Papakostas George I, Petersen Timothy, Mischoulon David, Green Cassandra H, Nierenberg Andrew A, Bottiglieri Teodoro, Rosenbaum Jerrold F, Alpert Jonathan E, Fava Maurizio
Depression Clinical and Research Program, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.
J Clin Psychiatry. 2004 Aug;65(8):1096-8. doi: 10.4088/jcp.v65n0811.
In the present study, we assessed the relationship between serum folate, vitamin B12, and homocysteine levels on the rate of relapse in outpatients with remitted major depressive disorder (MDD) during a 28-week continuation phase of treatment with fluoxetine.
Seventy-one outpatients (mean +/- SD age = 40.2 +/- 11.1 years; 56.3% women) with MDD (as assessed with the Structured Clinical Interview for DSM-III-R) who had remitted and who were enrolled in the continuation phase of treatment with fluoxetine had serum folate, vitamin B12, and homocysteine measurements completed at baseline (prior to acute-phase treatment). Patients were followed for 28 weeks of continued treatment with fluoxetine 40 mg/day to monitor for depressive relapse. Folate levels were classified as either low (< or = 2.5 ng/mL) or normal. Vitamin B12 levels were classified as either low (< or = 200 pg/mL) or normal. Homocysteine levels were classified as either elevated (> or = 13.2 micromol/L) or normal. With the use of separate logistic regressions, we then assessed the relationship between folate, vitamin B12, and homocysteine level status and relapse. The study was conducted from November 1992 to January 1999.
The presence of low serum folate levels (p =.004), but not low B12 (p >.05) or elevated homocysteine levels (p >.05), was associated with relapse during continuation treatment with fluoxetine. The relapse rates for patients with (N = 7) and without (N = 64) low folate levels were 42.9% versus 3.2%, respectively.
Low serum folate levels were found to place patients with remitted MDD at risk for depressive relapse during the continuation phase of treatment with fluoxetine.
在本研究中,我们评估了血清叶酸、维生素B12和同型半胱氨酸水平与缓解期重度抑郁症(MDD)门诊患者在为期28周的氟西汀持续治疗阶段复发率之间的关系。
71例MDD门诊患者(通过DSM-III-R结构化临床访谈评估),已缓解且参加氟西汀持续治疗阶段,在基线时(急性期治疗前)完成血清叶酸、维生素B12和同型半胱氨酸测量。患者接受28周的40mg/天氟西汀持续治疗以监测抑郁复发情况。叶酸水平分为低(≤2.5ng/mL)或正常。维生素B12水平分为低(≤200pg/mL)或正常。同型半胱氨酸水平分为升高(≥13.2μmol/L)或正常。然后使用单独的逻辑回归分析,我们评估了叶酸、维生素B12和同型半胱氨酸水平状态与复发之间的关系。该研究于1992年11月至1999年1月进行。
血清叶酸水平低(p = 0.004)与氟西汀持续治疗期间的复发相关,而维生素B12水平低(p>0.05)或同型半胱氨酸水平升高(p>0.05)则不然。叶酸水平低(N = 7)和叶酸水平正常(N = 64)的患者复发率分别为42.9%和3.2%。
发现在氟西汀持续治疗阶段,血清叶酸水平低会使缓解期MDD患者有抑郁复发的风险。