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Study protocol of a randomized, double-blind, placebo-controlled, multi-center trial to treat antipsychotic-induced weight gain: the Metformin-Lifestyle in antipsychotic users (MELIA) trial
被引:4
|作者:
de Boer, Nini
[1
]
Guloksuz, Sinan
[2
,3
]
van Baal, Caroline
[4
]
Willebrands, Leonie
[1
]
Deenik, Jeroen
[1
,2
,5
]
Vinkers, Christiaan H.
[6
,7
,8
]
Winter-van Rossum, Inge
[1
]
Zinkstok, Janneke
[1
]
Wilting, Ingeborg
[9
]
Zantvoord, Jasper B.
[6
,7
]
Backx, Frank
[10
]
Swildens, Wilma E.
[11
,12
]
Schouw, Marieke
[11
]
Bogers, Jan
[13
]
Hulshof, Folkwin
[14
]
de Knijff, Rudolf
[14
]
Duindam, Peter
[14
]
Veereschild, Mike
[14
]
Bak, Maarten
[2
,15
]
Frederix, Geert
[16
]
de Haan, Lieuwe
[6
,7
,17
]
van Os, Jim
[1
,2
,18
]
Cahn, Wiepke
[1
,11
]
Luykx, Jurjen J.
[1
,14
,19
]
机构:
[1] Univ Utrecht, Univ Med Ctr Utrecht, UMC Utrecht Brain Ctr, Dept Psychiat, HP A01-126,POB 85500, NL-3508 GA Utrecht, Netherlands
[2] Maastricht Univ, Sch Mental Hlth & Neurosci, Dept Psychiat & Neuropsychol, Med Ctr, Maastricht, Netherlands
[3] Yale Univ, Sch Med, Dept Psychiat, New Haven, CT USA
[4] Univ Utrecht, Univ Med Ctr Utrecht, Julius Ctr, Dept Biostat & Res Support, Utrecht, Netherlands
[5] GGz Cent Mental Hlth, Amersfoort, Netherlands
[6] Univ Amsterdam, Amsterdam Univ, Dept Psychiat, Med Ctr, Amsterdam, Netherlands
[7] Univ Amsterdam, Amsterdam Univ, Dept Anat & Neurosci, Med Ctr, Amsterdam, Netherlands
[8] GGZinGeest Mental Hlth, Amsterdam, Netherlands
[9] Univ Utrecht, Univ Med Ctr Utrecht, Dept Clin Pharm, Utrecht, Netherlands
[10] Univ Utrecht, Univ Med Ctr Utrecht, Dept Rehabil Physiotherapy Sci & Sport, Utrecht, Netherlands
[11] Altrecht Mental Hlth Care Inst, Utrecht, Netherlands
[12] Inholland Univ Appl Sci, Dept Nursing, Interprofess Mental Hlth Care, Amsterdam, Netherlands
[13] GGZ Rivierduinen, Oegstgeest, Netherlands
[14] GGNet Mental Hlth, Warnsveld, Netherlands
[15] Mondriaan Mental Hlth, Maastricht, Netherlands
[16] Univ Utrecht, Univ Med Ctr Utrecht, Julius Ctr, Dept Publ Hlth, Utrecht, Netherlands
[17] Arkin GGZ, Amsterdam, Netherlands
[18] Kings Coll London, Inst Psychiat Psychol & Neurosci, Dept Psychosis Studies, London, England
[19] Univ Utrecht, Univ Med Ctr Utrecht, UMC Utrecht Brain Ctr, Dept Translat Neurosci, Utrecht, Netherlands
关键词:
Antipsychotic-induced weight gain (AiWG);
Schizophrenia;
Metformin;
Lifestyle;
SEVERE MENTAL-ILLNESS;
METABOLIC SYNDROME;
PHYSICAL-ACTIVITY;
SCHIZOPHRENIA;
RISK;
QUESTIONNAIRE;
INTERVENTION;
ORGANIZATION;
INDIVIDUALS;
INSTRUMENT;
D O I:
10.1186/s12888-020-02992-4
中图分类号:
R749 [精神病学];
学科分类号:
100205 ;
摘要:
Background: Antipsychotic-induced Weight Gain (AiWG) is a debilitating and common adverse effect of antipsychotics. AiWG negatively impacts life expectancy, quality of life, treatment adherence, likelihood of developing type-2 diabetes and readmission. Treatment of AiWG is currently challenging, and there is no consensus on the optimal management strategy. In this study, we aim to evaluate the use of metformin for the treatment of AiWG by comparing metformin with placebo in those receiving treatment as usual, which includes a lifestyle intervention. Methods: In this randomized, double-blind, multicenter, placebo-controlled, pragmatic trial with a follow-up of 52 weeks, we aim to include 256 overweight participants (Body Mass Index (BMI) > 25 kg/m(2)) of at least 16 years of age. Patients are eligible if they have been diagnosed with schizophrenia spectrum disorder and if they have been using an antipsychotic for at least three months. Participants will be randomized with a 1:1 allocation to placebo or metformin, and will be treated for a total of 26 weeks. Metformin will be started at 500 mg b.i.d. and escalated to 1000 mg b.i.d. 2 weeks thereafter (up to a maximum of 2000 mg daily). In addition, all participants will undergo a lifestyle intervention as part of the usual treatment consisting of a combination of an exercise program and dietary consultations. The primary outcome measure is difference in body weight as a continuous trait between the two arms from treatment inception until 26 weeks of treatment, compared to baseline. Secondary outcome measures include: 1) Any element of metabolic syndrome (MetS); 2) Response, defined as >= 5% body weight loss at 26 weeks relative to treatment inception; 3) Quality of life; 4) General mental and physical health; and 5) Cost-effectiveness. Finally, we aim to assess whether genetic liability to BMI and MetS may help estimate the amount of weight reduction following initiation of metformin treatment. Discussion: The pragmatic design of the current trial allows for a comparison of the efficacy and safety of metformin in combination with a lifestyle intervention in the treatment of AiWG, facilitating the development of guidelines on the interventions for this major health problem.
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