TY - JOUR
T1 - ZNF804A Gene Variants Have a Cross-diagnostic Influence on Psychosis and Treatment Improvement in Mood Disorders
AU - Calabrò, Marco
AU - Mandelli, Laura
AU - Crisafulli, Concetta
AU - Di Nicola, Marco
AU - Colombo, Roberto
AU - Janiri, Luigi
AU - Lee, Soo-Jung
AU - Jun, Tae-Youn
AU - Wang, Sheng-Min
AU - Masand, Prakash S.
AU - Patkar, Ashwin A.
AU - Han, Changsu
AU - Pae, Chi-Un
AU - Serretti, Alessandro
PY - 2020
Y1 - 2020
N2 - Objective: Genetic variations in the gene encoding zinc finger protein 804A gene (ZNF804A) have been associated with major depression and bipolar disorder. In this work we focused on the potential influence of ZNF804A variations on the risk of developing specific sub-phenotypes as well as the individual response to available treatments. Methods: We used two samples of different ethnic origin: a Korean sample, composed by 242 patients diagnosed with major depression and 132 patients diagnosed with bipolar disorder and 326 healthy controls; an Italian sample composed 151 major depression subjects, 189 bipolar disorder subjects and 38 outpatients diagnosed for a primary anxiety disorder. Results: Our analyses reported an association of rs1344706 with psychotic phenotype in the cross-diagnostic pooled sample (geno p = 4.15 × 10−4, allelic p = 1.06 × 10−4). In the cross-diagnosis Italian sample but not in the Korean one, rs7597593 was involved with depressive symptoms improvement after treatment (geno p = 0.025, allelic p = 0.007). Conclusion: The present study evidenced the role of ZNF804A alterations in symptoms improvement after treatment. Both manic and depressive symptoms seem to be modulated by ZNF804A, though the latter was observed in the bipolar pooled sample only. The role of this factor is likely related to synaptic development and maintenance; however, further analyses will be needed to better understand the molecular mechanics involved with ZNF804A.
AB - Objective: Genetic variations in the gene encoding zinc finger protein 804A gene (ZNF804A) have been associated with major depression and bipolar disorder. In this work we focused on the potential influence of ZNF804A variations on the risk of developing specific sub-phenotypes as well as the individual response to available treatments. Methods: We used two samples of different ethnic origin: a Korean sample, composed by 242 patients diagnosed with major depression and 132 patients diagnosed with bipolar disorder and 326 healthy controls; an Italian sample composed 151 major depression subjects, 189 bipolar disorder subjects and 38 outpatients diagnosed for a primary anxiety disorder. Results: Our analyses reported an association of rs1344706 with psychotic phenotype in the cross-diagnostic pooled sample (geno p = 4.15 × 10−4, allelic p = 1.06 × 10−4). In the cross-diagnosis Italian sample but not in the Korean one, rs7597593 was involved with depressive symptoms improvement after treatment (geno p = 0.025, allelic p = 0.007). Conclusion: The present study evidenced the role of ZNF804A alterations in symptoms improvement after treatment. Both manic and depressive symptoms seem to be modulated by ZNF804A, though the latter was observed in the bipolar pooled sample only. The role of this factor is likely related to synaptic development and maintenance; however, further analyses will be needed to better understand the molecular mechanics involved with ZNF804A.
KW - Bipolar disorder
KW - Major depressive disorder
KW - Psychotic disorders
KW - Symptoms improvement
KW - ZNF804A
KW - Bipolar disorder
KW - Major depressive disorder
KW - Psychotic disorders
KW - Symptoms improvement
KW - ZNF804A
UR - https://publicatt.unicatt.it/handle/10807/325018
UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85086667514&origin=inward
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85086667514&origin=inward
U2 - 10.9758/cpn.2020.18.2.231
DO - 10.9758/cpn.2020.18.2.231
M3 - Article
SN - 1738-1088
VL - 18
SP - 231
EP - 240
JO - Clinical Psychopharmacology and Neuroscience
JF - Clinical Psychopharmacology and Neuroscience
IS - 2
ER -