• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

沙特阿拉伯迈马麦地区成年人中血红蛋白病(β-地中海贫血和镰状细胞特征)的流行情况。

Prevalence of Hemoglobinopathies (β-Thalassemia and Sickle Cell Trait) in the Adult Population of Al Majma'ah, Saudi Arabia.

机构信息

Department of Medical Laboratory Sciences, College of Applied Medical Sciences, Majmaah University, Al Majma'ah, Riyadh Province, Saudi Arabia.

Premarital Screening Center, King Khaled General Hospital, Al Majma'ah, Riyadh Province, Saudi Arabia.

出版信息

Hemoglobin. 2020 Jan;44(1):47-50. doi: 10.1080/03630269.2020.1729175. Epub 2020 Feb 24.

DOI:10.1080/03630269.2020.1729175
PMID:32091272
Abstract

Despite the high prevalence of hemoglobinopathies in Saudi Arabia, the prevalence data in some regions are lacking. Updating the epidemiological survey of hemoglobinopathies at regular intervals is necessary to develop effective prevention and control strategies. Therefore, the primary aim of this study was to determine the prevalence of selected hemoglobinopathies in Saudi adults attending premarital screening at the King Khaled General Hospital (KKGH), Al Majma'ah, Saudi Arabia. The current retrospective study was approved by the Central Institutional Review Board (IRB) of the Ministry of Health (with central IRB log #2019-0039E) and was carried out at the above hospital. The data of the premarital couples, who attended the premarital screening center at KKGH from 1 October 2016 to 30 September 2019, was included in this study. A cation exchange high performance liquid chromatography (HPLC) system was used for screening of the selected hemoglobinopathies. In total, 3755 cases including 1953 (52.01%) males and 1802 (47.99%) females, were screened for hemoglobinopathies. Abnormal hemoglobin (Hb) fractions were observed in 38 (1.01%) cases. The prevalence of β-thalassemia (β-thal) trait was 0.69% (26/3755) and that of sickle cell trait 0.32% (12/3755). Our results showed that the prevalence of β-thal trait is higher than that of sickle cell trait in the adult population of Al Majma'ah. Further comprehensive programs should be carried out to determine the prevalence of hemoglobinopathies in various provinces and cities of Saudi Arabia and other countries. This will help to maintain the updated records of the disease incidence for improving the control measures.

摘要

尽管血红蛋白病在沙特阿拉伯很常见,但一些地区缺乏流行数据。定期更新血红蛋白病的流行病学调查对于制定有效的预防和控制策略是必要的。因此,本研究的主要目的是确定在沙特阿拉伯 Al Majma'ah 参加婚前检查的成年人群中选定的血红蛋白病的流行率。这项回顾性研究得到了沙特卫生部中央机构审查委员会(IRB)的批准(中央 IRB 编号为 2019-0039E),并在上述医院进行。该研究纳入了 2016 年 10 月 1 日至 2019 年 9 月 30 日期间在 King Khaled 综合医院婚前检查中心就诊的婚前夫妇的数据。本研究采用阳离子交换高效液相色谱(HPLC)系统对选定的血红蛋白病进行筛查。共有 3755 例患者(包括 1953 例男性和 1802 例女性)接受了血红蛋白病筛查。在 38 例(1.01%)患者中观察到异常血红蛋白(Hb)片段。β-地中海贫血(β-thal)表型的患病率为 0.69%(26/3755),镰状细胞表型的患病率为 0.32%(12/3755)。我们的研究结果表明,在 Al Majma'ah 的成年人群中,β-地中海贫血表型的患病率高于镰状细胞表型。应该进一步开展全面的项目来确定沙特阿拉伯各省市和其他国家的血红蛋白病流行率。这将有助于保持疾病发病率的最新记录,从而改善控制措施。

相似文献

1
Prevalence of Hemoglobinopathies (β-Thalassemia and Sickle Cell Trait) in the Adult Population of Al Majma'ah, Saudi Arabia.沙特阿拉伯迈马麦地区成年人中血红蛋白病(β-地中海贫血和镰状细胞特征)的流行情况。
Hemoglobin. 2020 Jan;44(1):47-50. doi: 10.1080/03630269.2020.1729175. Epub 2020 Feb 24.
2
Six-year outcome of the national premarital screening and genetic counseling program for sickle cell disease and β-thalassemia in Saudi Arabia.沙特阿拉伯镰状细胞病和β地中海贫血国家婚前筛查与遗传咨询项目的六年成果。
Ann Saudi Med. 2011 May-Jun;31(3):229-35. doi: 10.4103/0256-4947.81527.
3
Prevalence and Regional Distribution of Beta-Hemoglobin Variants in Saudi Arabia: Insights from the National Premarital Screening Program".沙特阿拉伯β-血红蛋白变异体的流行情况和地域分布:来自全国婚前筛查计划的见解。
J Epidemiol Glob Health. 2024 Sep;14(3):1242-1248. doi: 10.1007/s44197-024-00281-x. Epub 2024 Jul 29.
4
Prevalence of beta-thalassemia trait in premarital screening in Al-Hassa, Saudi Arabia.沙特阿拉伯哈萨地区婚前筛查中β地中海贫血特征的患病率。
Ann Saudi Med. 2006 Jan-Feb;26(1):14-6. doi: 10.5144/0256-4947.2006.14.
5
Marked regional variations in the prevalence of sickle cell disease and β-thalassemia in Saudi Arabia: findings from the premarital screening and genetic counseling program.沙特阿拉伯镰状细胞病和β地中海贫血患病率的显著地区差异:婚前筛查与遗传咨询项目的结果
J Epidemiol Glob Health. 2011 Dec;1(1):61-8. doi: 10.1016/j.jegh.2011.06.002. Epub 2011 Jul 28.
6
Evaluation of high performance liquid chromatography (HPLC) pattern and prevalence of beta-thalassaemia trait among sickle cell disease patients in Lagos, Nigeria.尼日利亚拉各斯镰状细胞病患者的高效液相色谱(HPLC)图谱评估及β地中海贫血特征的患病率
Pan Afr Med J. 2014 May 22;18:71. doi: 10.11604/pamj.2014.18.71.4239. eCollection 2014.
7
Distribution of hemoglobinopathy disorders in Saudi Arabia based on data from the premarital screening and genetic counseling program, 2011-2015.基于 2011-2015 年婚前检查和遗传咨询计划的数据,沙特阿拉伯的血红蛋白病分布情况。
J Epidemiol Glob Health. 2018 Mar;7 Suppl 1(Suppl 1):S41-S47. doi: 10.1016/j.jegh.2017.12.001. Epub 2017 Dec 15.
8
Hemoglobinopathies: An update on the prevalence trends in Southern Saudi Arabia.血红蛋白病:沙特阿拉伯南部患病率趋势的最新更新。
Saudi Med J. 2021 Jul;42(7):784-789. doi: 10.15537/smj.2021.42.7.20210273.
9
Prevalence of hemoglobinopathies in rural Bengal, India.印度孟加拉邦农村地区血红蛋白病的患病率。
Hemoglobin. 2012;36(1):57-63. doi: 10.3109/03630269.2011.621007. Epub 2011 Oct 17.
10
"Minor" hemoglobinopathies: a risk factor for asthma.“轻度”血红蛋白病:哮喘的一个风险因素。
Eur Ann Allergy Clin Immunol. 2005 May;37(5):177-82.

引用本文的文献

1
Systematic Literature Review Shows Gaps in Data on Global Prevalence and Birth Prevalence of Sickle Cell Disease and Sickle Cell Trait: Call for Action to Scale Up and Harmonize Data Collection.系统文献综述显示镰状细胞病和镰状细胞性状的全球患病率及出生患病率数据存在差距:呼吁采取行动扩大并统一数据收集工作。
J Clin Med. 2023 Aug 25;12(17):5538. doi: 10.3390/jcm12175538.
2
Sickle Cell Anaemia among Tharu Population Visiting the Outpatient Department of General Medicine in a Secondary Care Centre: A Descriptive Cross-sectional Study.在二级保健中心的普通内科门诊就诊的塔鲁族人群中的镰状细胞贫血症:一项描述性横断面研究。
JNMA J Nepal Med Assoc. 2022 Sep 1;60(253):774-776. doi: 10.31729/jnma.7651.
3
Screening of Extended Family Members of Thalassemia Major Children as a Thalassemia Preventive Strategy.
对重型地中海贫血患儿的家族成员进行筛查,作为地中海贫血的预防策略。
Ethiop J Health Sci. 2022 Nov;32(6):1203-1210. doi: 10.4314/ejhs.v32i6.18.
4
Molecular Determination of Vascular Endothelial Growth Factor, miRNA-423 Gene Abnormalities by Utilizing ARMS-PCR and Their Association with Fetal Hemoglobin Expression in the Patients with Sickle Cell Disease.利用扩增阻滞突变系统聚合酶链反应(ARMS-PCR)对镰状细胞病患者血管内皮生长因子、miRNA-423基因异常进行分子检测及其与胎儿血红蛋白表达的关联研究
Curr Issues Mol Biol. 2022 Jun 1;44(6):2569-2582. doi: 10.3390/cimb44060175.
5
Hemoglobinopathies: An update on the prevalence trends in Southern Saudi Arabia.血红蛋白病:沙特阿拉伯南部患病率趋势的最新更新。
Saudi Med J. 2021 Jul;42(7):784-789. doi: 10.15537/smj.2021.42.7.20210273.
6
Biochemical and molecular analysis of the beta-globin gene and LCR region on Saudi β-thalassemia patients.沙特β地中海贫血患者β珠蛋白基因和LCR区域的生化与分子分析
Saudi J Biol Sci. 2020 Nov;27(11):3106-3112. doi: 10.1016/j.sjbs.2020.08.044. Epub 2020 Sep 4.
7
Novel genetic therapeutic approaches for modulating the severity of β-thalassemia (Review).用于调节β地中海贫血严重程度的新型基因治疗方法(综述)
Biomed Rep. 2020 Nov;13(5):48. doi: 10.3892/br.2020.1355. Epub 2020 Sep 2.