What this is
- This scoping review investigates () and its associations with physical health, sleep quality, and weight status in adults.
- It synthesizes findings from 30 studies published over the last decade, focusing on adult populations aged 18 and older.
- The review identifies inconsistent relationships between and various health outcomes, highlighting the need for further research.
Essence
- is associated with higher body mass index (BMI), less physical activity, and poorer sleep quality, but not with Type 2 diabetes mellitus (T2DM).
Key takeaways
- likely leads to higher BMI in adults, with 16 of 27 studies reporting a positive relationship. This suggests that may contribute to obesity-related health risks.
- Physical activity levels are inconsistently reported, with only four of six studies finding a significant association between and reduced physical activity. This indicates that more representative studies are needed.
- Thirteen studies found significant links between and poor sleep quality, primarily through self-reported measures. This underscores the need for further longitudinal research to clarify these associations.
Caveats
- The review is limited by the variability in diagnostic criteria for across studies, which may affect the reliability of findings.
- Most studies included were observational and cross-sectional, limiting the ability to draw causal conclusions about and health outcomes.
- Many studies had small sample sizes and were not representative of the general adult population, which may skew results.
Definitions
- Night Eating Syndrome (NES): An eating disorder characterized by recurrent episodes of night eating, leading to distress and functional impairment.
AI simplified
1. Introduction
Night eating syndrome (NES) is an eating disorder characterised by recurrent episodes of night eating evident through excess consumption of food after the evening meal or nocturnal ingestions after awakening from sleep, which cause significant dysfunction and distress [1,2]. Although the aetiology of NES is poorly understood, the syndrome is thought to result from a desynchronisation of mood, sleep, satiety, and circadian rhythms of food ingestion [2,3]. Moreover, NES has a substantial association with concurrent psychiatric diagnoses and comorbidities; these can include binge eating disorder, bulimia nervosa, generalised anxiety disorder and substance use disorder [4]. Consequently, individuals with NES often experience significant distress and impairments in normal functioning [1,2,3]. With a prevalence of 1.5% in the general population of the United States [3], NES creates a substantial burden to the healthcare system, detrimentally impacting quality of life and increasing morbidity [2,3,4,5]. Whilst its morbidity is suspected to be moderate due to known associations with medical and psychiatric conditions, we found no specific statistics regarding NES and mortality.
In addition to its mental health impacts, people with NES may also experience comorbidities such as sleep disorders and sleep apnoea, and metabolic conditions such as diabetes or hypercholesterolemia [2,4]. These problems are known to increase cardio-vascular and metabolic risk in the adult population and are associated with significant mortality and morbidity [4]. As with other EDs characterised by episodes of excess consumption, such as binge eating disorder [1], NES is also associated with increased body weight, and this further adds to the risk of metabolic syndrome and other physical health problems associated with obesity [2,4].
Research to date regarding the association between NES and Body Mass Index (BMI; kg/m2), physical health and sleep conditions is inconsistent [6,7,8]. Additionally, the majority of research on NES has been conducted within clinical settings [9,10,11] or in adolescent populations [12,13]. As such, there is a lack of knowledge regarding NES and physical health problems within more general and adult population groups [9,14,15]. To our knowledge, however, there has not been a scoping review or systematic review investigating the association of these physical health problems with NES. Thus, this review adopted a scoping review methodology to broadly investigate the extant literature, assessing associations of NES with physical health conditions, physical activity, sleep, and weight status in adult population samples of 18 years of age or older. We elected to conduct a scoping review as our research question was broad and we planned to optimise the inclusivity of articles to determine future directions in empirical and review research methodologies. This review searched articles from the past decade in order to focus on contemporary and up-to-date knowledge.
2. Materials and Methods
2.1. Search Processes
This scoping review was conducted according to PRISMA-ScR (Preferred Reporting Items for Systematic Reviews and Meta-Analyses-Scoping Review) guidelines [16]. The search was conducted through the use of PubMed, Medline (OVID) and SCOPUS to identify relevant articles published within the last 10 years (until 2013). Search terms including “Night eating* OR “NES” and Boolean phrases were used to refine the search. Additionally, the age of participants was restricted to 18 years and above, to ensure only adult participants were included. The abstracts and titles of the remaining articles were then used to screen for articles that were of relevance. Additionally, all articles selected by title and abstract were read to ensure relevance to NES.
2.2. Study Selection
Articles were included in this scoping review according to the following inclusion criteria: published in the English language, reported on participants with NES who were over the age of 18 years, published in peer-reviewed journals and published in the last decade (since 2013). Articles were excluded if the full text was not available. References from systematic reviews and meta-analyses were also examined to identify additional original studies. We chose to review the impacts of NES on adult populations as a large proportion of the existing literature has been conducted on adolescent populations [12,13]. Articles were then screened based on title, abstract or full text due to irrelevance to topic question or where text was not fully available.
2.3. Data Extraction
After reviewing the results of the initial search based on inclusion and exclusion criteria, data were extracted and compiled into table format. Data included author names, publication dates, study designs, sample size, participant demographics and outcomes. Two authors (SS and PH) reached consensus on data that were extracted and included in these tables.
3. Results
3.1. Study Characteristics
Figure 1 summaries the process of article selection for this review. The search of the PubMed Data base provided a total of 625 citations. Furthermore, nine additional studies which met the inclusion criteria were identified by reviewing the references of selected papers. After adjusting for duplicates, 630 records were screened. Of these, 607 articles were excluded as they were irrelevant to the topic. Upon reviewing the abstracts of articles obtained through a search on Medline (OVID) and SCOPUS, five additional relevant articles were included. After the screening process, 30 studies [17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46] assessing NES met the inclusion criteria and were thus included in this scoping review. The need for further research into NES within adult populations is reiterated through the limited number of relevant studies yielded through this search.
Search flow.
3.2. Relevant Studies
As shown in Table 1, only five studies investigated NES in a representative participant sample [26,27,32,37,44], whilst fourteen studies reported on university students [17,19,24,25,33,34,35,39,40,41,42,43,45,46] and ten studies reported on patients within outpatient clinics [18,20,21,22,23,28,29,30,36,38]. Most studies [17,19,20,21,22,23,24,25,26,28,29,30,32,34,36,37,39,42,43,44,45,46] compared participants who met NES diagnostic criteria with those who did not; however, some studies used no comparison groups [35,40,41], sex [31], age [27] or BMI groups as a comparison [18,38].
| Pub Date, Author | Study Design | Sample Size | Location | Comparison | Participant Features | Age in Years (Mean Age) | Sex | Other Features | Criteria/Questionaries Used | Cut-Off for NES Criteria | Main Results |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 2017. Yahia N et al. [] [17] | Case–control | 413 | USA | Any NES (mild, moderate and full) (n = 51)No NES (n = 362) | Central Michigan University students | 18–26(20.6 ± 1.68 SD) | 323 females,90 males | Self-reported | NEDQ, PSQI, IPAQ-S | Categorised via NEDQ | Relation between NES, sleep duration (= 0.023) and higher PSQI score (= 0.007).Relation between NES and BMI, eating habits, physical activity and smoking status (NS).pp |
| 2021Sutcu C et al. [] [18] | Cross-sectional | 420 | Turkey | Normal weight: BMI 18.50–24.99 (n = 105)Overweight: BMI 25–29.99 (n = 105)Obese: BMI 30–39.99 (n = 105)Morbidly obese: BMI > 40 (n = 105) | Endocrinology outpatient clinic | 18–65(42 ± 12 SD) | 288 females, 132 males | Face-to-Face interview | NEQ, BMI, waist circumference | ≥25 on NEQ | Relation between NES and waist circumference (< 0.05).Relation between NES and morbid obesity (< 0.001).pp |
| 2020Riccobono G et al. [] [19] | Cross-sectional | 1136 | Italy | NES (n = 60)No NES (n = 1076) | Italian university students | MD (25.97 ± 10.78 SD) | 774 females, 360 males | Self-reported | NEQ, MEQ, BMI, SPAQ | ≥25 on NEQ | Relation between NEQ and MEQ scores are significantly inversely correlated (< 0.01).Relation between BMI and NES (NS).p |
| 2014Kucukgoncu S et al. [] [20] | Cross-sectional | 155 | Turkey | NES (n = 33)No NES (n = 122) | Patients with depression in outpatient clinic | 18–60 (35.80 ± 8.78 SD) | 125 females, 30 males | Clinical interviews | NEQ, structural clinical interview for DSM-IV axis I diagnosis, PSQI | ≥25 on NEQ | Relation between NES and Global PSQI scores (< 0.001).Relation between NES and BMI (= 0.041).pp |
| 2016Geliebter A et al. [] [21] | Cross-sectional | 84 | USA | NES/subthreshold NES (n = 30)No NES (n = 54) | Pts referred for poly-somnography at the Sleep Disorders Institute | 18–81 (43.2 ± 13.3 SD) | 34 females, 50 males | Self-reported | NEDQ, BMI, AHI | Categorised via NEDQ | Relation between NES and BMI, OSA or AHI (NS). |
| 2015Saraçlı Ö et al. [] [22] | Cross-sectional | 1188 | Turkey | NES (n = 97)No NES (n = 336) | Psychiatric out-patients | 18 + (37.75 ± 12.02 SD) | 777 females, 411 males | Clinical interview | DSM-iV, NEQ, BMI | ≥25 on NEQ | Relation between NES and BMI (NS). |
| 2017Dorflinger LM et al. [] [23] | Cross-sectional | 110 | USA | NES (n = 12)No NES (n = 98) | MOVE! weight management program, veterans | MD (61.6 ± 8.5 SD) | 11 females, 99 males | Self-reported | NEQ, ISI, BMI | ≥25 on NEQ | Relation between NEQ score and ISI (< 0.001).Relation between NEQ score and higher BMI (< 0.05).pp |
| 2018Kandeger A et al. [] [24] | Cross-sectional | 383 | Turkey | NES (n = 20)No NES (n = 363) | University students | 17–37 (21.1 ± 0.1 SD) | 230 females, 153 males | Self-reported | NEQ, MEQ, ISI, BMI | ≥25 on NEQ | Relation between NES and BMI (< 0.01).Relation between NES and ISI scores (< 0.001).pp |
| 2014Meule A et al. [] [25] | Cross-sectional | 729 | Germany | NES (n = 11)No NES (n = 718)NEQ > 25 (n = 9)NEQ > 30 (n = 2) | University students | 18–47 (23.55 ± 3.89 SD) | 561 females, 168 males | Online self-reported | NEQ, MES, BMI | ≥25 on NEQ | Relation between NES and BMI (< 0.01).p |
| 2021Matsui K et al. [] [26] | Cross-sectional | 8348 | Japan | No NES (n = 8024)Nocturnal ingestions (n = 208)Evening hyperphagia (n = 119) | General Japanese population | 16–79 (MD) | 4182 females, 4166 males | Online self-reported | NEQ, BMI, ISI | ≥25 on NEQ | Relation between evening hyperphagia and BMI (< 0.05), average sleep duration of < 6 h (< 0.001), later sleep–wake schedule (< 0.001), ISI score of 8–14 points (< 0.05), and ISI score of 15–28 points (< 0.001).Relation between nocturnal ingestions and earlier sleep–wake schedule (< 0.001), ISI score of 8–14 points (< 0.001) and ISI score of 15–28 points (< 0.001). Relation between nocturnal ingestions and BMI (NS).pppppppp |
| 2014Meule A et al. [] [27] | Cross-sectional | 2317 | Germany | 21–30 years (n = 332)31–40 years (n = 335)41–50 years (n = 450)51–60 years (n = 437)61–70 years (n = 399)> 70 years (n = 364) | Representative sample of German adults | 21–92 (51.45 ± 16.97 SD) | 1245 females, 1072 males | Self-reported | NEQ, BMI | No cut-off | Weak positive relation between BMI and NES (< 0.001).p |
| 2014Hood MM et al. [] [28] | Cross-sectional | 194 | USA | NES (n = 13)No NES (n = 181) | Endocrinology clinic outpatients with T2DM | 18–65 (58.4 ± 13.0 SD) | 135 females, 59 males | Self-reported | DSM5, NEQ, PSQI, ESS, MEQ, BMI | ≥25 on NEQ | Relation between NES and poorer sleep quality (< 0.001), more daytime sleepiness (= 0.002) and shorter sleep duration (= 0.009). Relation between NEQ scores and HbA1C (= 0.2).Relation between NES and BMI, age (NS).pppp |
| 2014Cleator J et al. [] [29] | Cross-sectional | 81 | UK | NES (n = 31)No NES (n = 50) | UK outpatient clinic, all Caucasian | 18–68 (44.6 ± 11.6 SD) | 46 females, 35 males | Self-reported | NEQ, NESHI, weight, BMI, comorbidities, sleep | ≥25 on NEQ | Relation between NES and weight (= 0.04).Relation between NES and BMI, T2DM, OSA and sleep duration (NS).p |
| 2022Lent MR et al. [] [30] | Cross-sectional | 1017 | USA | NES (n = 48)No NES (n = 969) | General internal medicine, primary care, or weight management clinics | 18 + (51.1 ± 15.0 SD) | 790 females, 227 males | Self-reported online | NEQ, BMI, frequency of naps (<1/wk, 2–3/wk or 4+/wk), MCTQ, IPAQ-SF | ≥25 on NEQ | Relation between NES and higher BMI (< 0.001), shorter sleep duration (< 0.001), napping < two times per week (= 0.002) and engaging in moderate-to-high physical activity (= 0.005).pppp |
| 2014Gallant A et al. [] [31] | Longitudinal cohort study | 615 | Canada | Women (n = 310)Men (n = 305) | Adults enrolled in QUALITY (Quebec Adiposity and Lifestyle Investigation in Youth) | 18+Females (40.3 ± 5.1 SD)Males (42.5 ± 5.9 SD) | 310 females, 305 males | Self-reported | NEQ, BMI, waist circumference, weight, ATP III criteria, bloods (BGL, lipids), BP | ≥25 on NEQ | Relation between BMI and NEQ in women (< 0.001) and in men (= 0.04).Relation between higher NEQ and low BP in women (< 0.05) and BP in men (NS).Relation between NEQ in men and larger waist circumference (< 0.05) and increased triglycerides (< 0.01).Relation between NEQ in women and larger waist circumference and increased triglycerides (NS).Relation between NEQ in men and women and metabolic syndrome or T2DM (NS).ppppp |
| 2014de Zwaan M et al. [] [32] | Cross-sectional | 2456 | German | NES (n = 27)No NES (n = 2432) | Representative sample of the German general population | 14–92 (48.1 ± 19.0 SD) | 1256 females, 1200 males | Self-reported | NEQ, BMI | ≥25 on NEQ | Relation between NES and BMI (= 0.018).p |
| 2017Nolan LJ et al. [] [33] | Cross-sectional | 722 | USA | Students (n = 254), community members (n = 468) | University students and community member | 25 +Student group (18.7 ± 0.1 SD)Community group (42.9 ± 0.6 SD) | 421 females, 301 males | Online self-reported | NEQ, NEDQ, BMI, PSQI | ≥25 on NEQ | Relation between NES and BMI (< 0.001).Relation between NES and PSQI (= 0.006).pp |
| 2014Meule A et al. [] [34] | Cross-sectional | 305 | German | NES (n = 4, 1.24%)No NES (n = 301) | University students | 18–47 (23.55 ± 3.89 SD) | MD | Online self-reported | NEQ, MES, r-MEQ, | ≥25 on NEQ | Relation between NES and BMI and BMI (< 0.001).p |
| 2017Aloi M et al. [] [35] | Cross-sectional | 444 | Italy | No comparison group | University students | 18+ (21.4 ± 2.3 SD) | 327 females and 247 males | Self-reported | NEQ, EDE-Q, PSQI, BMI | ≥25 on NEQ | Relation between NEQ and BMI (NS).Relation between NEQ and age (NS).Relation between NEQ and PSQI (< 0.001).p |
| 2014Antelmi E et al. [] [36] | Cross-sectional | 120 | Italy | NES (n = 20)No NES (n = 100) | Resting leg syndrome in patients | 18+ (63.8 ± 11.5 SD) | 83 females, 37 males | Telephone | NEQ, ESS, BMI | ≥25 on NEQ | Relation between NES and BMI was significantly higher in RLS patients (= 0.023).Relation between NES and insomnia complaints and ESS (NS).Relation between NES and concomitant disease (HTN, CVD, DM, etc.) (NS).p |
| 2018Olejniczak D et al. [] [37] | Cross-sectional | 611 | Poland | NEQ ≥25 (n = 12)NEQ ≥30 (n = 4)No NES (n = 595) | General population | 19–30 (22.7) | 611 females, 0 males | Self-reported | NEQ, BMI | ≥25 on NEQ | Relation between NES and higher BMI (= 0.022).p |
| 2020Kara Y et al. [] [38] | Case-control | 421 | Turkey | NES (n = 92)No NES (n = 329)class I obesity (n = 150) class II obesity (n = 141)class III obesity (n = 130) | Obesity outpatient clinic | 18+Class I (49.49 ± 12.49)Class II (48.43 ± 11.81)Class III (49.05 ± 11.40) | 349 females, 72 males | Self-reported | NEQ, BMI, waist and hip circumference | ≥18 on NEQ | Relation between NES and BMI and waist–hip ratio (NS). |
| 2014Runfola CD et al. [] [39] | Cross-sectional | 1636 | USA | NES (n = 67)No NES (n = 1569) | University students, athletes | 18–26 (20.9 ± 1.7 SD) | 972 females, 664 males | Self-reported | NEQ, EDE-Q, EAT-II, HRQOL, BMI | ≥25 on NEQ | Relation between BMI and NES (NS).Relation between NES and lower HRQOL (< 0.001).p |
| 2018He J et al. [] [40] | Cross-sectional | 1237 | China | No comparison group | University students | 18+ (19.96 ± 1.36 SD) | 670 females, 567 males | Self-reported | NEQ, BMI, EDI | No cut-off | Relation between BMI and NEQ (NS). |
| 2014. Yeh SS et al. [] [41] | Cross-sectional | 330 | Australia | No comparison group | College students(48.4%), university staff, friends, and colleagues | 18–87 (27.42 ± 10.36 SD) | 223 females, 107 males | Self-reported | NEQ, PSQI, BMI | ≥25 on NEQ | Relation between NES and BMI (< 0.01) and reduced sleep duration (< 0.01).pp |
| 2022. El Ayoubi LM et al. [] [42] | Cross-sectional | 404 | Lebanon | No NES (n = 239)Mild NES (n = 75)Moderate NES (n = 59)Full NES (n = 31) | University students, 72% female | 291 females, 113 males | Self-reported online | NEDQ, GHQ-12, BMI | Categorised via NEDQ | NEDQ and BMI (< 0.0001).NEDQ and GHQ (< 0.0001).pp | |
| 2023Hamdan M et al. [] [43] | Cross-sectional | 475 | Palestine | NES (n = 141)No NES (n = 334) | University students | 18–25 (19.8 ± 1.4 SD) | 253 females, 197 males | Self-reported | NEQ, BMI,SF-IPAQ, Medical profile (Chronic diseases and duration) | ≥25 on NEQ | NES and BMI (NS).NES and medical history (NS).NES and physical activity (NS).NES and chronic disease (NS). |
| 2023. Kim W et al. [] [44] | Cross-sectional | 34434 | Korea | NES (n = 197)No NES (n = 344144) | Representative sample of the Korean general population | 19 + (MD) | 17729 females, 16705 males, | 2019 Korea Community Health Survey(KCHS) | NEQ, 3-level EuroQoL-5 Dimension Index (EQ-5D-3L) | ≥25 on NEQ | NES and lower HRQOL (< 0.001).p |
| 2022. Suna G et al. [] [45] | Cross-sectional | 568 | Turkey | NES (n = 24)No NES (n = 544) | University students | 18–25 (20.32 ± 1.61 SD) | 447 females, 121 males | Self-reported | PSQI, NEQ, BMI, WHR | ≥25 on NEQ | NES and higher PSQI (= 0.001).p |
| 2022. Hamurcu P. [] [46] | Cross-sectional | 846 | Turkey | No NES (n = 273)NES (n = 573) | University students | MD (21.4 ± 3.1 SD) | 712 females, 134 males | Self-reported online | NEQ, PSQI, World Health Organization Quality of Life Short Form (WHOQOL-BREF-TR) | ≥25 on NEQ | NES and WHOQOL-BREF-TR (< 0.001).p |
3.3. Diagnostic Criteria
A variety of tools were used to diagnose NES. including the Other Specified Feeding or eating disorders (OSFED) section of the Diagnostic and Statistical Manual of Mental Disorders, 5th edition (DSM5) [1], Night Eating Questionnaire (NEQ) [47], Night Eating Diagnostic Questionnaire (NEDQ) [48], Eating Disorder Examination Questionnaire (EDE-Q) [49], Night Eating Syndrome History and Inventory (NESHI) [50] and Eating Among Teens Survey (EAT-II) [51]. The discrepancies between the diagnostic criteria used reiterates the need for further research to obtain accurate data regarding the diagnosis and the complications of NES.
The NEQ can be used as a continuous measure to assess the severity of NES symptoms via a 14-item questionnaire [47]. This questionnaire characterises morning hunger, timing of first food consumption, food craving and control of overeating behaviour before bedtime and during nocturnal awakenings, quantity consumed after dinner, initial insomnia, frequency of nocturnal awakenings and ingestion of food, mood disturbance and awareness of these episodes. Participants in most studies were divided into NES and non-NES groups through a cut-off of 25 or more in the NEQ, which has a positive predictive value (PPV) of 40.7% [47]. Meule et al. [25], however, also utilised a cut-off of 30 or more in the NEQ, increasing the PPV to 72.7% [47]. Additionally, some studies did not include comparison groups and explored the relationship between NEQ results and associated features on a continuum [27,31,33,35,40,41].
Additionally, only one study utilised an additional self-reported questionnaire, NESHI, to confirm the diagnosis of NES obtained through the NEQ [29]. The NESHI [50] is a semi-structured interview assessing a typical 24 h food intake, as well as information on average weekly nocturnal ingestions, sleep routine, mood symptoms, weight and diet history, medical history about NES symptoms and previous treatment [52]. Furthermore, three studies utilised the NEDQ as the sole measure to classify diagnostic criteria for NES [17,21,42]. The NEDQ is a 22-item questionnaire which employs a hierarchical scoring method to allocate participants into four categories (normal, mild, moderate and full syndrome) based on the number of symptoms of NES that are present [48].
3.4. Weight Status
Twenty-seven studies examined the association between NES and weight status. Findings concerning the relationship between NES and BMI provided inconclusive and contradictory results, 11 studies reported no significant relationship [17,19,21,22,28,29,35,38,39,40,43] and 15 studies reported a statistically significant positive relationship [18,20,23,24,25,27,30,31,32,33,34,36,37,41,42]. One study reported a significant relationship with evening hyperphagia and no relationship with nocturnal ingestions [26].
Additionally, three studies observed other indicators of weight status, including weight (kg) [29], waist-to-hip ratio [38] and waist circumference [31]. Gallant et al. [31] and Kara et al. [38] reported no significant relationship between NES and waist circumference in men and women and waist–hip ratio. In contrast, Kara et al. [38] noted a significant relationship between NES and waist–height ratio. Similarly, Cleator et al. [29] observed a significant positive relation between NES and increased weight.
These inconsistencies may be accounted for by demographic features of participants, which may moderate the association between NES and weight status. Age was noted to moderate the relationship between NES and BMI in one study, which used age as a variable to investigate the impact of NEQ scores on BMI [27]. A significant positive association was reported within participants aged between 31 and 60 years; however, this association was not observed in the other age groups [27]. Consistent with previous studies investigating younger population samples [33,40], six studies [17,19,35,39,40,43] observed no significant relation between NES and BMI when reporting on a sample of college students. In contrast, Kandeger et al. [24], Meule et al. [25] and El Ayoubi et al. [42] reported a significant relationship between NES and BMI when reporting on university students in Turkey, Germany and Lebanon, respectively. Discrepancies between university-aged students and general adult samples [31,37] reiterate the need for further research into NES within adult populations to improve screening and management.
3.5. Physical Activity
Only six studies [17,30,39,43,44,46] explored the impact of NES on physical activity, with four studies [30,39,44,46] reporting a significant association and two studies [17,43] reporting no significant relationship. Levels of physical activity were assessed via the International Physical Activity Questionnaire—Short-form (IPAQ-S) [53], World Health Organization Quality of Life Turkish Short Form (WHOQOL-BREF-TR) [54] and HRQOL scores [6]. Two of the studies which utilised the WHOQOL-BREF-TR and HRQOL did not specifically discuss the physical domains [44,46].
Yahia et al. [17] attributed this lack of relationship between physical activity in NES and non-NES to the reduced age of participants (mean age: 20.6 ± 1.68 years). This was reiterated by Hamdan et al. [43], who reported no significant relation between NES and any level of physical activity (sedentary, moderate or high) in a university student sample. This contrasted with Hamurcu et al. [46] and Runfola et al. [39], who reported a significant relation in a population of university students (mean age = 21.4 ± 3.1 and 20.9 ± 1.7 years, respectively), although competitive athletes comprised 59.6% of the sample size for Runfola et al. Lent et al. [30] reported a significant relationship between higher NEQ scores and engaging in moderate-to-vigorous physical activity, although the mean age of participants was older (mean age: 51.1 ± 15 years). Similar results were obtained by Kim et al. when exploring a representative sample of the Korean general population [44].
Furthermore, Yahia et al. [17] reported on a small sample size of largely female participants, whilst Runfola et al. [39] reported on a larger sample size (n = 1636) of both men and women. Lent et al. [30], like Yahia et al. [17], reported on a largely female population sample (66.7%), and like Runfola et al. [39], this study utilised a large sample size (n = 1017). Although a larger sample was used in Runfola et al. [39], the majority of participants were athletes, who are not representative of the general population. These inconsistencies highlight the need for further research within large, general-population samples.
3.6. Quality of Sleep
Thirteen studies explored the impact of NES on quality of sleep [17,20,23,24,26,28,29,30,33,35,36,41,45]. This was primarily achieved through self-reported questionnaires, such as the Pittsburgh Sleep Quality Index (PSQI) [55], Morningness–Eveningness Questionnaire (MEQ) [56], Insomnia severity index (ISI) [57] and Epworth Sleepiness Scale (ESS) [58]. In contrast, Geliebter et al. [21] utilised polysomnography to objectively assess sleep quality via the Apnoea–Hypopnoea Index (AHI) [59] and diagnose obstructive sleep apnoea (OSA). All studies using the PSQI, MEQ and ESS revealed significant relationships between poor sleep quality and NES, whilst the AHI did not. Although objective data were obtained, Geliebter et al. [21] were limited in providing further information addressed through questionnaires, such as sleep duration, daytime sleepiness and impact of quality of life [11]. Moreover, several studies [17,20,28,33,35,41,45] analysed sleep quality over a month using the PSQI, thus increasing their reliability. These findings support the need for further longitudinal research into the interrelation between NES and aspects of sleep to develop effective screening and management of sleep problems which result from NES.
3.7. Medical Conditions
Five studies [21,28,29,31,36,42,43] investigated the impact of NES on chronic health conditions, including Type 2 diabetes Mellitus (T2DM) [28,29,31,36], metabolic syndrome [31], OSA [21,29] and cardiovascular disease [31,36]. Two additional studies reported on “chronic diseases” and NES, both reporting no significant relationship, although no specifications were reported regarding which conditions [42,43].
Of the four studies exploring the relationship between NES and T2DM [28,29,31,36], only Hood et al. [28] reported significant correlation between NEQ scores and HbA1C. In contrast, Cleator et al. [29,30] and Antelmi et al. [36] reported no significant relation between NES and T2DM, as well as other concomitant diseases, including hypertension, cardiovascular disease and thyroid pathologies. Similarly, Gallant et al. [31] identified no significant relation between NEQ in men and women and metabolic syndrome or T2DM when exploring biochemical markers (glucose, HDL cholesterol, triglycerides). Furthermore, only Gallant et al. [31] examined the interrelation between cardiac health, metabolic syndrome and NES, reporting that higher NEQ scores were associated with lower blood pressure in women and a larger waist circumference and higher triglycerides in men. None of the four studies investigating NES and T2DM were conducted on samples representative of the general population; two of the studies [28,29] were conducted within endocrinology outpatient clinics and another was conducted in restless leg syndrome patients from a sleep centre [36]. Furthermore, due to the small sample sizes used in studies examining the association between medical conditions and NES [28,29,31,36], these results may not be clinically significant for the general population.
Two studies [21,29] explored the impact of NES on obstructive sleep apnoea (OSA) using self-reported data on small sample sizes. Both studies reported no significant association between OSA and NES. Additionally, Geliebter et al. [21] did not observe any significant relationship between NES and AHI. Tools to assess OSA varied; Geliebter et al. [21] utilised polysomnography to diagnose OSA, with the threshold criterion of an AHI greater than or equal to 5; Cleator et al. [29], however, did not report how a diagnosis of OSA was made. Further exploration of large samples of participants representative of the general population and clearly defined methods of diagnosing OSA will provide an improved understanding of NES and its relationship with OSA.
4. Discussion
This scoping review investigated the associations between NES and Body Mass Index (BMI; kg/m2), physical health and sleep conditions. Thirty studies were identified that reported on associations between physical health problems and NES over the past decade [17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46]. Whilst there were inconsistencies in representative and larger-sample studies, NES appeared to be associated with higher BMI, less physical activity and poorer sleep quality. It was not, however, associated with T2DM. Inconsistencies and the lack of association with T2DM may have been because of smaller and less-representative population samples. This review also identified a number of limitations of the extant research.
4.1. Weight Status
This review found a positive relationship between NES and BMI in 16 of 27 studies [18,20,23,24,25,26,27,30,31,32,33,34,36,37,41,42]. Additionally, three studies observed other indicators of weight status, including weight (kg) [29], waist-to-hip ratio [38] and waist circumference [31], which are regarded as more sensitive universal screening tool than BMI to detect increased metabolic risk [60]. An explanation for the inconsistency in results is the use of different measurement methods. Furthermore, demographic features, most notably age, may have moderated associations [61]. For example, Nolan et al. [33] reported a significant relationship for community participants (mean age: 42.9 ± 0.6 years), but not for college students (mean age:18.7 ± 0.1years). However, Nolan et al. [33] did not further explore age as a moderator. Notably, six studies [17,19,36,39,40,43] reporting on a sample of college students and two studies [33,40] investigating younger population samples found no significant relation between NES and BMI.
4.2. Physical Activity
Six studies [17,30,39,43,44,46] reported incongruous findings when exploring the relationship between NES and physical activity. This may result from the use of different tools when assessing physical activity, differences in sample sizes and the exploration of different age groups. Of the six studies, only one study utilised a large representative sample of the general population (n = 34,434) [44]. As such, further research into representative populations of adults may glean a better understanding of the interaction between NES and physical activity.
4.3. Quality of Sleep
Sleep quality was assessed in 13 studies [17,20,23,24,26,28,29,30,33,35,36,41,45]. All studies which utilized self-reported questionnaires reported a significant association between NES and sleep quality, whilst Geliebter et al. [21], who used objective measures, did not. These inconsistencies may result from the use of subjective versus objective measures to assess sleep quality. The NEQ [47], which was the primary tool used to diagnose NES, strongly endorses symptoms related to nocturnal ingestions and sleep (for example, “trouble falling asleep”, “trouble staying asleep” and “waking up at night”), which are also assessed in self-reported questionnaires assessing sleep quality, such as the PSQI [55] and ISI [57]. These results reiterate the need for more objective measures in conjunction with subjective questionaries to assess the association of sleep quality and NES.
4.4. Medical Conditions
This scoping review found four studies [28,29,31,36] which explored the relationship between NES and T2DM, of which only one reported a significant relationship 28. Only Gallant et al. reported on metabolic syndrome, reporting no significant relationship [31]. Neither of the two studies exploring the association between NES and cardiovascular disease reported a significant relationship [31,36]. Both studies investigating the relationship between NES and OSA identified no significant relationship [21,29].
Although the results were largely congruent, the population samples examined within these studies were not representative of a general adult sample. For example, Hood et al. [28] reported on a largely African American sample population (58%), whilst Cleator et al. [29] reported only on Caucasians. Consequently, it is crucial to conduct further research to assess the impact of NES on cardiac and metabolic health within larger representative sample populations. These inconsistencies reiterate the need for further investigation of the impact of NES on glycaemic control and metabolic functioning in patients with T2DM.
4.5. Strengths and Limitations
Strengths and limitations of this scoping review
A scoping review was appropriate as we investigated a broad research topic rather than a single research question. Three data base searches were conducted, dating from 2013; whilst this provided a contemporary focus, it is possible that relevant earlier papers and unpublished grey literature research were missed. Two authors (SS and PH) reached consensus on data that were extracted. However, because we performed a scoping review rather than a systematic review, there was no critical appraisal of studies, no application of PICO framework, no estimation of bias in the studies and no meta-analysis performed.
Strengths and limitations of the extant literature
A limitation of the extant research is the variety of diagnostic instruments and criteria used to diagnose NES. Some studies utilised only one method to assess NES, while others used a combination of interview, DSM criteria and questionnaires. Twenty-seven studies [18,19,20,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,43,44,45,46] utilised the NEQ [47] as the diagnostic criterion for NES and three studies [17,21,42] used the NEDQ [48]. Other measures of NES used in these studies included the EDE-Q [49], NESHI [50] and EAT-II [51]; however, these were used as adjuncts to the NEQ [47] and NEDQ [48].
A further limitation is that most studies were observational rather than experimental, with the majority of the literature reviewed in this scoping review being cross-sectional studies. There was a mixed quality of samples, with five large representative samples [26,27,32,37,44], but many (i.e., 25 studies) smaller and less representative samples.
5. Conclusions
NES is an emerging area for clinical investigation, evaluation and intervention. It is evident through this review that there is a need for further research into NES and its associated features within a representative adult population sample. While few studies have been conducted, data are inconsistent, and thus it is imperative to conduct further research to accurately understand the complex interaction between NES and its associated features. By conducting further research on NES within general population samples, improved diagnostic measures and management plans can be developed to improve the overall health of the community.
Acknowledgments
We acknowledge Lily Collison, Senior Librarian, Western Sydney University, Campbelltown campus, for her technical support in conducting the scoping review.
Author Contributions
S.J.S., H.M. and P.H.; methodology, P.H. and H.M.; software, S.J.S.; validation, P.H. and H.M.; formal analysis, S.J.S.; investigation, S.J.S.; resources, S.J.S.; data curation, S.J.S.; writing—original draft preparation, S.J.S.; writing—review and editing, S.J.S., P.H. and H.M.; visualization, S.J.S.; supervision, P.H. and H.M.; project administration, P.H.; funding acquisition, P.H. All authors have read and agreed to the published version of the manuscript.
Institutional Review Board Statement
Not applicable.
Informed Consent Statement
Not applicable.
Data Availability Statement
Not applicable.
Conflicts of Interest
P.H. has been a consultant to Takeda Pharmaceuticals. S.J.S. and H.M. declare no conflict of interest.
Funding Statement
This research received no external funding.
Footnotes
References
Associated Data
Data Availability Statement
Not applicable.