Publication:
The limitation of factor IX coagulant activity determination in the diagnosis of hemophilia B carriers

dc.contributor.authorSaranya Rurgkhumen_US
dc.contributor.authorWerasak Sasanakulen_US
dc.contributor.authorSukanya Chotsuppakarnen_US
dc.contributor.authorPakaimas Pintaditen_US
dc.contributor.authorAmpaiwan Chuansumriten_US
dc.contributor.otherResearch Centeren_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-07-24T03:04:42Z
dc.date.available2018-07-24T03:04:42Z
dc.date.issued2002-11-01en_US
dc.description.abstractA preliminary study of factor IX coagulant activity (FIX:C) for determining hemophilia B carriers was conducted at the Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital in Bangkok. Twenty-eight females (8 obligate, 20 potential carriers) from 17 hemophilia B families were enrolled in the study. Additionally, 25 normal females were included. They were not pregnant and not using oral contraceptives. Then, three cut-off levels of FIX:C including 50 per cent which was the commonly used level; 57 per cent which was the mean-2 SD of normal females and 75 per cent which was the level reported by Knobe and Ljung in 1999 were used for the diagnosis of hemophilia B carriers. The sensitivities of these three cut-off levels were 12.5 per cent (1/8) for 50 per cent, 37.5 per cent (3/8) for 57 per cent and 50 per cent (4/8) for 75 per cent. Also, the specificities were 100 per cent (25/25) for both 50 and 57 per cent, and 96 per cent (24/25) for 75 per cent. Although the low cut-off levels of 50 per cent and 57 per cent had low sensitivities, they yielded a high specificity (100%) compared to the higher level of 75 per cent. In the present study, the sensitivity of the cut-off level at 75 per cent was much lower than that of the study by Knobe and Ljung (93%) since the presented sample size of obligate carriers was rather small. So, enrollment of more subjects should be further carried out. In conclusion, FIX:C determination alone showed a limitation in the diagnosis of hemophilia B carriers. The addition of genetic analysis of linkage analysis or mutation detection is required for a definite diagnosis.en_US
dc.identifier.citationJournal of the Medical Association of Thailand. Vol.85, No.SUPPL. 4 (2002)en_US
dc.identifier.issn01252208en_US
dc.identifier.other2-s2.0-0036881835en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/20338
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0036881835&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleThe limitation of factor IX coagulant activity determination in the diagnosis of hemophilia B carriersen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0036881835&origin=inwarden_US

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