Serum high concentrations of homocysteine and low levels of folic acid and vitamin B 12 are significantly correlated with the categories of coronary artery diseases
Ma et al. BMC Cardiovascular Disorders (2017) 17:37
DOI 10.1186/s12872-017-0475-8
RESEARCH ARTICLE
Open Access
Serum high concentrations of homocysteine
and low levels of folic acid and vitamin B12
are significantly correlated with the
categories of coronary artery diseases
Yan Ma1, Duanliang Peng1, Chenggui Liu2*, Chen Huang2 and Jun Luo1
Abstract
Background: Homocysteine (Hcy) has been considered as an independent risk factor for coronary artery disease
(CAD). Folic acid and vitamin B12 are two vital regulators in Hcy metabolic process. We evaluated the correlations
between serum Hcy, folic acid and vitamin B12 with the categories of CAD.
Methods: Serum Hcy, folic acid and vitamin B12 from 292 CAD patients, including 73 acute myocardial infarction
(AMI), 116 unstable angina pectoris (UAP), 103 stable angina pectoris (SAP), and 100 controls with chest pain
patients were measured, and the data were analyzed by SPSS software.
Results: Compared to SAP patients, patients with AMI and UAP had higher Hcy levels with approximately average
elevated (4-5) μmol/L, while SAP patients were approximately higher 8 μmol/L than controls. However, the levels of
folic acid and vitamin B12 had opposite results, which in AMI group was the lowest, while in controls was the
highest. CAD categories were positively correlated with Hcy (r = 0.286, p < 0.001), and negatively correlated with folic
acid (r = -0.297, p < 0.001) and vitamin B12 (r = -0.208, p < 0.001). There were significant trend toward increase in the
prevalence of high Hcy, low folic acid and vitamin B12 from controls, to SAP, to UAP, and to AMI.
Conclusions: The present study provide the valuable evidence that high concentrations of Hcy and low levels of folic
acid and vitamin B12 are significantly correlated with CAD categories.
Keywords: Homocysteine, Folic acid, Vitamin B12, Coronary artery disease, Atherosclerosis, Endothelial dysfunction
Background
Coronary artery disease (CAD) is seriously to harm people’s healthy disease in borth developed and developing
countries, which was predominantly caused by atherosclerosis with endothelial dysfunction [1, 2]. Despite best
efforts, available therapies protect only 30–40% of individuals at risk, and no therapeutic cure is anticipated for
those who currently suffer from the disease [3]. The
endothelium is a single layer of cells lining all blood vessels. It plays an important role in many physiological
functions, including the control of blood cell trafficking,
* Correspondence:
2
Department of Clinical Laboratory, Chengdu Women’s and Children’s
Central Hospital, Chongqing Medical University, No. 1617 Ri Yue Avenue,
Qingyang District, Chengdu 610091, China
Full list of author information is available at the end of the article
vasomotor tone, vessel permeability, and hemostatic balance. Endothelial cells produce a wide variety of substances in response to various physical and chemical
stimuli, including vasodilator substances, and vasoconstrictor substances [4].
Researches have confirmed that endothelial dysfunction, as an impairment of endothelium-dependent relaxation of blood vessels, occur as the initial event in
the pathogenesis of atherosclerosis, which considered
to be the initiating factor and the key point of cardiovascular disease [5, 6]. Moreover, endothelial dysfunction also play the important role in all stages and
categories of CAD from stable angina pectoris (SAP)
to unstable angina pectoris (UAP), and to acute myocardial infarction (AMI) [7]. Early warning and immediate risk stratification of patients with different
© The Author(s). 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0
International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and
reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to
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(http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
Ma et al. BMC Cardiovascular Disorders (2017) 17:37
categories of CAD is frequently a challenging task in
the current.
A large number of studies have confirmed that serum
high homocysteine (Hcy) concentration (morm than
15 μmol/L), which is called hyperhomocysteinemia
(HHcy), has been associated with endothelial dysfunction of atherosclerotic CAD owing to oxidative stress
[8], endoplasmic reticulum stress [9], involved inflammation [10], increased level of asymmetric dimethylarginine
(ADMA) [11] and so on [12–14]. Elevated ADMA can
results in decreasing endothelium-derived nitric oxide
concentration and bioavailability [15]. Nitric oxide as a
most important mediator of endothelium-dependent relaxation, is a potent vasodilator, which plays a key role
in normal vascular physiology in preserving the vessel
wall in a quiescent state by inhibition of inflammation,
thrombosis, and cellular proliferation [16]. Decreased nitric oxide bioavailability would result in the abnormal
thrombosis, vasorelaxation, and atherosclerosis, thereby
promoting the occurrence and development of CAD [17].
Folic acid and vitamin B12 play an important role in
regulating the metabolic process of Hcy [18]. Current
studies have shown that supplement folic acid, vitamin
B12 in patients with HHcy could reduce Hcy levels [19].
Folic acid supplementation not only may be useful in reducing Hcy level in high risk patients with HHcy [20],
but also can significantly improve endothelial dysfunction in patients with CAD [21]. On the other hand, folic
acid deficiency or/and vitamin B12 deficiency would result in HHcy [22–24]. Vitamin B12 deficiency and HHcy
are related to cardiovascular risk factors in patients with
CAD [25]. However, the correlations of CAD categories
with Hcy, folic acid, vitamin B12 have not been reported.
Therefore, we evaluate the correlations between CAD
categories and each of the metabolic parameters, anthropometric variables, life style habits and traditional
cardiovascular risk factors in CAD patients and controls
with chest pain patients.
Methods
This study included 292 CAD patients (203 male and 89
female) aged 36–85 (62.54 ± 14.52) years, and 100 controls
with chest pain symptom (69 male and 31 female) aged
38–87 (60.93 ± 15.65) years, from the Sichuan Academy of
Medical Sciences & Sichuan Provincial People’s Hospital.
There were no statistically significant difference in age
(means ± SD, t = 0.94, p = 0.348) and gender (male to
female ratio, χ2 = 0.01, p = 0.922) between CAD group
and controlled group.
All enrolled CAD patients had been confirmed by coronary angiography and were diagnosed to be103 SAP,
116 UAP, 73 AMI according to 2007 ACC/AHA guidelines. 100 controls with chest pain patients in the same
period were confirmed by coronary angiography too.
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