The incidence of venous thromboembolism among Factor V Leiden carriers: a community-based cohort study

被引:60
作者
Heit, JA
Sobell, JL
Li, H
Sommer, SS
机构
[1] Mayo Clin & Mayo Fdn, Sect Haematol Res, Dept Internal Med, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Div Cardiovasc Dis, Rochester, MN 55905 USA
[3] Mayo Clin & Mayo Fdn, Dept Psychiat, Rochester, MN 55905 USA
[4] Mayo Clin & Mayo Fdn, Dept Hlth Sci Res, Div Clin Epidemiol, Rochester, MN 55905 USA
[5] Mayo Clin & Mayo Fdn, Dept Hlth Sci Res, Div Biostat, Rochester, MN 55905 USA
[6] Mayo Clin & Mayo Fdn, Dept Biochem & Mol Biol, Rochester, MN 55905 USA
关键词
Factor V Leiden; venous thromboembolism;
D O I
10.1111/j.1538-7836.2004.01117.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
While Factor V (FV) Leiden is a risk factor for venous thromboembolisin (VTE), the incidence of VTE among FV Leiden carriers is uncertain. The objective of the study was to estimate the overall age-specific and pregnancy-related VTE incidence and the relative risk among FV Leiden carriers. In a community-based sample of 3424 south-eastern Minnesota residents, 230 (6.7%) were genotyped as FV Leiden carriers; 220 carriers (mean age = 68 years) could be matched to a noncarrier on age, gender, ethnicity and length of medical history. We performed a retrospective cohort study of carriers and noncarriers by reviewing the complete medical records in the community for demographic and baseline characteristics, pregnancies and live births, and first lifetime VTE. Over 14 722 person-years, 24 (10.9%) carriers developed VTE [overall incidence = 163 (95% CI 104, 242) per 100 000 person-years]. VTE incidence rates for ages 15-29, 30-44, 45-59 and greater than or equal to60 years were 0, 61, 244 and 764 per 100 000 person-years, respectively (cumulative VTE incidence at age 65 years = 6.3%). VTE incidence for carriers did not differ significantly from that for non-carriers except for those greater than or equal to60 years old (relative risk = 3.6; 95% Cl 2.0, 6.0). There were 311 live births among 130 women carriers; no VTE events occurred during pregnancy or postpartum [incidence = 0 (95% CI 0, 1186) per 100 000 women-years). Most FV Leiden carriers do not develop VTE. Among all carriers, those ! 60 years old are at the highest risk for VTE. The incidence of VTE among asymptornatic women carriers during pregnancy is low and insufficient to warrant prophylaxis.
引用
收藏
页码:305 / 311
页数:7
相关论文
共 46 条
[1]   A POPULATION-BASED PERSPECTIVE OF THE HOSPITAL INCIDENCE AND CASE-FATALITY RATES OF DEEP-VEIN THROMBOSIS AND PULMONARY-EMBOLISM - THE WORCESTER DVT STUDY [J].
ANDERSON, FA ;
WHEELER, HB ;
GOLDBERG, RJ ;
HOSMER, DW ;
PATWARDHAN, NA ;
JOVANOVIC, B ;
FORCIER, A ;
DALEN, JE .
ARCHIVES OF INTERNAL MEDICINE, 1991, 151 (05) :933-938
[2]   MUTATION IN BLOOD-COAGULATION FACTOR-V ASSOCIATED WITH RESISTANCE TO ACTIVATED PROTEIN-C [J].
BERTINA, RM ;
KOELEMAN, BPC ;
KOSTER, T ;
ROSENDAAL, FR ;
DIRVEN, RJ ;
DERONDE, H ;
VANDERVELDEN, PA ;
REITSMA, PH .
NATURE, 1994, 369 (6475) :64-67
[3]   THE MECHANISM OF INACTIVATION OF HUMAN PLATELET FACTOR VA FROM NORMAL AND ACTIVATED PROTEIN C-RESISTANT INDIVIDUALS [J].
CAMIRE, RM ;
KALAFATIS, M ;
CUSHMAN, M ;
TRACY, RP ;
MANN, KG ;
TRACY, PB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (35) :20794-20800
[4]   FAMILIAL THROMBOPHILIA DUE TO A PREVIOUSLY UNRECOGNIZED MECHANISM CHARACTERIZED BY POOR ANTICOAGULANT RESPONSE TO ACTIVATED PROTEIN-C - PREDICTION OF A COFACTOR TO ACTIVATED PROTEIN-C [J].
DAHLBACK, B ;
CARLSSON, M ;
SVENSSON, PJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (03) :1004-1008
[5]   INHERITED RESISTANCE TO ACTIVATED PROTEIN-C IS CORRECTED BY ANTICOAGULANT COFACTOR ACTIVITY FOUND TO BE A PROPERTY OF FACTOR-V [J].
DAHLBACK, B ;
HILDEBRAND, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (04) :1396-1400
[6]   A prospective study of venous thromboembolism in relation to factor V Leiden and related factors [J].
Folsom, AR ;
Cushman, M ;
Tsai, MY ;
Aleksic, N ;
Heckbert, SR ;
Boland, LL ;
Tsai, AW ;
Yanez, ND ;
Rosamond, WD .
BLOOD, 2002, 99 (08) :2720-2725
[7]   Prothrombin and factor V mutations in women with a history of thrombosis during pregnancy and the puerperium. [J].
Gerhardt, A ;
Scharf, RE ;
Beckmann, MW ;
Struve, S ;
Bender, HG ;
Pillny, M ;
Sandmann, W ;
Zotz, RB .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (06) :374-380
[8]   ACTIVATED PROTEIN-C RESISTANCE CAUSED BY ARG506GLN MUTATION IN FACTOR VA [J].
GREENGARD, JS ;
SUN, X ;
XU, X ;
FERNANDEZ, JA ;
GRIFFIN, JH ;
EVATT, B .
LANCET, 1994, 343 (8909) :1361-1362
[9]   PARAMETERS AFFECTING THE YIELD OF DNA FROM HUMAN-BLOOD [J].
GUSTAFSON, S ;
PROPER, JA ;
BOWIE, EJW ;
SOMMER, SS .
ANALYTICAL BIOCHEMISTRY, 1987, 165 (02) :294-299
[10]   An unknown genetic defect increases venous thrombosis risk, through interaction with protein C deficiency [J].
Hasstedt, SJ ;
Bovill, EG ;
Callas, PW ;
Long, GL .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (02) :569-576