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Blood, 15 September 2008, Vol. 112, No. 6, pp. 2173-2174.
MPDs: it's all in the familyJOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE
Dameshek was wrong.1 In this issue of Blood, in a landmark epidemiologic study, Landgren and colleagues demonstrate that first-degree relatives (parents, siblings, and offspring) of Swedish myeloproliferative disorder (MPD) patients have a 5- to 7-fold increased risk of developing an MPD.
Landgren and colleagues took a different approach. They exploited the interlocking Swedish healthcare and population databases, for which every resident is assigned a unique registration number. In this way, between 1958 and 2005, they were able to collect data on 11 039 MPD patients (6217 PV, 2838 ET, 1172 PMF, and 812 MPD not otherwise specified) with 24 577 first-degree relatives, and 43 550 matched controls with 99 542 first-degree relatives, giving their observations substantial statistical power. Not only was there an increased risk of acquiring an MPD among the first-degree relatives, but the risk also did not differ for a particular MPD, although the low number of PMF patients made the predictions for it less reliable. Furthermore, the risk among the first-degree relatives of patients with a particular MPD was not restricted to that MPD. Among the first-degree relatives, a higher risk was also observed for siblings, suggesting the possibility of recessive inheritance, although most smaller studies support an autosomal-dominant inheritance with variable penetrance.4–6 Importantly, in keeping with the female predominance in PV and ET, there was a higher risk for female relatives and the relatives of female probands compared with their male counterparts. In contrast to a smaller study,4 no evidence was found for anticipation, although anticipation has been a feature of other familial hematologic neoplasms. There was no increased risk among the first-degree relatives for acute myeloid leukemia or myelodysplastic syndrome, but there was a borderline risk for chronic myeloid leukemia (CML) and a significantly increased risk for chronic lymphocytic leukemia (CLL), malignant melanoma, and brain cancer. What conclusions can be drawn from this study? First, since a relatively genetically homogenous population was studied, the observations may not be totally applicable to other population groups. For example, in the United States, the age of MPD onset is lower, particularly in women with PV or ET. Second, given the high risk for an MPD in first-degree relatives, the term sporadic should be applied cautiously when a new MPD patient is encountered. In this regard, the familial MPDs are clinically similar to their sporadic counterparts with the exception that the frequency of JAK2 V617 expression is reduced in familial PV.4,5 Third, Dameshek was actually partially correct.7 While a higher risk for acquisition of a hematologic malignancy is seen in families in which there is a hematologic malignancy,8 acquisition of the same type of malignancy at such a high frequency is unusual, supporting the contention that PV, ET, and PMF have a common genetic basis. In this regard, the risk for acquiring CLL as well as CML should probably be considered as part of the general tendency for familial aggregation of hematologic malignancies and not specific to the MPD, particularly since CML is rarely familial. Fourth, the increase in ET prevalence, which coincided in part with a switch by Swedish hematologists from using the PVSG diagnostic criteria to the World Health Organization (WHO) MPD diagnostic criteria, probably reflects the unacceptable insensitivity of the WHO diagnostic criteria for recognizing PV. This is unfortunate, because PV is the ultimate phenotypic expression of the JAK2 V617F mutation. Finally, the data of Landgren et al serve to remind us that in MPDs, phenotype is driven as much and possibly more by as-yet-undefined genetic influences as it is by those that have been defined.
Footnotes
Conflict-of-interest disclosure: The author declares no competing financial interests.
REFERENCES
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