CJCP
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2017 Vol.  19 No.  7
Published: 2017-07-25

CLINICAL RESEARCH
CASE ANALYSIS
EXPERIMENTAL RESEARCH
REVIEW
CLINICAL RESEARCH
729 OU-YANG Li-Xue, YANG Fan
Diagnostic value of baseline serum luteinizing hormone level for central precocious puberty in girls

Objective To evaluate the diagnostic value of baseline serum luteinizing hormone (LH) level for central precocious puberty (CPP) in girls. Methods A total of 279 girls with precocious puberty were subjected to assessment of growth and development, bone age determination, baseline LH test, and follicle-stimulating hormone (FSH) test, gonadotropin-releasing hormone stimulation test, and other related examinations. Of the 279 patients, 175 were diagnosed with CPP and 104 with premature thelarche (PT). The receiver operating characteristic (ROC) curve was used to evaluate the diagnostic value of baseline LH and FSH levels and their peak levels for CPP, and the correlation between the baseline LH level and the peak LH level was analyzed. Results The CPP group had signifcantly higher bone age, baseline LH and FSH levels, peak LH and FSH levels, and ratio of peak LH level to peak FSH level than the PT group (P < 0.01). The ROC curve proved that baseline LH level and peak LH level had good diagnostic values for CPP. Among the three bone age subgroups in the CPP group (7.0-9.0 years, 9.0-11.0 years, and > 11.0 years), baseline LH level showed the best diagnostic value in the > 11.0 years subgroup, with the largest area under the ROC curve. At a baseline LH level of 0.45 IU/L, the Youden index reached the peak value, and the sensitivity and specifcity were 66.7% and 80% respectively, for the diagnosis of CPP. At a peak LH level of 9.935 IU/L, the Youden index reached the peak value, and the sensitivity and specifcity were 74.8% and 100% respectively, for the diagnosis of CPP. The baseline LH level was positively correlated with the peak LH level (r=0.440, P < 0.01). Conclusions Baseline LH level can be used as an primary screening index for the diagnosis of CPP. It has a certain diagnostic value for CPP at different bone ages, and may be used as a monitoring index during the treatment and follow-up.

2017 Vol. 19 (7): 729-733 [Abstract] ( 3235 ) [HTML 1KB] [PDF 1318KB] ( 951 )
734 CHENG Ying, GUO Li, DENG Mei, SONG Yuan-Zong
Clinical feature and genetic analysis of a family affected by congenital bile acid synthesis defect type 2: identifcation of 2 novel mutations in AKR1D1 gene Hot!
Congenital bile acid synthesis defect type 2 (CBAS2) is an autosomal recessive disorder caused by biallelic mutations of AKR1D1 gene, which encodes the Δ4-3-oxo-steroid 5β-reductase. Cholestatic jaundice is the main clinical manifestation, accompanied by malabsorption of fat and fat-soluble vitamins. This paper reported the clinical and genetic features of a CBAS2 patient definitely diagnosed by AKR1D1 genetic analysis. An 8-monthold male infant was referred to the hospital with the complaint of jaundiced skin and sclera over 7 months. On physical examination, growth retardation and malnutrition were discovered besides mild jaundice of the skin and sclera. The liver was palpable 8 cm below the right subcostal margin with medium texture, and the spleen was not enlarged. On liver function test, elevated levels of bilirubin (predominantly conjugated bilirubin) and transaminases were detected, but serum total bile acids and γ-glutamyl transpeptidase levels were within the normal ranges. Liver histopathologic analysis showed disorganized bile ducts, obvious multinucleated giant cells, significant cholestasis in hepatocytes, together with portal and interstitial fibrosis and lymphocytic infiltration. Via next generation sequencing analysis and Sanger sequencing confirmation, the infant proved to be a compound heterozygote of the AKR1D1 variants c.579+2delT and c.853C > T(p.Q285X), two novel mutations originated from his mother and father, respectively. CBAS2 was thus definitely diagnosed, and chenodeoxycholic acid was given orally. As a result, the abnormal liver function and hepatomegaly were improved gradually. On a follow-up 3 months later, a soft liver was palpable 2.5 cm below the right subcostal margin, and all liver function indices recovered to normal ranges.
2017 Vol. 19 (7): 734-740 [Abstract] ( 2994 ) [HTML 1KB] [PDF 2956KB] ( 685 )
741 YANG Jing-Hui, ZHANG Jing-Hui, ZHANG Yin-Hong, XU Xiao-Zhi, CHEN Hong, LI Yuan, JIANG Yan, WANG Zheng, ZHU Bao-Sheng, LI Li
Analysis of treatment efficacy for congenital hypothyroidism in some regions of Yunnan Province, China
Objective To observe the effects of initial doses and treatment timing of levothyroxine (L-T4) on the clinical effcacy in children with congenital hypothyroidism (CH). Methods This study included 98 children who had an abnormal level of thyroid stimulating hormone (TSH) in neonatal screening in four regions of Yunnan Province and who fnally had a confrmed diagnosis of CH. They received treatment with L-T4 and were divided into standard dose group (10-15 μg/kg per day) and low dose group ( < 10 μg/kg per day) by the therapeutic dose of L-T4. Meanwhile, these patients were also classifed into two treatment groups based on the starting time of L-T4 treatment, namely under 2 months old group and more than 2 months old group. The thyroid function and physical and neural development were examined before and after treatment. Results Compared with the low dose group, the standard dose group had a signifcantly lower TSH level and a signifcantly higher free thyroxine (FT4) level at 2 weeks after treatment (P < 0.05). There were no signifcant differences in TSH and FT4 levels at other time points after treatment between the standard and low dose groups (P > 0.05). The physical and neural development were not signifcantly different between the two dose groups before and at all time points after treatment (P > 0.05). At all time points after treatment, the levels of TSH and FT4 and physical development were not signifcantly different between the different starting time groups (P > 0.05). However, the Gesell score was signifcantly higher in the under 2 months old group than in the more than 2 months old group at all time points after treatment (P < 0.05). Conclusions The standard dose group has a better treatment outcome than the low dose group, whereas the symptoms of hyperthyroidism deserve close attention. The treatment timing is vital to the neurodevelopment of children with CH. Once diagnosed, the patients should receive treatments immediately.
2017 Vol. 19 (7): 741-747 [Abstract] ( 3082 ) [HTML 1KB] [PDF 1029KB] ( 674 )
748 ZHANG Lei, AN Mei-Yu, ZHU Bing, SHEN Wan-Dong, TAN Shu-Jiang, JI Xiao-Juan, TIAN Jie, LIU Xiao-Yan
Screening and follow-up for congenital heart disease in children aged 0-3 years in rural areas of Chongqing, China
Objective To examine the incidence of congenital heart disease (CHD) in children aged 0-3 years in the rural areas of Chongqing, and to determine the suitable "screening-diagnosis-follow-up" system and screening indicators for CHD in these areas. Methods Children aged 0-3 years from rural areas of the Fuling Disctrict of Chongqing were selected by cluster sampling. Using the "screening-diagnosis-evaluation system" employed at the levels of village/town, district/county, and province/city, the children were screened for seven indicators, i.e., family history of CHD, dyspnea, cyanosis, unique facial features, other congenital malformations, heart murmurs, and blood oxygen saturation (SpO2 < 95%). Children who were positive for one or more indicators accepted echocardiography (ECG) for the diagnosis of CHD. CHD patients were evaluated for disease progression, given guided treatments, and followedup by pediatric cardiologists. Results Screening was performed for 10005 out of the 10 281 children enrolled in the study (97.32% response rate). Among the 175 children who were positive for the indicators, 166 underwent ECG and 60 (0.6‰) were diagnosed with CHD, including 46 cases of simple CHD (76.65%), 11 cases of combined CHD (18.33%), and 3 cases of complex CHD (5.00%). Of the 7 screening indicators, heart murmur had the largest area under the ROC curve for the diagnosis of CHD. In addition, a combination of screening indicators (heart murmur, unique facial features, and other congenital malformations) was most effective for screening out CHD. The CHD patients were given surgical or intervention treatments, and followed up for 6 to 18 months. Ten patients improved without treatment, 13 patients received interventional or surgical treatment, 1 patient died of non-cardiac reasons. The remaining 36 patients were subjected to further follow-up. Conclusions Heart murmur alone and in combination with unique facial features and other congenital malformations are valuable tools for CHD screening in children aged 0-3 years. The "village/towndistrict/county-province/city" screening-diagnosis-evaluation systems are useful for the early detection, diagnosis, and treatment of CHD in infants and young children from the rural areas of Chongqing.
2017 Vol. 19 (7): 748-753 [Abstract] ( 3590 ) [HTML 1KB] [PDF 1000KB] ( 626 )
754 LIU Yi, ZHU Bei, ZHUO Lin, HE Ming-Yu, XU Yang, WANG Tong-Tong, CAI Qing-Qing, HU Bin, XU Ji-Cheng, ZHANG Wen-Hui
Risk factors for congenital heart disease in Chinese neonates: a Meta analysis
Objective To investigate the major risk factors for congenital heart disease (CHD) in Chinese neonates and to provide a reference for the prevention of CHD. Methods A literature search was performed to collect the case-control studies on the risk factors for CHD in Chinese neonates published in 2001-2016. The relevant data were extracted accordingly. The quality of included studies was assessed by Newcastle-Ottawa Scale. Sensitivity analysis was conducted using different models to analyze the same data. The publication bias was assessed by Egger's test. Results A total of 17 case-control studies involving 2 930 cases and 4 952 controls were included. The Meta analysis showed that the major risk factors for CHD in Chinese neonates were as follows:mother with advanced age (OR=2.649, 95%CI:1.675-4.189), cold or fever (OR=4.558, 95%CI:2.901-7.162), medication use in early pregnancy (OR=3.961, 95%CI:2.816-5.573), passive smoking (OR=2.766, 95%CI:1.982-3.859), abnormal childbearing history (OR=2.992, 95%CI:1.529-5.856), noise exposure (OR=3.030, 95%CI:1.476-6.217), radiation exposure (OR=2.363, 95%CI:1.212-4.607), decoration (OR=4.979, 95%CI:3.240-7.653), gestational diabetes (OR=5.090, 95%CI:3.132-8.274), and pet raising (OR=2.048, 95%CI:1.385-3.029). Conclusions Mothers with advanced age, cold or fever, medication use in early pregnancy, passive smoking, abnormal childbearing history, noise exposure, radiation exposure, decoration, gestational diabetes, and pet raising may increase the risk of CHD in Chinese neonates.
2017 Vol. 19 (7): 754-758 [Abstract] ( 4169 ) [HTML 1KB] [PDF 993KB] ( 1255 )
759 LIU Jin, YAN Hong, CHEN Xiao-Geng, MU Ya-Ping
Effects of Huaiqihuang granules on immune function in children with severe Mycoplasma pneumoniae pneumonia

Objective To observe the effects of Huaiqihuang granules on the immune function in children with severe Mycoplasma pneumoniae pneumonia. Methods Pediatric inpatients with severe Mycoplasma pneumoniae pneumonia were randomly divided into Huaiqihuang granule treatment group (n=51) and conventional treatment group (n=47). The Huaiqihuang granule treatment group was orally administered Huaiqihuang granules in addition to the conventional treatment, while the conventional treatment group received conventional treatment only. Levels of serum IgA, IgG, and IgM, percentages of CD4+ and CD8+ T lymphocyte subsets, and CD4+/CD8+ ratio were examined in the two groups. The incidence rate of respiratory tract re-infection within three months following treatment was compared between the two groups. Results The levels of serum IgA, IgG, and IgM, the percentage of CD4+ T lymphocytes, and the CD4+/CD8+ ratio were significantly higher in the Huaiqihuang granule treatment group than in the conventional treatment group three months after treatment (P  < 0.05). In contrast, the percentage of CD8+ T lymphocytes was signifcantly lower in the Huaiqihuang granule treatment group than in the conventional treatment group (P  < 0.05). In addition, the incidence rate of respiratory tract re-infection within three months following treatment was signifcantly lower in the Huaiqihuang granule treatment group than in the conventional treatment group (P  < 0.05). Conclusions Huaiqihuang granules can regulate immune functions and reduce the incidence of short-term respiratory tract re-infection in children with severe Mycoplasma pneumoniae pneumonia.

2017 Vol. 19 (7): 759-762 [Abstract] ( 3615 ) [HTML 1KB] [PDF 982KB] ( 738 )
763 LIN Shu-Xiang, WANG Wei, GUO Wei, YANG Hong-Jiang, MA Bai-Cheng, FANG Yu-Lian, XU Yong-Sheng
A molecular epidemiological study of KI polyomavirus and WU polyomavirus in children with acute respiratory infection in Tianjin, China

Objective To investigate the relationship of KI polyomavirus (KIPyV) and WU polyomavirus (WUPyV) with acute respiratory infection in children in Tianjin, China. Methods A total of 3 730 nasopharyngeal secretions were collected from hospitalized children with acute respiratory infection in Tianjin Children's Hospital from January 2011 to December 2013. Viral nucleic acid was extracted, and virus infection (KIPyV and WUPyV) was determined by PCR. Some KIPyV-positive and WUPyV-positive PCR products were subjected to sequencing. Sequencing results were aligned with the known gene sequences of KIPyV and WUPyV to construct a phylogenetic tree. Amplifed VP1 fragments of KIPyV were inserted into the cloning vector (PUCm-T) transformed into E. coli competent cells. Positive clones were identifed by PCR and sequencing. The nucleotide sequences were submitted to GenBank. In addition, another seven common respiratory viruses in all samples were detected by direct immunofluorescence assay. Results In the 3 730 specimens, the KIPyV-positive rate was 12.14% (453/3 730) and the WUPyV-positive rate was 1.69% (63/3730). The mean infection rate of KIPyV was signifcantly higher in June and July, while the mean infection rate of WUPyV peaked in February and March. Most of the KIPyV-positive or WUPyV-positive children were < 3 years. The co-infections with KIPyV, WUPyV, and other respiratory viruses were observed in the children. The coinfection rate was 2.31% (86/3 730) and there were nine cases of co-infections with WUPyV and KIPyV. Thirty-fve KIPyV-positive and twelve WUPyV-positive PCR products were sequenced and the alignment analysis showed that they had high homology with the known sequences (94%-100% vs 95%-100%). The VP1 gene sequences obtained from two KIPyV strains in this study were recorded in GenBank with the accession numbers of KY465925 and KY465926. Conclusions For some children with acute respiratory infection in Tianjin, China, the acute respiratory infection may be associated with KIPyV and WUPyV infections. KIPyV infection is common in summer, and WUPyV infection in spring. The epidemic strains in Tianjin have a high homology with those in other regions.

2017 Vol. 19 (7): 763-769 [Abstract] ( 3571 ) [HTML 1KB] [PDF 538KB] ( 736 )
770 TANG Rong, AO Xiang, ZHONG Yong, WANG Rui-Ling, ZHOU Qiao-Ling
Values of combination of urinary L-FABP and NGAL in early diagnosis of acute kidney injury after cardiac surgery in children
Objective To investigate the values of combination of urinary liver-type fatty acid-binding protein (L-FABP) and neutrophil gelatinase-associated lipocalin (NGAL) in early diagnosis of acute kidney injury (AKI) after cardiac surgery in children. Methods A total of 97 children with congenital heart disease undergoing cardiopulmonary bypass surgery were enrolled. Serum and urine samples were collected before and after surgery. Levels of serum creatinine (Scr), urinary L-FABP, and urinary NGAL from AKI group (n=18) and non-AKI group (n=79) were measured, and the postoperative dynamic changes in these markers were compared between the two groups. The receiver operating characteristic (ROC) curve and the area under ROC curve (AUC) were used to assess the values of these markers alone or in combination in the prediction of postoperative AKI. Results The levels of urinary L-FABP and NGAL in the AKI group were signifcantly higher than those in the non-AKI group at 2 and 6 hours after surgery, and the changes in their concentrations were earlier than Scr. The AUCs of urinary L-FABP alone in predicting AKI at 2 and 6 hours after surgery were 0.921 and 0.896 respectively, and those of urinary NGAL alone were 0.908 and 0.928 respectively. Those of their combination were 0.942 and 0.929 respectively. Conclusions Urinary L-FABP and NGAL signifcantly increase in the early stage of AKI after cardiac surgery in children, which are signifcantly earlier than the changes in Scr. They can be used to predict the occurrence of AKI in the early stage. A combination of the two biomarkers can further improve the accuracy of diagnosis.
2017 Vol. 19 (7): 770-775 [Abstract] ( 3586 ) [HTML 1KB] [PDF 1081KB] ( 778 )
776 CHEN Yan-Zhao, LIU Zhi-Ping, ZHOU Ke-Ying, LI Bo
Value of serum miR-17-92 cluster in diagnosis of retinoblastoma

Objective To investigate the value of serum miR-17-92 cluster in the diagnosis of retinoblastoma (RB). Methods Serum samples were collected from 20 children with RB and 20 healthy controls. Quantitative real-time PCR was used to measure the expression of miR-17-92 cluster. The expression of miR-17-92 cluster was compared between children with different stages of RB and the changes in the expression of miR-17-92 cluster after multimodality therapy were analyzed. The receiver operating characteristic (ROC) curve was used to investigate the value of serum miR-17-92 cluster in the diagnosis of RB. Results Compared with the healthy controls, the children with RB had signifcantly higher relative expression of miR-17-3P, miR-17-5P, miR-18a, and miR-20a in serum (P < 0.05), and miR-18a showed the greatest increase. There were no signifcant differences in the relative expression of miR-19a, miR-19b-1, and miR-92a-1 between children with RB and healthy controls (P > 0.05). There were no signifcant differences in the expression of miR-17-5P, miR-17-3P, miR-18a, and miR-20a between the children with early-to-moderate stage of RB and those with advanced stage of RB (P >  0.05), but there were signifcant reductions after multimodality therapy (P < 0.05). In the diagnosis of RB, the areas under the ROC curve (AUCs) for serum miR-17-3P, miR-17-5P, miR-18a, and miR-20a were 0.770, 0.755, 0.828, and 0.665 respectively, and miR-18a had the largest AUC, with a sensitivity of 90% and a specifcity of 65%. Conclusions miR-17-3P, miR-17-5P, miR-18a, and miR-20a are highly expressed in the serum of children with RB, and miR-18a may be used as a new marker for the diagnosis of RB.

2017 Vol. 19 (7): 776-780 [Abstract] ( 2831 ) [HTML 1KB] [PDF 1043KB] ( 613 )
781 SUN Qing, XIE Yao, ZHAO Wei-Hong, HUA Ying, WU Peng-Hui, LI Shuo, LU Xin-Tian
Adverse effects of high-dose methotrexate therapy
Objective To investigate the adverse effects of high-dose methotrexate (HDMTX) therapy, and to provide a theoretical basis for optimizing clinical treatment. Methods A retrospective analysis was performed for the clinical data of 120 children with acute lymphoblastic leukemia or non-Hodgkin lymphoma who underwent 601 times of HDMTX therapy. The adverse effects of various systems were analyzed according to the WHO criteria for the classifcation of adverse effects of anticancer drugs. Results Almost all the children experienced bone marrow suppression, and 93.3% had granulocytopenia. The most common adverse effects in the digestive system and urinary system were elevated glutamic-pyruvic transaminase (60.4%) and proteinuria (9.2%) respectively. For skin symptoms, skin erythema had the highest incidence rate (7.2%). The adverse effects in the nervous system (hyperpathia, numbness of extremities, or headache) were only observed in 7 cases. Serious adverse effects were only seen in the blood system and digestive system. Compared with the 3 g/m2 methotrexate (MTX) group, the 5 g/m2 HDMTX group had a signifcantly higher 24-hour plasma MTX concentration, signifcant reductions in hemoglobin and platelet count, and signifcantly higher incidence rates of oral mucositis, proteinuria, and skin symptoms (P < 0.05). Conclusions Serious adverse effects of HDMTX therapy mainly involve the blood system and digestive system, and the adverse effects such as bone marrow suppression, oral mucositis, proteinuria, and skin symptoms occur in a dose-dependent manner.
2017 Vol. 19 (7): 781-785 [Abstract] ( 4052 ) [HTML 1KB] [PDF 992KB] ( 800 )
786 GUO Jing-Min, SHI Xiao-Xi, YANG Shi-Wei, QIAN Qin-Fang, HUANG Yan, XIE Yan-Qin, OU Ping
Efficacy of clonidine transdermal patch in treatment of moderate to severe tic disorders in children

Objective To investigate the difference in the efficacy between clonidine transdermal patch and haloperidol tablets in the treatment of moderate to severe tic disorders in children. Methods A total of 134 children with moderate to severe tic disorders were randomly divided into clonidine group (n=70) and haloperidol group (n=64). The clonidine and haloperidol groups were treated with clonidine transdermal patch and haloperidol tablets respectively, and the treatment lasted for 8 weeks in both groups. The Yale Global Tic Severity Scale (YGTSS) was used to evaluate the conditions of the children before and after treatment, and the adverse events during the treatment were recorded. Results The haloperidol group had a signifcantly better treatment outcome than the clonidine group after one week of treatment (P < 0.05); the treatment outcome showed no signifcant difference between the two groups after 3, 5, and 8 weeks of treatment (P > 0.05). The clonidine group had signifcantly less reductions in the motor tics, vocal tics, and function impairment scores and total score of YGTSS than the haloperidol group after one week of treatment (P < 0.05); there were no signifcant differences in YGTSS score reductions between the two groups after 3, 5, and 8 weeks of treatment (P > 0.05). The clonidine group had a signifcantly lower overall incidence of adverse events than the haloperidol group (8% vs 37%; P < 0.01). Conclusions Clonidine transdermal patch and haloperidol are both effective in the treatment of moderate to severe tic disorders in children. The clonidine transdermal patch, despite slow action, has comparable effcacy and fewer adverse effects compared with haloperidol.

2017 Vol. 19 (7): 786-789 [Abstract] ( 3782 ) [HTML 1KB] [PDF 980KB] ( 916 )
790 TANG Ni, MAO Man-Yun, ZHAI Rui, CHEN Xiang, ZHANG Jiang-Lin, ZHU Wu, LI Jie
Clinical characteristics of urticaria in children versus adults
Objective To study the clinical characteristics of urticaria in children versus adults, and to provide reference for the etiological analysis, disease evaluation, and treatment of urticaria in children. Methods The clinical data of 2411 patients with urticaria who visited the Department of Dermatology at Xiangya Hospital of Central South University from January 2013 to May 2017 were collected to study their socio-demographic characteristics. The clinical characteristics of urticaria were compared between the 68 children and 672 adults of the 740 patients with complete follow-up data. Results Among the 411 pediatric patients, 314 (76.4%) had acute urticaria; among the 2 000 adult patients, 896 (44.8%) had chronic spontaneous urticaria. The causes of acute urticaria in children included infection (41%, 16/39). The accompanying symptoms of acute urticaria in children mainly included abdominal pain and diarrhea (44%, 17/39), while those in adults mainly included chest distress and shortness of breath (32%, 11/34). Compared with the adult patients, the pediatric patients had signifcantly lower chronic urticaria activity scores before and after treatment (P < 0.05), a signifcantly higher rate of response to second-generation antihistamines (82.1% vs 62.2%; P < 0.05), and a signifcantly higher proportion of individuals with a personal and family history of urticaria (P < 0.05). Conclusions Acute urticaria is more commonly seen than chronic urticaria in children with urticaria, and the main accompanying symptoms are abdominal pain and diarrhea, which are different from adults with urticaria. Chronic urticaria has a better treatment outcome in children than in adults. The most frequently seen cause of acute urticaria is infection in children. Atopic children may be susceptible to urticaria.
2017 Vol. 19 (7): 790-795 [Abstract] ( 3626 ) [HTML 1KB] [PDF 998KB] ( 869 )
796 FAN Li, LIU Heng, WANG Yu-Chuan, CHEN Li, ZHOU Jing-Jing, CUI Yu-Xia
Association of serum vitamin D level with severity and treatment in children with Henoch-Schönlein purpura

Objective To investigate the association of serum vitamin D[25-(OH)D3] level with the severity and treatment in children with Henoch-Schönlein purpura (HSP). Methods A total of 50 children with newly-diagnosed HSP between January and December, 2015 were enrolled as HSP group, and 49 healthy children were enrolled as control group. Fasting serum samples were collected, and ELISA was used to measure serum 25-(OH)D3 level. According to the serum 25-(OH)D3 level, the HSP group were further divided into normal group (> 20 ng/mL) (n=9), insuffciency group (15-20 ng/mL) (n=15), defciency group (≤ 15 ng/mL) (n=25), and severe defciency group (≤ 5 ng/mL) (n=1). The general data, clinical manifestations, hormone therapy, course of disease before admission, and length of hospital stay were compared between groups. Results The HSP group had a signifcantly lower serum 25-(OH)D3 level than the control group (16±6 ng/mL vs 29±5 ng/mL; P  < 0.01). Compared with the normal and insuffciency groups, the defciency and severe deficiency groups had significant increases in the incidence rate of renal involvement, rate of hormone application, and median length of hospital stay (P  < 0.05), while there was no signifcant difference in course of disease before admission (P  > 0.05). Conclusions Children with HSP have a low serum 25-(OH)D3 level, and such children may have a high risk of renal involvement, a high rate of hormone application, and a prolonged length of hospital stay. However, further studies are needed to investigate whether vitamin D supplementation is helpful to the treatment of HSP and can shorten the course of disease in children with HSP.

2017 Vol. 19 (7): 796-799 [Abstract] ( 3833 ) [HTML 1KB] [PDF 987KB] ( 638 )
800 YU Ren-Qiang, ZHAO Xin, CHEN Dao-Zhen, LIAO Xiang-Peng, ZHOU Qin
Vitamin D level at birth and influencing factors in preterm infants

Objective To investigate vitamin D level at birth and possible influencing factors in preterm infants. Methods A total of 600 preterm infants were enrolled, and venous blood samples were collected within 24 hours after birth to measure the serum level of 25-hydroxyvitamin D[25(OH)D]. The effect of sex, birth weight, birth season, gestational age, mother's age, body mass index (BMI) in early pregnancy, delivery mode, and complications during pregnancy on serum 25(OH)D level was analyzed. Results The rates of vitamin D defciency, insuffciency, and suffciency were 42.0%, 38.7%, and 19.3% respectively. The preterm infants born in summer and autumn had a signifcantly higher serum 25(OH)D level than those born in winter (P  < 0.05) and a signifcantly lower incidence rate of vitamin D defciency than those born in spring and winter (P  < 0.003). Compared with those whose mothers were aged < 30 years, the infants whose mothers were aged ≥ 30 years had a signifcantly higher serum 25(OH)D level (P  < 0.05) and a signifcantly lower incidence rate of vitamin D defciency (P  < 0.017). Compared with those whose mothers were overweight or had normal body weight, the infants whose mothers were obese had a signifcantly lower serum 25(OH)D level (P  < 0.05) and a signifcantly higher incidence rate of vitamin D defciency (P  < 0.006). Compared with those whose mothers had no preeclampsia, the infants whose mothers had preeclampsia during pregnancy had a signifcantly lower serum 25(OH)D level (P  < 0.05) and a signifcantly higher incidence rate of vitamin D defciency (P  < 0.017). The multivariate analysis showed that birth in winter and spring, mother's age < 30 years, and early-pregnancy BMI ≥ 28 kg/m2 were risk factors for vitamin D defciency (P  < 0.05). Conclusions There is a high prevalence of vitamin D defciency in preterm infants. Vitamin D supplementation should be given to the preterm infants with high-risk factors for vitamin D defciency.

2017 Vol. 19 (7): 800-805 [Abstract] ( 3290 ) [HTML 1KB] [PDF 1052KB] ( 825 )
806 YANG Xiao, PENG Wei, ZHU Li-Na, ZHANG Xiao-Ai, WANG Yan
Association between IL-6 C-572G and susceptibility to spontaneous preterm birth
Objective To investigate the association between the genetic polymorphism of IL-6 C-572G and susceptibility to spontaneous preterm birth (SPTB). Methods The subjects were from Beijing and the surrounding areas of Beijing. This case-control study enrolled 569 SPTB infants, including 56 extremely preterm ( < 28 weeks of gestation), 166 very preterm (28-31+6 weeks of gestation) and 347 moderate to late preterm infants (32 to 36+6 weeks of gestation). A total of 673 term infants were enrolled as the control group. The latest Sequenom MassARRAY®SNP detection technique was used for the typing of single nucleotide polymorphism of IL-6 C-572G. Results Compared with the CC genotypes, the IL-6 C-572G G-positive genotype (CG+GG genotype) was signifcantly associated with an increased susceptibility to moderate to late SPTB (OR=1.35, 95%CI:1.01-1.80, P=0.04). Conclusions Among the Chinese population, IL-6 C-572G polymorphism is associated with susceptibility to moderate to late SPTB.
2017 Vol. 19 (7): 806-811 [Abstract] ( 2729 ) [HTML 1KB] [PDF 1050KB] ( 597 )
733
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2017 Vol. 19 (7): 733-733 [Abstract] ( 1375 ) [HTML 1KB] [PDF 763KB] ( 511 )
740
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2017 Vol. 19 (7): 740-740 [Abstract] ( 1413 ) [HTML 1KB] [PDF 761KB] ( 517 )
785
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2017 Vol. 19 (7): 785-785 [Abstract] ( 1357 ) [HTML 1KB] [PDF 763KB] ( 450 )
836
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2017 Vol. 19 (7): 836-836 [Abstract] ( 1320 ) [HTML 1KB] [PDF 883KB] ( 400 )
CASE ANALYSIS
812 QIAN Miao, HAN Shu-Ping, YU Zhang-Bing, CHEN Xiao-Hui
Poor weight gain, recurrent metabolic alkalosis and hypokalemia in a neonate
The study reports a female neonate with a gestational age of 29+2 weeks and a birth weight of 1 210 g. Ten minutes after birth, the neonate was admitted to the hospital due to shortness of breath. Several days after birth, the neonate presented with hyperglycemia, polyuria, and poor weight gain, accompanied by azotemia, hypochloremic metabolic alkalosis, hypokalemia, and hyponatremia. Laboratory examinations showed elevated levels of aldosterone, renin, and angiotensin Ⅱ. Gene detection revealed SLC12A1 gene mutation. Neonatal Bartter syndrome was thus confrmed. The neonate was treated with sodium and potassium supplements, and was followed up for 8 months. During the follow-up, the mental and neural development of the neonate was almost normal at the corrected age, and regular reexaminations showed slight metabolic alkalosis and almost normal electrolyte levels. For the neonates who have the symptoms of unexplainable polyurine and electrolyte disorders, it is important to examine the levels of aldosterone, renin and angiotensin. A defnite diagnosis of neonatal Bartter syndrome can be made based on the presence of SLC12A1 gene mutation.
2017 Vol. 19 (7): 812-815 [Abstract] ( 3134 ) [HTML 1KB] [PDF 992KB] ( 849 )
816 TIAN Mao-Qiang, LIU Shu-Yi, LI Juan, SHU Xiao-Mei
Hypertension and intermittent convulsions for one month in a school-age child
Childhood polyarteritis nodosa (PAN) is a rare systemic vasculitis and the delayed diagnosis and treatment will cause high incidence of sequelae and high mortality. This article reports a girl with childhood PAN due to posterior reversible encephalopathy syndrome (PRES). The girl aged ten years was admitted to the hospital due to hypertension and convulsions for one month. She had complaints of headache, vomiting, and blurred vision before convulsions. At six months before admission, a mass was observed in the neck. The physical examination showed that she had hypertension and no abnormal fndings in the central nervous system. The brain magnetic resonance imaging manifested long T1 and T2 signals, high signal intensities on fluid-attenuated inversion recovery (FLAIR) images, and iso-signal intensity on diffusion-weighted imaging in the white matter of the left occipital lobe. Therefore, the cause of convulsions was considered as PRES. Mass biopsy suggested PAN and no fndings supported tuberculosis. The right kidney atrophy was observed by ultrasound examination. Emission computed tomography of the kidney showed multiple vascular stenosis and no blood perfusion in the right kidney, so PAN was confrmed. These fndings suggest that PAN should be considered in patients with vasculitis who had involvements of multiple systems after excluding common vasculitis, such as Kawasaki disease and Henoch-Schönlein purpura. Biopsy and angiography should be performed as early as possible for timely diagnosis and treatment.
2017 Vol. 19 (7): 816-819 [Abstract] ( 2940 ) [HTML 1KB] [PDF 1407KB] ( 639 )
EXPERIMENTAL RESEARCH
820 SHEN Dong-Dong, YUAN Fei, HOU Jiang-Hong
Effect of annexin A2 on EGFR/NF-κB signal transduction and mucin expression in human airway epithelial cells treated with Mycoplasma pneumoniae

Objective To investigate the effect of annexin A2 (AnxA2) on epithelial growth factor receptor (EGFR)/nuclear factor-κB (NF-κB) signal transduction and mucin expression in human airway epithelial H292 cells treated with Mycoplasma pneumoniae (MP). Methods H292 cells were divided into control group, MP group, NC-siRNA+MP group, and AnxA2 siRNA+MP group. The cells in the MP group were incubated with 5 μg/mL MP antigen for 2 hours. The cells in the NC-siRNA+MP and AnxA2 siRNA+MP groups were transfected with NC-siRNA and AnxA2 siRNA for 24 hours, followed by MP antigen stimulation for 2 hours. The MTT method was used to measure cell viability; quantitative real-time PCR was used to measure the mRNA expression of AnxA2; Western blot was used to measure the protein expression of AnxA2, phosphorylated EGFR (p-EGFR), and phosphorylated p65 NF-κB (p-p65 NF-κB); ELISA was used to measure the secretion of mucin 5AC (MUC5AC) and mucin 5B (MUC5B). Results The MP and NC-siRNA+MP groups had lower cell viability than the control group (P  < 0.05). The AnxA2 siRNA+MP group had higher cell viability than the MP and NC-siRNA+MP groups and lower cell viability than the control group (P  < 0.05). The MP and NC-siRNA+MP groups had signifcantly higher mRNA and protein expression of AnxA2 than the AnxA2 siRNA+MP group (P  < 0.05). Compared with the control group, the MP and NC-siRNA+MP groups had significant increases in the protein expression of p-EGFR, p-p65 NF-κB, MUC5AC, and MUC5B (P  < 0.05); the AnxA2 siRNA+MP group had lower protein expression than the MP and NC-siRNA+MP groups, but higher protein expression than the control group (P  < 0.05). Conclusions AnxA2 is involved in the airway lesion induced by MP antigen via mediating EGFR/NF-κB signaling activation and mucin expression in human airway epithelial cells.

2017 Vol. 19 (7): 820-825 [Abstract] ( 2871 ) [HTML 1KB] [PDF 1075KB] ( 652 )
826 ZHU Lian, XU Zhi-Liang
Effect of high-fat diet on expression of transient receptor potential vanilloid 1 in respiratory tract and dorsal root ganglion of mice

Objective To investigate the effect of high-fat diet on the expression of transient receptor potential vanilloid 1 (TRPV1) in the respiratory system and the dorsal root ganglion (DRG) of mice, as well as its effect on the excitability of sensory neurons. Methods A total of 20 C57BL/6 mice were randomly divided into normal-diet (ND) group and high-fat diet (HFD) group, with 10 mice in each group. The mice were given corresponding diets and body weights were monitored. After 7 weeks of feeding, lung tissue, bronchial tissue, and DRG at thoracic segments 3-4 were collected and immunohistochemical staining was performed. A patch clamp was used to measure the number of action potentials and TRPV1 current intensity in the DRG. Results After 7 weeks of feeding, the HFD group had signifcantly greater mean weight gain than the ND group (6.4±2.6 g vs 2.3±0.5 g; P  < 0.001). The HFD group had signifcantly higher expression of TRPV1 in the bronchus, pulmonary alveoli, and DRG than the ND group (P  < 0.05). Compared with the ND group, the HFD group had signifcant increases in the TRPV1 current intensity and number of action potentials in the DRG (P  < 0.05). Conclusions High-fat diet induces a signifcant increase in body weight and leads to high expression of TRPV1 and high excitability in the respiratory system and the peripheral sensory neurons. This suggests that TRPV1 may be an important factor in the physiopathological mechanisms of bronchial hyperresponsiveness.

2017 Vol. 19 (7): 826-831 [Abstract] ( 3523 ) [HTML 1KB] [PDF 1419KB] ( 542 )
REVIEW
832 WANG Ni-Na, YE Qi-Dong
Advances in targeted therapy for childhood acute myeloid leukemia
At present, acute myeloid leukemia (AML) accounts for about 15%-20% of childhood acute leukemia. Although overall survival rate is increasing with the help of risk stratification, stratification of chemotherapy, and supportive treatment, conventional pharmacotherapy still has a limited clinical effect and certain limitations in improving remission rate in previously untreated patients and reducing recurrence after remission. With the development of precision medicine, the mechanisms of targeted therapy, including abnormal activation of AML-related signaling pathways and epigenetic modifcation, have been found in recent years. Molecular-targeted drugs can therefore act on specifc receptors and target genes to improve clinical effect and the prognosis of AML patients.
2017 Vol. 19 (7): 832-836 [Abstract] ( 3802 ) [HTML 1KB] [PDF 1073KB] ( 717 )
837 LIU Ya-Ting, LU Si-Guang
Research advances in immunological pathogenesis of immunoglobulin A vasculitis
Immunoglobulin A (IgA) vasculitis is the most common leukocytoclastic small-vessel vasculitis in children and mainly involves the small vessels in the skin, joints, digestive tract, and kidneys. Its pathogenesis is still unclear. Currently, it is believed that environmental factors can cause autoimmune dysfunction and lead to the deposition of IgA-containing immune complexes on the wall of arterioles on the basis of genetic factors. This article reviews the research advances in the role of immune factors in the pathogenesis of IgA vasculitis.
2017 Vol. 19 (7): 837-840 [Abstract] ( 3358 ) [HTML 1KB] [PDF 990KB] ( 680 )
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