<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">PSYCH</journal-id><journal-title-group><journal-title>Psychology</journal-title></journal-title-group><issn pub-type="epub">2152-7180</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/psych.2019.1012106</article-id><article-id pub-id-type="publisher-id">PSYCH-95183</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Social Sciences&amp;Humanities</subject></subj-group></article-categories><title-group><article-title>
 
 
  The Lower Prolactin Serum Level Is a Characteristic of Anorexia Nervosa with Depression
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Jihui</surname><given-names>Yue</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Minfeng</surname><given-names>Cheng</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Hong</surname><given-names>Wang</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Shenglin</surname><given-names>Wen</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Psychology, Fifth Affiliated Hospital, Sun Yat-sen University, Zhuhai, China</addr-line></aff><pub-date pub-type="epub"><day>05</day><month>09</month><year>2019</year></pub-date><volume>10</volume><issue>12</issue><fpage>1615</fpage><lpage>1621</lpage><history><date date-type="received"><day>19,</day>	<month>May</month>	<year>2019</year></date><date date-type="rev-recd"><day>17,</day>	<month>September</month>	<year>2019</year>	</date><date date-type="accepted"><day>20,</day>	<month>September</month>	<year>2019</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  This study was designed to explore the relationship between anorexia nervosa and depression and to evaluate the role that endocrine hormones play in anorexia nervosa with functional hypothalamic amenorrhea and comorbid depression. In this study, thyroid hormones and sex hormones were compared between 30 first-episode drug-naive female patients with anorexia nervosa with depression (AND), and 20 female patients with anorexia nervosa with no depression (ANND). There were no differences between anorexia nervosa participants with and without depression in thyroid hormones levels. Patients with AND had significantly lower prolactin serum levels; patients with AND had a median [P25, P75] prolactin level of 213.0 uIU/ml [12.1-268.2] vs. 446.6 uIU/ml [119.1-35.5] for patients with ANND. There were no differences in other sex hormones between the two groups. Our data suggested that a lower prolactin serum level is a characteristic of first-episode neuroleptic-naive patients with AND.
 
</p></abstract><kwd-group><kwd>Anorexia Nervosa</kwd><kwd> Prolactin</kwd><kwd> Depression</kwd><kwd> Amenorrhea</kwd><kwd> Body Mass Index</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Anorexia nervosa (AN) is a potentially life-threatening disorder typically seen in adolescent girls  (Stergioti et al., 2013) . Its diagnosis primarily depends on the clinical manifestation, which is characterized by a serious disturbance in eating behavior, along with cognitive distortions about body shape or body weight. Serious medical complications affect almost every organ system including electrolyte disorders, hematologic disorders, endocrine changes, and severe bone loss  (American Psychiatric Association, 2013) . Although the disorder has been studied from the multifactorial model to a complex developmental model  (Garner, 1993;   Kaye et al., 2009;   Herpertz-Dahlmann et al., 1997) , the etiology of AN remains elusive. AN is associated with a lifelong trajectory and the continued appearance of multiple risk factors over the entire disease time course  (Gicquel, 2013) .</p><p>Adolescents with functional hypothalamic amenorrhea show a higher incidence of subclinical symptoms of AN, including psychosomatic discomfort, and mild depressive traits  (Bomba et al., 2007) . Functional hypothalamic amenorrhea might represent part of the AN biological spectrum, and a link between these two conditions might exist, possibly related to the degree of psychological and/or hormonal dysfunction  (Bomba et al., 2014) . Elevated transaminases are common in severely malnourished patients with AN  (Hanachia et al., 2013) . In addition, with the exception of the reports, four risk factors including young age, low body mass index (BMI), the pure restrictive form of the disease, and male sex were observed.</p><p>The presence of suicidal thoughts and self-injurious behaviors in patients with eating disorders is well known. A significant percentage of adolescents with eating disorders present negative emotions and suicidal ideation  (Varela-Besteiro et al., 2017) . Self-criticism is a significant problem in depression and eating disorders  (Thew et al., 2017) .</p><p>The limitations of studies on patients with AN and comorbid depression have received little attention. Therefore, we performed this study to evaluate endocrine hormones levels in the presence of these conditions in an attempt to further explore the relationship between AN and depression and to evaluate the role that endocrine hormones play in AN and comorbid depression.</p></sec><sec id="s2"><title>2. Materials and Methods</title><p>First-episode inpatients (n = 50) with AN were recruited from inpatient units of the Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong Province, PR China. Most patients were hospitalized for diagnostic or therapeutic purposes for endocrinology-related symptoms. All subjects were adolescent girls presented with severely malnourish and functional hypothalamic amenorrhea. Ethical written informed consent was obtained from all patients in accordance with protocols approved by the Clinical Research Ethics Committee of the Third Affiliated Hospital of Sun Yat-sen University.</p><p>A total of 50 first-episode patients presented with AND; the patients were diagnosed according to the DSM-IV criteria. The patients were divided into two groups based on the presence of comorbid depression: 30 patients with AND, and 20 patients with ANND. A chemiluminescence immunoassay (SIEMENS Advia Centaur XP) was used to measure endocrine hormones levels prior to any medication after hospitalization. Endocrine hormones, including free triiodothyronine, free unbound thyroxine, thyroid stimulating hormone, prolactin, follicle-stimulating hormone, luteinizing hormone, and estradiol were recorded at admission prior to any medication after hospitalization.</p><p>The exclusion criteria for all subjects were as follows: 1) depression that was clearly due to substance abuse, and any other type of psychiatric disturbance; 2) a history of antipsychotic therapy or other medication; 3) physical illnesses including any with cerebral or endocrine pathology; and 4) premenopausal or pregnant women.</p><p>All statistical analyses were conducted with Statistical Program for the Social Sciences (SPSS) software (version 22.0, Chicago, IL, USA). Comparisons between the AN and AND groups were evaluated by Student’s t-test or Mann-Whitney test. The statistical signiﬁcance was set at p &lt; 0.05.</p></sec><sec id="s3"><title>3. Results</title><p>The two groups were similar with regard to age, body mass index, and duration of AN (see <xref ref-type="table" rid="table1">Table 1</xref>). There were no differences between anorexia nervosa participants with and without depression in thyroid hormones levels.</p><p>The two groups differed with regard to prolactin (see <xref ref-type="table" rid="table1">Table 1</xref> and <xref ref-type="fig" rid="fig1">Figure 1</xref>). AND patients had a median [P<sub>25</sub>, P<sub>75</sub>] prolactin level of 213.0 uIU/mL [12.1 - 268.2] vs. 446.6 uIU/mL [119.1 - 635.5] for Group ANND patients (p = 0.004). There were no differences in other sex hormones between the two groups.</p></sec><sec id="s4"><title>4. Discussion</title><p>In our study, 60% of the participants showed depression. Patients with AN often report feeling markedly less well, and this may be associated with changes in</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Demographic and endocrine hormones values at admission</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >ANND (n = 20)</th><th align="center" valign="middle" >AND (n = 30)</th><th align="center" valign="middle" >p value</th></tr></thead><tr><td align="center" valign="middle" >Mean age (&#177;SD)</td><td align="center" valign="middle" >16.2 (3.1)</td><td align="center" valign="middle" >15.5 (2.0)</td><td align="center" valign="middle" >0.267</td></tr><tr><td align="center" valign="middle" >Body mass index(&#177;SD)</td><td align="center" valign="middle" >12.6 (1.7)</td><td align="center" valign="middle" >13.3 (1.8)</td><td align="center" valign="middle" >0.083</td></tr><tr><td align="center" valign="middle" >Duration of AN<sup>a</sup> (P<sub>25</sub>, P<sub>75</sub>)</td><td align="center" valign="middle" >7 (6 - 12)</td><td align="center" valign="middle" >8 (6 - 12)</td><td align="center" valign="middle" >0.299</td></tr><tr><td align="center" valign="middle" >Free triiodothyronine<sup>b</sup> (&#177;SD)</td><td align="center" valign="middle" >2.9 (0.8)</td><td align="center" valign="middle" >2.9 (0.7)</td><td align="center" valign="middle" >0.716</td></tr><tr><td align="center" valign="middle" >Free unbound thyroxine<sup>c</sup> (&#177;SD)</td><td align="center" valign="middle" >13.8 (2.5)</td><td align="center" valign="middle" >12.9 (2.4)</td><td align="center" valign="middle" >0.215</td></tr><tr><td align="center" valign="middle" >Thyroid stimulating hormone<sup>d</sup> (&#177;SD)</td><td align="center" valign="middle" >1.5 (0.8)</td><td align="center" valign="middle" >1.8 (1.0)</td><td align="center" valign="middle" >0.190</td></tr><tr><td align="center" valign="middle" >Prolactin<sup>e</sup> (P<sub>25</sub>, P<sub>75</sub>)</td><td align="center" valign="middle" >446.6 (119.1 - 635.5)</td><td align="center" valign="middle" >213.0 (12.1 - 268.2)</td><td align="center" valign="middle" >0.004</td></tr><tr><td align="center" valign="middle" >Follicle stimulating hormone<sup>f</sup> (P<sub>25</sub>, P<sub>75</sub>)</td><td align="center" valign="middle" >0.5 (0.0 - 1.8)</td><td align="center" valign="middle" >0.7 (0.2-2.0)</td><td align="center" valign="middle" >0.437</td></tr><tr><td align="center" valign="middle" >Luteinizing hormone<sup>g</sup> (P<sub>25</sub>, P<sub>75</sub>)</td><td align="center" valign="middle" >0.0 (0.0 - 0.1)</td><td align="center" valign="middle" >0.0 (0.0 - 0.4)</td><td align="center" valign="middle" >0.558</td></tr><tr><td align="center" valign="middle" >Estradiol<sup>h</sup> (P<sub>25</sub>, P<sub>75</sub>)</td><td align="center" valign="middle" >15.9 (6.6 - 106.6)</td><td align="center" valign="middle" >29.8 (20.9 - 86.4)</td><td align="center" valign="middle" >0.735</td></tr></tbody></table></table-wrap><p><sup>a</sup>Duration of AN given in months. <sup>b</sup>Reference free triiodothyronine serum level: 3.10 - 6.80 pmol/L. <sup>c</sup>Reference free unbound thyroxine serum level: 12.30 - 20.20 pmol/L. <sup>d</sup>Reference thyroid stimulating hormone serum level: 0.27 - 4.20 uIU/mL. <sup>e</sup>Reference prolactin serum level, women who are menopausal: 59 - 619 uIU/mL. <sup>f</sup>Reference follicle stimulating hormone serum levels, women who are menopausal: 26.72 - 133.41 mIU/mL. <sup>g</sup>Reference luteinizing hormone serum levels, women who are menopausal: 1.78 - 92.10 mIU/mL. <sup>h</sup>Reference estradiol serum levels, women who are menopausal: &lt;10 - 28 pg/mL.</p><p>steroid hormones  (Rigaud et al., 2010;   Wassif et al., 2011) . Individuals with AN have been observed to have lower levels of emotion expression  (Davies et al., 2011;   Rhind et al., 2014) . Age was not associated with poor emotion expression, but characteristics involving lower BMI, social anhedonia, and depression were associated with poor emotion expression  (Lang et al., 2016) . The evidence for depression in patients with AN associated with increased levels of pro-inflammatory mediators has been less clear. Metabolic disturbances in AN would lead to a pattern of immune disturbances distinct from that of depression. Loss of adipose tissue may attenuate cytokine production and thus modulate the experience of illness  (Pisetsky et al., 2014) . The AN subjects had low concentrations of insulin-like growth factor-1, relative hypercortisolemia, leptin, insulin, amylin, and incretins; and high concentrations of ghrelin, peptide YY, and adiponectin. These changes might affect neurocognition, anxiety, depression, and the psychopathology of AN  (Misra &amp; Klibanski, 2014) .</p><p>In this study, all subjects were adolescent girls who presented with severe malnourishment and functional hypothalamic amenorrhea. The data on the hormonal functions are intriguing. Low levels of luteinizing hormone and follicle-stimulating hormone at baseline remained low at 1-year follow-up in AN subjects; and, resumption of menses did not depend on BMI but on restoration of hypothalamic-pituitary-ovarian function  (Golden et al., 1997) . We can assume that hormonal imbalance resulted from an altered hypothalamic-pituitary tone secondary to aforementioned structural brain changes and hypothalamic-pituitary-ovarian dysfunction associated with worsened malnutrition.</p><p>We found significant differences in prolactin serum levels between AND and ANND patients at admission. Patients with AND had lower prolactin serum levels than those in the ANND group. The results showed that decreased prolactin serum levels, which were caused by depression, were related to emotion. Research shows that prolactin can affect the dopaminergic activity (DA) and change the DA receptor sensitivity  (Aihara et al., 2004) . The results indicate that the difference in serum prolactin levels between groups could result from the specific pattern of prolactin secretion with alterations in DA. It was not a change in BMI but depression that played a role in treatment outcomes of patients with eating disorders  (Fewell et al., 2017) . Therefore, alleviating a depressive symptom could be considered as a first-line treatment option for patients with AN with depression.</p><p>Our study is limited by an inevitable selection bias because the study sample consisted of patients from our hospital. In addition, the study group consisted only of females, and there was a lack of clinical data after treatment. Such a sample may not be representative of all patients with AN with depression. In addition, this study did not include a depression control group; we cannot conclude that reduced prolactin serum levels are specific to AN or apparent in depression disorders in general. The results must be confirmed in a multicenter study before deﬁnite conclusions can be drawn.</p></sec><sec id="s5"><title>5. Conclusion</title><p>In summary, this study included adolescent girls who presented with severe malnourishment and functional hypothalamic amenorrhea. Patients with AND had lower prolactin serum levels than those patients with ANND. A better understanding of clinical characteristics of AN with depression would provide better treatment for patients with these problems.</p></sec><sec id="s6"><title>Contributors</title><p>Wen Shenglin designed the study. Yue Jihui and Wang Hong collected the original data. Cheng Minfeng managed and analyzed the data. Yue Jihui wrote the manuscript. Wen Shenglin revised the paper. All authors contributed to and have approved the ﬁnal manuscript.</p></sec><sec id="s7"><title>Acknowledgements</title><p>The study was supported by grants from the Technology Project of Guangdong Province, China (No. 2014A 020212530).</p></sec><sec id="s8"><title>Conflicts of Interest</title><p>No conﬂict of interest declared.</p></sec><sec id="s9"><title>Cite this paper</title><p>Yue, J. H., Cheng, M. F., Wang, H., &amp; Wen, S. L. (2019). The Lower Prolactin Serum Level Is a Characteristic of Anorexia Nervosa with Depression. Psychology, 10, 1615-1621. https://doi.org/10.4236/psych.2019.1012106</p></sec><sec id="s10"><title>NOTES</title></sec></body><back><ref-list><title>References</title><ref id="scirp.95183-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Aihara, K., Shimada, J., Miwa, T., Tottori, K., Burris, K. D., Yocca, F. D., Horie, M., &amp; Kikuchi, T. (2004). 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