Wenwei Guang
Anhui Medical University
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Featured researches published by Wenwei Guang.
Fertility and Sterility | 2003
Xiaobin Wang; Changzhong Chen; Lihua Wang; Dafang Chen; Wenwei Guang; Jonathan L. French
OBJECTIVE To examine rates of conception and pregnancy loss and their relations with time to clinical pregnancy and reproductive outcomes. DESIGN A prospective observational study. SETTING Population-based cohort in China. PATIENT(S) Five hundred eighteen healthy newly married women who intended to conceive. Upon stopping contraception, daily records of vaginal bleeding and daily first-morning urine specimens were obtained for < or =1 year or until a clinical pregnancy was achieved. Daily urinary hCG was assayed to detect early pregnancy loss (EPL). INTERVENTION(S) None. MAIN OUTCOME MEASURE(S) Conception, pregnancy loss, and time to clinical pregnancy. RESULT(S) The conception rate per cycle was 40% over the first 12 months. Of the 618 detectable conceptions, 49 (7.9%) ended in clinical spontaneous abortion, and 152 (24.6%) in EPL. Early pregnancy loss was detected in 14% of all the cycles without clinically recognized pregnancy, but the frequencies were lower among women with delayed time to clinical pregnancy. Early pregnancy loss in the preceding cycle was associated with increased odds of conception (odds ratio [OR], 2.6; 95% confidence interval [CI], 1.8-3.9), clinical pregnancy (OR, 2.0; 95% CI, 1.3-3.0), and EPL (OR, 2.4; 95% CI, 1.4-4.2) but was not associated with spontaneous abortion, low birth weight, or preterm birth in the subsequent cycle. CONCLUSION(S) We demonstrated substantial EPL in the non-clinically pregnant cycles and a positive relation between EPL and subsequent fertility.
American Journal of Human Genetics | 2001
Xin Xu; Zhian Fang; Binyan Wang; Changzhong Chen; Wenwei Guang; Yongtang Jin; Jianghua Yang; Steve Lewitzky; Avram Aelony; Alex Parker; Joanne M. Meyer; Scott T. Weiss; Xiping Xu
A genomewide screen for quantitative-trait loci (QTLs) that underlie asthma was performed on 533 Chinese families with asthma, by the unified Haseman-Elston method. Nine asthma-related phenotypes were studied, including forced expiratory volume in 1 s (FEV1), forced vital capacity (FVC), airway responsiveness as indicated by methacholine (MTCH)-challenge test, serum total immunoglobulin E (TIgE), serum-specific immunoglobulin E, eosinophil count in peripheral blood, and skin-prick tests with three different allergens (cockroach, Dermatophagoides pteronyssinus, and D. farinae). Our study showed significant linkage between airway responsiveness to MTCH and D2S1780 on chromosome 2 (P<.00002) and provided suggestive evidence (P<.002) for six additional possible QTLs: D10S1435 and D22S685, for FEV1; D16S412, for FVC; D19S433, for airway responsiveness to MTCH; D1S518, for TIgE; and D4S1647, for skin reactivity to cockroach. No significant or suggestive evidence of linkage for the other four traits was found.
Occupational and Environmental Medicine | 2004
Lin Wang; Xiaobin Wang; Weixu Wang; C Chen; A G Ronnennberg; Wenwei Guang; Aiqun Huang; Zhian Fang; Tonghua Zang; Xin Xu
Background: Dysmenorrhoea is the most common gynaecological disorder in women of reproductive age. Despite the association between stress and pregnancy outcomes, few studies have examined the possible link between stress and dysmenorrhoea. Aims and Methods: Using a population based cohort of Chinese women, the independent effect of women’s perceived stress in the preceding menstrual cycle on the incidence of dysmenorrhoea in the subsequent cycle was investigated prospectively. The analysis included 1160 prospectively observed menstrual cycles from 388 healthy, nulliparous, newly married women who intended to conceive. The perception of stress and the occurrence of dysmenorrhoea in each menstrual cycle were determined from daily diaries recorded by the women. Results: After adjustment for important covariates, the risk of dysmenorrhoea was more than twice as great among women with high stress compared to those with low stress in the preceding cycle (OR = 2.4; 95% CI 1.4 to 4.3). The risk of dysmenorrhoea was greatest among women with both high stress and a history of dysmenorrhoea compared to women with low stress and no history of dysmenorrhoea (OR = 10.4, 95% CI 4.9 to 22.3). Stress in the follicular phase of the preceding cycles had a stronger association with dysmenorrhoea than stress in the luteal phase of the preceding cycles. Conclusion: This study shows a significant association between stress and the incidence of dysmenorrhoea, which is even stronger among women with a history of dysmenorrhoea.
Clinical and Experimental Hypertension | 2004
Guo Huang; Houxun Xing; Ke Hao; Shaojie Peng; Di Wu; Wenwei Guang; Aiqun Huang; Xiumei Hong; Yuanping Wang; Yan Feng; Yan Zhang; Jianping Li; Changzhong Chen; Binyan Wang; Xuejun Zhang; Dong Li; Yunxian Yu; Jing Liu; Guoying Zhu; Yong Huo; Dafang Chen; Yongtai Hou; Xiaobin Wang; Xin Xu; Tianhua Niu; Xiping Xu
Background: There is considerable variability in individual response to antihypertensive agents. The reason for this is not known, but may be related to individual genetic variability. This study examined whether the therapeutic efficacy of benazepril on essential hypertension is modified by β2 adrenergic receptor gene (ADRB2) Arg16Gly (R16G) polymorphism. Methods and Results: We conducted a family‐based study of 321 and 610 hypertensive subjects from Yuexi and Huoqiu Counties of Anhui, China, respectively. Both systolic and diastolic blood pressures (SBP and DBP) before and after a 15‐day benazepril treatment were measured. ADRB2 R16G genotypes were determined for all subjects. ADRB2 G16 allele frequency was found to be 41.0% and. 47.4% in Huoqiu and Yuexi, respectively. In Yuexi family‐based association test (FBAT) revealed that the G16 allele was associated with a greater DBP decrease in response to a 15‐day benazepril treatment (Z = 2.12, P = 0.03), and the data were consistent with a dominant inheritance model. A similar trend was observed in Huoqiu Chinese, but the magnitudes of effects were smaller and did not reach statistical significance. The FBAT results were further confirmed by using a generalized estimating equation model. Conclusion: Our family‐based study provided the first evidence that ADRB2 R16G polymorphism may play an important role in DBP response to benazepril treatment, although the magnitude of the effect appears to be modified by other risk factors such as plasma lipid and glucose profiles.
Annals of Epidemiology | 2004
Dong Li; Houxun Xing; Ke Hao; Shaojie Peng; Di Wu; Wenwei Guang; Aiqun Huang; Yuanping Wang; Yan Zhang; Yunxian Yu; Jianping Li; Changzhong Chen; Binyan Wang; Guoying Zhu; Yong Huo; Dafang Chen; Alayne G. Ronnenberg; Tianhua Niu; Xiping Xu
PURPOSE Essential hypertension, as a complex disorder with unknown etiology cause, is a major public health problem worldwide. Patients need constant drug therapy to maintain their blood pressure in a normal range. However, the current facts suggest that the treatment is not optimized in a large number of patients, and as a result they are at risk for compliance resulting in uncontrolled blood pressure. Genetic and environmental factors associated with individual variation in response to anti-hypertensive drug remain largely unknown. METHODS In order to illustrate the existence and to attempt to identify the factors modifying drug effect, we conducted a large-scale follow-up study in two Chinese rural counties differing in both genetic background and residential environment. Hypertensive patients were treated with benazepril, a commonly used angiotensin converting enzyme inhibitor, for 15 days, and the end-point effect was evaluated. RESULTS We found that there were large and significant differences in drug response between subjects from two counties, even after adjustment for known factors. The responses to benazepril, measured in diastolic blood pressure drop, in male patients from Yuexi was twice as effective as their counterparts from Huoqiu. CONCLUSIONS These results suggest that adjustment of treatment regimen is necessary to improve efficacy, and it could be done at the population level to make it more feasible and affordable.
Epidemiology | 2005
Scott A. Venners; Susan A. Korrick; Xin Xu; C Chen; Wenwei Guang; Aiqun Huang; Larisa Altshul; Melissa J. Perry; Lingling Fu; Xiaobin Wang
Previous studies of pregnancy losses and 1,1,1-trichloro-2,2-bis(p-chlorophenyl)ethane (DDT) were limited because they did not include losses prior to clinical detection of pregnancy and because exposures were measured after the pregnancies of interest. The authors examined the association of preconception serum total DDT (sum of DDT isomers and metabolites) concentration and subsequent pregnancy losses in 388 newly married, nonsmoking, female textile workers in China between 1996 and 1998. Upon stopping contraception, subjects provided daily urine specimens and records of vaginal bleeding for up to 1 year or until clinical pregnancy. Daily urinary human chorionic gonadotropin was assayed to detect conception and early pregnancy losses, and pregnancies were followed to detect clinical spontaneous abortions. There were 128 (26%) early pregnancy losses in 500 conceptions and 36 (10%) spontaneous abortions in 372 clinical pregnancies. Subjects were grouped in tertiles by preconception serum total DDT concentration (group 1: 5.5-22.9 ng/g; group 2: 23.0-36.5 ng/g; group 3: 36.6-113.3 ng/g). Compared with group 1, group 2 had adjusted relative odds of early pregnancy losses of 1.23 (95% confidence interval (Cl): 0.72,2.10), and group 3 had adjusted odds of 2.12 (9ii% Cl: 1.26, 3.57). The relative odds of early pregnancy losses associated with a 10-ng/g increase in serum total DDT were 1.17 (95% Cl: 1.05, 1.29). The small number of spontaneous abortions following clinical detection of pregnancy were not associated with serum total DDT. In this population, there was a positive, monotonic, exposure-response association between preconception serum total DDT and the risk of subsequent early pregnancy losses.
American Journal of Epidemiology | 2004
Scott A. Venners; Xiaobin Wang; Changzhong Chen; Lihua Wang; Dafang Chen; Wenwei Guang; Aiqun Huang; Louise Ryan; John F. O’Connor; Bill L. Lasley; James W. Overstreet; Allen J. Wilcox; Xiping Xu
Journal of Nutrition | 2004
Alayne G. Ronnenberg; Richard J. Wood; Xiaobin Wang; Houxun Xing; C Chen; Dafang Chen; Wenwei Guang; Aiqun Huang; Lihua Wang; Xiping Xu
American Journal of Epidemiology | 2005
Scott A. Venners; Susan A. Korrick; Xiping Xu; Changzhong Chen; Wenwei Guang; Aiqun Huang; Larisa Altshul; Melissa J. Perry; Lingling Fu; Xiaobin Wang
Journal of Nutrition | 2003
Alayne G. Ronnenberg; Xiaobin Wang; Houxun Xing; C Chen; Dafang Chen; Wenwei Guang; Aiqun Guang; Lihua Wang; Louise Ryan; Xiping Xu