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Effects of AMPD1 gene C34T polymorphism on cardiac index, blood pressure and prognosis in patients with cardiovascular diseases: a meta-analysis
BMC Cardiovascular Disorders volume 17, Article number: 174 (2017)
The meta-analysis was aimed to evaluate the effects of AMPD1 gene C34T polymorphism on cardiac function indexes, blood pressure and prognosis in patients with cardiovascular diseases (CVD).
Eligible studies were retrieved through a comprehensive search of electronic databases and manual search. Then the high-quality studies met the rigorous inclusion and exclusion criteria, as well as related to the subject was selected for the study. Comprehensive data analyses were conducted using STATA software 12.0.
The study results revealed that CVD patients with CT + TT genotype of AMPD1 C34T polymorphism presented elevated left ventricular ejection fraction (LVEF) (%) and reduced left ventricular end diastolic dimension (LVEDD) (mm) as compared with CC genotype, moreover, the subgroup analysis found that the LVEF (%) was markedly higher in heart failure (HF) patients carrying CT + TT genotype than CC genotype. Besides, the systolic blood pressure (SBP) (mmHg) in CVD patients with CT + TT genotype was obviously decreased in contrast with the CC genotype. Patients suffered from HF with different genotypes (CT + TT and CC) of AMPD1 C34T polymorphism exhibited no significant differences in total survival rate and cardiac survival rate.
Our current meta-analysis indicated that the T allele of AMPD1 gene C34T polymorphism may be correlated with LVEF, LVEDD and SBP, which plays a protective role in the cardiac functions and blood pressure in CVD patients, but had no effects on total survival rate and cardiac survival rate for HF.
Cardiovascular disease (CVD), a series of diseases involving the heart or blood vessels of people, has become one of the predominant causes of morbidity and mortality worldwide threatening human health according to W.H.O statistics [1,2,3]. At present, CVD remains the first reason of great number of deaths and disabilities in China, and nearly 3 million individuals died each year from CVD, which approximately accounts for 42% of all deaths in 2010 . In general, CVD, including coronary artery diseases (CAD), heart failure (HF), myocardial infarction and so on, are multifactorial disorders frequently sharing or coexisting risk elements like hypertension, dyslipidemia, overweight, and physical inactivity, which could partially illustrate the etiology of CVD [5, 6]. Apart from the above, mounting evidence has indicated that genetic polymorphisms in some special genes also have important impact on the pathogenesis of CVD, which provided solid foundations to elucidate the essence of clinical phenotype diversity and individual clinical treatment [7, 8].
The AMPD1 gene encodes the adenosine monophosphate deaminase (AMPD), a crucial enzyme in purine nucleotide and energy metabolism especially in skeletal muscle, as well as in cardiac muscle, with the function of catalyzing adenosine monophosphate to inosine monophosphate [9, 10]. To our knowledge, The AMPD1 gene is prevalently localized in chromosome 1 in the region p13 ~ 21 with 20 kb spanning in length, and consisting of 16 exons and 15 introns . Under most conditions, there is a common polymorphism of the nonsense mutation with a C-to-T transition at position 34 of AMPD1, contributing to the appearance of a premature stop codon, which leads to some related metabolic muscle diseases due to the AMPD activity deficiency . While several recent studies also suggested that AMPD1 may play essential roles in the initiation and development of CVD, for instance, it has been demonstrated that AMPD1 allele mutation play a protective role during congestive heart failure (CHF) development, which contributed to prolong possibility of survival without cardiac transplantation , meanwhile, it can alleviate the aortic stiffness and inflammation for patients with CAD . Therefore, it was reasonably speculated that AMPD1 as a possible candidate gene is related to CVD. But the effect of AMPD1 C34T polymorphism in CVD remains controversial, like Collins RP and his team, who have yielded conflicting results stating that the mutant T allele of AMPD1was deleterious in both HF and post-MI patients who had myocardial infarction histories . Besides, de Groote P et al. did not find any impacts of AMPD1 genetic mutation on the prognosis and survival in CHF patients . Therefore, there appears a need for a meta-analysis to investigate the relationship between the AMPD1 gene C34T variant and CVD risk regarding the aspects of cardiac indexes, blood pressure and prognosis, and thereby deriving a more plausible estimation for CVD.
Published literatures about AMPD1 gene C34T polymorphism and CVD were retrieved by using following ten English and Chinese databases (including PubMed, Springerlink, Wiley, Web of Science, EBSCO, Ovid, SicenceDirect, Wanfang, China National Knowledge Infrastructure and VIP) from inception through March 2017 with the following search terms: (“AMPD1” OR “Adenosine monophosphate deaminase 1”) and (“Cardiovascular disease” OR “CVD” OR “CAD” OR “heart failure” OR “myocardial infarction” OR “heart disease”). In addition, we also carried out a manual search to find potential relevant studies.
Inclusion and exclusion criteria
The inclusion criteria were as follows: (1) associations of AMPD1 gene C34T polymorphism with blood pressure, cardiac function and prognosis in CVD patients; (2) studies in which could obtain the parameters (blood pressure, cardiac indexes and prognosis) of CVD patients carrying CT + TT and CC genotypes of AMPD1 gene C34T polymorphism and calculate WMD (95%CI) and HR (95%CI); (3) unlimited sample size; (4) reliable detection of polymorphic loci; (5) with the same or overlapping data published by the same authors, the most recent or complete articles with the largest sample size; (6) only English or Chinese publications. Literatures that did not conform to the above inclusion criteria or involve one of the following criteria must be eliminated: (1) the literature with only overview and summary (without data) or meeting abstracts; (2) articles with insufficient data; (3) unpublished documents; (4) duplicated publications.
Two researchers independently searched and reviewed to extract available literature data based on the selection criteria. Disagreements were handled by discussions. The following major information was collected: (1) first author’s name; (2) publication year; (3) age, gender ethnicity and country of subjects; (4) type of diseases; (5) genotyping technology; (6) sample size of the CVD patients carried with different genotypes of AMPD1 gene C34T polymorphism; (7) LVEF (%), LVEDD (mm), SBP (mmHg), diastolic blood pressure (DBP) (mmHg), total survival rate and the cardiovascular incidence in patients with different genotypes of AMPD1 gene C34T polymorphism.
Meta-analysis was performed by STATA 12.0 (StataCorp, College Station, TX, USA) software. Kaplan-Meier survival curves were used for HR and 95%CI calculation with the aid of software Engauge Digitizer Version 4.1 (http://sourceforge.net/) and the method . Parameters, such as LVEF (%), LVEDD (mm), SBP (mmHg), DBP (mmHg), total survival rate and cardiovascular incidence in CVD patients with CT + TT and CC genotypes of AMPD1 gene C34T polymorphism were evaluated using weighted mean difference (WMD) or hazard ratio (HR) and 95% confidence interval (95%CI), and Z test was used to compare the significance of the combined effects . The Cochran’s Q-statistic (P h < 0.05 was considered significant) and I 2 tests (I 2 > 50%) were used to measure heterogeneity between the studies. The random-effects model was used for significant heterogeneity, while the fixed-effects model was conducted when no significant heterogeneity was existed [18, 19]. Heterogeneity sources were analyzed using subgroup (with or without HF) analysis. The sensitivity analysis was aimed to assess the impact of each single study on the overall estimate. Possible publication bias was tested by Egger’s linear regression analysis . P < 0.05 was statistically significant difference.
Baseline characteristics of included studies
A total of 206 studies related to AMPD1 gene polymorphism and CVD (165 English studies and 41 Chinese articles) were retrieved in the initial literature search, of which 108 unrelated articles falling short of titles or abstracts were removed, and the remaining 94 articles were used for further screening. Then, 80 studies of these 94 papers were excluded after more detailed reviewing the full texts, 6 articles with insufficient data and 2 duplicates were removed. Finally, only 8 articles were considered eligible to be incorporated into the meta-analysis [10, 13,14,15, 21,22,23,24]. The flow diagram of the literature selection process is shown in Fig. 1. The included researches which involved 2805 CVD cases all published between 1999 and 2014, including 192 consecutive stable CAD cases, 97 CAD with HF cases, 104 CAD without HF cases, 908 CHF cases, 1395 HF cases and 109 CHD cases. Baseline characteristics of the included studies are shown in Table 1.
Correlation of AMPD1 gene C34T polymorphism with cardiac function indexes (LVEF and LVEDD)
In this study, no significant heterogeneity was discovered, and accordingly, the fixed effect model was adopted (LVEF: I 2 = 0.00%, P h = 0.566; LVEDD: I 2 = 58.6%, P h = 0.064). The meta-analysis showed that, as compared with CC genotype, LVEF (%) was significantly increased in CT + TT genotype (WMD = 0.74, 95%CI: 0.36 ~ 1.12, P < 0.001, Fig. 2a), while LVEDD (mm) was markedly reduced (WMD = −1.31, 95%CI: -2.60 ~ −0.02, P = 0.047, Fig. 2b). The results of subgroup analysis revealed that HF patients with CT + TT genotype had higher LVEF than CC genotype (WMD = 0.73, 95%CI: 0.36 ~ 1.11, P < 0.001, Fig. 3a), and, interestingly, LVEDD was turned out to be irrelevant to different genotypes (CT + TT and CC) in CVD patients with or without HF (all P > 0.05, Fig. 3b).
Correlation of AMPD1 gene C34T polymorphism with blood pressure (SBP and DBP)
No heterogeneity was found among the studies (SBP: I 2 = 0%, P h = 0.578; DBP: I 2 = 0%, P h = 0.529), and accordingly, the fixed effect model was used. SBP (mmHg) was significantly lower in CVD patients with the CT + TT genotype compared with CC genotype by meta-analysis (WMD = −3.87, 95%CI: -7.01 ~ −0.74, P = 0.016, Fig. 2c), however, there were no such differences in DBP (mmHg) (WMD = −0.61, 95%CI: -2.71 ~ −1.48, P = 0.567, Fig. 2d). Subgroup analysis demonstrated that different genotypes (CT + TT and CC) of AMPD1 gene C34T polymorphism in CVD patients with or without HF had no impact on SBP and DBP (both P > 0.05, Fig. 3c, d).
Effects of AMPD1 gene C34T polymorphism on total survival rate and cardiac survival rate
Effects of AMPD1 gene C34T polymorphism on total survival rate were studied in 4 literatures, and it was considerably heterogeneous among the 4 studies (I 2 = 76.6%, P h = 0.001), thus the random effects model was selected. Two studies were about the effects of AMPD1 gene C34T polymorphism on cardiac survival rate, and it was proved to be with heterogeneity (I 2 = 39.4%, P h = 0.176), and the fixed effect model was preferred. Among 4 studies, two suggested that AMPD1 gene C34T polymorphism of (CT + TT) enhanced the total survival rate of patients, while the other two found that it had no effects on the total survival rate and cardiac survival rate. Meta-analysis results showed that there were no distinctly differences in total survival rate and cardiac survival rate in CAD patients with different AMPD1 gene C34T polymorphism genotypes (Total survival rate: HR = 0.93, 95%CI: 0.54 ~ 1.59, P = 0.780; Cardiac survival rate: HR = 1.05, 95%CI: 0.82 ~ 1.33, P = 0.713, Fig. 2e, f).
Sensitivity analysis and publication bias
Sensitivity analysis verified that all included studies presented no evident impacts on pooled WMD (Fig. 4a-d), as well as the pooled HR (Fig. 5e, f). Egger linear regression analysis indicated that there were no publication bias in the correlation of different genotypes (CT + TT and CC) of the AMPD1 gene C34T polymorphism with cardiac indexes (LVEF and LVEDD), blood pressure (SBP and DBP) and cardiac survival rate (all P < 0.05, Fig. 5a-e), while the total survival rate had a publish bias (P = 0.008, Fig. 5f).
The present meta-analysis has combined and reanalyzed 8 publications involving 2805 cases of patients with CVD, to assess the effect of AMPD1 gene C34T polymorphism on LVEF (%), LVEDD (mm), SBP (mmHg), DBP (mmHg), total and cardiac survival rate of CVD.
Our study showed that LVEF (%) in CVD patients with T allele of AMPD1 gene C34T polymorphism was significantly increased in comparison to those patients with CC genotype. On the contrary, the CVD patients with CT + TT genotype had a greater reduction of LVEDD (mm) than those with CC genotype. In addition, our subgroup analysis according to the patients with or without HF verified that the LVEF was markedly higher in HF patients who carried with CT + TT genotype than CC genotype. As is known to all, abnormalities of left ventricle (LV) function or structure has been a common event among most CVD patients, demonstrating a negative influence on cardiovascular prognosis [25, 26]. While LVEF is well-recognized as an important determinant of a person’s cardiac function to be clinically applied for the evaluation of the severity of heart systolic function, and in particular, it is typically low when the patients with the systolic form of congestive heart failure . As for LVEDD, it has widely accepted as a sensitive indication for measurement of the left ventricular remodeling for patients with CVD . More importantly, the myocardial remodeling, which is marked by changes in LVEF and LV volumes, could be functioned as a practical prognosis indicator to guide clinicians’ diagnose . Probably, there is an explanation for this finding that this polymorphic variant of AMPD1 C34T could weaken the AMPD activity, and promote the elevated circulating levels of adenosine, a crucial protective agent, which was in part the consequence of the attenuation of myocardial fibrosis and ventricular remodeling, and thus contributing to less severe CVD [13, 30]. Consistently, both Safranow K et al.  and Gastmann A et al.  pointed out the tendency that LVEDD values in patients with CAD or CHF who carried the mutant T allele of AMPD1 was smaller, further indicating that the AMPD1 C34T polymorphism might affect different types of ventricular remodeling among CVD. Interestingly, no relevance of AMPD1 gene C34T polymorphism to LVEF (%) had been found in our 5 included researches [13,14,15, 21, 24], which might be partially limited by the small sample size. To our knowledge, high blood pressure (BP), or together with other risk elements could maximize the cardiovascular risk to a certain extent . In the present study, we also revealed that being carrier of the T allele in AMPD1 C34T polymorphism is remarkably correlated with lower levels of SBP, indicating that T allele carriers of this SNP may benefit for CVD individuals, as it have a decreased risk of developing the CVD pathologic state through a lower value of SBP. As shown by Safranow K, T allele carriers tended to have lower SBP than wild type in patients with CAD and HF, especially in ischemic HF patients, what might account for the lower fasting serum glucose or the higher creatinine clearance due to the T allele in patients with HF . Moreover, fasting serum glucose has been conformed to be positively correlated with SBP in a previous research . Therefore, the relatively increased LVEF and reduced LVEDD (or LV volumes) in CVD patients indirectly indicated that the T mutant allele of AMPD1 variant performed a protective effect on cardiac function recovery.
In addition, the present meta-analysis further explored the possibility of a relative survival and cardiovascular incidence benefit for the AMPD1 genetic mutation in HF patients, but failed to find any significant differences between different genotypes (CT + TT and CC) of this polymorphism and total survival rate and cardiac survival rate. It may therefore be possible that adenosine concentration in plasma (or muscle) of different genotypes showed no differences although T allele could induce the synthesis of myocardial adenosine [32, 33]. Moreover, the adenosine concentration in patients with T allele was only markedly increased after exercise as suggested previously, hence, the protective role of T allele might exert protective functions through increasing the local secretion of adenosine due to the short half-life of adenosine [34, 35]. Our result was broadly consistent with Kolek MJ group, who reported the AMPD1 genotype had no statistically influences on the survival of HF . Similarly, no influence of the functional AMPD1 C34T polymorphism has been demonstrated by De Groote P et al. on the major clinical parameters and cardiac survival in consecutive white patients with stable CHF linked to left ventricular systolic dysfunction .
There are several limitations of the current meta-analysis need to be pointed out. First, as we know, heart failure can be caused by atherosclerotic and non-atherosclerotic factors, but we couldn’t conduct a subgroup analysis due to the fact that the included studies didn’t analyze the effects of AMPD1 gene C34T polymorphism on cardiac index, blood pressure and prognosis in patients with HF based on the etiology.. Second, heterogeneity in our study may influence the reliability of our results, although subgroup analysis was conducted to detect the heterogeneity source, as well as sensitivity analysis was introduced to appraise the stability of the results. Third, the data extracted from each record were based on unadjusted estimates, which may lead to misleading results. Fourth, we did not obtain all desired information from all materials because of the small number of studies. Fifth, the relatively small sample size of our study might have negative impact on the power of our meta-analysis. Lastly, the limited English and Chinese studies might also lead to language bias despite no evidence of publication bias from our statistical tests.
In conclusion, our meta-analysis suggested that T allele of AMPD1 gene C34T polymorphism was correlated with LVEF (%), LVEDD (mm) and SBP (mmHg) of CVD, which plays a protective role in the recovery of ventricular remodeling and cardiac function, as well as blood pressure, but has no influences on the total survival rate and cardiac survival rate of HF patients. Further well-designed researches with large sample size and complete clinical data are needed to test and verify our findings.
adenosine monophosphate deaminase 1
coronary artery diseases
congestive heart failure
diastolic blood pressure
left ventricular end diastolic dimension
left ventricular ejection fraction
systolic blood pressure
Biglu MH, Ghavami M, Biglu S. Cardiovascular diseases in the mirror of science. J Cardiovasc Thorac Res. 2016;8(4):158–63.
Cooney M, Cooney MT, Maher V, Khan B, Leong T, Graham I. Improvement in the estimation of cardiovascular risk by carotid intima-medial thickness: a report from the Dublin Cardiohealth station study. Prev Med Rep. 2015;2:725–9.
Ding S, Huang H, Xu Y, Zhu H, Zhong C. MiR-222 in cardiovascular diseases: physiology and pathology. Biomed Res Int. 2017;2017:4962426.
Xu S, Jiayong Z, Li B, Zhu H, Chang H, Shi W, et al. Prevalence and clustering of cardiovascular disease risk factors among Tibetan adults in China: a population-based study. PLoS One. 2015;10(6):e0129966.
Perretta-Tejedor N, Fernandez-Mateos J, Garcia-Ortiz L, Gomez-Marcos MA, Recio-Rodriguez JI, Agudo-Conde C, et al. Association of VAV2 and VAV3 polymorphisms with cardiovascular risk factors. Sci Rep. 2017;7:41875.
Zaw KK, Nwe N, Hlaing SS. Prevalence of cardiovascular morbidities in Myanmar. BMC Res Notes. 2017;10(1):99.
Sharma S, Garg I, Ashraf MZ. TLR signalling and association of TLR polymorphism with cardiovascular diseases. Vasc Pharmacol. 2016;87:30–7.
Xuan Y, Wang L, Zhi H, Li X, Wei P. Association between 3 IL-10 Gene polymorphisms and cardiovascular disease risk: systematic review with meta-analysis and trial sequential analysis. Medicine. 2016;95(6):e2846.
Wang L, Mo X, Xu Y, Zuo B, Lei M, Li F, Jiang S, Deng C, Xiong Y: Molecular characterization and expression patterns of AMP deaminase1 (AMPD1) in porcine skeletal muscle. Comp Biochem Physiol B, Biochem Mol Biol 2008, 151(2):159-166.
Tousoulis D, Kioufis S, Siasos G, Oikonomou E, Zaromitidou M, Maniatis K, et al. The impact of AMPD1 gene polymorphism on vascular function and inflammation in patients with coronary artery disease. Int J Cardiol. 2014;172(3):e516–8.
Sabina RL, Morisaki T, Clarke P, Eddy R, Shows TB, Morton CC, et al. Characterization of the human and rat myoadenylate deaminase genes. J Biol Chem. 1990;265(16):9423–33.
Fischer S, Drenckhahn C, Wolf C, Eschrich K, Kellermann S, Froster UG, et al. Clinical significance and neuropathology of primary MADD in C34-T and G468-T mutations of the AMPD1 gene. Clin Neuropathol. 2005;24(2):77–85.
Loh E, Rebbeck TR, Mahoney PD, DeNofrio D, Swain JL, Holmes EW. Common variant in AMPD1 gene predicts improved clinical outcome in patients with heart failure. Circulation. 1999;99(11):1422–5.
Collins RP, Palmer BR, Pilbrow AP, Frampton CM, Troughton RW, Yandle TG, et al. Evaluation of AMPD1 C34T genotype as a predictor of mortality in heart failure and post-myocardial infarction patients. Am Heart J. 2006;152(2):312–20.
de Groote P, Lamblin N, Helbecque N, Mouquet F, Hermant X, Amouyel P, et al. The impact of the AMPD1 gene polymorphism on exercise capacity, other prognostic parameters, and survival in patients with stable congestive heart failure: a study in 686 consecutive patients. Am Heart J. 2006;152(4):736–41.
Parmar MK, Torri V, Stewart L. Extracting summary statistics to perform meta-analyses of the published literature for survival endpoints. Stat Med. 1998;17(24):2815–34.
Chen H, Manning AK, Dupuis J. A method of moments estimator for random effect multivariate meta-analysis. Biometrics. 2012;68(4):1278–84.
Jackson D, White IR, Riley RD. Quantifying the impact of between-study heterogeneity in multivariate meta-analyses. Stat Med. 2012;31(29):3805–20.
Zintzaras E, Ioannidis JP. Heterogeneity testing in meta-analysis of genome searches. Genet Epidemiol. 2005;28(2):123–37.
Egger M, Davey Smith G, Schneider M, Minder C. Bias in meta-analysis detected by a simple, graphical test. BMJ. 1997;315(7109):629–34.
Safranow K, Czyzycka E, Binczak-Kuleta A, Rzeuski R, Skowronek J, Wojtarowicz A, et al. Association of C34T AMPD1 gene polymorphism with features of metabolic syndrome in patients with coronary artery disease or heart failure. Scand J Clin Lab Invest. 2009;69(1):102–12.
Agewall S, Norman B. Association between AMPD1 gene polymorphism and coagulation factors in patients with coronary heart disease. Pathophysiol Haemost Thromb. 2006;35(6):440–4.
Kolek MJ, Carlquist JF, Thaneemit-Chen S, Lazzeroni LC, Whiting BM, Horne BD, et al. The role of a common adenosine monophosphate deaminase (AMPD)-1 polymorphism in outcomes of ischemic and nonischemic heart failure. J Card Fail. 2005;11(9):677–83.
Gastmann A, Sigusch HH, Henke A, Reinhardt D, Surber R, Gastmann O, et al. Role of adenosine monophosphate deaminase-1 gene polymorphism in patients with congestive heart failure (influence on tumor necrosis factor-alpha level and outcome). Am J Cardiol. 2004;93(10):1260–4.
Hoke U, Thijssen J, van Bommel RJ, van Erven L, van der Velde ET, Holman ER, et al. Influence of diabetes on left ventricular systolic and diastolic function and on long-term outcome after cardiac resynchronization therapy. Diabetes Care. 2013;36(4):985–91.
Bak SH, Ko SM, Jeon HJ, Yang HS, Hwang HK, Song MG. Assessment of global left ventricular function with dual-source computed tomography in patients with valvular heart disease. Acta Radiol. 2012;53(3):270–7.
Breathett K, Allen LA, Udelson J, Davis G, Bristow M. Changes in Left Ventricular Ejection Fraction Predict Survival and Hospitalization in Heart Failure With Reduced Ejection Fraction. Circulation Heart failure. 2016;9(10):e002962.
Olsson DP, Eck Arvstrand C, Sartipy U, Holzmann MJ. Acute kidney injury after valvular heart surgery and early changes in cardiac function and structure. Cardiorenal Med. 2014;4(3–4):201–9.
Yeh JK, Hsiao YC, Jian CR, Wang CH, Wen MS, Kuo CT, et al. Comparison of baseline versus Posttreatment left ventricular ejection fraction in patients with acute Decompensated heart failure for predicting cardiovascular outcome: implications from single-center systolic heart failure cohort. PLoS One. 2016;11(1):e0145514.
Wakeno M, Minamino T, Seguchi O, Okazaki H, Tsukamoto O, Okada K, et al. Long-term stimulation of adenosine A2b receptors begun after myocardial infarction prevents cardiac remodeling in rats. Circulation. 2006;114(18):1923–32.
Qian Y, Lin Y, Zhang T, Bai J, Chen F, Zhang Y, et al. The characteristics of impaired fasting glucose associated with obesity and dyslipidaemia in a Chinese population. BMC Public Health. 2010;10:139.
Tarnopolsky MA, Parise G, Gibala MJ, Graham TE, Rush JW. Myoadenylate deaminase deficiency does not affect muscle anaplerosis during exhaustive exercise in humans. J Physiol. 2001;533(Pt 3):881–9.
Andreassi MG, Botto N, Laghi-Pasini F, Manfredi S, Ghelarducci B, Farneti A, et al. AMPD1 (C34T) polymorphism and clinical outcomes in patients undergoing myocardial revascularization. Int J Cardiol. 2005;101(2):191–5.
Kalsi KK, Yuen AH, Rybakowska IM, Johnson PH, Slominska E, Birks EJ, Kaletha K, Yacoub MH, Smolenski RT: Decreased cardiac activity of AMP deaminase in subjects with the AMPD1 mutation--a potential mechanism of protection in heart failure. Cardiovasc Res 2003, 59(3):678-684.
Norman B, Sabina RL, Jansson E. Regulation of skeletal muscle ATP catabolism by AMPD1 genotype during sprint exercise in asymptomatic subjects. J Appl Physiol. 2001;91(1):258–64.
We thank all subjects who participated in this study. We acknowledge the helpful comments on this paper received from our reviewers.
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Feng, A., Liu, Z., Zhou, S. et al. Effects of AMPD1 gene C34T polymorphism on cardiac index, blood pressure and prognosis in patients with cardiovascular diseases: a meta-analysis. BMC Cardiovasc Disord 17, 174 (2017) doi:10.1186/s12872-017-0608-0
- Cardiovascular diseases
- Cardiac indexes
- Blood pressure