کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
4179582 1276557 2007 5 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Sustained Low-Grade Pro-inflammatory State in Unmedicated, Remitted Women with Major Depressive Disorder as Evidenced by Elevated Serum Levels of the Acute Phase Proteins C-reactive Protein and Serum Amyloid A
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی روانپزشکی بیولوژیکی
پیش نمایش صفحه اول مقاله
Sustained Low-Grade Pro-inflammatory State in Unmedicated, Remitted Women with Major Depressive Disorder as Evidenced by Elevated Serum Levels of the Acute Phase Proteins C-reactive Protein and Serum Amyloid A
چکیده انگلیسی

BackgroundMajor depressive disorder (MDD) shows increased coronary artery disease (CAD) risk of unknown mechanism(s). MDD is more common in women than men; CAD diagnosis can be difficult in women. Elevations of the inflammatory markers C-reactive protein (CRP) and serum amyloid A (SAA) predict increased CAD risk in populations; few data on these markers exist in MDD, particularly in remitted patients.MethodsWe measured fasting am serum CRP (high sensitivity, CRPhs) and SAA in 18 unmedicated, remitted women with MDD (mean age 41 ± (SD)12, body mass index (BMI) 25.2 ± 4.1 kg/m2) and 18 BMI-matched healthy control subjects (age 36 ± 10, BMI 25.3 ± 3.8 kg/m2) on 2 separate occasions, ≥ 6 days apart.ResultsRepeat SAA and CRPhs measurements strongly correlated across study days (SAA: r = .83, p < .001; CRPhs: r = .94, p < .001). Both SAA (5.30 ± 3.39 vs. 2.84 ± 1.87 mg/L, p < .005) and CRPhs (3.23 ± 3.17 vs. 1.12 ± 1.45 mg/L; p < .01) were significantly elevated in MDD women versus controls.ConclusionsElevated SAA and CRPhs in remitted, unmedicated women with MDD indicate a pro-inflammatory state unrelated to current depressive symptoms or pharmacotherapy. These findings suggest that inflammatory mechanisms may in part underlie findings of increased CAD risk in MDD.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Biological Psychiatry - Volume 62, Issue 4, 15 August 2007, Pages 309–313
نویسندگان
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