and its complications. Dan Med J 2012;59:A4505.

30) Thompson J, Nitiahpapand R, Bhatti P, Kourliouros A. Vitamin D deficiency and atrial fibrillation. Int J Cardiol 2015;184:159-62.

31) Zhang Z, Yang Y, Ng CY, Wang D, Wang J, Li G, et al. Meta-analysis of Vitamin D Deficiency and Risk of Atrial Fibrillation. Clin Cardiol 2016;39:537-43.

32) Huang WL, Yang J, Yang J, Wang HB, Yang CJ, Yang Y. Vitamin D and new-onset atrial fibrillation: A metaanalysis of randomized controlled trials. Hellenic J Cardiol 2018;59:72-77.

33) Xiang W, Kong J, Chen S, Cao LP, Qiao G, Zheng W, et al. Cardiac hypertrophy in vitamin D receptor knockout mice: role of the systemic and cardiac renin-angiotensin systems. Am J Physiol Endocrinol Metab 2005;288:E125-32.

34) Frustaci A, Chimenti C, Bellocci F, Morgante E, Russo MA, Maseri A. Histological substrate of atrial biopsies in patients with lone atrial fibrillation. Circulation 1997;96:1180-4.

35) Cardin S, Li D, Thorin-Trescases N, Leung TK, Thorin E, Nattel S. Evolution of the atrial fibrillation substrate in experimental congestive heart failure: angiotensindependent and -independent pathways. Cardiovasc Res 2003;60:315-25.

36) Oz F, Cizgici AY, Oflaz H, Elitok A, Karaayvaz EB, Mercanoglu F, et al. Impact of vitamin D insufficiency on the epicardial coronary flow velocity and endothelial function. Coron Artery Dis 2013;24:392-7.

37) Canning MO, Grotenhuis K, de Wit H, Ruwhof C, Drexhage HA. 1-alpha,25-Dihydroxyvitamin D3 (1,25(OH)(2)D(3)) hampers the maturation of fully active immature dendritic cells from monocytes. Eur J Endocrinol 2001;145:351-7.

38) Maisel WH, Rawn JD, Stevenson WG. Atrial fibrillation after cardiac surgery. Ann Intern Med 2001;135:1061-73.

Keywords : Atrial fibrillation, cardiac surgery, meta-analysis, Vitamin D
Viewed : 4896
Downloaded : 985