Yang Rongsong, Yang Yinan, Dong Xiangyu, Wu Xiangyang, Wei Yalin
Department of Pediatric Cardiology, Lanzhou University Second Hospital, Lanzhou 730030, China.
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Zhonghua Er Ke Za Zhi. 2014 Aug;52(8):625-9.
To determine the relationship between the serum sulfur dioxide, homocysteine and the pulmonary arterial pressure in children with congenital heart defects who generated a pulmonary arterial hypertension syndrome (PAH-CHD), and analyze their role in the pathological process of the disease.
This was a prospective cohort study, children with systemic pulmonary shunt CHD were selected. The patients were divided into three groups: the CHD with no PAH group:n = 20, 10 males, 10 females, 5 with ventricular septal defect (VSD), 8 with atrial septal defect (ASD) and 7 with patent ductus arteriosus (PDA), mean age (1.9 ± 1.8) years; the CHD with mild PAH group:n = 20, 10 males, 10 females, 12 with VSD, 6 with ASD, and 2 with PDA, mean age (1.0 ± 0.8) year; the CHD with moderate or severe PAH group:n = 20, 8 males, 12 females, 12 with VSD, 6 with ASD, and 1 with PDA, 1 with ASD+VSD, mean age (1.8 ± 1.6) year. Twenty healthy children were enrolled from outpatient department as the control group [included 8 males, 12 females, mean age (1.9 ± 1.5) years]. The homocysteine and SO2 concentrations in the serum samples were detected by a modified high performance liquid chromatographic method with fluorescence detection (HPLC-FD), then, multiple comparisons among the groups were performed with analysis of variance, and the pearson correlation.
The serum homocysteine concentrations were respectively (11.0 ± 2.7) , (11.7 ± 2.5), (12.0 ± 2.1), (14.3 ± 3.2) µmol/L in the control group, CHD with no PAH group, CHD with mild PAH group, and CHD with moderate or severe PAH group. According to the multiple comparisons, the CHD with moderate or severe PAH group had the highest level (P all < 0.05) .While the comparison within the control group, CHD with none PAH group, and CHD with mild PAH group, the differences were not significant (P all > 0.05). The serum sulfur dioxide strength (concentrated as SO3(2-)) were respectively (10.6 ± 2.4), (8.9 ± 2.3), (7.3 ± 2.9), (4.3 ± 2.1) µmol/L in the control group, CHD with none PAH group, CHD with mild PAH group, and CHD with moderate or severe PAH group. CHD with moderate or severe PAH group had the highest level of serum sulfur dioxide (P < 0.05) . The pearson correlation analysis indicated that in the CHD children, the serum homocysteine were positively correlated with the pulmonary arterial pressure (r = 0.481, P < 0.01), while, the sulfur dioxide were negatively correlated with pulmonary arterial pressure (r = -0.553, P < 0.01).In all children, the serum homocysteine levels were negatively correlated with the sulfur dioxide (r = -0.231, P = 0.039).
The PAH-CHD children had higher homocysteine levels and lower sulfur dioxide levelsl, which demonstrated the disturbance of homocysteine-sulfur dioxide pathway in the sulfur containing amino acids metabolish in the disease. The homocysteine may become a biological marker which reflecting the severities of the PAH-CHD, while the sulfur dioxide can be a new target for the therapy of PAH-CHD.
探讨先天性心脏病合并肺动脉高压综合征(PAH-CHD)患儿血清二氧化硫、同型半胱氨酸与肺动脉压的关系,并分析其在疾病病理过程中的作用。
本研究为前瞻性队列研究,选取体肺分流型先天性心脏病患儿。将患者分为三组:无PAH的CHD组:n = 20,男10例,女10例,室间隔缺损(VSD)5例,房间隔缺损(ASD)8例,动脉导管未闭(PDA)7例,平均年龄(1.9±1.8)岁;轻度PAH的CHD组:n = 20,男10例,女10例,VSD 12例,ASD 6例,PDA 2例,平均年龄(1.0±0.8)岁;中度或重度PAH的CHD组:n = 20,男8例,女12例,VSD 12例,ASD 6例,PDA 1例,ASD + VSD 1例,平均年龄(1.8±1.6)岁。选取门诊20例健康儿童作为对照组[男8例,女12例,平均年龄(1.9±1.5)岁]。采用改良高效液相色谱荧光检测法(HPLC-FD)检测血清样本中的同型半胱氨酸和SO2浓度,然后进行方差分析和Pearson相关性分析进行组间多重比较。
对照组、无PAH的CHD组、轻度PAH的CHD组和中度或重度PAH的CHD组血清同型半胱氨酸浓度分别为(11.0±2.7)、(11.7±2.5)、(12.0±2.1)、(14.3±3.2)μmol/L。经多重比较,中度或重度PAH的CHD组水平最高(P均<0.05)。而对照组、无PAH的CHD组和轻度PAH的CHD组组内比较,差异无统计学意义(P均>0.05)。对照组、无PAH的CHD组、轻度PAH的CHD组和中度或重度PAH的CHD组血清二氧化硫强度(以SO3(2-)计)分别为(10.6±2.4)、(8.9±2.3)、(7.3±2.9)、(4.3±2.1)μmol/L。中度或重度PAH的CHD组血清二氧化硫水平最高(P<0.05)。Pearson相关性分析表明,在CHD患儿中,血清同型半胱氨酸与肺动脉压呈正相关(r = 0.481,P<0.01),而二氧化硫与肺动脉压呈负相关(r = -0.553,P<0.01)。在所有儿童中,血清同型半胱氨酸水平与二氧化硫呈负相关(r = -0.231,P = 0.039)。
PAH-CHD患儿同型半胱氨酸水平较高,二氧化硫水平较低,提示该病含硫氨基酸代谢中的同型半胱氨酸-二氧化硫途径存在紊乱。同型半胱氨酸可能成为反映PAH-CHD严重程度的生物学标志物,而二氧化硫可成为PAH-CHD治疗的新靶点。