HAPTOGLOBIN PHENOTYPES AND GENE-FREQUENCIES IN BIPOLAR DISORDER - AN ASSOCIATION STUDY IN FAMILY-HISTORY SUBGROUPS

Citation
L. Fananas et al., HAPTOGLOBIN PHENOTYPES AND GENE-FREQUENCIES IN BIPOLAR DISORDER - AN ASSOCIATION STUDY IN FAMILY-HISTORY SUBGROUPS, Human heredity, 47(1), 1997, pp. 27-32
Citations number
15
Categorie Soggetti
Genetics & Heredity
Journal title
ISSN journal
00015652
Volume
47
Issue
1
Year of publication
1997
Pages
27 - 32
Database
ISI
SICI code
0001-5652(1997)47:1<27:HPAGIB>2.0.ZU;2-#
Abstract
Several studies have shown that major depression is accompanied by sig nificantly increased plasma levels of positive acute-phase proteins su ch as haptoglobin (Hp). A significant higher frequency of the HP1 all ele has recently been detected in patients with unipolar major depress ion. Pursuing the hypothesis that certain unipolar and bipolar disorde rs may be genetically related, this study analyzed Hp genotype and all ele frequencies in bipolar patients, taking into account their family history of major affective disorders. An increase of HP1 allele frequ ency was found in the subgroup of patients with family history of excl usively unipolar disorder (70% in patients vs. 38% in controls, chi(2) = 8.34, p = 0.004). The relative risk for the HP1 carriers in this s ubgroup was 3.8 (chi(2) = 7.29, p = 0.007). These results suggest a ge netic and etioIogical heterogeneity in the bipolar disorder.