基因缺失型13例,分別為- ?αα 3 . 7 基因型11例 7 3 . 3 3 % ) ? - α 4 . 2 基因型1例 6 . 6 7 % )以及-SEA基因型1例( 6 . 6 7 % ); <img src="/qkimages/24c9/24c9202504/24c920250415-1-l.jpg" with="12px" style="vertical-align: middle;"> 基因非缺失型2例,均為WSM雜合突變。地中海貧血攜帶者中MCV、MCH2項指標均異常僅有1例(篩查陽性率 6 . 6 7 % )。結(jié)論:重慶市人類精子庫捐精志愿者地中海貧血篩查結(jié)果具有區(qū)域性(籍貫以川渝地區(qū)為主)和人群分布差異性(健康育齡男性),地中海貧血攜帶率較低,因地中海貧血對供精出生子代具有重要的影響,建議人類精子庫在捐精志愿者中開展地中海貧血基因篩查。-龍源期刊網(wǎng)" />

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重慶市人類精子庫488例捐精志愿者地中海貧血篩查情況及基因型分析

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【中圖分類號】R69【文獻標志碼】A【收稿日期】2024-12-09

Thalassemia screening and genotype analysis in 488 sperm donors in Chongqing Human Sperm Bank

ShengWeiqiong,HuangJing,ZhangTianfeng,ZhangYi,HuangHua, Wang Hong,Jia Guoqing,Kang Chengjiang

(Human Sperm Bank,Chongqing Research Institute for Population and Family Planning Scienceand Technology)

【AbstractObetiveToivesgatetheariagftetalasmiageneinspedonorsinCongqing,Cnabyalyigethalas semi screeningandgene mutation typesofspermdonors inChongqing Human SpermBank(CHSB),andtoprovideareferencefor thalasemiascreeninginspermdonors inChongqing.Methods:Bloodsamples werecolectedfrom488spermdonors inCHSBdoos withalltestsqualifiedduringthequarantine)fromDecember2021toAugust2024.Acompletebloodcountanalysisasperforedto measure the mean corpuscular volume(MCV)and mean corpuscular hemoglobin(MCH).Polymerase chain reaction(PCR)/agarose gel electrophoresis was used to detect deletional α -thalassemia mutations.PCR and DNA reverse dot blot hybridization were used to detect 3 common non-deletional α -thalassemia mutations and 17 common β -thalassemia mutations.The test results were then analyzed. Results:Amongthe 488 sperm donorsaged 2 5 . 6 4 ± 4 . 9 5 years,15( 3 . 0 7 % ,allHannationality)tested positive for thalassemia.This carriage rate was lower than that of the thalassemia population in Chongqing ( 9 . 2 4 % ).Among the 15 thalassemia carriers,13had deletional α -gene mutations(-α3.7 genotype in11 cases[73.33%], -α4.2 genotype in 1 case[6.67 % ],and -SEA genotype in1 case I 1),and 2 had non-deletional α -gene mutations (both with the WSM heterozygous mutation).There was only1 case of abnormal MCV and MCH2 indicators among thalassemia carriers(screening positive rate was 6 . 6 7 % ).Conclusion:Thalassemia screening inspermdonorsin CHSBrevealsalowthalassemiacariagerate,reflectinggeogaphic(predominantly Sichuanand Chongqingorigins)anddemographic(healthymenofchildbearingpotential)characteristics.Giventhesignificantimpactofthalassmiaonteoffspring conceived through spermdonation,itisrecommendedtoconductthalassemiagenesreeingamong spermdonorsinhuman sperm banks.

【Key words】Chongqing;sperm donor;thalassemia;genotype analysis

人類精子庫是以治療不育癥及預(yù)防遺傳病和提供生殖保險等為目的,利用超低溫冷凍技術(shù),采集、檢測、保存和提供精子并進行相關(guān)研究的公益性機構(gòu)。(剩余9826字)

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