We tested the hypothesis that allelic variation of 5-HTT linked polymorphic region (5-HTTLPR) could influence illness onset and recurrence in 129 bipolar and 128 unipolar recurrent patients. Among bipolar patients, homozygotes for the short variant showed an earlier age at onset and a lower recurrence rate than heterozygotes and homozygotes for the long variant. Unipolar patients showed a trend toward the same difference. Data support a role for 5-HTTLPR in course of affective illness. © 2002 Elsevier Science B.V./ECNP. All rights reserved.

Serotonin transporter promoter genotype and illness recurrence in mood disorders

Smeraldi E.;Benedetti F.;
2002-01-01

Abstract

We tested the hypothesis that allelic variation of 5-HTT linked polymorphic region (5-HTTLPR) could influence illness onset and recurrence in 129 bipolar and 128 unipolar recurrent patients. Among bipolar patients, homozygotes for the short variant showed an earlier age at onset and a lower recurrence rate than heterozygotes and homozygotes for the long variant. Unipolar patients showed a trend toward the same difference. Data support a role for 5-HTTLPR in course of affective illness. © 2002 Elsevier Science B.V./ECNP. All rights reserved.
2002
5-HTTLPR; Antidepressant response; Bipolar; Depression; Functional polymorphism; Illness onset and recurrence; Unipolar
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11768/90492
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