Patel Parizad, Shah Avani, Mishra Kanchan, Ghosh Kanjaksha
Surat Raktadan Kendra & Research Centre, Udhna Magdalla Road, Nr. Chosath Joganio Mata Temple, Surat, Gujarat 395002 India.
Indian J Hematol Blood Transfus. 2019 Jan;35(1):144-148. doi: 10.1007/s12288-018-0970-9. Epub 2018 Jun 7.
Macrothrombocytopenia is being increasingly described across the globe. There is paucity of data on the prevalence of this condition from different parts of India. 10,047 healthy college students from the city of Surat in western India were investigated for macrothrombocytopenia i.e. those with Mean platelet Volume of > 11 fL and platelet count of less than 150 × 10/L. ABO blood groups, complete blood counts, peripheral smear examination and haemoglobinopathy work up was also done. Siblings and parents of the macrothrombocytopenic individuals were also studied when available. Bleeding assessment tool of International society of thrombosis and haemostasis were applied to see if there were excessive bleeding in macrothrombocytropenia patients. One hundred and ninety-six students (1.95%) had asymptomatic macrothrombocytopenia. More female students ( < 0.0001) had this condition and blood group A was under represented ( = 0.019) with this condition. Prevalence of macrothrombocytopenia was not related to ethnic subgroups to which the students belonged to, nor was it linked to presence of any haemoglobinopathy gene. In 38 of the 52, 1st degree relatives studied macrothrombocytopenia was confirmed at least in one of them. Excessive bleeding in none of the individuals with macrothrombocytopenia was noted. Asymptomatic macrothrombocytopenia is rare in western parts of India and affects 1.95% of the healthy population. Females were over represented with this condition raising a suspicion of X linked dominant inheritance. Underrepresentation of blood group A in this condition requires further study.
巨血小板减少症在全球范围内的报道日益增多。印度不同地区关于这种疾病患病率的数据匮乏。对来自印度西部苏拉特市的10047名健康大学生进行了巨血小板减少症调查,即平均血小板体积>11 fL且血小板计数低于150×10⁹/L的学生。还进行了ABO血型、全血细胞计数、外周血涂片检查和血红蛋白病检查。巨血小板减少症患者的兄弟姐妹和父母在有条件时也进行了研究。应用国际血栓与止血学会的出血评估工具来观察巨血小板减少症患者是否有过度出血情况。196名学生(1.95%)患有无症状巨血小板减少症。患有这种疾病的女生更多(P<0.0001),且A型血的学生在这种疾病中的占比偏低(P=0.019)。巨血小板减少症的患病率与学生所属的种族亚组无关,也与任何血红蛋白病基因的存在无关。在研究的52名一级亲属中,有38名至少有一人被确诊为巨血小板减少症。未发现巨血小板减少症患者有过度出血情况。无症状巨血小板减少症在印度西部较为罕见,影响1.95%的健康人群。女性在这种疾病中的占比过高,引发了对X连锁显性遗传的怀疑。这种疾病中A型血占比偏低需要进一步研究。