| Literature DB >> 31481903 |
Ewa Tumiel1, Adam Wichniak1, Marek Jarema1, Michał Lew-Starowicz1,2.
Abstract
Background: People suffering from schizophrenia are notably vulnerable to cardiometabolic risk factors (CMRF), such as obesity, high blood pressure, hyperglycemia and insulin resistance, high serum triglycerides, and low serum high-density lipoprotein (HDL), which are related to increased mortality and decreased quality of life. The increased risk of "metabolic syndrome" (MS) is related to low physical activity, an unhealthy diet, and side effects of antipsychotic drugs. Nonpharmacological interventions seem to be important in the prevention and therapy of MS. Aim: This paper provides an overview of published studies and a critical analysis of pilot programs involving nonpharmacological measures aimed at prevention and treatment of CMRF in patients with schizophrenia. Material and Method: We searched the PubMed, PsycARTICLES, and Cochrane Library databases to identify clinical trials. We included full-text studies that met the following criteria: age > 18 years, a diagnosis of schizophrenia or schizoaffective disorder, and monitored parameters associated with MS.Entities:
Keywords: cardiometabolic risk factors; diet; exercise; metabolic syndrome; psychotherapy; schizophrenia
Year: 2019 PMID: 31481903 PMCID: PMC6709656 DOI: 10.3389/fpsyt.2019.00566
Source DB: PubMed Journal: Front Psychiatry ISSN: 1664-0640 Impact factor: 4.157
Figure 1Flow diagram for the search results.
Short-term non-pharmacological interventions for the treatment of cardiometabolic risk factors in people with schizophrenia.
| Authors (year) | Study sample (N) | Drop-out % | Study group and design of the study | Intervention | Outcome measures, assessment tools | Duration (weeks) | Effects (statistically significant) |
|---|---|---|---|---|---|---|---|
|
| 64 | 0 | RCT | Seven educational and motivational meetings. | Body weight; BMI; WC | 12 | Significant differences between the experimental group and a control after the intervention: |
|
| 25 | 24 | Control group | HIT(n = 12) vs. CG (n = 7) | VO2peak; e | 8 | HIT Group: |
|
| 16 | 0 | No control group, no randomization | Daily measurement of the activity using a pedometer. | BMI; weight; HR; BP; 6-MWT | 10 | The correlation between the number of steps and lengthening the distance in 6-MWT |
|
| 24 | 8,3 | No control group, no randomization | Cycling 90 min/week | Weight; BMI; muscle mass; total fat; visceral fat | 12 | Improving cardiovascular fitness as indicated by the step test (t = 4.093, p = 0.001) |
|
| 20 | 20 | No control group, no randomization | HIIT | BMI; body weight; HR; BP; PP; MAP; PP; WC; HC; WC/HC; | 8 | Body weight: 75.17 vs. 73.72 (p = 0.022) |
|
| 32 | 19 | No control group, no randomization | Training at the gym | BMI; WC; BP; 6-MWT; vertical jump | 10 | Improvement in the IPAQ score: 459 vs. 945 (p > 0.001) |
|
| 30 | 3 | Control group (healthy) (n = 15) | Personalized diet | BMI; body weight; WC; HC; WC/HC; glucose; lipid profile; leptin; ghrelin; insulin; HOMA-IR; body fat percentage | 8 | p < 0.05 |
|
| 13 | 31 | Schizophrenia/Schizoaffective disorder | Moderate-to-vigorous intensity exercise | Skinfolds; BMI; WC; lipid profile; HR; BP; maximum exercise test on an electronically braked cycle ergometer | 12 | 2-fold increase in the duration of training |
|
| 63 | ND | Control group n = 30 | Mild/intensity exercises | WC; HC; WHR; Body weight; BMI; BP | 10 | Body weight: 78,1 vs. 76,7 (p < 0.01) |
|
| 63 | 38 | Control group | 24 weeks | Wpeak; VO2peak; BMI; body fat percentage; WC; RR; lipid profile; glucose | 24 | Increased Wpeak of 7.6% (P < 0.01) |
|
| 8 | 0 | No control group, no randomization | Walking 30 min/day. | Body weight; BMI; VO2 max; 6-MWT | 24 | Body weight: 75,5 vs. 73,7 (2.4%, p < 0,05) |
|
| 17 | 18% | No control group, no randomization | Walking/jogging with increasing intensity 3x/week. | Glucose; AST, ALT, bilirubin; lipid profile; EKG; body weight; BP; HR; | 10 | Increase in HR: 84.9 vs. 90.6 (p = 0.05) |
|
| 265 | 29% | Control group (standard care) | 3 groups: | Body weight; BMI; WC; HR; BP; HDL-C; TG; glucose; HbA1c | 48 | Group C showed favorable |
|
| 185 | ND | No control group, | Fitness program: | Weight; BMI; fat percentage; circumference (abdomen, thigh, pelvis, arm) | 36 | The mean BMI at the end of study was reduced to 28.39 ± 4.6, which was significantly lower (t = 3.352; p = 0.002) than at baseline. |
|
| 183 | Schizophrenia | Individual guidance, group sessions | Weight, height, WC, body fat percentage (fat%), | 120 | Significant improvement in consumption of soft drinks (P = 0.001) and fast food (P = 0.009) | |
|
| 54 | Schizophrenia | Individual guidance, group sessions | Weight; height; WC; body fat percentage (fat%); | 120 | WC 11.4 (0.7–22.1) p = 0.037 (only women) | |
|
| 19 | 0 | No control group | Group exercise | TG; total cholesterol; LDL; HDL | 12 | No significant changes |
|
| 33 | 0 | Training group n = 18 | Week moderate intensity | Body weight | 8 | Reduced bodyweight by 2.3 kg |
|
| 33 | 21% | Control group n = 17 | Two groups: | RER | 12 | Significantly increased: peak VO2, VCO2, watts, VE, and dyspnea score |
|
| 6 | 0 | Chronic paranoid schizophrenia (n = 4) | Treadmills | Body weight, BMI, VO2max ml/kg/min | 6 | 17% improvement in cardiovascular fitness on average (change in VO2max |
BP, blood pressure; HR, heart rate; PP, pulse pressure; RR, the inverse of heart rate; MAP, mean arterial pressure; HRV, heart rate variability; RER, respiratory exchange ratio; SBP, systolic blood pressure; DBP, diastolic blood pressure; BMI, body mass index; WC, waist circumference; HC, hit circumference; WHR, waist/hip ratio; VAI, visceral adiposity index; 6-MWT, 6-min walking test; VO2 max/VO2peak, maximal/peak oxygen uptake; Wpeak, peak power output; VE, peak minute ventilation; Vt, peak tidal volume; PetCO2, tidal carbon dioxide pressure; VCO2, rate of carbon dioxide production at peak; OGTT, oral glucose tolerance test; HIT, high aerobic intensity training; HIIT, High Intensity Interval Training; CG, computer games; CG, control group; Hs-CRP, high-sensitivity serum C-reactive protein; HOMA-IR and HOMA-β, homeostatic model assessment-measured insulin resistance and β- cells; HbA1c, glycated hemoglobin; BDNF, brain-derived neurotrophic factor; TNF-α, tumor necrosis factor; IL-6, interleukin 6; AST, aspartate aminotransferase; ALT, alanine transaminase; RCT, Random Control Trial; e net, net mechanical efficiency of walking; HDL, high-density lipoproteins; LDL, low-density lipoprotein; TG, triglyceride; EGG, electrocardiography; PANSS, Positive and Negative Syndrome Scale; PANS, Positive and Negative Affect Schedule; BDI, Beck Depression Inventory; BAI, The Beck Anxiety Inventory; SIAS, Social Interaction Anxiety Scale; GAF, Global Assessment of Functioning; SOFAS, Social and Occupational Functioning Assessment Scale; CGI-S, The Clinical Global Impression-Severity scale; WHODAS 2.0, WHO Disability Assessment Schedule 2.0; WHOQOL-BREF, Brief Form of World Health Organization Quality of Life Questionnaire; HRQOL, Health-Related Quality of Life; IPAQ, The International Physical Activity Questionnaire; CDSS, The Calgary Depression Scale for Schizophrenia; GLTEQ, Godin Shephard Leisure Time Exercise Questionnaire; MADRS, Montgomery–Åsberg Depression Rating Scale; BPRS, The Brief Psychiatric Rating Scale; MSPSS, Multidimensional Scale of Perceived Social Support; CSQ-8, The Client Satisfaction Questionnaire; SANS, The Scale for the Assessment of Negative Symptoms; MOS Short-Form 36, The Short Form (36) Health Survey.