Genetic Aspects of Scurvy and the European Famine of 1845–1848

Nutrients

Joris R. Delanghe²  Marc L. De Buyzere¹  Marijn M. Speeckaert³ 

[1] Department of Cardiology, Ghent University Hospital, B 9000 Ghent, Belgium; E-Mail:;Department of Laboratory Medicine, Ghent University Hospital, B 9000 Ghent, Belgium;Department of Nephrology, Ghent University Hospital, B 9000 Ghent, Belgium; E-Mail:

关键词: haptoglobin;    iron;    polymorphism;    scurvy;    vitamin C;   

DOI  :  10.3390/nu5093582

来源: mdpi

【 摘 要 】

The view of scurvy being exclusively a nutritional disorder needs to be updated. Genetic polymorphisms of HFE and haptoglobin (Hp) may explain the geographic variability of mortality caused by the European famine of the mid-19th century. In this period, potatoes had fallen victim to the potato blight and Ireland was more severely hit than continental Europe. Hereditary hemochromatosis is a genetic disorder with mutations in the HFE gene, characterized by iron overload (with a reduced vitamin C stability) and with a predominance of affected men. The Irish have the world’s highest frequency of the C282Y mutation and the particular iron metabolism of the Irish helps to understand the size of the catastrophe and the observed overrepresentation of male skeletons showing scurvy. Hp is a plasma α₂-glycoprotein characterized by 3 common phenotypes (Hp 1-1, Hp 2-1 and Hp 2-2). When the antioxidant capacity of Hp is insufficient, its role is taken over by hemopexin and vitamin C. The relative number of scurvy victims corresponds with the Hp 2-2 frequency, which is associated with iron conservation and has an impact on vitamin C stability. As iron is more abundant in males, males are overrepresented in the group of skeletons showing scurvy signs.

【 授权许可】

CC BY   
© 2013 by the authors; licensee MDPI, Basel, Switzerland.