Eating disorder

饮食失调
  • 文章类型: Journal Article
    这项研究的目的是确定腹腔疾病(CD)患者中避免/限制性食物摄入障碍(ARFID)的患病率,并评估代谢并发症,疾病控制,饮食依从性,以及与症状和生活质量指标的相关性。
    这是一项对137名成人CD患者的回顾性研究,他们在2018年至2020年之间在CD诊所完成了ARFID调查。人口统计,临床结果,标准化饮食评估,并回顾了乳糜泻症状日记和无麸质饮食问卷的影响。测量的主要结果是基于患者报告的调查响应的怀疑ARFID的比率。
    78名患者(57%)符合疑似ARFID标准。年龄没有差异,性别,身体质量指数,微量营养素缺乏,或患有或不患有ARFID的骨骼疾病。与非ARFID患者相比,ARFID患者在活检活动或对无麸质饮食的依从性方面没有差异。食物和社会负担对无麸质饮食问卷的影响最能预测ARFID。
    ARFID很常见,对CD患者影响很大。虽然有些饮食行为肯定是由于他们的CD,有或没有怀疑ARFID的患者在疾病控制方面没有明显差异,这表明这些不适应的行为不是疾病控制所必需的。我们没有发现代谢并发症增加,但这是两年的快照.我们需要进一步了解社会和食物对在这项调查中得分高的患者的影响,以防止进一步的缺陷和损害,长期有害的饮食行为。
    UNASSIGNED: The objective of this study was to identify the prevalence of avoidant/restrictive food intake disorder (ARFID) in patients with celiac disease (CD) and assess metabolic complications, disease control, diet adherence, and correlation with symptom and quality-of-life metrics.
    UNASSIGNED: This was a retrospective study of 137 adult patients with CD who completed an ARFID survey in the CD clinic between 2018 and 2020. Demographics, clinical results, standardized diet assessment, and results of Celiac Disease Symptom Diary and Impact of a Gluten-free Diet Questionnaire were reviewed. The primary outcome measured was the rate of suspected ARFID based on patient-reported survey responses.
    UNASSIGNED: Seventy-eight patients (57%) met suspected ARFID criteria. There were no differences in age, gender, body mass index, micronutrient deficiencies, or bone disease in those with or without ARFID. Patients with ARFID did not have a difference in biopsy activity or better adherence to a gluten-free diet compared with non-ARFID patients. Food and social burden on Impact of a Gluten-free Diet Questionnaire was most predictive of ARFID.
    UNASSIGNED: ARFID is common and has a high impact in patients with CD. Although some eating behavior is certainly due to their CD, there was no distinct difference in disease control between those with or without suspected ARFID, suggesting these maladaptive behaviors are not necessary for disease control. We did not find increased metabolic complications, but this was a 2-year snapshot. We need to further understand the social and food impacts on patients who score high on this survey to prevent further deficiencies and impaired, long-term detrimental eating behaviors.
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  • 文章类型: Journal Article
    背景:精神病理学障碍通常是进食障碍(ED)的共病诊断。我们旨在评估意大利高中青少年人群中与ED相关的精神病理学特征和症状的存在。
    方法:招募了一个高中青少年样本,收集人口统计学和临床数据。两份自我报告问卷,饮食失调量表-3(EDI-3)和青少年精神病理学评估问卷(Q-PAD),被管理。
    结果:纳入548名青少年(333F/215M;16.89±0.85岁)。与临床或高度临床关注的ED相关的症状在一系列个体中普遍存在,百分比从身体不满意的26.82%到感受缺陷的51.83%不等。Q-PAD评估的结果表明存在心理困扰,导致不适或具有挑战性的情况,需要对青少年进行潜在干预的比例从2.93%的心理社会风险到23.77%的焦虑。这些百分比显示了性别之间的差异(F>M,p<0.001)。我们的研究还强调了ED的症状与家庭中的生活方式因素之间的关联。我们观察到Q-PAD测量值与EDI-3得分之间的相关性,包括Q-PAD和EDI-3身体不满之间的正相关(r=0.7),Q-PAD人际冲突与EDI-3人际问题呈负相关(r=0.6),Q-PAD自尊与幸福感和EDI-3无效性复合(r=-0.7)。
    结论:记录了高中青少年中ED症状和心理困扰的相当普遍。这些条件是相互关联的,表明全面解决这些问题的重要性。早期发现对于改善治疗结果和实施预防策略至关重要。
    BACKGROUND: Psychopathological disorders are often comorbid diagnosis in eating disorders (EDs). We aimed to assess the presence of psychopathological traits and symptoms associated with EDs in an Italian high school adolescent population.
    METHODS: A sample of high school adolescents was enrolled, and demographic and clinical data were collected. Two self-report questionnaires, the Eating Disorder Inventory-3 (EDI-3) and the Questionnaire for the Assessment of Psychopathology in Adolescence (Q-PAD), were administered.
    RESULTS: 548 adolescents (333 F/215 M; 16.89 ± 0.85 years) were included. Symptoms associated with EDs of clinical or high clinical concern were prevalent in a range of individuals, with percentages varying from 26.82% for body dissatisfaction to 51.83% for Interoceptive Deficits. The findings from the Q-PAD assessment indicated the presence of psychological distress, leading to discomfort or challenging situations requiring potential intervention in a percentage of adolescents ranging from 2.93% for psychosocial risks to 23.77% for anxiety. These percentages showed differences between genders (F > M, p < 0.001). Our study also highlighted an association between symptoms of EDs and lifestyle factors within families. We observed correlations between Q-PAD measures and EDI-3 scores, including a positive correlation between Q-PAD and EDI-3 body dissatisfaction (r = 0.7), Q-PAD interpersonal conflicts and EDI-3 interpersonal problems (r = 0.6) and a negative correlation between Q-PAD self-esteem and well-being and EDI-3 ineffectiveness Composite (r=-0.7).
    CONCLUSIONS: a substantial prevalence of ED symptoms and psychological distress among high school adolescents were recorded. These conditions are interrelated, suggesting the importance of addressing them comprehensively. Early detection is essential to improve treatment outcomes and to implement preventive strategies.
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  • 文章类型: Journal Article
    背景/目标:迄今为止,已经进行了一些系统评价和荟萃分析,表明精英运动员饮食失调的患病率高以及相关的危险因素。然而,与查找和比较这些评论相关的大量时间负担,方法和抽样重点各不相同,可能是告知政策和最佳实践以及指导未来研究的障碍。这篇综述旨在提供有关精英运动员饮食失调(包括身体形象问题和饮食失调)的患病率和危险因素的已发表综述的证据摘要。方法:五个数据库(CINAHL,PsycINFO,MEDLINE,Scopus,和SPORTDiscus)系统搜索符合以下纳入标准的同行评审系统评价和荟萃分析:(1)调查患病率和饮食紊乱的危险因素,(2)包括优秀运动员的样本,和(3)可用英语。纳入的研究使用AMSTAR2进行数据提取和偏倚风险评估。结果:最初的搜索确定了1828篇文章,这些文章经过标题和摘要筛选,然后是全文,留下24项系统评价(包括10项荟萃分析)。饮食失调在精英运动员中普遍存在,包括男性和女性以及跨运动类型。与非运动员对照相比,精英运动员饮食失调和饮食失调的风险较高,但身体形象问题的风险较低。确定了几个风险因素,包括女性,在精益运动中竞争,经历职业变化。很少有评论或荟萃分析检查了运动环境中的感知压力,大多数人都有很大的偏见风险。结论:精英运动员有饮食失调的风险,所有这些都应考虑进行一级预防和筛查。需要进一步研究特定运动与一般压力和风险中介,以更好地为干预措施提供信息。
    Background/Objectives: Several systematic reviews and meta-analyses have been conducted to date indicating a high prevalence of disordered eating in elite athletes and associated risk factors. However, the substantial time burden associated with locating and comparing these reviews, which are varied in methodology and sampling focus, may be a barrier for informing policy and best practice as well as directing future research. This umbrella review aimed to provide a summary of evidence across published reviews regarding the prevalence and risk factors for disordered eating (including body image concerns and eating disorders) in elite athletes. Methods: Five databases (CINAHL, PsycINFO, MEDLINE, Scopus, and SPORTDiscus) were systematically searched for peer-reviewed systematic reviews and meta-analyses that met the following inclusion criteria: (1) investigated prevalence and risk factors for disordered eating, (2) included a sample of elite athletes, and (3) available in English. The included studies underwent data extraction and risk of bias assessment using the AMSTAR 2. Results: The initial search identified 1828 articles that were screened for title and abstract and then full text, leaving 24 systematic reviews (including 10 meta-analyses). Disordered eating was prevalent across elite athletes, including males and females and across sport type. Elite athletes were at elevated risk for disordered eating and eating disorders but at lower risk for body image concerns versus non-athlete controls. Several risk factors were identified, including female gender, competing in lean sports, and experiencing career changes. Few reviews or meta-analyses examined perceived pressures within the sporting environment, and most had substantial risk of bias concerns. Conclusions: Elite athletes are at risk for the spectrum of disordered eating, and all should be considered for primary prevention and screening. Further research is needed regarding sport-specific versus general pressures and mediators of risk to better inform interventions.
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  • 文章类型: Journal Article
    与溃疡性结肠炎(UC)风险相关的厌食症和贪食症的证据有限且不一致。这项研究的目的是利用双向,双样本孟德尔随机化(MR)分析,以预测神经性厌食症和神经性贪食症与UC之间的因果关系。
    全基因组关联研究(GWAS)提供了来自英国生物库的厌食症和贪食症的数据,利用单核苷酸多态性(SNP)作为工具变量。此外,与UC的遗传关联是从各种来源收集的,包括FinnGen生物库,英国生物银行和国际炎症性肠病遗传学联合会(IIBDGC)。本研究中使用的主要分析方法是逆方差加权(IVW)方法。要评估水平多效性,研究人员进行了MR-Egger回归和MR-PRESSO全局测试分析.此外,使用CochranQ检验评估异质性。
    这项研究发现,遗传预测的贪食症(OR=0.943,95%CI:0.893-0.996;p=0.034)与IIBDGC数据集中的UC风险之间存在负相关,这表明暴食症患者发生UC的风险降低约5.7%.在其他两个数据集中未观察到关联。相反,遗传预测的厌食症未发现与UC有因果关系.在双向孟德尔随机化中,IIBDGC数据集中的UC与厌食症的风险呈负相关(OR=0.877,95%CI:0.797-0.965;p=0.007),提示UC患者发生厌食症的风险降低约12.3%,但与贪食症没有因果关系。
    遗传预测的贪食症可能与UC的发作呈负相关,而遗传预测的厌食症与UC的发展没有因果关系。相反,遗传预测的UC可能与厌食症的发展呈负相关。
    UNASSIGNED: Evidence for anorexia and bulimia in relation to the risk of ulcerative colitis (UC) is limited and inconsistent. The objective of this research was to utilize bi-directional, two-sample Mendelian randomization (MR) analysis to predict the causal association between anorexia nervosa and bulimia nervosa with UC.
    UNASSIGNED: The genome-wide association studies (GWAS) provided data for anorexia and bulimia from the UK Biobank, utilizing single-nucleotide polymorphisms (SNP) as instrumental variables. Additionally, genetic associations with UC were collected from various sources including the FinnGen Biobank, the UK Biobank and the International Inflammatory Bowel Disease Genetics Consortium (IIBDGC). The main analytical approach utilized in this study was the inverse-variance-weighted (IVW) method. To evaluate horizontal pleiotropy, the researchers conducted MR-Egger regression and MR-PRESSO global test analyses. Additionally, heterogeneity was assessed using the Cochran\'s Q test.
    UNASSIGNED: This study found a negative association between genetically predicted bulimia (OR = 0.943, 95% CI: 0.893-0.996; p = 0.034) and the risk of UC in the IIBDGC dataset, indicating that individuals with bulimia have approximately a 5.7% lower risk of developing UC. No association was observed in the other two datasets. Conversely, genetically predicted anorexia was not found to be causally associated with UC. In bi-directional Mendelian randomization, UC from the IIBDGC dataset was negatively associated with the risk of anorexia (OR = 0.877, 95% CI: 0.797-0.965; p = 0.007), suggesting that UC patients have approximately a 12.3% lower risk of developing anorexia, but not causally associated with bulimia.
    UNASSIGNED: Genetically predicted bulimia may have a negative association with the onset of UC, while genetically predicted anorexia does not show a causal relationship with the development of UC. Conversely, genetically predicted UC may have a negative association with the development of anorexia.
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  • 文章类型: Editorial
    暂无摘要。
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  • 文章类型: Journal Article
    背景:青少年饮食失调(ED)的评估很大程度上依赖于自我报告,然而,对症状的存在和/或严重性的持续缺乏认识可能是ED的内在因素.这项研究考察了半结构化访谈的心理测量学特性,饮食失调检查(PEDE)的父版本,开发用于系统地评估护理人员的症状报告。
    方法:多站点,对寻求神经性厌食症(AN)和亚综合征性AN治疗的青年患者(N=522;年龄范围:12~18岁)的临床样本进行了评估,使用针对青年患者的进食障碍检查(EDE)和针对辅助护理人员的PEDE报告.
    结果:四个PEDE分量表的内部一致性与EDE的既定范围相当。在每种度量的相应子量表之间发现了显着的中型相关性和差至中等水平的一致性。对于PEDE,EDE四因素模型的验证性因子分析提供了较差的拟合;探索性因子分析表明3因素模型更适合PEDE.
    结论:研究结果表明,PEDE具有与原始EDE相当的心理测量特性。护理人员视角的增加可以提供增量信息,可以帮助评估青年中的AN。未来的研究有必要在更广泛的诊断性ED样本中建立PEDE的心理测量特性。
    饮食失调的评估主要依靠自我报告;然而,在患有神经性厌食症的青少年中,否认症状或症状严重程度可能会使评估复杂化,并延迟该人群的治疗。父母饮食失调检查(PEDE)是第一个正式开发的半结构化访谈,旨在通过纳入照顾者的观点来改善儿童饮食失调评估。在这项研究中,大量神经性厌食症青少年样本完成了自我报告访谈(饮食失调检查或EDE),其父母完成了PEDE。PEDE似乎一直在衡量父母对孩子饮食失调症状的报告。两次访谈的结果彼此相关,但并不完全一致。这表明在饮食失调评估中,PEDE可以提供护理人员的额外信息,这些信息可能会减少诊断混乱,并导致对患有神经性厌食症的青少年进行早期干预.
    BACKGROUND: Assessment of eating disorders (ED) in youth relies heavily on self-report, yet persistent lack of recognition of the presence and/or seriousness of symptoms can be intrinsic to ED. This study examines the psychometric properties of a semi-structured interview, the parent version of the Eating Disorder Examination (PEDE), developed to systematically assess caregiver report of symptoms.
    METHODS: A multi-site, clinical sample of youth (N = 522; age range: 12 to 18 years) seeking treatment for anorexia nervosa (AN) and subsyndromal AN were assessed using the Eating Disorder Examination (EDE) for youth and the PEDE for collateral caregiver report.
    RESULTS: Internal consistencies of the four PEDE subscales were on par with established ranges for the EDE. Significant medium-sized correlations and poor to moderate levels of agreement were found between the corresponding subscales on each measure. For the PEDE, confirmatory factor analysis of the EDE four-factor model provided a poor fit; an exploratory factor analysis indicated that a 3-factor model better fits the PEDE.
    CONCLUSIONS: Findings suggest that the PEDE has psychometric properties on par with the original EDE. The addition of the caregiver perspective may provide incremental information that can aid in the assessment of AN in youth. Future research is warranted to establish psychometric properties of the PEDE in broader transdiagnostic ED samples.
    Assessments for eating disorders rely primarily on self-report; yet, the denial of symptoms or symptom severity among adolescents with anorexia nervosa can complicate assessment and delay treatment in this population. The Parent Eating Disorder Examination (PEDE) is the first semi-structured interview formally developed to improve childhood eating disorder assessment by including caregiver perspectives. In this study, a large sample of adolescents with anorexia nervosa completed a self-report interview (the Eating Disorder Examination or EDE) and their parents completed the PEDE. The PEDE appeared to measure parents’ report of their child’s eating disorder symptoms consistently. Results from both interviews were related to one another but did not completely agree. This suggests that in an eating disorder assessment, the PEDE can provide additional information from caregivers that might reduce diagnostic confusion and lead to earlier intervention for youth with anorexia nervosa.
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  • 文章类型: Journal Article
    目标:垂直袖状胃切除术(VSG)后,饮食行为在体重恢复中的作用尚不清楚。这项研究旨在检查VSG对过度体重减轻(EWL)和五个饮食相关变量(食物成瘾,去抑制,对饥饿的易感性,饮食限制,和体重问题),同时在手术前和术后八个月探索它们的关联。
    方法:从魁北克一家医疗中心招募了76名接受VSG的参与者,加拿大。测量包括体重指数(BMI),饮食失调检查(体重问题),耶鲁食物成瘾量表(食物成瘾),和三因素饮食问卷(去抑制,对饥饿的易感性,和饮食限制)。在手术前(T0)和手术后八个月(T8)之间进行T检验,并检查了T0和T8之间、T0内和T8内的相关性。
    结果:T8时平均EWL为63.43%±13.14。T0和T8之间的比较显示食物成瘾的显着减少,去抑制,和饥饿易感性(p=0.001-0.005)。在饮食限制和体重方面没有观察到显着差异。T0时的BMI与T8时的EWL呈负相关(r=-0.45)。在T0内,观察到食物成瘾和饮食限制之间呈负相关(r=-0.42),在T8内由负变为正(r=0.35)。
    结论:这项研究证实,VSG对减肥有效,并且与不良饮食行为的减少有关。手术后,食物成瘾程度较高的个体表现出更多的饮食限制,这表明需要在那些对食物有强烈渴望的人中保持克制。然而,体重问题仍然很高,即使在体重显著减轻后,表明仅靠减肥可能不足以改变。手术后的医疗随访侧重于整体福祉和生活方式的适应将是一个重要的补充。
    OBJECTIVE: Following vertical sleeve gastrectomy (VSG), the role of eating behaviors in weight regain remains unclear. This study aimed to examine the effects of VSG on excess weight loss (EWL) and five eating-related variables (food addiction, disinhibition, susceptibility to hunger, dietary restraint, and weight concern) while exploring their associations before and eight months post-surgery.
    METHODS: A sample of 76 participants who underwent VSG was recruited from a healthcare center in Quebec, Canada. Measurements included body mass index (BMI), the Eating Disorder Examination (weight concern), the Yale Food Addiction Scale (food addiction), and the Three-Factor Eating Questionnaire (disinhibition, susceptibility to hunger, and dietary restraint). T-tests were conducted between pre-surgery (T0) and eight-month post-surgery (T8), and correlations were examined between T0 and T8, within T0, and within T8.
    RESULTS: The mean EWL was 63.43% ± 13.14 at T8. Comparisons between T0 and T8 showed a significant decrease in food addiction, disinhibition, and susceptibility to hunger (p = 0.001-0.005). No significant differences were observed for dietary restraint and weight concerns. BMI at T0 was negatively correlated with EWL at T8 (r = -0.45). Within T0, a negative correlation was observed between food addiction and dietary restraint (r = -0.42), which changed from negative to positive within T8 (r = 0.35).
    CONCLUSIONS: This study confirmed that VSG is effective for weight loss and associated with a reduction in maladaptive eating behaviors. Postsurgery, individuals with greater food addiction exhibited more dietary restraint, suggesting a need for restraint among those experiencing a strong drive toward food. However, weight concerns remained high even after significant weight loss, indicating that weight loss alone may not be sufficient for change. A postsurgery medical follow-up focusing on overall well-being and lifestyle adaptation would be a crucial complement.
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  • 文章类型: Journal Article
    据推测,神经性厌食症(AN)的发病机理涉及多个生物系统。然而,可靠的AN生物标志物尚未建立。本研究旨在鉴定与AN相关的具有统计学意义和临床意义的外周生物标志物。进行了系统的文献检索,以确定从开始到2022年6月30日以英语发表的研究。我们进行了两级随机效应荟萃分析,以检查在52种不同的生物标志物中AN和对照组之间的差异,发现酰化生长素释放肽,促肾上腺皮质激素(ACTH),羧基末端胶原交联(CTX),胆固醇,皮质醇,去酰基生长素释放肽,ghrelin,生长激素(GH),obestatin,与非AN对照相比,AN病例的可溶性瘦素受体水平显着升高。相反,C反应蛋白(CRP),CD3阳性,CD8,肌酐,雌二醇,卵泡刺激素(FSH),游离甲状腺素,游离三碘甲状腺原氨酸,葡萄糖,胰岛素,胰岛素样生长因子1(IGF-1),瘦素,黄体生成素,淋巴细胞,与非AN对照组相比,AN中的催乳素水平显着降低。我们的发现表明,外周生物标志物可能与AN的病理生理学有关,比如适应饥饿的过程。对外周生物标志物的科学研究可能最终在AN的个性化临床护理中取得突破。
    The pathogenesis of anorexia nervosa (AN) has been hypothesized to involve several biological systems. However, reliable biomarkers for AN have yet to be established. This study was aimed to identify statistically significant and clinically meaningful peripheral biomarkers associated with AN. A systematic literature search was conducted to identify studies published in English from inception until 30 June 2022. We conducted two-level random-effects meta-analyses to examine the difference between AN and comparison groups across 52 distinct biomarkers and found that acylated ghrelin, adrenocorticotropic hormone (ACTH), carboxy-terminal collagen crosslinks (CTX), cholesterol, cortisol, des-acyl ghrelin, ghrelin, growth hormone (GH), obestatin, and soluble leptin receptor levels were significantly higher in cases of AN compared with those in non-AN controls. Conversely, C-reactive protein (CRP), CD3 positive, CD8, creatinine, estradiol, follicle-stimulating hormone (FSH), free thyroxine, free triiodothyronine, glucose, insulin, insulin-like growth factor 1 (IGF-1), leptin, luteinizing hormone, lymphocyte, and prolactin levels were significantly lower in AN compared with those in non-AN controls. Our findings indicate that peripheral biomarkers may be linked to the pathophysiology of AN, such as processes of adaptation to starvation. Scientific investigation into peripheral biomarkers may ultimately yield breakthroughs in personalized clinical care for AN.
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  • 文章类型: Editorial
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  • 文章类型: Journal Article
    神经性厌食症(AN)是一种复杂的神经精神疾病。本系统综述综合了来自各种研究的证据,以评估和研究AN患者的基因多态性与心理和神经生物学因素之间的关联。
    跨PubMed的系统搜索,PsycINFO,Scopus,和WebofScience数据库,随着手动搜索,进行了。审查方案经PROSPERO(CRD42023452548)批准。在1,250篇文章中,11符合纳入标准。使用纽卡斯尔-渥太华量表(NOS)工具评估合格文章的质量。系统审查遵循PRISMA指南。
    5-羟色胺能系统,特别是5-HTTLPR多态性,始终与腹侧注意力网络中改变的连通性相关联,抑制控制受损,对AN的敏感性增加。5-HTTLPR多态性影响奖励处理,动机,推理,工作记忆,抑制,和AN患者的预后预测。多巴胺能系统,涉及像COMT这样的基因,DRD2、DRD3和DAT1调节奖励,动机,和决策。这些多巴胺能基因的遗传变异与AN患者的心理表现和临床严重程度有关。在人群中,BDNF基因的Val66Met多态性影响人格特征,饮食行为,和情绪反应。像OXTR这样的基因,TFAP2B,KCTD15与社会认知有关,情绪处理,身体形象问题,和AN患者的人格维度。
    多个基因与AN的易感和/或严重程度有关联。这种遗传因素有助于AN的复杂性,并导致其临床表现的更高多样性。因此,进行更广泛的研究以阐明神经性厌食症病理的潜在机制对于提高我们的认识和开发针对该疾病的有针对性的治疗干预措施至关重要.系统审查注册:[https://clinicaltrials.gov/],标识符[CRD42023452548]。
    UNASSIGNED: Anorexia nervosa (AN) is a complex neuropsychiatric disorder. This systematic review synthesizes evidence from diverse studies to assess and investigate the association between gene polymorphisms and psychological and neurobiological factors in patients with AN.
    UNASSIGNED: A systematic search across PubMed, PsycINFO, Scopus, and Web of Science databases, along with manual searching, was conducted. The review protocol was approved by PROSPERO (CRD42023452548). Out of 1,250 articles, 11 met the inclusion criteria. The quality of eligible articles was assessed using the Newcastle-Ottawa Scale (NOS) tool. The systematic review followed the PRISMA guidelines.
    UNASSIGNED: The serotoninergic system, particularly the 5-HTTLPR polymorphism, is consistently linked to altered connectivity in the ventral attention network, impaired inhibitory control, and increased susceptibility to AN. The 5-HTTLPR polymorphism affects reward processing, motivation, reasoning, working memory, inhibition, and outcome prediction in patients with AN. The dopaminergic system, involving genes like COMT, DRD2, DRD3, and DAT1, regulates reward, motivation, and decision-making. Genetic variations in these dopaminergic genes are associated with psychological manifestations and clinical severity in patients with AN. Across populations, the Val66Met polymorphism in the BDNF gene influences personality traits, eating behaviors, and emotional responses. Genes like OXTR, TFAP2B, and KCTD15 are linked to social cognition, emotional processing, body image concerns, and personality dimensions in patients with AN.
    UNASSIGNED: There was an association linking multiple genes to the susceptibly and/or severity of AN. This genetic factor contributes to the complexity of AN and leads to higher diversity of its clinical presentation. Therefore, conducting more extensive research to elucidate the underlying mechanisms of anorexia nervosa pathology is imperative for advancing our understanding and potentially developing targeted therapeutic interventions for the disorder.Systematic review registration: [https://clinicaltrials.gov/], identifier [CRD42023452548].
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