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Thalassemia: current approach to an old disease.地中海贫血:针对一种古老疾病的当前治疗方法。
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Prevalence of thalassaemia in schoolchildren in north-eastern Badia, Jordan.约旦东北部巴迪亚地区学龄儿童地中海贫血的患病率
East Mediterr Health J. 1999 Nov;5(6):1165-70.
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Appraisal of sickle-cell and thalassaemia genes in Saudi Arabia.沙特阿拉伯镰状细胞病和地中海贫血基因评估
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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。

Prevalence of beta-thalassemia trait in premarital screening in Al-Hassa, Saudi Arabia.

作者信息

Al-Suliman Ahmad

机构信息

Medical Department, King Fahad Hospital, Hofuf Saudi, Arabia.

出版信息

Ann Saudi Med. 2006 Jan-Feb;26(1):14-6. doi: 10.5144/0256-4947.2006.14.

DOI:10.5144/0256-4947.2006.14
PMID:16521869
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6078547/
Abstract

BACKGROUND

The Al-Hassa area is one of the regions in Saudi Arabia where hemoglobinopathies are prevalent. The Saudi Ministry Of Heath designed a protocol for premarital testing after the royal decree in December 2003. The protocol was implemented in a February 2004 order. The aim of this study was to determine the prevalence of beta-thalassemia trait among subjects coming for premarital screening in the Al-Hassa area.

SUBJECTS AND METHODS

From February 2004 to November 2004, healthy subjects coming to six marriages consultation centers in the Al-Hassa area underwent routine mandatory tests. Subjects were considered to have beta-thalassemia trait if they had a mean corpuscular volume (MCV) <80 fL and/or a mean corpuscular hemoglobin (MCH) <27 pg and a hemoglobin A2 level >3.2%. Venous blood was taken into an EDTA tube and the complete blood count and red blood cell indices were measured by a Coulter automated cell counter on the same day of hemoglobin collection. Electrophoresis was done on cellulose acetate.

RESULTS

All Saudi participants (n=8918), including 4218 (47.3%) males and 4700 (52.7%) females were screened. The prevalence of beta-thassemia trait with high hemoglobin A2 and microcytic hypochromic anemia was 3.4% (307/8918).

CONCLUSION

In countries with a high prevalence of hemoglobinopathies, a premarital screening program is helpful for identification and prevention of high-risk marriages. With a 3.4% prevalence of beta-thalassemia trait in premarital couples, future comprehensive programs are needed to know the actual prevalence of beta-thalassemia in Al-Hassa.

摘要

背景

哈萨地区是沙特阿拉伯血红蛋白病流行的地区之一。沙特卫生部在2003年12月发布皇家法令后制定了婚前检测方案。该方案于2004年2月开始实施。本研究的目的是确定在哈萨地区进行婚前筛查的人群中β地中海贫血特征的患病率。

研究对象与方法

2004年2月至2004年11月,前往哈萨地区六个婚姻咨询中心的健康受试者接受了常规强制检测。如果受试者的平均红细胞体积(MCV)<80 fL和/或平均红细胞血红蛋白(MCH)<27 pg且血红蛋白A2水平>3.2%,则被认为具有β地中海贫血特征。将静脉血采集到乙二胺四乙酸(EDTA)管中,并在采集血红蛋白的同一天用库尔特自动血细胞计数器测量全血细胞计数和红细胞指数。在醋酸纤维素上进行电泳。

结果

共筛查了所有沙特参与者(n = 8918),其中男性4218名(47.3%),女性4700名(52.7%)。血红蛋白A2升高且伴有小细胞低色素性贫血的β地中海贫血特征的患病率为3.4%(307/8918)。

结论

在血红蛋白病高发国家,婚前筛查计划有助于识别和预防高危婚姻。婚前夫妇中β地中海贫血特征的患病率为3.4%,未来需要开展综合计划以了解哈萨地区β地中海贫血的实际患病率。