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Medication-Induced Weight Change Across Common Antidepressant Treatments : A Target Trial Emulation Study.
Petimar, Joshua; Young, Jessica G; Yu, Han; Rifas-Shiman, Sheryl L; Daley, Matthew F; Heerman, William J; Janicke, David M; Jones, W Schuyler; Lewis, Kristina H; Lin, Pi-I D; Prentice, Carly; Merriman, John W; Toh, Sengwee; Block, Jason P.
Affiliation
  • Petimar J; Department of Population Medicine, Harvard Medical School and Harvard Pilgrim Health Care Institute, and Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts (J.P., J.G.Y.).
  • Young JG; Department of Population Medicine, Harvard Medical School and Harvard Pilgrim Health Care Institute, and Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts (J.P., J.G.Y.).
  • Yu H; Department of Population Medicine, Harvard Medical School and Harvard Pilgrim Health Care Institute, Boston, Massachusetts (H.Y., S.L.R.-S., P.-I.D.L., S.T., J.P.B.).
  • Rifas-Shiman SL; Department of Population Medicine, Harvard Medical School and Harvard Pilgrim Health Care Institute, Boston, Massachusetts (H.Y., S.L.R.-S., P.-I.D.L., S.T., J.P.B.).
  • Daley MF; Institute for Health Research, Kaiser Permanente Colorado, Denver, Colorado (M.F.D.).
  • Heerman WJ; Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee (W.J.H.).
  • Janicke DM; Department of Clinical and Health Psychology, College of Public Health and Health Professions, University of Florida, Gainesville, Florida (D.M.J.).
  • Jones WS; Division of Cardiology, Duke University Department of Medicine, and Duke University Medical Center, Duke Clinical Research Institute, Durham, North Carolina (W.S.J.).
  • Lewis KH; Department of Epidemiology and Prevention, Division of Public Health Sciences, Wake Forest University School of Medicine, Winston-Salem, North Carolina (K.H.L.).
  • Lin PD; Department of Population Medicine, Harvard Medical School and Harvard Pilgrim Health Care Institute, Boston, Massachusetts (H.Y., S.L.R.-S., P.-I.D.L., S.T., J.P.B.).
  • Prentice C; Faith Family Medical Center, Nashville, Tennessee (C.P.).
  • Merriman JW; Department of Medicine, College of Medicine, University of Florida, Gainesville, Florida (J.W.M.).
  • Toh S; Department of Population Medicine, Harvard Medical School and Harvard Pilgrim Health Care Institute, Boston, Massachusetts (H.Y., S.L.R.-S., P.-I.D.L., S.T., J.P.B.).
  • Block JP; Department of Population Medicine, Harvard Medical School and Harvard Pilgrim Health Care Institute, Boston, Massachusetts (H.Y., S.L.R.-S., P.-I.D.L., S.T., J.P.B.).
Ann Intern Med ; 177(8): 993-1003, 2024 Aug.
Article in En | MEDLINE | ID: mdl-38950403
ABSTRACT

BACKGROUND:

Antidepressants are among the most commonly prescribed medications, but evidence on comparative weight change for specific first-line treatments is limited.

OBJECTIVE:

To compare weight change across common first-line antidepressant treatments by emulating a target trial.

DESIGN:

Observational cohort study over 24 months.

SETTING:

Electronic health record (EHR) data from 2010 to 2019 across 8 U.S. health systems.

PARTICIPANTS:

183 118 patients. MEASUREMENTS Prescription data determined initiation of treatment with sertraline, citalopram, escitalopram, fluoxetine, paroxetine, bupropion, duloxetine, or venlafaxine. The investigators estimated the population-level effects of initiating each treatment, relative to sertraline, on mean weight change (primary) and the probability of gaining at least 5% of baseline weight (secondary) 6 months after initiation. Inverse probability weighting of repeated outcome marginal structural models was used to account for baseline confounding and informative outcome measurement. In secondary analyses, the effects of initiating and adhering to each treatment protocol were estimated.

RESULTS:

Compared with that for sertraline, estimated 6-month weight gain was higher for escitalopram (difference, 0.41 kg [95% CI, 0.31 to 0.52 kg]), paroxetine (difference, 0.37 kg [CI, 0.20 to 0.54 kg]), duloxetine (difference, 0.34 kg [CI, 0.22 to 0.44 kg]), venlafaxine (difference, 0.17 kg [CI, 0.03 to 0.31 kg]), and citalopram (difference, 0.12 kg [CI, 0.02 to 0.23 kg]); similar for fluoxetine (difference, -0.07 kg [CI, -0.19 to 0.04 kg]); and lower for bupropion (difference, -0.22 kg [CI, -0.33 to -0.12 kg]). Escitalopram, paroxetine, and duloxetine were associated with 10% to 15% higher risk for gaining at least 5% of baseline weight, whereas bupropion was associated with 15% reduced risk. When the effects of initiation and adherence were estimated, associations were stronger but had wider CIs. Six-month adherence ranged from 28% (duloxetine) to 41% (bupropion).

LIMITATION:

No data on medication dispensing, low medication adherence, incomplete data on adherence, and incomplete data on weight measures across time points.

CONCLUSION:

Small differences in mean weight change were found between 8 first-line antidepressants, with bupropion consistently showing the least weight gain, although adherence to medications over follow-up was low. Clinicians could consider potential weight gain when initiating antidepressant treatment. PRIMARY FUNDING SOURCE National Institutes of Health.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Weight Gain / Antidepressive Agents Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Ann Intern Med Year: 2024 Type: Article

Full text: 1 Database: MEDLINE Main subject: Weight Gain / Antidepressive Agents Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Ann Intern Med Year: 2024 Type: Article