| Literature DB >> 29615407 |
Laura Chiavaroli1,2, Cyril W C Kendall1,2,3, Catherine R Braunstein1,2, Sonia Blanco Mejia1,2, Lawrence A Leiter1,2,4,5,6, David J A Jenkins1,2,4,5,6, John L Sievenpiper1,2,4,5,6.
Abstract
OBJECTIVE: Carbohydrate staples such as pasta have been implicated in the obesity epidemic. It is unclear whether pasta contributes to weight gain or like other low-glycaemic index (GI) foods contributes to weight loss. We synthesised the evidence of the effect of pasta on measures of adiposity.Entities:
Keywords: body weight; glycaemic index; glycemic index; pasta; systematic review and meta-analysis; weight loss
Mesh:
Substances:
Year: 2018 PMID: 29615407 PMCID: PMC5884373 DOI: 10.1136/bmjopen-2017-019438
Source DB: PubMed Journal: BMJ Open ISSN: 2044-6055 Impact factor: 2.692
Figure 1Literature search. BMI, body mass index; GI, glycaemic index.
Summary of trial characteristics
| Trial characteristics* | All | Neutral energy balance | Negative energy balance |
| Trial no (n) | 32 | 23 | 9 |
| Trial size (total, range) | 2448 (8–250) | 1989 (8–250) | 459 (13–123) |
| Male:female† (%) | 40:60 | 47:53 | 27:73 |
| Age (years) | 50 (40–58) | 52.0 (42.1–59.5) | 49.5 (34.2–53.0) |
| Metabolic phenotype (OW/OB:DM:CHD) (%) | 66:31:3 | 57:39:4 | 89:11:0 |
| Setting (IP:OP) (%) | 3:97 | 4:96 | 0:100 |
| Baseline body weight (kg)‡ | 85.5 (80.0–91.9) | 84.1 (79.5–87.5) | 92.5 (86.1–93.9) |
| Baseline BMI (kg/m2)§ | 30.4 (28.2–32.0) | 29.5 (27.4–31.4) | 31.7 (30.1–32.9) |
| Study design (C:P) (%) | 19:81 | 26:74 | 0:100 |
| Dose pasta (servings/week)¶ | 3.3 (2.3–3.5) | 3.4 (2.9–4.1) | 2.3 (2.3–3.5) |
| GI in pasta/LGI group | 49.0 (44.0–55.1) | 46.5 (49.9–55.5) | 44.0 (42.3–49.4) |
| GI in higher-GI group | 62.5 (61.6–63.2) | 63.3 (60.1–64.4) | 61.0 (59.2–66.6) |
| Calorie reduction in pasta/LGI group (kcal)** | −179 (−90 to −448) | −165 (−74 to −313) | −447 (−134 to −594) |
| Calorie reduction in higher-GI group (kcal)** | −181 (−93 to −401) | −160 (−40 to −248) | −470 (−172 to −561) |
| Feeding control (Met:Suppl:DA) (%) | 6:44:50 | 4:48:48 | 11:33:56 |
| Follow-up duration (weeks) | 12 (9–21) | 12 (6–24) | 12 (10–21) |
| Funding sources | 47:9:25:19 | 44:13:26:17 | 56:0:22:22 |
*Median (IQR), unless otherwise indicated.
†24/32 trials provided data on sex.
‡30/32 trials reported baseline body weight.
§28/32 trials reported baseline BMI.
¶11/32 trials provided data from which dose could be approximated.
**20/32 trials provided data from which to approximate changes in caloric intake.
A, agency; AI, agency and industry; BMI, body mass index; C, cross-over design; CHD, coronary heart disease; DA, dietary advice; DM, diabetes; GI, glycaemic index; I, industry; IP, inpatient; LGI, low glycaemic index; Met, metabolic; NR, not reported; OB, obese; OP, outpatient; OW, overweight; P, parallel design; Suppl, supplemented/provision of certain food.
Figure 2Forest plot of randomised controlled trials investigating the effects of pasta in the context of low-GI dietary patterns on body weight (kg). n=2448. Data are expressed as mean differences represented by a square and 95% CIs by the line through the square. 95% CIs exceeding the plot’s bounds are represented by an arrowhead. Pooled effect estimates are represented by diamonds and were estimated with the use of generic inverse variance random effects models. Between-study heterogeneity was assessed by the Cochran Q statistic, where P<0.10 is considered statistically significant, and quantified by the I2 statistic, where I2≥50% is considered evidence of substantial heterogeneity. CHD, coronary heart disease; CHO, carbohydrate; GI, glycaemic index; HGI, higher-glycaemic index diet; LGI, low-glycaemic index diet; MUFA, monounsaturated fatty acid; Pro, protein.
Figure 3Plot of the pooled effect estimates from randomised controlled trials investigating the effects of pasta in the context of low-GI dietary patterns on global and abdominal markers of adiposity. Pooled effect estimates are represented by diamonds and were estimated with the use of generic inverse-variance random-effects models. Between-study heterogeneity was assessed by the Cochran Q statistic, where P<0.10 is considered statistically significant, and quantified by the I2 statistic where I2 ≥50% is considered evidence of substantial heterogeneity. BMI, body mass index; GI, glycaemic index; HGI, higher-glycaemic index diet; LGI, low-glycaemic index diet.