Volume 4, Issue 6 p. 995-1014
Systematic review
Open Access

Change in emotional eating after bariatric surgery: systematic review and meta-analysis

L. Y. Wong

L. Y. Wong

Department of Medicine (Austin), University of Melbourne, Melbourne, Victoria, Australia

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N. Zafari

N. Zafari

Department of Medicine (Austin), University of Melbourne, Melbourne, Victoria, Australia

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L. Churilov

L. Churilov

Department of Medicine (Austin), University of Melbourne, Melbourne, Victoria, Australia

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L. Stammers

L. Stammers

Department of Medicine (Austin), University of Melbourne, Melbourne, Victoria, Australia

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S. Price

S. Price

Department of Medicine (Austin), University of Melbourne, Melbourne, Victoria, Australia

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E. I. Ekinci

E. I. Ekinci

Department of Medicine (Austin), University of Melbourne, Melbourne, Victoria, Australia

Department of Endocrinology, Austin Health, Melbourne, Victoria, Australia

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P. Sumithran

Corresponding Author

P. Sumithran

Department of Medicine (Austin), University of Melbourne, Melbourne, Victoria, Australia

Department of Endocrinology, Austin Health, Melbourne, Victoria, Australia

Correspondence to: Dr P. Sumithran, Level 1, Centaur Building, Repatriation Hospital, 300 Waterdale Road, Heidelberg Heights, Victoria 3081 Australia (e-mail: [email protected])Search for more papers by this author
First published: 16 July 2020
Citations: 8

Funding information

No funding

Abstract

en

Background

The effect of bariatric surgery on ‘emotional eating’ (EE) in people with obesity is unclear. This systematic review and meta-analysis aimed to examine changes in self-reported emotional eating behaviour after bariatric surgery.

Methods

Fifteen electronic databases were searched from inception to August 2019. Included studies encompassed patients undergoing primary bariatric surgery, quantitatively assessed EE, and reported EE scores before and after surgery in the same participants. Studies were excluded if they were not in English or available in full text. The systematic review and meta-analysis were conducted according to the PRISMA guidelines. Random-effects models were used for quantitative analysis. Study quality was assessed using the National Heart, Lung, and Blood Institute quality assessment tool for before–after (pre–post) studies with no control group.

Results

Some 23 studies containing 6749 participants were included in the qualitative synthesis, with follow-up of from 2 weeks to 48 months. EE scores decreased to 12 months after surgery. Results were mixed beyond 12 months. Quantitative synthesis of 17 studies (2811 participants) found that EE scores decreased by a standardized mean difference of 1·09 (95 per cent c.i. 0·76 to 1·42) 4–18 months after surgery, indicating a large effect size.

Conclusion

Bariatric surgery may mitigate the tendency to eat in response to emotions in the short to medium term.

Abstract

es

Antecedentes

El efecto de la cirugía bariátrica sobre la “alimentación emocional” (emotional eating, EE) en personas con obesidad no esta claro. Esta revisión sistemática y metaanálisis tuvo como objetivo examinar los cambios en el comportamiento de la alimentación emocional referida por los mismos pacientes después de cirugía bariátrica.

Métodos

Se realizó una búsqueda en 15 bases de datos electrónicas desde el inicio de las mismas hasta agosto de 2019. Los estudios seleccionados incluían pacientes con cirugía bariátrica primaria, EE evaluada de forma cuantitativa, y descripción de las puntuaciones de EE antes y después de la cirugía en los mismos participantes. Se excluyeron estudios que no estuvieran publicados en inglés o si no se disponía del texto completo. Esta revisión sistemática y metaanálisis se llevó a cabo de acuerdo con las recomendaciones PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses). Se utilizó un modelo de efectos aleatorios para el análisis cuantitativo. La calidad de los estudios individuales se evaluó utilizando la herramienta de evaluación de la calidad NHLBI para estudios de antes-después (pre-post) sin grupo control.

Resultados

Se incluyeron un total de 23 estudios con 6.749 participantes en la síntesis cualitativa, y un seguimiento de 2 semanas a 48 meses. Las puntuaciones EE disminuyeron a los 12 meses postoperatorios. Los resultados fueron variados más allá de los 12 meses. La síntesis cuantitativa de 17 estudios (2.811 participantes) encontró que las puntuaciones EE disminuyeron con una diferencia de medias ponderada de 1,09 (i.c. del 95% 0,76, 1,42) a los 4-18 meses tras la operación, lo que indica una magnitud de efecto grande.

Conclusión

La cirugía bariátrica puede atenuar la tendencia a comer en respuesta a las emociones en el corto y medio plazo.

Introduction

Bariatric surgery is the most effective treatment for obesity, resulting in a mean weight loss of 26–38 per cent at 3–5 years, compared with 0–3 per cent for lifestyle interventions1, 2. Although the exact mechanisms are not understood completely, it is thought that postoperative neurohormonal changes promote sustained weight loss by contributing to control of hunger and enhanced meal-induced satiety, particularly after sleeve gastrectomy (SG) and Roux-en-Y gastric bypass (RYGB). The efficacy of bariatric surgery relative to pharmaceutical modulation of hunger and satiety (mean placebo-subtracted weight losses of 3–8 per cent at 12 months3) raises the possibility that bariatric surgery has wider-ranging effects on eating behaviour. This is supported by reports of alterations in food preferences (such as reduced appeal of sweet, fatty foods) and reduced cravings after bariatric surgery4, 5.

Consumption of highly palatable foods in response to emotional states (‘emotional eating’) affects 15–47 per cent of the general population, and as much as 63 per cent of people with obesity6. This is concerning, as emotional eating is associated with food preoccupation7, loss of control over eating8, 9, overeating10-12 and reduced success of obesity treatment13. It is not clear whether emotional eating behaviour is altered after bariatric surgery, owing to considerable heterogeneity between studies in methods of assessing eating behaviour, types of bariatric surgery performed, and timing of postoperative follow-up.

This systematic review and meta-analysis aimed to review comprehensively emotional eating changes following bariatric surgery in studies that used pre–post assessments of eating behaviour. It was hypothesized that emotional eating scores would be lower after bariatric surgery than before surgery.

Methods

This systematic review and meta-analysis was guided by the PRISMA statement14 and MOOSE guidelines15. It was registered on PROSPERO (identification number CRD42019134042).

Eligibility criteria

Studies were considered eligible if they included patients of any age and sex undergoing primary bariatric surgery, quantitatively assessed emotional eating, and reported emotional eating scores before and after surgery in the same participants. Studies were excluded if they included only revisional surgery, did not include human participants, were not in the English language, or were not published as full-text versions (for example, conference abstracts).

Search strategy

Fifteen databases (Table S1, supporting information) were searched up to 16 August 2019 by one author and a clinical librarian. The following search terms were adapted for each source and included Medical Subject Headings (MeSH) and keywords such as ‘emotion* eat*’, ‘comfort eat*’, ‘stress eat’, ‘eating behaviour’, ‘bariatric surgery’, ‘sleeve gastrectomy’, ‘RYGB’, ‘biliopancreatic diversion’, ‘LAGB’ and ‘gastric band*’. No limits were placed on year of publication, publication status, study design, sample size, language or full-text availability. Animal studies were excluded. The search results from all the databases were downloaded and electronically managed using EndNote X9™ (Clarivate Analytics, Philadelphia, Pennsylvania, USA).

Study selection

Duplicates were removed and references imported into Rayyan16 (http://rayyan.qcri.org) for screening of titles and abstracts by two authors independently. Relevant full-text articles were retrieved, and two authors independently reviewed each according to the inclusion and exclusion criteria. Conflicts were resolved by consensus following discussion. Additional papers were found via hand-searches of reference lists of full-text papers and key systematic reviews.

Data extraction

A data extraction sheet was created and one author extracted the following information: study characteristics (author, year of publication); design (aim, sample size, setting, type of intervention, follow-up, tools used to identify emotional eating); participant characteristics (age, sex, BMI); description of surgery; and emotional eating scores before and after surgery. In addition, 11 authors were contacted to retrieve mean(s.d.) values of emotional eating assessments, of whom five responded. Graphical outcome data for two studies were estimated using PlotDigitizer™ 2.6.8 (SourceForge; Slashdot Media, La Jolla, California, USA)17.

Quality assessment

Two authors independently assessed study quality using the National Heart, Lung, and Blood Institute (NHLBI) ‘quality assessment tool for before–after (pre–post) studies with no control group’18, to give each an overall quality rating of poor, fair or good. Disagreements were resolved by consensus.

Statistical analysis

Meta-analysis was conducted using Review Manager™ 5.3 (The Cochrane Collaboration, The Nordic Cochrane Centre, Copenhagen, Denmark)19. The primary outcome was the standardized mean difference (SMD) of emotional eating scores after surgery. Review Manager™ facilitates the input of data in several formats (for example, mean, mean difference (MD), standard deviation (s.d.), standard error, 95 per cent c.i., P value), which can be converted into SMD and 95 per cent c.i. for quantitative synthesis. Study outcomes were calculated to two decimal places, unless otherwise reported in the original study. Studies were pooled for meta-analysis if sufficient outcome data could be obtained or estimated, and if postsurgical assessment occurred within 4–18 months (the longest time point was used if multiple were reported). This time frame was chosen as maximum weight loss occurs up to 1–2 years after bariatric surgery.

As emotional eating was assessed using a number of different tools, quantitative assessment outcomes were reported as SMDs to facilitate comparison between different scales. Effect sizes were considered small, medium and large for SMDs of 0·2, 0·5 and 0·8 respectively20. Pooled estimates of study outcomes were obtained using an inverse-variance weighted random-effects model. All studies that satisfied inclusion criteria for quantitative synthesis were included in one meta-analysis, followed by prespecified subgroup analyses based on type of surgery. To avoid confounding between- and within-study variability, subgroup analyses by surgical type were based on individual questionnaires that were used in more than one study: the Dutch Eating Behaviour Questionnaire (DEBQ), and the 18- and 21-item revisions of the Three-Factor Eating Questionnaire (TFEQ). For studies that divided participants receiving the same operation into subgroups, subgroups were combined to form one group using the sample size and mean(s.d.) values for meta-analysis. Heterogeneity was quantified using the I2 test, where values greater than 25 per cent, more than 50 per cent and above 75 per cent represent low, moderate and high heterogeneity respectively21. Publication bias was evaluated by visual interpretation of funnel plots and Egger's regression test, with significance set at P < 0·050. Statistical analyses were conducted in Review Manager™ 5.3 and STATA® version IC15.1 (StataCorp, College Station, Texas, USA).

Sensitivity analysis

A number of sensitivity analyses were performed. These were undertaken initially to assess the robustness of the conclusion by changing the eligibility criteria (removing studies that contained only participants aged 18 years or less, those that included only female patients, and those rated as poor quality). Between-study heterogeneity was assessed by stratifying studies based on the questionnaire used to assess emotional eating, and by sequentially excluding individual studies from meta-analysis one at a time. Finally, studies were excluded if reported presurgery or postsurgery mean(s.d.) values indicated that emotional eating scores were not distributed normally (if mean minus 3 standard deviations included negative values). Effect sizes, statistical significance and heterogeneity were examined for each analysis to determine whether the summary estimates differed meaningfully from the main analysis.

Results

Screening of databases resulted in 1275 citations, and hand-searching provided an additional five articles. After duplicates were removed, 949 studies remained. Title and abstract screening yielded 80 studies, of which 234, 22-43 were included in the qualitative synthesis and 17 in the meta-analysis (Fig1).

Details are in the caption following the image
PRISMA diagram for the review

Study characteristics

An overview of the study characteristics is provided in Table 1. Twenty were prospective cohort studies4, 22-40, one41 was a retrospective cohort study, and two42, 43 were RCTs. One RCT42 randomized patients with a BMI of 50–60 kg/m2 to either duodenal switch or gastric bypass, and the other43 randomized patients to either lifestyle intervention or usual care after bariatric surgery. A total of 6749 (range 9–4569; mean 293; median 71) surgical participants were involved. One study41 was conducted in an adolescent population, and the remainder included only adults. The mean age range was 16·9–47·1 years and mean preoperative BMI ranged from 36 to 57 kg/m2. Every study had a predominantly female population (range 65–100 per cent). The vast majority of patients underwent RYGB (19 studies, 6140 patients)4, 23-36, 38, 39, 41, 42, seven studies (381 patients)4, 22, 26, 30, 32, 36, 40 investigated SG, three (48 patients)28, 36, 38 examined laparoscopic adjustable gastric banding (LAGB), two (121 patients)37, 43 included vertical banded gastroplasty (VBG), and one each duodenal switch (29 patients)42, biliopancreatic diversion (BPD) (26 patients)28 and anastomosis gastric bypass (4 patients)32.

Table 1. Characteristics of studies included in the qualitative analysis
Reference Setting No. of women* Age (years)‡ Baseline BMI (kg/m2)‡ Procedure†
Alfonsson et al.34 Sweden (n.r.) 101 of 129 (78·3) 42·8(10·52) 42·95(3·98) RYGB (129)
Van der Zwaal et al.35 Netherlands (multicentre) 14 of 14 (100) 44·3(6) 45·2(6·7) RYGB (14)
Monpellier et al.24 Netherlands (single-centre) 3733 of 4569 (81·7) 47·1(10·7) 44·4(5·7) RYGB (4569)
Pepino et al.36 USA (single-centre) 39 of 44 (89) 42·8(10·8) 47·7(8·0) Mixed (RYGB 25, SG 8, LAGB 11)
Subramaniam et al.32 Malaysia (multicentre) 37 of 57 (65) 39·40(10·01) 45·52(9·94) Mixed (RYGB 30, SG 23, 1 anastomosis, gastric bypass–mini gastric bypass 4)
Pepino et al.38 USA (single-centre) 27 of 27 (100) LAGB: 46·8(13·9)¶ LAGB: 48·5(10·5)¶ LAGB (10)
RYGB: 42·1(8·4)¶ RYGB: 46·3(7·7)¶ RYGB (17)
Nance et al.4 USA (single-centre) RYGB: 20 of 23 (87) RYGB: 43·0(9·6) RYGB: 46·9(7·5) RYGB (23)
SG: 7 of 8 (88) SG: 36·6(9·0) SG: 53·3(8·7) SG (8)
Van Hout et al.37 Netherlands (single-centre) 80 of 91 (88) 38·6(8·3) 45·7(5·1) VBG (91)
Papalazarou et al.43 Greece (single-centre) 30 of 30 (100) Lifestyle intervention: 32·7(6·2)¶ Lifestyle intervention: 48·5(8·1)¶ VBG (30)
Usual care group: 33·4(7·7)¶ Usual care group: 49·8(6·2)¶
Holsen et al.40 USA (multicentre) 16 of 18 (89) 38·4(10·1) 41·8(4·5) SG (18)
Järvholm et al.41 Sweden (multicentre) 55 of 82 (67) 16·9(1·15) 45·4(6·08) RYGB (82)
Willmer et al.33 Sweden (multicentre) 63 of 63 (100) 39(5·5) 39·2(3·3) RYGB (63)
Laurenius et al.31 Sweden (n.r.) 28 of 43 (65) 42·6(9·7) 44·5(4·9) RYGB (43)
Turkmen et al.29 Sweden (single-centre) 9 of 9 (100) 31·4(7·41) 47·2(8·85) RYGB (9)
Søvik et al.42 Norway and Sweden (multicentre) RYGB: 23 of 31 (74) RYGB: 35·2(7·0) RYGB: 54·8(3·24) RYGB (31)
DS: 19 of 29 (66) DS: 36·1(5·26) DS: 55·2(3·49) DS (29)
Bryant et al.23 UK (n.r.) 9 of 12 (75) 36(2) 45·3(1·9) RYGB (12)
Petereit et al.25 Lithuania (single-centre) 128 of 180 (71·1) 42·7(10·5) 45·2(6·4) RYGB (180)
Woodard et al.27 USA (single-centre) 28 of 35 (80) 48(11)¶ 48·7(8·3)¶ RYGB (35)
Nasirzadeh et al.26 Canada (multicentre) 658 of 844# (81·2) 45 (38–53)§ 48·6(7·8) Mixed (RYGB 760, SG 84)
Castellini et al.28 Italy (single-centre) LAGB: 23 of 27 (85) LAGB: 43·85(11·36) LAGB: 44·79(5·3) LAGB (27)
RYGB: 28 of 30 (93) RYGB: 43·63(9·83) RYGB: 49·49(6·76) RYGB (30)
BPD: 24 of 26 (92) BPD: 48·84(8·36) BPD: 50·57(6·55) BPD (26)
Dymek et al.39 USA (single-centre) 26 of 32 (81) 39·1(8·47) 56·7(11·5) RYGB (32)
Weineland et al.30 Sweden (single-centre) 171 of 186 (91·9) 42·2(9·3) 36·2(3·6) Mixed (SG 130, RYGB 56)
Sioka et al.22 Greece (single-centre) < 3 months: 7 of 10 (70) < 3 months: 38·2(10·76) < 3 months: 43·68(8·29) SG (110)
3–6 months: 11 of 11 (100) 3–6 months: 38(9·96) 3–6 months: 43·85(5·69)
6–12 months: 7 of 11 (64) 6–12 months: 42·1(10·9) 6–12 months: 45·85(6·13)
1–2 years: 31 of 39 (79) 1–2 years: 39·56(9·15) 1–2 years: 46·05(5·83)
2–3 years: 19 of 23 (83) 2–3 years: 40·39(9·68) 2–3 years: 46·52(6·81)
> 3 years: 11 of 16 (69) > 3 years 38·63(10·83) > 3 years: 44·81(5·63)
  • Values in parentheses are *percentages and †number of patients. ‡Values are mean(s.d.) unless indicated otherwise; §values are mean (i.q.r.). ¶Data converted from originally reported outcome data into mean(s.d.) values using Review Manager 5.3. #Of a total 844 participants, only 810 had their sex recorded (658 women and 152 men). n.r., Not reported; RYGB, Roux-en-Y gastric bypass; SG, sleeve gastrectomy; LAGB, laparoscopic adjustable gastric band; VBG, vertical banded gastroplasty; DS, duodenal switch; BPD, biliopancreatic diversion.

Assessment of emotional eating

Details of outcomes are summarized in Table 2. The timing of postsurgical assessment ranged from 3 days to 48 months, with the most common final duration of follow-up being 12 months (7 studies)23, 25, 27-29, 34, 40. The most common measure of emotional eating was the DEBQ44, used in nine studies4, 24, 32, 35-38, 40, 43. The 21- and 18-item revisions of the original 51-item TFEQ (TFEQ-R2145 and TFEQ-R18)46, 47 were used in six29, 31, 33, 40-42 and three23, 25, 27 studies respectively. The remaining seven studies used a mix of questionnaires, including the Emotional Eating Scale (EES)26, 28, 39, General Food Craving Questionnaire – Trait (GFCQ-T)34, 35, the Yale Emotional Overeating Questionnaire (EOQ)30, and dietician interview22, in which eating patterns were defined by the International Federation for the Surgery of Obesity and Metabolic Disorders (IFSO) European Accreditation Council for Bariatric Surgery.

Table 2. Emotional eating outcomes of studies included in the qualitative analysis
Change from preop. baseline/control§ Trends after surgery§
Reference Questionnaire Assessment time points (months) Outcome* MD P MD P No. analysed of total enrolled (retention rate)#
34 GFCQ-T Preop. 2·27(1·03) n.a. n.a. 129 of 177 (72·9)
1 1·39(0·72) −0·88 (−1·10, −0·66)** < 0·001 n.a. 129 of 177 (72·9)
35 DEBQ and GFCQ-T Preop. DEBQ: 2·53(0·86) n.a. n.a. 14 of 20 (70)
GFCQ-T: 2·97(1·37)
> 24 DEBQ: 2·10(0·72) DEBQ: −0·43 (−1·05, 0·19)** 0·034 n.a. 14 of 20 (70)
GFCQ-T: 2·14(0·80) GFCQ-T: −0·83 (−1·71, 0·05)** 0·035
24 DEBQ Preop. 2·43(0·82) n.a. n.a. 2028 of 4829 (42·0)
15 1·94(0·77) −0·49 (−0·54, −0·44)** ≤ 0·001 n.a. 1939 of 4829 (40·2)
24 2·09(0·78) −0·34 (−0·39, −0·29)** 15 versus 24 months: 0·15 (0·10, 0·20)** ≤ 0·001 1401 of 4829 (29·0)
36 2·27(0·82) −0·16 (−0·25, −0·07)** 24 versus 36 months: 0·18 (0·09, 0·27)** > 0·05 388 of 4829 (8·0)
48 2·35(0·86) −0·08 (−0·24, 0·08)** 36 versus 48 months: 0·08 (−0·09, 0·25)** > 0·05 112 of 4829 (2·3)
36 DEBQ Preop. 2·73(0·97)†† n.a. n.a. 44 of 51 (86)
After about 20% (range 15–28%) surgery-induced weight loss (within 9 months) 1·95(0·80)†† −0·78 (−1·15, −0·41)** < 0·001 n.a. 44 of 51 (86)
32 DEBQ Preop. 2·06(0·94) n.a. n.a. 57 of 80 (71)
3 1·64(0·80) −0·42 (−0·78, −0·06)** n.a. 45 of 80 (56)
6 1·81(0·81) −0·25 (−0·63, 0·13)** 3 versus 6 months: 0·17 (−0·19, 0·53)** 36 of 80 (45)
38 DEBQ Preop. RYGB: 2·8(0·8) n.a. n.a. RYGB: 17 of 17 (100)††
LAGB: 3·2(1·0) LAGB: 10 of 10 (100)††
After about 20% surgery-induced weight loss (within 9 months) RYGB: 1·9(0·7) RYGB: −0·90 (−1·41, −0·39)** n.a. RYGB: 17 of 17 (100)††
LAGB: 2·3(1·0) LAGB: −0·90 (−1·78, −0·023)** < 0·001 LAGB: 10 of 10 (100)††
4 DEBQ Preop. SG: 2·8(0·9) n.a. n.a. SG: 8 of 8 (100)††
RYGB: 2·6(0·9) RYGB: 23 of 23 (100)††
After about 20% surgery-induced weight loss SG: 2·2(0·6) SG: −0·6 (−1·04, −0·16)** n.a. SG: 8 of 8 (100)††
RYGB: 1·8(0·7) RYGB: −0·80 (−1·66, 0·07)** RYGB: 23 of 23 (100)††
37 DEBQ Preop. 2·4(0·8) n.a. n.a. 81 of 91 (89)
6 1·9(0·8) −0·50 (−0·75, −0·25)** ≤ 0·01 n.a. 81 of 91 (89)
12 2·0(0·8) −0·40 (−0·65, −0·15)** ≤ 0·01 6 versus 12 months: 0·10 (−0·15, 0·35)** > 0·05 81 of 91 (89)
24 2·2(0·9) −0·20 (−0·46, 0·06)** > 0·05 12 versus 24 months: 0·20 (0·06, 0·46)** > 0·05 81 of 91 (89)
43 DEBQ Preop. Usual care: 3·2(0·77)** n.a. n.a. Usual care: 15 of 15 (100)††
Lifestyle: 3·6(0·77)** Lifestyle: 15 of 15 (100)††
3 Usual care: 2·6(0·39)** −0·60 (−1·0, −0·16)** n.a. Usual care: 15 of 15 (100)††
Lifestyle: 2·6(0·39)** −1·00 (−1·44, −0·56)** Lifestyle: 15 of 15 (100)††
12 Usual care: 2·5(0·77)** −0·70 (−1·13, −0·15)** 3 versus 12 months: −0·10 (−0·54, 0·34)** Usual care: 15 of 15 (100)††
Lifestyle: 2·5(0·39)** −1·10 (−1·54, −0·66)** 3 versus 12 months: −0·10 (−0·38, 0·18)** Lifestyle: 15 of 15 (100)††
36 Usual care: 3·2(0·39)** −0·00 (−0·44, 0·44)** 12 versus 36 months: 0·65 (0·58, 0·72)** Usual care: 15 of 15 (100)††
Lifestyle: 3·1(0·39)** −0·50 (−0·94, −0·06)** 12 versus 36 months: 0·60 (0·32, 0·88)** Lifestyle: 15 of 15 (100)††
40 DEBQ and TFEQ-R21 Preop. DEBQ: 3·2(0·7) n.a. n.a. 18 of 20 (90)
TFEQ-R21: 60·2(24·8)
12 DEBQ: 1·9(0·9) DEBQ: −1·30 (−1·83, −0·77)** < 0·001 n.a. 18 of 20 (90)
TFEQ-R21: 27·5(22·4) TFEQ-R21: −32·70 (−44·16, -21·24)** < 0·001
41 TFEQ-R21 Preop. Mixed model: 40·6 (35·4, 45·8)† n.a. n.a. 81 of 82 (99)
12 Mixed model: 20·8 (15·7, 25·8)† Mixed model: −19·9 (−27·7, −12·0)† n.a. 81 of 82 (99)
24 Mixed model: 24·9 (19·6, 30·2)† Mixed model: −15·7 (−24·2, −7·3)† 12 versus 24 months, mixed model: 4·1 (−4·1, 12·3)† 73 of 82 (89)
33 TFEQ-R21 Preop. 15·2(n.r.) n.a. n.a. 52 of 63 (83)
9 9·9(n.r.) −5·31 (−6·66, −3·96) ≤ 0·001 n.a. 52 of 63 (83)
31 TFEQ-R21 Preop. 53·7 (46·8, 60·7)†‡‡ n.a. n.a. 43 of 47 (91)
6 weeks 27·4 (20·4, 34·5)†‡‡ −26·3 (−36·9, −15·6)** < 0·001 n.a. RYGB: 42 of 47 (89)
12 27·1 (19·3, 34·8)†‡‡ −26·6 (−36·6, −16·6)** < 0·001 6 weeks versus 12 months: −0·30 (−10·40, 9·77)** RYGB: 27 of 47 (57)
24 38·8 (29·8, 47·9)†‡‡ −14·90 (−21·99, −7·81)** 0·046 12 versus 24 months: 11·70 (3·92, 19·50)** RYGB: 34 of 47 (72)
29 TFEQ-R21 Preop. 47·90(27·56) n.a. n.a. 9 of 9 (100)**
6 32·06(27·46) −15·84 (−42·0, 10·36)** n.a. 8 of 9 (89)§§
12 33·76 (23·96) −14·14 (−38·63, 10·35)** 6 versus 12 months: −1·70 (−25·94, 29·34)** 8 of 9 (89)§§
42 TFEQ-R21 Preop. RYGB: 44·4 (34·1, 54·8)†¶¶ n.a. n.a. RYGB: 31 of 31 (100)
DS: 50·0 (39·8, 60·2)†¶¶ DS: 29 of 29 (100)
12 RYGB: 36·4 (26·1, 46·8)†¶¶ RYGB: −8·00 (−22·04, 6·04)** < 0·05 n.a. RYGB: 31 of 31 (100)
DS: 28·8 (18·1, 39·5)†¶¶ DS: −21·20 (−35·34, −7·06)** < 0·05 DS: 29 of 29 (100)
24 RYGB: 35·1 (25·2, 45·0)†¶¶ RYGB: −9·30 (−23·04, 4·44)** < 0·05 12 versus 24 months (RYGB): −1·3 (−15·0, 12·4)** 0·853 RYGB: 31 of 31 (100)##
DS: 32·5 (22·2, 42·9)†¶¶ DS: −17·5 (−31·4, −3·6)** < 0·05 12 versus 24 months (DS): 3·7 (−11·2, 18·6)** DS: 29 of 29 (100)##
23 TFEQ-R18 Preop. 58·89 (33·15) n.a. n.a. 12 of 14 (86)
3 days 61·11 (31·25) 2·22 (−25·06, 29·50)** > 0·05 n.a. 12 of 14 (86)
2 37·04 (24·77) −21·85 (−46·63, 2·93)** > 0·05 3 days versus 2 months: −24·07 (−47·94, 3·15)** 12 of 14 (86)
12 37·37 (24·48) −21·52 (−46·19, 3·152)** > 0·05 2 versus 12 months: 0·33 (−20·52, 21·18)** 12 of 14 (86)
25 TFEQ-R18 Preop. 28·2(n.r.) n.a. n.a. 180 of 180 (100)‡‡
12 17·2(n.r.) < 0·001 n.a. 180 of 180 (100)‡‡
27 TFEQ-R18 Preop. 56(6)‡ n.a. n.a. 35 of 35 (100)‡‡
12 25(5)‡ −51·0 (−66·3, −35·7)** < 0·001 n.a. 35 of 35 (100)‡‡
26 EES Preop. n.r. n.a. n.a. 698 of 844 (82·7)
12 n.r. Preop. versus 12 months: −21·4 (−23·7, −19·1) < 0·01 n.a. 549 of 844 (65·0)
24 n.r. Preop. versus 24 months: −20·1 (−22·7, −17·4) < 0·01 12 versus 24 months: 2·0 (0·1, 3·9) < 0·05 382 of 844 (45·3)
36 n.r. Preop. versus 36 months: −21·4 (−25·3, −17·5) < 0·01 12 versus 36 months: 4·9 (1·9, 8·0) < 0·01 240 of 844 (28·4)
24 versus 36 months: 0·2 (−2·3, 2·7) > 0·05
28 EES Preop. LAGB: 46·25(9·88) n.a. n.a. LAGB: 27 of 30 (90)
RYGB: 43·14(12·43) RYGB: 30 of 31 (97)
BPD: 46·76(10·01) BPD: 26 of 30 (87)
12 LAGB: 1·30(1·03) LAGB: −44·95 (−48·70, −41·20)** n.a. LAGB: 27 of 30 (90)
RYGB: 0·75(0·73) RYGB: −42·39 (−46·85, −37·93)** RYGB: 30 of 31 (97)
BPD: 0·79(0·51) BPD: −45·97 (−49·82, −42·12)** BPD: 26 of 30 (87)
39 EES Preop. EES anger subscale: 13·9(10·3) n.a. n.a. 32 of 32 (100)
EES anxiety subscale: 11·3(8·0)
EES depression subscale: 8·9(5·3)
2 weeks EES anger subscale: 5·3(8·4) EES anger subscale: −8·60 (−13·2, −4·00)** n.a. 32 of 32 (100)
EES anxiety subscale: 4·7(7·3) EES anxiety subscale: −6·60 (−10·35, −2·85)**
EES depression subscale: 3·8(5·3) EES depression subscale: −5·10 (−7·70, −2·50)**
6 EES anger subscale: 5·1(9·5) EES anger subscale: −8·80 (−14·3, −3·31)** EES anger subscale, 2 weeks versus 6 months: −0·20 (−5·28, 4·88) 20 of 32 (63)
EES anxiety subscale: 5·4(7·8) EES anxiety subscale: −5·9 (−1·5, −10·3)** EES anxiety subscale, 2 weeks versus 6 months: 0·70 (−3·55, 4·95)
EES depression subscale: 2·5(4·2) EES depression subscale: −6·40 (−9·00, −3·80)** EES depression subscale, 2 weeks versus 6 months: −1·30 (−3·90, 1·30)
30 EOQ Preop. 1·28(1·05) n.a. n.a. 32 of 186 (17·2)
6 0·83(0·88) −0·45 (−0·92, 0·03)** n.a. 32 of 186 (17·2)
22 Interview assessment by dietician††† Preop. < 3 months: 0% n.a. n.a. < 3 months: 10***
3–6 months: 46·8%¶¶ 3–6 months: 11***
6–12 months: 19·5%¶¶ 6–12 months: 11***
1–2 years: 9·0%¶¶ 1–2 years: 39***
2–3 years: 14·5%¶¶ 2–3 years: 23***
> 3 years: 6·0%¶¶ > 3 years: 16***
Postop. < 3 months: 10%¶¶ n.r. n.a. < 3 months: 10***
3–6 months: 0%¶¶ 3–6 months: 11***
6–12 months: 0%¶¶ 6–12 months: 11***
1–2 years: 2·5%¶¶ 1–2 years: 39***
2–3 years: 0%¶¶ 2–3 years: 23***
> 3 years: 12·4%¶¶ > 3 years: 16***
  • *Values are mean(s.d.) unless indicated otherwise; values are †mean (95 per cent c.i.) and ‡mean(s.e.). §Values are mean difference (MD) (95 per cent c.i.) unless indicated otherwise; ¶values are mean (95 per cent c.i.). #Values in parentheses are percentages. **Data converted using Review Manager 5.3 from originally reported outcome data into standard deviation, MD and/or 95 per cent confidence intervals. ††Data received through personal email communication with author. ‡‡For purposes of analysis, retention rate assumed to be 100 per cent as the number of people excluded or loss to follow-up was not reported explicitly; retention rate may be overestimated. §§Ambiguous interpretation of data from study; number of analysed participants may be either eight or nine. ¶¶Results converted electronically from a graphical to numerical format using PlotDigitizer. ##Two participants were lost to follow-up at 24 months, but it was not mentioned which groups this occurred in, or numbers used for analysis. ***Study had a total of 23 dropouts/exclusions, but did not state in which groups these dropouts occurred; these patients were excluded from analysis. †††Interview assessment by dietician according to International Federation for the Surgery of Obesity and Metabolic Disorders (IFSO) European Accreditation Council for Bariatric Surgery (proportion classified as ‘emotional eaters’). GFCQ-T, General Food Craving Questionnaire – Trait; n.a., not applicable; DEBQ, Dutch Eating Behaviour Questionnaire; RYGB, Roux-en-Y gastric bypass; LAGB, laparoscopic adjustable gastric band; SG, sleeve gastrectomy; TFEQ-R21/R18, Three-Factor Eating Questionnaire – Revised 21/18; n.r., not reported; DS, duodenal switch; EES, Emotional Eating Scale; BPD, biliopancreatic diversion; EOQ, Emotional Overeating Questionnaire.

Risk of bias

Using the NHLBI quality assessment tool18, four studies28, 37, 40, 41 were rated as good, 134, 25-27, 29, 31-33, 36, 38, 39, 42, 43 as fair, and six22-24, 30, 34, 35 as poor (Table 3). Many papers did not clearly define the study population, period of recruitment, specific inclusion or exclusion criteria, or ethnicity. The overall retention rate ranged from 2·3 to 100 per cent, with eight studies24, 26, 30-32, 34, 35, 39 reporting loss to follow-up of more than 20 per cent of participants (Table 2). Six studies4, 25, 27, 38, 42, 43 did not report the number of participants lost or excluded from follow-up.

Table 3. Quality assessment of included studies according to the National Heart, Lung, and Blood Institute quality assessment tool for before–after (pre–post) studies with no control group
Reference 1 2 3 4 5 6 7 8 9 10 11 12 Quality rating (of 11)
34 Y N Y ? ? N Y ? N Y N n.a. Poor (4)
23 Y N N ? ? Y Y ? Y Y N n.a. Poor (5)
28 N Y Y N ? Y Y ? Y Y N n.a. Good (6)
39 Y N N ? ? Y Y ? N Y N n.a. Fair (4)
40 Y Y N ? ? N Y ? Y Y N n.a. Good (5)
41 Y Y N N ? Y Y ? Y Y N n.a. Good (6)
31 Y N N ? ? Y Y ? Y Y N n.a. Fair (5)
24 Y N ? N ? N Y ? N Y N n.a. Poor (3)
4 Y N N ? Y Y Y ? Y Y N n.a. Fair (6)
26 Y Y Y Y ? N Y ? N Y N n.a. Fair (6)
43 Y Y N ? ? N Y ? ? Y N n.a. Fair (4)
36 Y N N ? ? Y Y ? Y Y N n.a. Fair (5)
38 Y N N ? ? Y Y ? ? Y N n.a. Fair (4)
25 Y Y Y N ? Y Y ? N Y N n.a. Fair (6)
22 Y Y Y Y ? Y N ? Y N N n.a. Poor (6)
42 Y Y N ? Y Y Y N Y Y N n.a. Fair (7)
32 N N Y ? ? N Y ? N Y N n.a. Fair (3)
29 Y N N Y ? Y Y ? Y Y N n.a. Fair (6)
35 Y N N ? ? N Y ? Y Y N n.a. Poor (4)
37 Y Y Y N ? Y Y ? Y Y N n.a. Good (7)
30 Y N Y Y ? N Y ? N N N n.a. Poor (4)
33 Y Y N ? ? N Y ? Y Y N n.a. Fair (5)
27 N N N ? ? N Y ? Y Y N n.a. Fair (3)
Total (of 23) 20 10 8 4 2 13 22 0 14 21 0 n.a.
  • 1. Was the study question or objective clearly stated?
  • 2. Were eligibility/selection criteria for the study population prespecified and described clearly?
  • 3. Were the participants in the study representative of those who would be eligible for the test/service/intervention in the general or clinical population of interest?
  • 4. Were all eligible participants that met the prespecified entry criteria enrolled?
  • 5. Was the sample size sufficiently large to provide confidence in the findings?
  • 6. Was the test/service/intervention clearly described and delivered consistently across the study population?
  • 7. Were the outcome measures prespecified, clearly defined, valid, reliable, and assessed consistently across all study participants?
  • 8. Were the people assessing the outcomes blinded to the participants' exposures/interventions?
  • 9. Was the loss to follow-up after baseline 20 per cent or less? Were those lost to follow-up accounted for in the analysis?
  • 10. Did the statistical methods examine changes in outcome measures from before to after the intervention? Were statistical tests done that provided P values for the pre-to-post changes?
  • 11. Were outcome measures of interest taken multiple times before the intervention and multiple times after the intervention (did they use an interrupted time-series design)?
  • 12. If the intervention was conducted at a group level (such as a whole hospital or community), did the statistical analysis take into account the use of individual-level data to determine effects at the group level?
  • Y, yes; N, no; ?, not reported or cannot be determined; n.a., not applicable.

Changes in emotional eating after bariatric surgery

A summary of findings is presented in Table 2. Most studies observed that emotional eating decreased in the first 3 months after RYGB31, 32, 39, VBG43, SG32 and one anastomosis gastric bypass32, compared with preoperative scores. Changes were seen as early as 2 weeks after surgery39. Reduced postoperative emotional eating was reported also in studies with a 6–9-month follow-up4, 33, 36-39. Three studies4, 36, 38 assessed emotional eating patterns using the DEBQ after approximately 20 per cent weight loss (which occurred 4–9 months after surgery), and reported significant decreases in emotional eating after RYGB, LAGB and SG. Eleven prospective cohort studies25-28, 31, 34, 37, 40-43 including a range of surgical modalities such as VBG, RYGB, SG and LAGB showed a significant decrease in emotional eating at 12 months after surgery. Four studies showed no change in emotional eating within the first year, of which two23, 29 had small sample sizes of 12 or fewer participants, one32 was the only study performed in Asia, and one30 assessed emotional overeating rather than emotional eating.

Longer-term studies tended to show mixed results beyond 12 months. Some24, 26, 31, 41, 42 found that emotional eating at 15, 24 and 36 months was still significantly reduced compared with baseline, whereas one small study35 of 14 patients did not see a significant reduction in emotional eating at 24 months after surgery. The only two studies37, 43 that examined VBG reported significant decreases in emotional eating at 3, 6 and 12 months that were no longer evident at 24 months37 or 36 months43. Only one study24 examined changes beyond 36 months and did not demonstrate significant changes in emotional eating at 48 months compared with before surgery. However, emotional eating scores at 48 months were available for only 112 (5·5 per cent) of 2028 participants with preoperative emotional eating assessments, implying significant risk of attrition bias for these results.

Longitudinal postoperative assessments of emotional eating

Twelve studies22-24, 26, 29, 31, 32, 37, 39, 41-43 assessed emotional eating at more than one postoperative time point. Generally, emotional eating scores did not significantly differ between any two time points within the first 12 months after surgery23, 29, 31, 32, 37, 39, 43. Some studies reported increases in emotional eating from 12 to 24 months26, 31, 37, 12 to 36 months43 and 15 to 24 months24 after operation, whereas two studies41, 42 did not. Longer-term studies also showed mixed results. One study24 found a significant increase in emotional eating from 24 to 36 months after RYGB, although this was not found in a study26 involving patients undergoing RYGB and SG.

Synthesis of results

A meta-analysis of 17 studies containing 2811 surgical participants showed that emotional eating improved after bariatric surgery by a SMD of 1·09 (95 per cent c.i. 0·76, 1·42), indicating a large effect size (Fig2). This effect remained consistent in sensitivity analyses following removal of studies consisting of non-adult or women-only cohorts, those in which emotional eating scores were not normally distributed, and fair and/or poor-quality studies (Table 4). A moderate-to-large effect size was also seen in meta-analyses involving only the revised TFEQ (SMD 0·90, 0·60 to 1·21; MD 24·65, 95 per cent c.i. 16·22 to 33·08 (score range 0–100)) (Figs 3 and 4), and DEBQ (SMD 0·74, 0·54 to 0·94; MD 0·63, 0·46 to 0·80 (score range: 0–5)) (Figs 5 and 6). Subgroup analysis by type of surgical intervention showed that emotional eating reductions were significant after RYGB, SG, duodenal switch, VBG and LAGB (Figs 3-6).

Details are in the caption following the image
Forest plot of the effect of bariatric surgery on emotional eating

Values are mean(s.d.). An inverse-variance random-effects model was used for meta-analysis. Standardized mean differences (SMDs) are shown with 95 per cent confidence intervals.

Table 4. Effect of sensitivity analysis on meta-analysis
Total no. of patients
Outcome of interest No. of studies Before surgery After surgery SMD I2 (%)
Age
Removal of studies with only age ≤ 18 years 16 2730 2592 1·11 (0·76, 1·47) 94
Sex
Removal of women-only studies 14 2745 2608 1·10 (0·73, 1·46) 94
Quality assessment
Good quality studies only 3 263 263 2·12 (0·34, 3·90) 98
Good and fair quality studies only 13 599 561 1·24 (0·69, 1·80) 94
Questionnaire used
TFEQ-R18 2 58 47 0·86 (0·45, 1·27) n.a.
TFEQ-R21 5 211 194 0·85 (0·54, 1·16) 47
DEBQ 8 2316 2206 0·81 (0·57, 1·04) 68
EES 1 83 83 5·71 (5·02, 6·40) n.a.
EOQ 1 32 32 0·46 (−0·04, 0·96) n.a.
GFCQ-T 1 129 129 0·99 (0·73, 1·25) n.a.
One-sample removed analysis
Alfonsson et al.34 16 2682 2544 1·10 (0·74, 1·47) 94
Bryant et al.23 16 2788 2661 1·11 (0·77, 1·46) 94
Castellini et al.28 16 2728 2590 0·79 (0·64, 0·94) 59
Holsen et al.40 16 2793 2655 1·06 (0·72, 1·40) 94
Järvholm et al.41 16 2730 2592 1·11 (0·76, 1·47) 94
Laurenius et al.31 16 2768 2646 1·08 (0·74, 1·43) 94
Monpellier et al.24 16 783 734 1·14 (0·70, 1·57) 93
Nance et al.4 16 2780 2642 1·10 (0·75, 1·45) 94
Papalazarou et al.43 16 2781 2643 1·08 (0·74, 1·42) 94
Pepino et al.36 16 2767 2629 1·11 (0·76, 1·46) 94
Pepino et al.38 16 2784 2646 1·08 (0·73, 1·42) 94
Subramaniam et al.32 16 2754 2637 1·14 (0·80, 1·49) 94
Søvik et al.42 16 2751 2613 1·13 (0·78, 1·49) 94
Turkmen et al.29 16 2802 2665 1·12 (0·78, 1·46) 94
van Hout et al.37 16 2730 2592 1·13 (0·77, 1·49) 94
Weineland et al.30 16 2779 2641 1·13 (0·78, 1·48) 94
Woodard et al.27 16 2776 2638 1·10 (0·75, 1·45) 94
Non-normally distributed studies
Removal of all studies where mean(3 s.d.) included negative values 1 30 30 1·26 (0·70, 1·81) n.a.
  • Values in parentheses are 95 per cent confidence intervals. SMD, standardized mean difference; TFEQ-R18/21, Three-Factor Eating Questionnaire – Revised 18/21; n.a. not applicable; DEBQ, Dutch Eating Behaviour Questionnaire; EES, Emotional Eating Scale; EOQ, Emotional Overeating Questionnaire; GFCQ-T, General Food Craving Questionnaire Trait.
Details are in the caption following the image
Forest plot of the effect of different types of bariatric surgery on emotional eating in studies using revised versions of the Three-Factor Eating Questionnaire: standardized mean differences

Values are mean(s.d.). An inverse-variance random-effects model was used for meta-analysis. Standardized mean differences (SMDs) are shown with 95 per cent confidence intervals. RYGB, Roux-en-Y gastric bypass; SG, sleeve gastrectomy; n.a., not applicable.

Details are in the caption following the image
Forest plot of the effect of different types of bariatric surgery on emotional eating in studies using revised versions of the Three-Factor Eating Questionnaire: mean differences

Values are mean(s.d.). An inverse-variance random-effects model was used for meta-analysis. Mean differences (MDs) are shown with 95 per cent confidence intervals. RYGB, Roux-en-Y gastric bypass; SG, sleeve gastrectomy; n.a., not applicable.

Details are in the caption following the image
Forest plot of the effect of different types of bariatric surgery on emotional eating in studies using the Dutch Eating Behaviour Questionnaire: standardized mean differences

Values are mean(s.d.). An inverse-variance random-effects model was used for meta-analysis. Standardized mean differences (SMDs) are shown with 95 per cent confidence intervals. RYGB, Roux-en-Y gastric bypass; SG, sleeve gastrectomy; VBG, vertical banded gastroplasty; LAGB, laparoscopic adjustable gastric banding; n.a., not applicable.

Details are in the caption following the image
Forest plot of the effect of different types of bariatric surgery on emotional eating in studies using the Dutch Eating Behaviour Questionnaire: mean differences

Values are mean(s.d.). An inverse-variance random-effects model was used for meta-analysis. Mean differences (MDs) are shown with 95 per cent confidence intervals. RYGB, Roux-en-Y gastric bypass; SG, sleeve gastrectomy; VBG, vertical banded gastroplasty; LAGB, laparoscopic adjustable gastric banding; n.a., not applicable.

Included studies had high heterogeneity (I2 = 93 per cent). Heterogeneity was moderate in sensitivity analyses that removed the study done by Castellini et al.28 (SMD 0·79, 95 per cent c.i. 0·64 to 0·94; I2 = 59 per cent) and which included studies using DEBQ only (SMD 0·81, 0·57 to 1·04; I2 = 68 per cent) (Table 4). Heterogeneity was low if only studies using TFEQ-R21 were included (SMD 0·85, 0·54 to 1·16; I2 = 47 per cent) (Table 4). No publication bias was detected from visual examination of a funnel plot of all included studies (Fig7) and from Egger's test (P = 0·092).

Details are in the caption following the image
Funnel plot with pseudo 95 per cent confidence limits

SMD, standardized mean difference.

Discussion

The main finding of this meta-analysis of 17 studies was that emotional eating improved 4–18 months after bariatric surgery by a SMD of 1·09 (95 per cent c.i. 0·76 to 1·42). Qualitative analysis indicated an improvement in emotional eating in the first 12 months after bariatric surgery25-28, 31, 34, 37, 39-43, and mixed findings thereafter. The observation in longitudinal studies that early postoperative changes in emotional eating may not be sustained in the longer term are consistent with findings from cross-sectional studies comparing patients at 24–68 months after LAGB with presurgical controls48 and patients at 7 years post-RYGB with control groups with obesity49, as well as with a 2016 systematic review by Opozda and colleagues50 which examined preoperative and postoperative emotional eating patterns, mostly after RYGB.

There are several reasons why emotional eating behaviour may improve after bariatric surgery. In preparation for surgery and for the first few postoperative months, most patients will have received comprehensive nutritional and psychobehavioural evaluation, education and support, including strategies to modify eating behaviour. This may strengthen their efforts to avoid consuming food in response to emotions, which may wane over time51. Emotional eating typically involves a preference for highly palatable foods52, whereas after bariatric surgery avoidance of high-fat/high-sugar foods may occur as a learnt response to postprandial discomfort or dumping syndrome53, 54. A conditioned avoidance might then override the desire to consume these foods. Longitudinal studies have found reduced activation of the medial frontal gyrus55, 56, insula55, 56 and mesolimbic reward regions5, 57, 58 in patients who had RYGB55, 58 and SG 1–6 months after surgery57. RYGB and SG are associated with changes in the release of several gut hormones, including increased postprandial release of glucagon-like peptide 1 and peptide YY, with reduced circulating acyl-ghrelin59-61. These changes contribute to alterations in neural activity62, but cannot fully account for the reported improvement in emotional eating, as this is also observed in patients who have LAGB but do not have these same postsurgical hormonal changes. Functional neuroimaging after LAGB demonstrates diminished activation of areas involved in food motivation and reward in response to images of food, and increased activity in areas involved in cognitive restraint63, 64. Reduced food reward may also diminish the effectiveness of consuming palatable food as a coping mechanism during times of emotional distress. Several studies have reported that in the short to medium term after bariatric surgery, some patients experience improvements in the emotional states (low self-esteem39, 65, depressive34, 39, 65 and anxiety32, 65 symptoms) that previously had led them to consume highly palatable foods.

Overall, this review is limited by a high number of poor- to fair-quality studies, as well as high heterogeneity between studies. There was large variability between types of bariatric surgery used, methods of outcome assessment, and duration and timing of postoperative follow-up. Further limitations common to many of the studies reviewed were their small sample size, short follow-up and high attrition rates. Most had observational designs, which did not allow assessment of causal relationships with risks of confounding. Only three studies4, 36, 38 considered weight loss as a confounder, assessing emotional eating after approximately 20 per cent weight loss. Few studies reported details of preoperative or postoperative management of participants, and whether this differed from standard practice. Where reported, there was wide variation in practice (weekly contact with a dietician to monitor bodyweight, review dietary intake, provide behavioural education and adjust recommended energy intake needed to achieve weight loss target4, 36, 38, preoperative education sessions27, advice from sports medicine specialists32, and psychological support26, 37, 41). These differences are likely to affect eating behaviour, and are sources of further confounding. All studies used subjective self-report questionnaires, which may be influenced by the requirement to recall negative emotions, food intake, and the association between the two, as well as socially desirable responses, whereby some participants may report changes in eating behaviour to reflect expectations of the clinicians66.

Despite the comprehensive search strategy, the present review may be subject to selective reporting bias. Emotional eating behaviours are often not the main study outcomes and may not have been mentioned in the title or abstract. The exclusion of non-English-language studies may also have introduced bias, as negative findings are more likely to be published in a local journal rather than an international English-language journal67. Most study populations comprised middle-aged Caucasian women, generally from westernized, industrialized countries (mainly in North America and Europe), and therefore cannot be generalized to other settings or underrepresented groups such as men, adolescents, older patients, or people with very high BMIs.

Acknowledgements

The authors thank Helen Baxter, clinical librarian at Austin Health, who helped to develop search strategies and performed computerized searches.

This work received no specific funding. E.I.E. was supported by research grants from the Sir Edward Weary Dunlop Medical Research Foundation. P.S. is supported by a David Bickart Clinical Research Fellowship from the University of Melbourne and an Investigator Grant from the National Health and Medical Research Council.

Disclosure: The authors declare no conflict of interest.

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