Meifang Xiao

Meifang Xiao


Research Focus & Metrics

Academic Career Length

9Years (2018-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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9 March 2024 in Chemical Engineering Journal
Verified
Journal Article
Closed access
YWYuexin Wang
Yuexin Wang
BSBo Shen
Bo Shen
NLNini Luo
Nini Luo
CLCai Li
Cai Li
HWHaiping Wu
Haiping Wu
QXQianfeng Xia
Qianfeng Xia

6 June 2024 in Analytica Chimica Acta
Verified
Journal Article
Closed access
GTGuozhen Tian
Guozhen Tian
JTJun Tan
Jun Tan
BLBiao Liu
Biao Liu
MXMeifang Xiao
Meifang Xiao
QXQianfeng Xia
Qianfeng Xia

5 January 2021 in Virologica Sinica
Verified
Journal Article
Closed access
PDF file
JDJiang Du
Jiang Du
LZLiyuan Zhang
Liyuan Zhang
XHXiaoyuan Hu
Xiaoyuan Hu
RPRuoyan Peng
Ruoyan Peng
GWGaoyu Wang
Gaoyu Wang
FYFeifei Yin
Feifei Yin

13 June 2022 in Frontiers in Genetics
Verified
Journal Article
Open access
MWMin Wang
Min Wang
XZXiaozhuang Zhang
Xiaozhuang Zhang
YZYubin Zhang
Yubin Zhang
MXMeifang Xiao
Meifang Xiao
Background: There are limited studies on the molecular profile of thalassemia in Hainan, the free trade island in China. Our aim was to reveal the prevalence and molecular mutation spectrum of thalassemia in different ethnic groups and regions of Hainan through a large sample study for the first time.Methods: A total of 231,596 individuals from 19 cities and counties in Hainan were screened by hematological parameter analysis, and further genetic analysis was performed on individuals with MCV less than 82 fL.Results: Totally, 31,780 (13.72%) subjects were diagnosed as thalassemia carriers. The overall prevalence of α-thalassemia, β-thalassemia, and α+β-thalassemia were 11.04%, 1.48%, and 1.20%, respectively. We further analyzed the molecular profiles of thalassemia in various ethnic groups and mainly compared the difference between Han and Li. The results showed that the frequency of thalassemia in the Li population (47.03%) was much higher than that in Han (9.37%). Except for β-thalassemia (1.31% of Li vs. 1.47% of Han), the frequencies of α-thalassemia (39.59% of Li vs. 7.35% of Han) and α+β-thalassemia (6.13% of Li vs. 0.56% of Han) in the Li were obviously higher than those in Han. The high-frequent genotypes of α-thalassemia in Han were αα/--SEA (25.55%), -α3.7/αα (22.17%), -α4.2/αα (21.59%), αWSα/αα (8.93%), and -α3.7/-α4.2 (4.17%) and those of Li were -α4.2/αα (17.24%), -α3.7/αα (17.16%), -α3.7/-α4.2 (15.09%), αWSα/αα (9.69%), and αWSα/-α3.7 (8.06%), respectively. The αα/--SEA was the highest genotype of α-thalassemia in Han but only accounted for 1.87% in Li. For β-thalassemia, the top three high-frequent genotypes in both Han and Li were βCD41/42(-TTCT)/βN, β-28(A>G)/βN, and βIVS-Ⅱ-654(C>T)/βN, but the frequency of βCD41/42(-TTCT)/βN in Li (90.96%) was much higher than that in Han (56.32%) and the data reported in other provinces of China. Additionally, the prevalence of thalassemia ranged from 8.16% to 34.35% in Hainan, Wuzhishan, Baoting, Qiongzhong, and Baisha have a higher prevalence than other areas.Conclusion: Our study revealed the characteristics of ethnic and regional differences in the prevalence of thalassemia in the childbearing age population of Hainan for the first time, indicating that the prevalence of thalassemia among Li nationality is the highest in China. Those findings will be useful for genetic counseling and the prevention of thalassemia.

21 April 2023 in PLOS Neglected Tropical Diseases
Verified
Journal Article
Open access
PDF file
GWGaoyu Wang
Gaoyu Wang
RFRuijia Fu
Ruijia Fu
LZLiyuan Zhang
Liyuan Zhang
LXLiying Xue
Liying Xue
AAAbdullah Y. Al-Mahdi
Abdullah Y. Al-Mahdi
FYFeifei Yin
Feifei Yin
Scrub typhus, caused by mite-borne Orientia tsutsugamushi (O. tsutsugamushi), is a major febrile disease in the Asia-Pacific region. The DNA load of O. tsutsugamushi in the blood was previously found to be significantly higher in patients with fatal disease than those with non-fatal disease and correlated with the duration of illness, presence of eschar, and hepatic enzyme levels. In this prospective observation study, we analyzed the association of bacterial DNA load with clinical features, disease severity, and genotype using real-time PCR targeting the 56 kDa TSA gene of O. tsutsugamushi in the blood samples of 117 surviving patients with scrub typhus who had not received appropriate antibiotic treatment. The median O. tsutsugamushi DNA load was 3.11×103 copies/mL (range, 44 to 3.3×106 copies/mL). The severity of patients was categorized as mild, moderate, and severe based on the number of dysfunctional organs, and no significant difference in O. tsutsugamushi DNA load was found among these groups. Patients infected with the Karp group showed a significantly higher O. tsutsugamushi DNA load than those in the Gilliam (P < 0.05) and TA763 (P < 0.01) groups. Patients belonging to the Li ethnic group showed a significantly higher DNA load than those in the Han ethnic groups. The blood bacterial DNA load of patients showed no significant difference between groups divided by gender, age, with or without eschar, or the season of disease onset. The highest body temperature recorded during fever onset was positively correlated with O. tsutsugamushi DNA load (ρ = 0.272, P  = 0.022). Correlation analyses indicated that the serum total bilirubin level was positively correlated with O. tsutsugamushi DNA load. In conclusion, the findings in this study demonstrated the association of DNA load of O. tsutsugamushi with the severity and genotype in patients with scrub typhus in Hainan, China.

4 February 2022 in Journal of Clinical Laboratory Analysis
Verified
Journal Article
Open access
PDF file
MWMin Wang
Min Wang
XZXiaozhuang Zhang
Xiaozhuang Zhang
YZYanhong Zhao
Yanhong Zhao
ZLZhe Lu
Zhe Lu
MXMeifang Xiao
Meifang Xiao
Background: Hainan has one of the high incidences of thalassemia in China, but the epidemiological data in the whole province has not been reported yet. The objective of our study was to reveal the true prevalence and molecular mutation spectrum of thalassemia in the population of Hainan who are of childbearing age.Methods: We screened 166,936 individuals from 19 cities and counties in Hainan by hematological parameters analysis, and further conducted genetic analysis for individuals whose MCV was less than 82fL.Results: In total, 21,619 (12.95%) subjects were diagnosed as thalassemia carriers or patients. The overall prevalence of α‐thalassemia, β‐thalassemia, and α+β‐thalassemia were 10.39%, 1.38%, and 1.18%, respectively. Eleven α‐thalassemia mutations and sixteen β‐thalassemia mutations were identified. The high‐frequent genotypes of α‐thalassemia were ‐α3.7/αα (19.70%), ‐α4.2/αα (19.39%), αα/‐‐SEA (15.60%), αWSα/αα (9.24%), and ‐α3.7/‐α4.2 (8.90%), and those of β‐thalassemia were βCD41/42(−TTCT)/βN (58.92%), β−28(A>G)/βN (16.05%), βIVS−Ⅱ−654(C>T)/βN (8.42%), βCD71/72(+A)/βN (6.03%), βCD17(A>T)/βN (5.47%), and βCD26 (GAG>AAG)/βN (2.69%). In addition, the frequencies and hematological profiles of many rare mutations of α‐ [Fusion, HKαα, αααanti4.2, IVS‐II‐55 (T>G), IVS‐II‐119 (−G,+CTCGGCCC)] and β‐globin genes [−50 (G>A), IVS‐Ⅱ‐81 (C>T)] in Hainan were reported for the first time.Conclusion: Our study revealed the high prevalence and extensive molecular spectrum of thalassemia in childbearing age population of Hainan, suggesting thalassemia in Hainan ranks second in prevalence among all regions in China. The findings will be useful for genetic counseling and prevention of thalassemia.