Objective: To evaluate the effect of the serotonin-norepinephrine re-uptake inhibitor desvenlafaxine on blood pressure and incidence of new onset hypertension in pooled short-term studies and in two longer-term, randomized withdrawal studies. Research design and methods: Data from patients randomly assigned to desvenlafaxine 10 mg to 400 mg/day or placebo in 11 short-term (8-12 weeks), fixed-dose, double-blind, placebo-controlled studies of major depressive disorder (MDD) were pooled for analysis; two desvenlafaxine randomized withdrawal studies (36 and 46 weeks) were analyzed separately. Main outcome measures: Outcomes included change from baseline in supine systolic blood pressure (SSBP) and supine diastolic blood pressure (SDBP), assessed using a mixed model repeated measures (MMRM) analysis, and incidence of hypertension (defined as three consecutive second SDBP measures >= 90 mm Hg AND increase of >= 10 mm Hg from baseline and/or SSBP >= 140 mm Hg AND increase of >= 10 mm Hg), analyzed using Cochran Mantel Hanzael tests. Potential predictors of change in SSBP and SDBP at LOCF were examined by including predictor variables in a regression model. Results: In the pooled, short-term studies, mean changes from baseline over time in SSBP and SDBP were statistically significant compared with placebo for the desvenlafaxine doses of 10 mg/day or greater for SSBP (p <= 0.0004; MMRM) and 25 mg/day or greater for SDBP (p <= 0.0449; MMRM). The proportion of patients with new onset hypertension differed significantly from placebo for the 50, 200, and 400 mg/day doses (1.9%, 2.4%, 4.8%, respectively, vs 0.8%; all p <= 0.0244). Predictors of change in BP included baseline SDBP, baseline SSBP, dose, body mass index, gender, age, race, and history of hypertension. Limitations: Data were pooled from studies which differed somewhat in study design and patient demographics. None of the studies were originally designed to examine treatment effects on BP. Study entry criteria limit generalization of these results to medically stable patients with a primary diagnosis of MDD. Conclusions: Short-term desvenlafaxine treatment was associated with small but statistically significant increases in SSBP and SDBP.
机构:
Virginia Commonwealth Univ, Dept Psychiat, Sch Med, Mood Disorders Inst, Richmond, VA 23298 USA
Virginia Commonwealth Univ, Inst Womens Hlth, Richmond, VA 23298 USAVirginia Commonwealth Univ, Dept Psychiat, Sch Med, Mood Disorders Inst, Richmond, VA 23298 USA
Kornstein, Susan G.
Fava, Maurizio
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Massachusetts Gen Hosp, Depress Clin & Res Program, Boston, MA 02114 USA
Harvard Univ, Massachusetts Gen Hosp, Sch Med, Boston, MA USAVirginia Commonwealth Univ, Dept Psychiat, Sch Med, Mood Disorders Inst, Richmond, VA 23298 USA
Fava, Maurizio
Jiang, Qin
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Wyeth Res, Collegeville, PA USAVirginia Commonwealth Univ, Dept Psychiat, Sch Med, Mood Disorders Inst, Richmond, VA 23298 USA
Jiang, Qin
Tourian, Karen A.
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Wyeth Res, Clin Res & Dev, Neurosci, Paris, FranceVirginia Commonwealth Univ, Dept Psychiat, Sch Med, Mood Disorders Inst, Richmond, VA 23298 USA
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Univ Virginia, Dept Psychiat & Neurobehav Sci, Charlottesville, VA USAUniv Virginia, Dept Psychiat & Neurobehav Sci, Charlottesville, VA USA
Clayton, Anita H.
Hwang, Eunhee
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Pfizer Inc, Collegeville, PA USAUniv Virginia, Dept Psychiat & Neurobehav Sci, Charlottesville, VA USA
Hwang, Eunhee
Kornstein, Susan G.
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Virginia Commonwealth Univ, Dept Psychiat, Richmond, VA USA
Virginia Commonwealth Univ, Inst Womens Hlth, Richmond, VA USAUniv Virginia, Dept Psychiat & Neurobehav Sci, Charlottesville, VA USA
Kornstein, Susan G.
Tourian, Karen A.
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Pfizer Inc, Collegeville, PA USAUniv Virginia, Dept Psychiat & Neurobehav Sci, Charlottesville, VA USA
Tourian, Karen A.
Cheng, Ru-fong
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Pfizer Inc, Collegeville, PA USAUniv Virginia, Dept Psychiat & Neurobehav Sci, Charlottesville, VA USA
Cheng, Ru-fong
Abraham, Lucy
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Pfizer Inc, Walton Oaks, EnglandUniv Virginia, Dept Psychiat & Neurobehav Sci, Charlottesville, VA USA
Abraham, Lucy
Mele, Linda
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机构:Univ Virginia, Dept Psychiat & Neurobehav Sci, Charlottesville, VA USA
Mele, Linda
Boucher, Matthieu
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Pfizer Canada Inc, Kirkland, PQ, CanadaUniv Virginia, Dept Psychiat & Neurobehav Sci, Charlottesville, VA USA
机构:
Virginia Commonwealth Univ, Dept Psychiat, Richmond, VA 23298 USA
Virginia Commonwealth Univ, Inst Womens Hlth, Richmond, VA 23298 USAVirginia Commonwealth Univ, Dept Psychiat, Richmond, VA 23298 USA
Kornstein, Susan G.
Clayton, Anita H.
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Univ Virginia, Dept Psychiat & Neurobehav Sci, Charlottesville, VA USA
Univ Virginia, Dept Obstet & Gynecol, Charlottesville, VA USAVirginia Commonwealth Univ, Dept Psychiat, Richmond, VA 23298 USA
Clayton, Anita H.
Bao, Weihang
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Pfizer Inc, Collegeville, PA USAVirginia Commonwealth Univ, Dept Psychiat, Richmond, VA 23298 USA
Bao, Weihang
Guico-Pabia, Christine J.
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CGP Strateg Solut LLC, Lansdale, PA USAVirginia Commonwealth Univ, Dept Psychiat, Richmond, VA 23298 USA
机构:
Virginia Commonwealth Univ, Dept Psychiat, Richmond, VA USA
Virginia Commonwealth Univ, Inst Womens Hlth, Richmond, VA USAUniv Complutense Madrid, CIBERSAM, Madrid, Spain
机构:
Pfizer Inc, New York, NY USA
Univ Penn, Ctr Clin Epidemiol & Biostat, Philadelphia, PA 19104 USA
Univ Penn, Ctr Pharmacoepidemiol Res & Training, Philadelphia, PA 19104 USAUniv Complutense Madrid, CIBERSAM, Madrid, Spain
Salas, Maribel
Mackell, Joan
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Pfizer Inc, New York, NY USAUniv Complutense Madrid, CIBERSAM, Madrid, Spain