کد مقاله کد نشریه سال انتشار مقاله انگلیسی ترجمه فارسی نسخه تمام متن
2628561 1136475 2015 5 صفحه PDF سفارش دهید دانلود کنید
عنوان انگلیسی مقاله
A randomized controlled trial of 6-week Chlorella vulgaris supplementation in patients with major depressive disorder
ترجمه فارسی عنوان
یک کارآزمایی بالینی تصادفی شده با مکمل Chlorella vulgaris 6 هفته ای در بیماران مبتلا به اختلال افسردگی شدید
کلمات کلیدی
موضوعات مرتبط
علوم پزشکی و سلامت پزشکی و دندانپزشکی طب مکمل و جایگزین
چکیده انگلیسی


• Ø Chlorella vulgaris extract (CVE) is an antioxidant-rich algal product.
• This study tested the effects of CVE supplementation in patients with depression.
• Six-week CVE supplementation improved anxiety, and physical and cognitive symptoms of depression.
• CVE was safe and well-tolerated during the study.

BackgroundMajor depressive disorder (MDD) is a widespread psychiatric disorder with incapacitating symptoms. Oxidative stress has been identified to play a role in the pathophysiology of MDD.ObjectiveTo evaluate the therapeutic effectiveness of a chemically defined and antioxidant-rich Chlorella vulgaris extract (CVE) as adjunct to standard treatment in patients suffering from MDD.MethodsSubjects with MDD diagnosis according to DSM-IV criteria who were receiving standard antidepressant therapy were assigned to add-on therapy with CVE (1800 mg/day; n = 42), or continued standard antidepressant therapy alone (n = 50) for a period of 6 weeks. Changes in the frequency of depressive symptoms were assessed using the Hospital Anxiety and Depression Scale (HADS) and Beck Depression Inventory II (BDI-II) scale.ResultsThere were significant reductions in total and subscale BDI-II and HADS scores in both CVE and control groups by the end of trial. The magnitude of reductions in total BDI-II score [−4.14 (−5.30 to −2.97)] as well as physical [−2.34 (−2.84 to −1.84)] and cognitive [−1.12 (−1.62 to −0.61)] subscales were significantly greater in the CVE versus control group, however, reduction of the affective symptoms was greater in the control compared with the CVE group [0.95 (0.18–0.72)]. Total HADS [−3.71 (−4.44 to −2.98)] as well as individual subscales of depression [−1.46 (−2.02 to −0.90)] and anxiety [−2.25 (−2.74 to −1.76)] were reduced to a greater degree in the CVE group. CVE was well tolerated and no serious adverse event was reported.ConclusionThis pilot exploratory trial provides the first clinical evidence on the efficacy and safety of adjunctive therapy with CVE in improving physical and cognitive symptoms of depression as well as anxiety symptoms in patients who are receiving standard antidepressant therapy.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Complementary Therapies in Medicine - Volume 23, Issue 4, August 2015, Pages 598–602
نویسندگان
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