Literature DB >> 29118561

Pilot study of the prevalence of binge eating disorder in non-alcoholic fatty liver disease patients.

Jinyu Zhang1, Omair Abbasi2, Lev Malevanchik3, Neena Mohan1, Richard Denicola1, Nicholas Tarangelo1, Dina Halegoua-De Marzio4.   

Abstract

BACKGROUND: Non-alcoholic fatty liver disease (NAFLD) is the most common liver disease in the United States. Binge eating disorder (BED) is the most common form of eating disorder. NAFLD and BED have similar risk factors, including obesity, insulin resistance, and metabolic syndrome. The aim of our study was to examine prevalence of BED in NAFLD patients.
METHODS: We administered the Binge Eating Scale (BES), a questionnaire validated to screen for BED, to NAFLD patients at our Fatty Liver Center. Demographics were retrieved retrospectively from our electronic medical record.
RESULTS: Of the total 95 NAFLD patients screened, 22 (23.1%) had binge eating tendencies; 6 of the 22 (6.3%) scored 27 or more points, suggestive of severe binge eating. Patient demographics included 59 females and 36 males (14 females and 8 males positive for BED). Liver disease severity and of metabolic syndrome presence were similar in both groups: 45 patients had steatosis, 25 steatohepatitis, and 24 cirrhosis, of which 10 steatosis, 5 steatohepatitis, and 7 cirrhosis patients screened positive for BED. Of the NAFLD patients with BED, 50.0% had insulin resistance, 68.2% hypertension, and 50.0% hyperlipidemia, whereas among non-BED NAFLD patients 58.9% had insulin resistance, 63.0% hypertension, and 67.1% hyperlipidemia.
CONCLUSIONS: This pilot study suggests that BED may have a higher prevalence among NAFLD patients than in the general population. Based on these preliminary results, further study into the prevalence of BED is recommended. More data is need to identify effects of BED on the progression of NAFLD and role of BED treatment.

Entities:  

Keywords:  Non-alcoholic fatty liver disease; binge eating disorder; metabolic syndrome

Year:  2017        PMID: 29118561      PMCID: PMC5670286          DOI: 10.20524/aog.2017.0200

Source DB:  PubMed          Journal:  Ann Gastroenterol        ISSN: 1108-7471


Introduction

Non-alcoholic fatty liver disease (NAFLD) is the most common liver disease in the United States. Obesity is a common and well documented risk factor for NAFLD, and as many as two thirds of patients with NAFLD are obese [1]. Estimates of the prevalence of NAFLD range from 6.3-33% worldwide, with a median of 20% in the general population [2]. The prevalence of non-alcoholic steatohepatitis (NASH) in the US general population has been estimated to be 2-12% and that of NAFLD to be 20-46% [1,3]. NAFLD is currently the third most frequent indication for liver transplantation, but it has been predicted to become the leading indication by 2020 [4-6]. Binge eating disorder (BED) was made an official diagnosis in 2013 with the release of the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-V) under the category of “Feeding and Eating Disorders.” However, it was also present in Appendix B of DSM-IV-TR as a “diagnosis needing more research”. BED is the most common eating disorder in the United States, with an estimated lifetime prevalence of 2.6% among adults—more than the prevalence of bulimia nervosa and anorexia nervosa combined. Patients with BED have recurrent episodes of binge eating, which occur on average at least once a week for three months, and are associated with marked distress (Table 1). Each episode can be defined as eating an amount of food that is definitely larger than what most people would eat in a similar, discrete period of time. A key aspect of binge eating is a sense of lack of control over eating during the episode. Patients may eat alone because of embarrassment at how much they are eating. After an episode, patients may feel very guilty, depressed, or disgusted with themselves. Unlike other eating disorders, individuals with BED do not often partake in inappropriate compensatory behaviors such as inducing vomiting or starvation [7]. Over 40% of patients with BED are obese [8].
Table 1

DSM-V (Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition) criteria for binge eating disorder

DSM-V (Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition) criteria for binge eating disorder The presence of BED has been associated with a greater risk for developing metabolic syndrome, independent of obesity [9]. BED patients are 13 times more likely to develop type 2 diabetes [10]. In addition, patients with BED have been found to have a lower health-related quality of life and increased healthcare costs when compared to non-BED patients [11]. In view of these issues, the prevalence and effects of BED in vulnerable patient populations have become a focus of research. Studies examining the prevalence of BED amongst patients with type 2 diabetes have found a rate between 1.4% and 25.6% [12-16]. Diabetes has also been noted to be an important risk factor in the prognosis of fatty liver disease [17]. Given the shared associations of diabetes and obesity between both BED and NAFLD, the aim of this study was to assess the prevalence and potential effects of BED amongst NAFLD patients.

Patients and methods

NAFLD patients seeking care at our tertiary Fatty Liver Center between September 2015 and October 2016 were approached following their visit to complete the Binge Eating Scale (BES) in person or were e-mailed a secure online form of the BES. Those that had already completed the BES in-clinic were excluded from the online group. In total, we had 36 patients complete the BES in-clinic and 59 complete online, totaling 95 patients. The BES is a 16-item screening questionnaire that assesses the range of severity of certain behavioral, emotional, and cognitive symptoms associated with BED, with a maximum of 46 points allotted to responses [18]. Since the BES was created prior to the creation of provisional criteria for BED in the DSM, it does not consider the frequency with which binge eating occurs, which is the fourth listed criterion for BED under DSM-V (DMS-V requires that binge eating occur, on average, at least once per week for three months). Therefore, the BES is best used as a screening tool [19]. The BES has been shown to have good internal consistency and validity in studies and across several languages [20-23]. The BES has also been frequently used to assess for BED in patients seeking bariatric surgery [24]. A score of 18 or above is considered positive for binge eating, while a score of 27 or above is indicative of severe binge eating. Using a cutoff of 17, the BES has been shown to have a sensitivity of 0.85-0.98 and a specificity of 0.48-0.75 [19,25-30]. Descriptive data—race, body mass index (BMI), degree of NAFLD (steatosis, NASH vs. cirrhosis), as well as past medical history for metabolic syndrome (insulin resistance, hyperlipidemia, and hypertension)—were retrieved retrospectively from our electronic medical record. Retrospective determination of degree of NAFLD was based on imaging studies (e.g., ultrasound, magnetic resonance imaging [MRI], computed tomography [CT]), biopsy, or Fibrosure test scores. Patients were determined to have insulin resistance if their hemoglobin a1C was greater than 5.7% (cutoff for prediabetes) in the past year, they were on diabetes medication, or were documented in the chart as having insulin resistance; hyperlipidemia if they were on statin therapy or documented in the chart as having hyperlipidemia; and hypertension if they were on blood pressure medications or documented in the chart as having hypertension.

Results

Of the 95 NAFLD patients screened, 22 (23.1%) had had binge eating tendencies, with 6 of the 22 (6.3%) scoring 27 or more points, suggestive of severe binge eating. Fifty-nine females and 36 males (14 females and 8 males screened positive for BED); 82 Caucasians, 8 African Americans, 2 Hispanics, and 3 Asians participated (20 Caucasians, 1 African American, and 1 Asian screened positive for BED). The severity of liver disease in both groups—based on biopsies, Fibrosure scores, and liver imaging including CT, ultrasound and MRI—showed 45 patients had hepatic steatosis, 25 NASH, and 24 cirrhosis, of which 10 hepatic steatosis, 5 NASH and 7 cirrhosis patients screened positive for BED. A total of 28 patients had biopsies performed. See Table 2 for demographic details. See Fig. 1-3 for severity of liver disease, prevalence of metabolic syndrome, and distribution of BMI.
Table 2

Patient demographics

Figure 3

Body mass index (BMI) in patients with non-alcoholic fatty liver disease

Figure 3 is a box and whisker plot of the BMI’s in the Non-BED NAFLD (negative binge eating) and BED NAFLD (positive binge eating) patients with non-alcoholic fatty liver disease. The P-value of 0.05 refers to a comparison of the mean BMI values. The “x” represents the mean BMI of each sample population.

Patient demographics Liver histology in patients with non-alcoholic fatty liver disease BED NAFLD (positive binge eating in patients with non-alcoholic fatty liver disease) Non-BED NAFLD (negative binge eating in patients with non-alcoholic fatty liver disease) Prevalence of metabolic syndrome in patients with non-alcoholic fatty liver disease BED NAFLD (positive binge eating in patients with non-alcoholic fatty liver disease) Non-BED NAFLD (negative binge eating in patients with non-alcoholic fatty liver disease) Body mass index (BMI) in patients with non-alcoholic fatty liver disease Figure 3 is a box and whisker plot of the BMI’s in the Non-BED NAFLD (negative binge eating) and BED NAFLD (positive binge eating) patients with non-alcoholic fatty liver disease. The P-value of 0.05 refers to a comparison of the mean BMI values. The “x” represents the mean BMI of each sample population. With respect to the presence of metabolic syndrome in both groups, of the binge eating NAFLD patients 50.0% had insulin resistance (defined as pre-diabetic and diabetic), 68.2% had hypertension, and 50.0% had hyperlipidemia; among the non-binge eating NAFLD patients 58.9% had insulin resistance, 63.0% had hypertension, and 67.1% had hyperlipidemia. The mean BMI for binge eating NAFLD patients was 36.6, median 35.5, range 24.6-53.9, whereas the mean BMI for non-binge eating NAFLD patients was 33.6, median 31.8, range 23.4-62.7. Statistical analysis included the two-tailed z-score for those that screened positive and those that screened negative in terms of insulin resistance, hypertension and hyperlipidemia. There was no significant difference in terms of insulin resistance (P=0.46), hypertension (P=0.65), and hyperlipidemia (P=0.1443). The two-tailed t-score was also determined for BMI. There was no significant difference in BMI between the positive screen and negative screen groups (P=0.05). With respect to sex, there was no significant difference between males and females: P=0.5448 for the negative screen group and P=0.078 for the positive screen group. The F-test was performed for differences in liver characteristics, i.e., steatosis, NASH, and cirrhosis: P=0.086. No significant variance was found among the different groups between those who screened positive and those who screened negative.

Discussion

To our knowledge, this is the first study to evaluate binge eating tendencies in patients with NAFLD. We found that 23.1% of our subjects screened positive on the BES. While the BES is best utilized as a screening tool and a positive screen is not necessarily equivalent to a diagnosis of BED, looking only at positive screens for BES, a study using the BES in an obese outpatient population found that 14.6% of men and 10.6% of women screened positive for BED [25]. Another cross-sectional study utilizing the BES in patients undergoing evaluation for bariatric surgery found that 17% of patients screened positive [20]. In both studies, the percentage of people who screened positive was well below our 23.1%. Two studies correlating the BES with a confirmed diagnosis of BED found that, if the cutoff score is raised to 27, the specificity of the BES increased to about 95% [25,26]. Utilizing the higher cutoff score, our study would screen 6.3% of NAFLD patients positive for BED, which is still above what is seen in the general population (2.6%) [8]. Analysis of our data is limited by the fact that BED is new to DSM-V, although it was characterized in DSM-IV and estimates in the existing literature are based on DSM-IV criteria. BMIs for those who completed the BES in-clinic (n=36) were taken at the time of BES completion, whereas for those who completed the BES online (n=59) the BMI was obtained as close as possible to the date of BES completion. Therefore, there may exist some discrepancy in BMI reporting between the two groups. While there were no statistically significant differences seen with regard to metabolic syndrome, analysis is limited by the retrospective nature of our data. However, all patients included in the study were seen in the liver clinic within the year prior to BES completion. While there was no significant variance in histology (steatosis, NASH, vs. cirrhosis), the analysis was limited by the retrospective nature of our data: we could only evaluate the examinations that had been previously performed, whether imaging or some other modality. Only close to one third of our patients had biopsies. In general, this study was intended to provide pilot data concerning the possibility of a greater prevalence of binge eating symptoms, if not BED, in the NAFLD population. Current criteria in the DMS-V for BED measure severity by the number of such episodes per week. The BES attempts to assess severity of BED by the presence of certain psychological, emotional, and behavioral symptoms; it does so by measuring how intense the symptoms feel to the patient and not by the frequency of events. Currently, no data exist on the connection between BED and NAFLD. Our study suggests that there could be a possible connection, given the percentage of positive screens in our sample population. Further case-controlled studies with a larger sample size are needed. This could be an important area of interest to explore further, as it would point to a need for additional assessment of eating patterns in the NAFLD population. Often patients turn to popular diet programs for weight loss, many of which rely on restrictive eating patterns. Dietary restraint has been shown to be a behavior that may perpetuate binge eating behavior, rather than preventing it [31]. Identifying such individuals and providing closer nutritional guidance along with addressing eating dysregulated eating behaviors may lead to better weight loss. Currently, psychotherapeutic interventions have shown efficacy for BED, including cognitive behavioral therapy and mindfulness, which is not standard in NAFLD treatment. In addition there is promising evidence supporting certain anticonvulsant therapies, stimulants, and appetite suppressants for the management of BED [32,33]. Our findings leave open the possibility that treatment of BED in a patient with BED and NAFLD could lead to an improvement in the patient’s liver disease. A larger multicenter cross-sectional study is needed to identify prevalence rates of BED in NAFLD. In addition, a case-controlled prospective study of NAFLD progression patients with and without comorbid BED would provide additional data concerning the effects of BED on fatty liver disease outcomes. What is already known: Nonalcoholic fatty liver disease (NAFLD) is the most common liver disease in the United States (US) Binge eating disorder (BED) carries an estimated prevalence of 2.6% among US adults; it is thereby the most common form of eating disorder BED patients are 13 times more likely to develop type 2 diabetes What the new findings are: BED may have a higher prevalence in patients with NAFLD compared to the general population More data will be needed to identify the effects of BED on the progression of NAFLD and the role of BED treatment
  31 in total

1.  A position statement on NAFLD/NASH based on the EASL 2009 special conference.

Authors:  Vlad Ratziu; Stefano Bellentani; Helena Cortez-Pinto; Chris Day; Giulio Marchesini
Journal:  J Hepatol       Date:  2010-05-07       Impact factor: 25.083

2.  [Validation of the French version of the Binge Eating Scale: Examination of its factor structure, internal consistency and construct validity in a non-clinical and a clinical population].

Authors:  P Brunault; P Gaillard; N Ballon; C Couet; P Isnard; S Cook; I Delbachian; C Réveillère; R Courtois
Journal:  Encephale       Date:  2016-03-24       Impact factor: 1.291

3.  Binge eating disorder: Evidence-based treatments.

Authors:  Christine M Peat; Kimberly A Brownley; Nancy D Berkman; Cynthia M Bulik
Journal:  Curr Psychiatr       Date:  2012-05

Review 4.  From NAFLD to NASH to cirrhosis-new insights into disease mechanisms.

Authors:  Alexander Wree; Lori Broderick; Ali Canbay; Hal M Hoffman; Ariel E Feldstein
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2013-08-20       Impact factor: 46.802

Review 5.  Binge eating in the bariatric surgery population: a review of the literature.

Authors:  Sara H Niego; Michele D Kofman; Jeffrey J Weiss; Allan Geliebter
Journal:  Int J Eat Disord       Date:  2007-05       Impact factor: 4.861

6.  Metabolic syndrome in obese men and women with binge eating disorder: developmental trajectories of eating and weight-related behaviors.

Authors:  Kerstin K Blomquist; Vanessa A Milsom; Rachel D Barnes; Abbe G Boeka; Marney A White; Robin M Masheb; Carlos M Grilo
Journal:  Compr Psychiatry       Date:  2012-04-05       Impact factor: 3.735

7.  Diagnosis of binge eating disorder: discrepancies between a questionnaire and clinical interview.

Authors:  C G Greeno; M D Marcus; R R Wing
Journal:  Int J Eat Disord       Date:  1995-03       Impact factor: 4.861

8.  Binge eating disorder and night eating syndrome in adults with type 2 diabetes.

Authors:  Kelly C Allison; Scott J Crow; Rebecca R Reeves; Delia Smith West; John P Foreyt; Vicki G Dilillo; Thomas A Wadden; Robert W Jeffery; Brent Van Dorsten; Albert J Stunkard
Journal:  Obesity (Silver Spring)       Date:  2007-05       Impact factor: 5.002

Review 9.  Binge-Eating Disorder in Adults: A Systematic Review and Meta-analysis.

Authors:  Kimberly A Brownley; Nancy D Berkman; Christine M Peat; Kathleen N Lohr; Katherine E Cullen; Carla M Bann; Cynthia M Bulik
Journal:  Ann Intern Med       Date:  2016-06-28       Impact factor: 25.391

10.  Binge eating and dietary restraint in obese patients.

Authors:  M D Marcus; R R Wing; D M Lamparski
Journal:  Addict Behav       Date:  1985       Impact factor: 3.913

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  5 in total

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Authors:  Ammar Albanna; Reem Hatem; Faisal A Nawaz; Ghadah A Al-Sharif; Mohammad Almoosa; Wid Kattan; Christos Tzivinikos; E Lila Amirali
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Authors:  Clémence M Canivet; Pascal Perney; Faredj Cherick; Magalie Orlowski; Stéphanie Patouraux; Béatrice Bailly-Maitre; Albert Tran; Antonio Iannelli; Philippe Gual; Rodolphe Anty
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