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<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Psychol.</journal-id>
<journal-title>Frontiers in Psychology</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Psychol.</abbrev-journal-title>
<issn pub-type="epub">1664-1078</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fpsyg.2024.1394954</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Psychology</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Health-related quality of life in severe hypersensitivity reactions: focus on severe allergic asthma and hymenoptera venom anaphylaxis&#x2014;a cross-sectional study</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name><surname>Ricciardi</surname> <given-names>Luisa</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
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<contrib contrib-type="author">
<name><surname>Silvestro</surname> <given-names>Orlando</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
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<contrib contrib-type="author">
<name><surname>Martino</surname> <given-names>Gabriella</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
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<contrib contrib-type="author" corresp="yes">
<name><surname>Catalano</surname> <given-names>Antonino</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="corresp" rid="c001"><sup>&#x002A;</sup></xref>
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<contrib contrib-type="author">
<name><surname>Vicario</surname> <given-names>Carmelo Mario</given-names></name>
<xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
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<name><surname>Lund-Jacobsen</surname> <given-names>Trine</given-names></name>
<xref ref-type="aff" rid="aff4"><sup>4</sup></xref>
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<contrib contrib-type="author">
<name><surname>Schwarz</surname> <given-names>Peter</given-names></name>
<xref ref-type="aff" rid="aff4"><sup>4</sup></xref>
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<contrib contrib-type="author">
<name><surname>Sapienza</surname> <given-names>Daniela</given-names></name>
<xref ref-type="aff" rid="aff5"><sup>5</sup></xref>
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<name><surname>Gangemi</surname> <given-names>Sebastiano</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
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<name><surname>Pioggia</surname> <given-names>Giovanni</given-names></name>
<xref ref-type="aff" rid="aff6"><sup>6</sup></xref>
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<contrib contrib-type="author">
<name><surname>Giorgianni</surname> <given-names>Concetto Mario</given-names></name>
<xref ref-type="aff" rid="aff5"><sup>5</sup></xref>
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<aff id="aff1"><sup>1</sup><institution>Department of Clinical and Experimental Medicine, University of Messina</institution>, <addr-line>Messina</addr-line>, <country>Italy</country></aff>
<aff id="aff2"><sup>2</sup><institution>Department of Health Sciences, University Magna Graecia of Catanzaro</institution>, <addr-line>Catanzaro</addr-line>, <country>Italy</country></aff>
<aff id="aff3"><sup>3</sup><institution>Department of Cognitive Science, Psychology, Education and Cultural Studies, University of Messina</institution>, <addr-line>Messina</addr-line>, <country>Italy</country></aff>
<aff id="aff4"><sup>4</sup><institution>Department of Endocrinology and Metabolism, Rigshospitalet</institution>, <addr-line>Copenhagen</addr-line>, <country>Denmark</country></aff>
<aff id="aff5"><sup>5</sup><institution>Department of Biomedical and Dental Sciences and Morphofunctional Imaging, University of Messina</institution>, <addr-line>Messina</addr-line>, <country>Italy</country></aff>
<aff id="aff6"><sup>6</sup><institution>Institute for Biomedical Research and Innovation (IRIB), National Research Council of Italy (CNR)</institution>, <addr-line>Messina</addr-line>, <country>Italy</country></aff>
<author-notes>
<fn fn-type="edited-by" id="fn0001">
<p>Edited by: Gianluca Castelnuovo, Catholic University of the Sacred Heart, Italy</p>
</fn>
<fn fn-type="edited-by" id="fn0002">
<p>Reviewed by: Alberto Sardella, University of Catania, Italy</p>
<p>Ada Ghiggia, University of Trieste, Italy</p>
</fn>
<corresp id="c001">&#x002A;Correspondence: Antonino Catalano, <email>catalanoa@unime.it</email></corresp>
</author-notes>
<pub-date pub-type="epub">
<day>23</day>
<month>08</month>
<year>2024</year>
</pub-date>
<pub-date pub-type="collection">
<year>2024</year>
</pub-date>
<volume>15</volume>
<elocation-id>1394954</elocation-id>
<history>
<date date-type="received">
<day>10</day>
<month>04</month>
<year>2024</year>
</date>
<date date-type="accepted">
<day>09</day>
<month>08</month>
<year>2024</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x00A9; 2024 Ricciardi, Silvestro, Martino, Catalano, Vicario, Lund-Jacobsen, Schwarz, Sapienza, Gangemi, Pioggia and Giorgianni.</copyright-statement>
<copyright-year>2024</copyright-year>
<copyright-holder>Ricciardi, Silvestro, Martino, Catalano, Vicario, Lund-Jacobsen, Schwarz, Sapienza, Gangemi, Pioggia and Giorgianni</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>
</license>
</permissions>
<abstract>
<sec id="sec1">
<title>Background</title>
<p>Growing evidence reveals the important role of clinical psychological factors in chronic-immune diseases. The aim of this study was to investigate Health-Related Quality of Life (HR-QoL), depression, anxiety, and alexithymia in patients with severe hypersensitivity reactions such as Severe Allergic Asthma (SAA) and Hymenoptera Venom Anaphylaxis (HVA).</p>
</sec>
<sec id="sec2">
<title>Methods</title>
<p>The Short-Form Health Survey-36 (SF-36), the Beck Depression Inventory Questionnaire (BDI-II), the Hamilton Anxiety Rating Scale (HAM-A) and the Toronto Alexithymia Scale (TAS-20) were used to assess HR-QoL and clinical psychological features of patients with SAA and HVA.</p>
</sec>
<sec id="sec3">
<title>Results</title>
<p>Overall, 78 patients were recruited. Patients with SAA (<italic>n</italic>&#x2009;=&#x2009;35) reported lower scores for physical functioning [65 (58&#x2013;75) vs. 90 (85&#x2013;95); <italic>p</italic>&#x2009;=&#x2009;&#x003C;0.001], role limitations due to physical health [25 (0&#x2013;50) vs. 62 (50&#x2013;75); <italic>p</italic>&#x2009;=&#x2009;0.004], bodily pain [47.5 (41.1&#x2013;61.3) vs. 55.5 (55&#x2013;96); <italic>p</italic>&#x2009;=&#x2009;0.001], general health [40 (30&#x2013;60) vs. 70 (50&#x2013;80); <italic>p</italic>&#x2009;=&#x2009;0.0003] and social functioning [50 (37.5&#x2013;62.5) vs. 62.5 (54.9&#x2013;75); <italic>p</italic>&#x2009;=&#x2009;0.007] while higher scores for depressive symptoms [14 (11&#x2013;15.4) vs. (9.5 (6&#x2013;15.4); <italic>p</italic>&#x2009;=&#x2009;0.05)] compared to HVA patients (<italic>n</italic>&#x2009;=&#x2009;43). All the dimensions of SF-36 were negatively correlated with anxiety (<italic>r</italic> from &#x2212;0.26 to &#x2212;0.66; <italic>p</italic><sup>all</sup>&#x2009;&#x003C;&#x2009;0.01) and depressive symptoms (<italic>r</italic> from &#x2212;0.44 to &#x2212;0.73; <italic>p</italic><sup>all</sup>&#x2009;&#x003C;&#x2009;0.001). Alexithymia was negatively correlated with vitality (<italic>r</italic>&#x2009;=&#x2009;&#x2212;0.28; <italic>p</italic>&#x2009;=&#x2009;0.02) and mental health (<italic>r</italic>&#x2009;=&#x2009;&#x2212;027; <italic>p</italic>&#x2009;=&#x2009;0.03). Additionally, patients with alexithymia (38% of participants) showed higher levels of depressive symptoms [9.5 (10&#x2013;19) vs. 14 (6&#x2013;13.9); <italic>p</italic>&#x2009;=&#x2009;0.005] and anxiety levels [31 (27.9&#x2013;35) vs. 24 (16&#x2013;33.9); <italic>p</italic>&#x2009;=&#x2009;0.02]; they also showed less vitality [40 (39.9&#x2013;50) vs. 55 (50&#x2013;60) <italic>p</italic>&#x2009;=&#x2009;0.01], social functioning [50 (37.5&#x2013;62.5) vs. 62.5 (50 vs. 75); <italic>p</italic>&#x2009;=&#x2009;0.01] and mental health [48 (44&#x2013;60) vs. 68 (56&#x2013;76); <italic>p</italic>&#x2009;=&#x2009;0.004].</p>
</sec>
<sec id="sec4">
<title>Conclusion</title>
<p>Clinical psychological features due to severe hypersensitive reactions may contribute to the patient&#x2019;s perceived HR-QoL. Focused clinical psychological interventions should be promoted to improve the clinical management of such conditions.</p>
</sec>
</abstract>
<kwd-group>
<kwd>clinical psychology</kwd>
<kwd>immunology</kwd>
<kwd>alexithymia</kwd>
<kwd>severe allergic asthma</kwd>
<kwd>hymenoptera venom anaphylaxis</kwd>
<kwd>H-R quality of life</kwd>
<kwd>severe hypersensitivity reactions</kwd>
<kwd>outdoor workers</kwd>
</kwd-group>
<counts>
<fig-count count="1"/>
<table-count count="1"/>
<equation-count count="0"/>
<ref-count count="77"/>
<page-count count="9"/>
<word-count count="7197"/>
</counts>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Psychology for Clinical Settings</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<sec sec-type="intro" id="sec5">
<label>1</label>
<title>Introduction</title>
<p>Empirical evidence suggests that chronic diseases may impact psychological well-being, increasing the risk of morbidity with incident psychopathologies, such as depression and anxiety (<xref ref-type="bibr" rid="ref15">Di Giuseppe and Conversano, 2022</xref>; <xref ref-type="bibr" rid="ref28">Isvoranu et al., 2021</xref>; <xref ref-type="bibr" rid="ref31">Lin et al., 2022</xref>). Chronic illness represents a challenge for patients and requires continuous adjustment in the management of daily life (<xref ref-type="bibr" rid="ref43">Merlo, 2019</xref>; <xref ref-type="bibr" rid="ref9">Braido, 2013</xref>; <xref ref-type="bibr" rid="ref69">van Houtum et al., 2015</xref>).</p>
<p>Asthma is a chronic respiratory disease characterized by persistent airway inflammation and airway stiffening, resulting in variable difficulty in breathing (<xref ref-type="bibr" rid="ref72">World Health Organization, 2019</xref>). Asthma appears with heterogeneous and variable symptomatology, including airway secretion, shortness of breath, wheezing, chest pain, and coughing attacks (<xref ref-type="bibr" rid="ref9">Braido, 2013</xref>; <xref ref-type="bibr" rid="ref34">Louis et al., 2023</xref>). For these reasons the <xref ref-type="bibr" rid="ref21">Global Initiative for Asthma (2023)</xref> classifies asthma based on the control of symptoms and distinguishes between well-controlled or uncontrolled asthma, the latter is characterized by the presence of frequent symptoms&#x2019; exacerbations, requiring timely use of oral corticosteroids (OCS) or hospitalization.</p>
<p>Severe Asthma (SA) is a subtype of difficult-to-treat asthma, characterized by poor symptoms control despite adherence to a correctly prescribed maximal inhaler with high-dose inhalant corticosteroids (ICS) and beta2 long-acting agents&#x2019; (LABA) treatment (<xref ref-type="bibr" rid="ref6">Bagnasco et al., 2021</xref>; <xref ref-type="bibr" rid="ref52">Ricciardi et al., 2023</xref>). Patients with SA represent about 5&#x2013;10% of the asthma population (<xref ref-type="bibr" rid="ref11">Chung et al., 2014</xref>). SA is characterized by low lung function, immune dysregulation, and frequent exacerbations, with life-threatening asthma attacks (<xref ref-type="bibr" rid="ref3">Backman et al., 2019</xref>). For these reasons, asthma is one of the major public health issues worldwide and causes a significant social and economic burden (<xref ref-type="bibr" rid="ref45">Mortimer et al., 2022</xref>; <xref ref-type="bibr" rid="ref33">L&#x00F3;pez-Tiro et al., 2022</xref>). Severe allergic asthma (SAA) patients have chronic allergic asthma due to immunoglobulin E (IgE)-mediated sensitization to inhalant allergens, prevalently Dust Mites or, in Southern Italy, to <italic>Parietaria Judaica</italic> pollens (<xref ref-type="bibr" rid="ref32">Liotta et al., 2023</xref>).</p>
<p>In this context we would mention the <italic>not-negligible</italic> incidence of asthma in workers, as occupational asthma represents an important environmental workplace disease, especially in outdoor workers. Several organic, inorganic and xenobiotic substances may provoke immunoreactions with consequences on the respiratory system, even resulting in occupational asthma (<xref ref-type="bibr" rid="ref68">Toletone et al., 2016</xref>; <xref ref-type="bibr" rid="ref54">Ru&#x00EB;ff et al., 2023</xref>). Previous literature has also highlighted how occupational asthma influences workers&#x2019; perceived quality of life of also concerning syndromes characterized by depression and anxiety (<xref ref-type="bibr" rid="ref63">Suarthana et al., 2023</xref>; <xref ref-type="bibr" rid="ref14">Del Roio et al., 2023</xref>).</p>
<p><xref ref-type="bibr" rid="ref22">Gruffydd-Jones et al. (2019)</xref> in a multinational survey, analyzing 1.598 patients with poor control of asthma symptoms despite long-term treatment, highlighted a significant reduction in work productivity with a negative impact on emotional well-being at work. Empirical evidence suggests that SA and occupational asthma are associated with low perceived Health-Related Quality of Life (HR-QoL) (<xref ref-type="bibr" rid="ref27">Hossny et al., 2017</xref>; <xref ref-type="bibr" rid="ref6">Bagnasco et al., 2021</xref>; <xref ref-type="bibr" rid="ref70">Wang et al., 2020</xref>), psychological distress (<xref ref-type="bibr" rid="ref50">Patella et al., 2022</xref>) and significant risk of psychiatric comorbidity, such as anxiety and depression (<xref ref-type="bibr" rid="ref53">Roche et al., 2022</xref>). Additionally, recent research (<xref ref-type="bibr" rid="ref60">Silvestro et al., 2023</xref>; <xref ref-type="bibr" rid="ref52">Ricciardi et al., 2023</xref>) suggests that patients with SA and SAA may present a low awareness to identify and describe one&#x2019;s feelings, experiencing a clinical condition known as alexithymia which negatively impacts the disease course (<xref ref-type="bibr" rid="ref47">Nemiah et al., 1976</xref>).</p>
<p>Hymenoptera venom allergy is a typical IgE-mediated disease, provoked by bees or wasps, causing several symptoms including urticaria, angioedema, flushing, itching, hypotension, and anaphylaxis (<xref ref-type="bibr" rid="ref62">Sturm et al., 2018</xref>): a systemic allergic reaction due to HVA may develop within minutes from a sting and in some cases, it can be potentially life-threatening leading to cardiorespiratory arrest (<xref ref-type="bibr" rid="ref57">Schiener et al., 2017</xref>). Although there is a lack of epidemiological data, a European multicenter study estimated that about 48.2% of severe hypersensitivity reactions in adults (&#x003E;18&#x2009;years old) are caused by insect stings (<xref ref-type="bibr" rid="ref74">Worm et al., 2014</xref>). Additionally, <xref ref-type="bibr" rid="ref49">Pastorello et al. (2001)</xref> reported a death range per year due to HVA from 0.03 to 0.48% out of a population of 1,000,000 subjects.</p>
<p>Patients who have experienced anaphylaxis following Hymenoptera stinging have been found to present psychological distress (<xref ref-type="bibr" rid="ref58">Schoeben et al., 2020</xref>; <xref ref-type="bibr" rid="ref51">Ricciardi et al., 2018</xref>; <xref ref-type="bibr" rid="ref8001">Giorgianni et al., 2024</xref>). HVA may cause, fear of being stung again by an insect, anxiety, uncertainty, restrictions in social life and everyday activities, therefore leading to a lower HR-QoL (<xref ref-type="bibr" rid="ref25">H&#x00F6;fer et al., 2023</xref>; <xref ref-type="bibr" rid="ref56">Schaarschmidt et al., 2018</xref>).</p>
<p>Few study have investigated HVA related to the role of occupational exposure, but it would be appropriate to provide useful information to high risk outdoor workers to correctly manage environmental exposure to hymenoptera stings. Observational studies on populations of HVA subjects have documented that outdoor workers have greatest risk of occasional hymenoptera (<xref ref-type="bibr" rid="ref68">Toletone et al., 2016</xref>). Since little evidence exists about the crucial role of clinical psychological factors in patients with severe hypersensitivity reactions, the present research study aims to: (1) investigate HR-QoL and clinical psychological characteristics in patients with a history of severe allergic diseases, including SAA and HVA; (2) analyze the clinical-psychological differences between SAA and HVA and (3) evaluate the associations of clinical-psychological features in these severe allergic diseases.</p>
<p>A greater understanding of the psychological complexity of patients suffering from SAA and HVA could promote a greater awareness of the integrated approach needed in such chronic diseases.</p>
</sec>
<sec sec-type="methods" id="sec6">
<label>2</label>
<title>Methods</title>
<sec id="sec7">
<label>2.1</label>
<title>Participants</title>
<p>This cross-sectional study included 78 patients with a history of severe hypersensitivity reactions, 35 with SAA and 43 with HVA, who referred to the Outpatients Clinic for Allergy and Clinical Immunology at the Department of Clinical and Experimental Medicine of the University Hospital of Messina, Italy between January and May 2022. All SAA patients were treated with Omalizumab, an anti-IgE biologic treatment, in addition to high dose ICS&#x2009;+&#x2009;LABA, while HVA patients were under venom allergen immunotherapy (VAIT), 6 with bee venom extract and 37 with wasp venom extract (ALK, Alutard, Milan). Exclusion criteria were age under 18&#x2009;years, cognitive decline, moderate to severe kidney or liver failure, heart failure with NYHA (New York Heart Association) class &#x2265;2, cancer, malabsorption, endocrine disorders of thyroid, parathyroid or adrenal glands, and known psychopathological diseases and psychotropic drugs assumption.</p>
</sec>
<sec id="sec8">
<label>2.2</label>
<title>Ethics statement</title>
<p>The research will be carried out following the Declaration of Helsinki (<xref ref-type="bibr" rid="ref73">World Medical Association, 2013</xref>). Ethical approval was obtained from the Ethics Committee of the University Hospital of Messina University (Protocol number 16/19). All patients were informed about privacy and the use of anonymous data for research purposes and signed an informed consent according to the European General Data Protection Regulation 2016/679.</p>
</sec>
<sec id="sec9">
<label>2.3</label>
<title>Clinical evaluation</title>
<p>A psychological assessment was conducted by a researcher in clinical psychology, performing a gold-standard clinical psychological interview and a psycho-diagnostics examination.</p>
<p>The Beck Depression Inventory, second edition (BDI-II), was administered to measure depressive symptoms (<xref ref-type="bibr" rid="ref8">Beck et al., 1996</xref>; <xref ref-type="bibr" rid="ref20">Ghisi et al., 2006</xref>). It consists of a self-report instrument, composed of 21 items scored on a four-point Likert scale. BDI-II detects both somatic-affective (e.g., agitation, sleep disorder, and loss of energy) and cognitive (e.g., pessimism, suicidal thoughts, self-criticalness) features of depression. In the present study, the Italian version of BDI-II was adopted, as it showed good proprieties and a bi-factorial structure with an <italic>&#x03B1;</italic> coefficient of 0.86 for cognitive/affective and 0.65 for somatic symptoms (<xref ref-type="bibr" rid="ref44">Montano and Flebus, 2006</xref>).</p>
<p>The Hamilton Anxiety Rating Scale (HAM-A) was used to assess the severity of anxiety symptoms (<xref ref-type="bibr" rid="ref23">Hamilton, 1959</xref>). It is a self-report questionnaire, consisting of 14 items scored on a five-point Likert scale. HAM-A presents a bi-factorial structure, detecting both somatic (e.g., respiratory, autonomic, gastrointestinal symptoms) and psychic components of anxiety (e.g., tension, fears and depressed mood). Previous research documented, good statistical proprieties, high reliability, and diagnostic accuracy for the Italian version of this scale (<xref ref-type="bibr" rid="ref38">Martino et al., 2021</xref>; <xref ref-type="bibr" rid="ref59">Scimeca et al., 2014</xref>).</p>
<p>The Italian version of the Short-Form Health Survey-36 (SF-36) was used to measure patients&#x2019; perceived HR-QoL. SF-36 is a self-administered questionnaire that detects eight dimensions of HR-QoL, comprising physical functioning, limitation due to physical role, bodily pain, general health, vitality, mental health, limitation due to emotional role and social functioning (<xref ref-type="bibr" rid="ref71">Ware and Sherbourne, 1992</xref>). SF-36 presents a range score from 0 to 100; a lower score indicates a poorer HR-QoL. Previous studies confirmed the psychometric qualities of the scale on Italian clinical samples, with reliability (Cronbach&#x2019;s <italic>&#x03B1;</italic>) for the eight factors ranging from 0.77 to 0.93 (<xref ref-type="bibr" rid="ref2">Apolone and Mosconi, 1998</xref>).</p>
<p>The Toronto Alexithymia Scale-20 (TAS-20) was used to assess alexithymic traits (<xref ref-type="bibr" rid="ref66">Taylor et al., 1997</xref>; <xref ref-type="bibr" rid="ref65">Taylor, 2000</xref>; <xref ref-type="bibr" rid="ref4">Bagby et al., 1994a</xref>). It consists of a self-report questionnaire, composed of 20 items scored on a five-point Likert scale. Three cut-off scores were identified to recognize alexithymic (&#x2265;61), borderline (51 to 60) and non-alexithymic (&#x2264;50) individuals (<xref ref-type="bibr" rid="ref5">Bagby et al., 1994b</xref>). TAS-20 presents a three-factor structure that comprises the main features of alexithymia: difficulty identifying feelings (DIF), difficulty describing feelings (DDF) and externally oriented thinking (EOT). In the present study, the Italian version of TAS-20 was used; previous research highlighted a good propriety and reliability of the three factors structure (Cronbach&#x2019;s <italic>&#x03B1;</italic>) considering a score of 0.86 for full scale and 0.83, 0.79, and 0.81 for DIF, DDF, EOT, respectively (<xref ref-type="bibr" rid="ref10">Bressi et al., 1996</xref>).</p>
</sec>
<sec id="sec10">
<label>2.4</label>
<title>Statistical analyses</title>
<p>Statistical analysis was performed using MedCalc software (version 10.2.0.0; Mariakerke, 173 Belgium). The Kolmogorov&#x2013;Smirnov test was used to verify the normal distribution of values of studied variables. The entire sample was divided into groups according to the allergic disease and the presence (TAS-20 scores &#x2265;61) or the absence of alexithymia and the Mann&#x2013;Whitney test was used to observe any differences in the level of anxiety, depressive symptoms and QoL. The <italic>&#x03C7;</italic><sup>2</sup> test was used to calculate differences in the proportion of categorical variables. Spearman correlation coefficient was applied to evaluate the degree of association between two variables. Finally, a multiple regression analysis was performed to explore the association between alexithymia, identified as the dependent variable, and the explanatory variables age, age at diagnosis, anxiety and depression. For all the tests used, the value of <italic>p</italic>&#x2009;&#x003C;&#x2009;0.05 was considered to indicate the statistical significance.</p>
</sec>
<sec id="sec11">
<label>2.5</label>
<title>Results</title>
<p>The main socio-demographic and clinical characteristics of recruited patients are reported in <xref ref-type="table" rid="tab1">Table 1</xref>. Overall, the median age of participants was 55&#x2009;yrs., and the prevalent gender was male (57%). Participants showed moderate anxiety levels, mild depressive symptoms, conceivable alexithymia and low perceived HR-QoL. The age at diagnosis was significantly higher in patients with HVA in comparison with patients with SAA [44 (38&#x2013;48.2) vs. 21 (13&#x2013;35), <italic>p</italic>&#x2009;=&#x2009;0.002, respectively]. Moreover, the HVA group presented a significant difference in the employment status in comparison with patients with SAA, particularly in the number of full-time workers (84% vs. 54%) respectively. Regarding clinical psychological features, both groups showed no significant differences in anxiety and alexithymia levels. However, the SAA group presented higher depressive symptoms levels in comparison with HVA patients [14 (11&#x2013;15.4) vs. (9.5 (6&#x2013;15.4); <italic>p</italic>&#x2009;=&#x2009;0.05)]. On the other hand, patients in the HVA group showed higher levels of externally oriented thinking [25 (23&#x2013;28) vs. 23 (20&#x2013;25); <italic>p</italic>&#x2009;=&#x2009;0.05]. Data on the SF-36 survey are reported in <xref ref-type="fig" rid="fig1">Figure 1</xref>; patients with SAA showed a lower score in physical functioning [65 (58&#x2013;75) vs. 90 (85&#x2013;95); <italic>p</italic>&#x2009;&#x003C;&#x2009;0.001], role limitations due to physical health [25 (0&#x2013;50) vs. 62 (50&#x2013;75); <italic>p</italic>&#x2009;=&#x2009;0.004], bodily pain [47.5 (41.1&#x2013;61.3) vs. 55.5 (55&#x2013;96); <italic>p</italic>&#x2009;=&#x2009;0.001], general health, [40 (30&#x2013;60) vs. 70 (50&#x2013;80); <italic>p</italic>&#x2009;=&#x2009;0.0003] and social functioning [50 (37.5&#x2013;62.5) vs. 62.5 (54.9&#x2013;75); <italic>p</italic>&#x2009;=&#x2009;0.007] in comparison to the HVA group. There were no statistically significant differences between the groups concerning vitality, role limitations due to emotional problems and mental health. Considering TAS-20 scores &#x2265;61, it was observed that 29 (38%) participants exhibited clinically significant levels of alexithymia. Taking into account the presence (TAS-20 scores &#x2265;61) or absence (TAS-20 &#x003C;61) of alexithymia, it was highlighted that patients with alexithymia presented higher levels of depression [9.5 (10&#x2013;19) vs. 14 (6&#x2013;13.9); <italic>p</italic>&#x2009;=&#x2009;0.005], anxiety, with particular regard to the psychic dimension [31 (27.9&#x2013;35) vs. 24 (16&#x2013;33.9); <italic>p</italic>&#x2009;=&#x2009;0.02] and lower scores in vitality [40 (39.9&#x2013;50) vs. 55 (50&#x2013;60); <italic>p</italic>&#x2009;=&#x2009;0.01], social functioning [50 (37.5&#x2013;62.5) vs. 62.5 (50 vs. 75); <italic>p</italic>&#x2009;=&#x2009;0.01] and mental health [48 (44&#x2013;60) vs. 68 (56&#x2013;76); <italic>p</italic>&#x2009;=&#x2009;0.004] to the patients without alexithymia.</p>
<table-wrap position="float" id="tab1">
<label>Table 1</label>
<caption>
<p>Main socio-demographic and clinical characteristics of participants.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th/>
<th align="center" valign="top">Total (<italic>n</italic>&#x2009;=&#x2009;78)</th>
<th align="center" valign="top">Severe allergic asthma (<italic>n</italic>&#x2009;=&#x2009;35)</th>
<th align="center" valign="top">Hymenoptera anaphylaxis (<italic>n</italic>&#x2009;=&#x2009;43)</th>
<th align="center" valign="top"><italic>p</italic></th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="middle">Age (yr)</td>
<td align="char" valign="middle" char="(">55 (50&#x2013;59)</td>
<td align="char" valign="middle" char="(">59 (54&#x2013;64)</td>
<td align="char" valign="middle" char="(">52 (46&#x2013;57)</td>
<td align="char" valign="middle" char=".">0.05</td>
</tr>
<tr>
<td align="left" valign="middle">Age at diagnosis (yr)</td>
<td align="char" valign="middle" char="(">38 (25&#x2013;45)</td>
<td align="char" valign="middle" char="(">21 (13&#x2013;35)</td>
<td align="char" valign="middle" char="(">44 (38&#x2013;48.2)</td>
<td align="char" valign="middle" char=".">0.002&#x002A;</td>
</tr>
<tr>
<td align="left" valign="middle">BMI (Kg/m<sup>2</sup>)</td>
<td align="char" valign="middle" char="(">26.3 (24.7&#x2013;27.9)</td>
<td align="char" valign="middle" char="(">27 (24&#x2013;30)</td>
<td align="char" valign="middle" char="(">25.8 (24.6&#x2013;27.3)</td>
<td align="char" valign="middle" char=".">0.4</td>
</tr>
<tr>
<td align="left" valign="middle">Gender [male (%)]</td>
<td align="char" valign="middle" char="(">45 (57)</td>
<td align="char" valign="middle" char="(">13 (37)</td>
<td align="char" valign="middle" char="(">32 (74)</td>
<td align="char" valign="middle" char=".">0.002&#x002A;</td>
</tr>
<tr>
<td align="left" valign="middle" char="." colspan="5">Education</td>
</tr>
<tr>
<td align="left" valign="middle">Primary school [<italic>n</italic> (%)]</td>
<td align="char" valign="middle" char="(">1 (1)</td>
<td align="char" valign="middle" char="(">1 (2)</td>
<td align="char" valign="middle" char="(">0(0)</td>
<td/>
</tr>
<tr>
<td align="left" valign="middle">Secondary school [<italic>n</italic> (%)]</td>
<td align="char" valign="middle" char="(">17 (22)</td>
<td align="char" valign="middle" char="(">7 (20)</td>
<td align="char" valign="middle" char="(">10 (23)</td>
<td/>
</tr>
<tr>
<td align="left" valign="middle">High school [<italic>n</italic> (%)]</td>
<td align="char" valign="middle" char="(">46 (59)</td>
<td align="char" valign="middle" char="(">19 (56)</td>
<td align="char" valign="middle" char="(">27 (63)</td>
<td/>
</tr>
<tr>
<td align="left" valign="middle">Bachelor&#x2019;s degree [<italic>n</italic> (%)]</td>
<td align="char" valign="middle" char="(">13 (17)</td>
<td align="char" valign="middle" char="(">7 (20)</td>
<td align="char" valign="middle" char="(">6 (14)</td>
<td/>
</tr>
<tr>
<td align="left" valign="middle">PhD or specialization [<italic>n</italic> (%)]</td>
<td align="char" valign="middle" char="(">1 (1)</td>
<td align="char" valign="middle" char="(">1(2)</td>
<td align="char" valign="middle" char="(">0(0)</td>
<td align="char" valign="middle" char=".">0.52</td>
</tr>
<tr>
<td align="left" valign="middle" char="." colspan="5">Marital status</td>
</tr>
<tr>
<td align="left" valign="middle">Single [<italic>n</italic> (%)]</td>
<td align="char" valign="middle" char="(">17 (22)</td>
<td align="char" valign="middle" char="(">8 (22)</td>
<td align="char" valign="middle" char="(">9 (21)</td>
<td/>
</tr>
<tr>
<td align="left" valign="middle">Married [<italic>n</italic> (%)]</td>
<td align="char" valign="middle" char="(">56 (72)</td>
<td align="char" valign="middle" char="(">24 (69)</td>
<td align="char" valign="middle" char="(">32 (74)</td>
<td/>
</tr>
<tr>
<td align="left" valign="middle">Divorced [<italic>n</italic> (%)]</td>
<td align="char" valign="middle" char="(">3 (4)</td>
<td align="char" valign="middle" char="(">1 (3)</td>
<td align="char" valign="middle" char="(">2 (5)</td>
<td/>
</tr>
<tr>
<td align="left" valign="middle">Widower [<italic>n</italic> (%)]</td>
<td align="char" valign="middle" char="(">2 (2)</td>
<td align="char" valign="middle" char="(">2 (6)</td>
<td align="char" valign="middle" char="(">0 (0)</td>
<td align="char" valign="middle" char=".">0.43</td>
</tr>
<tr>
<td align="left" valign="middle" char="." colspan="5">Employment status</td>
</tr>
<tr>
<td align="left" valign="middle">Full time [<italic>n</italic> (%)]</td>
<td align="char" valign="middle" char="(">55 (70)</td>
<td align="char" valign="middle" char="(">19 (54)</td>
<td align="char" valign="middle" char="(">36 (84)</td>
<td/>
</tr>
<tr>
<td align="left" valign="middle">Unemployed [<italic>n</italic> (%)]</td>
<td align="char" valign="middle" char="(">7 (9)</td>
<td align="char" valign="middle" char="(">4 (11)</td>
<td align="char" valign="middle" char="(">3 (8)</td>
<td/>
</tr>
<tr>
<td align="left" valign="middle">Pensioner [<italic>n</italic> (%)]</td>
<td align="char" valign="middle" char="(">12 (16)</td>
<td align="char" valign="middle" char="(">10 (29)</td>
<td align="char" valign="middle" char="(">2 (4)</td>
<td/>
</tr>
<tr>
<td align="left" valign="middle">Housewife [<italic>n</italic> (%)]</td>
<td align="char" valign="middle" char="(">4 (5)</td>
<td align="char" valign="middle" char="(">2 (6)</td>
<td align="char" valign="middle" char="(">2 (4)</td>
<td align="char" valign="middle" char=".">0.01&#x002A;</td>
</tr>
<tr>
<td align="left" valign="middle" char="." colspan="5">Anxiety levels</td>
</tr>
<tr>
<td align="left" valign="middle">HAMA score</td>
<td align="char" valign="middle" char="(">29 (25&#x2013;32.6)</td>
<td align="char" valign="middle" char="(">31 (23&#x2013;36)</td>
<td align="char" valign="middle" char="(">28 (20.8&#x2013;33.6)</td>
<td align="char" valign="middle" char=".">0.39</td>
</tr>
<tr>
<td align="left" valign="middle">HAMA somatic symptom score</td>
<td align="char" valign="middle" char="(">14 (11&#x2013;16)</td>
<td align="char" valign="middle" char="(">15 (12&#x2013;17)</td>
<td align="char" valign="middle" char="(">12 (8.4&#x2013;16.2)</td>
<td align="char" valign="middle" char=".">0.13</td>
</tr>
<tr>
<td align="left" valign="middle">HAMA psychic symptom score</td>
<td align="char" valign="middle" char="(">15 (13.4&#x2013;16)</td>
<td align="char" valign="middle" char="(">15 (12&#x2013;17.4)</td>
<td align="char" valign="middle" char="(">15 (13.4&#x2013;17)</td>
<td align="char" valign="middle" char=".">0.89</td>
</tr>
<tr>
<td align="left" valign="middle" char="." colspan="5">Depression severity</td>
</tr>
<tr>
<td align="left" valign="middle">BDI-II score</td>
<td align="char" valign="middle" char="(">12 (9.4&#x2013;14)</td>
<td align="char" valign="middle" char="(">14 (11&#x2013;15.4)</td>
<td align="char" valign="middle" char="(">9.5 (6&#x2013;14.6)</td>
<td align="char" valign="middle" char=".">0.05&#x002A;</td>
</tr>
<tr>
<td align="left" valign="middle" char="." colspan="5">Alexithymia</td>
</tr>
<tr>
<td align="left" valign="middle">TAS-20 total score</td>
<td align="char" valign="middle" char="(">59 (55&#x2013;62)</td>
<td align="char" valign="middle" char="(">56 (45&#x2013;63)</td>
<td align="char" valign="middle" char="(">61 (56&#x2013;65)</td>
<td align="char" valign="middle" char=".">0.12</td>
</tr>
<tr>
<td align="left" valign="middle">DIF</td>
<td align="char" valign="middle" char="(">19 (16&#x2013;22)</td>
<td align="char" valign="middle" char="(">18 (13&#x2013;23)</td>
<td align="char" valign="middle" char="(">19.5 (16&#x2013;22)</td>
<td align="char" valign="middle" char=".">0.48</td>
</tr>
<tr>
<td align="left" valign="middle">DDF</td>
<td align="char" valign="middle" char="(">15 (13.3&#x2013;16)</td>
<td align="char" valign="middle" char="(">15 (11&#x2013;16)</td>
<td align="char" valign="middle" char="(">16 (13&#x2013;18)</td>
<td align="char" valign="middle" char=".">0.29</td>
</tr>
<tr>
<td align="left" valign="middle">EOT</td>
<td align="char" valign="middle" char="(">24 (23&#x2013;25.6)</td>
<td align="char" valign="middle" char="(">23 (20&#x2013;25)</td>
<td align="char" valign="middle" char="(">25 (23&#x2013;28)</td>
<td align="char" valign="middle" char=".">0.05&#x002A;</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p>Values are expressed as median (IQR). HAMA-A, Hamilton anxiety rating scale; BDI-II, Beck Depression Inventory II Edition; TAS-20, Toronto Alexithymia Scale 20-item; DIF, difficulty identifying feelings; DDF, difficulty describing feelings; EOT, externally oriented thinking.</p>
</table-wrap-foot>
</table-wrap>
<fig position="float" id="fig1">
<label>Figure 1</label>
<caption>
<p>Difference in HR-QoL between group with SAA and group with HVA.</p>
</caption>
<graphic xlink:href="fpsyg-15-1394954-g001.tif"/>
</fig>
<p>Overall, the number of explored clinical psychological morbidities was positively related to age (<italic>r</italic>&#x2009;=&#x2009;0.48; <italic>p</italic>&#x2009;&#x003C;&#x2009;0.01), BMI (<italic>r</italic>&#x2009;=&#x2009;0.34; <italic>p</italic>&#x2009;=&#x2009;0.003) anxiety (<italic>r</italic>&#x2009;=&#x2009;0.32; <italic>p</italic>&#x2009;=&#x2009;0.01), depression (<italic>r</italic>&#x2009;=&#x2009;025; <italic>p</italic>&#x2009;=&#x2009;0.04); conversely, it was negatively associated with HR-QoL: physical functioning (<italic>r</italic>&#x2009;=&#x2009;&#x2212;036; <italic>p</italic>&#x2009;=&#x2009;0.004), limitations due to physical health (<italic>r</italic>&#x2009;=&#x2009;&#x2212;0.37; <italic>p</italic>&#x2009;=&#x2009;0.003), bodily pain (<italic>r</italic>&#x2009;=&#x2009;&#x2212;0.35; <italic>p</italic>&#x2009;=&#x2009;0.005) and general health (<italic>r</italic>&#x2009;=&#x2009;&#x2212;0.38; <italic>p</italic>&#x2009;=&#x2009;0.003). At correlation analysis, all the dimensions of SF-36 were negatively associated with age (<italic>r</italic> from &#x2212;0.2 to &#x2212;0.57; <italic>p</italic><sup>all</sup>&#x2009;&#x003C;&#x2009;0.05), anxiety, both somatic and psychic (<italic>r</italic> from &#x2212;0.26 to &#x2212;0.66; <italic>p</italic><sup>all</sup>&#x2009;&#x003C;&#x2009;0.01) and depressive symptoms (<italic>r</italic> from &#x2212;0.44 to &#x2212;0.73; <italic>p</italic><sup>all</sup>&#x2009;&#x003C;&#x2009;0.001). Similar associations were observed when analyzing these variables in both groups separately. Moreover, considering the entire sample, TAS-20 was negatively correlated with vitality (<italic>r</italic>&#x2009;=&#x2009;&#x2212;0.28; <italic>p</italic>&#x2009;=&#x2009;0.02) and mental health (<italic>r</italic>&#x2009;=&#x2009;&#x2212;027; <italic>p</italic>&#x2009;=&#x2009;0.03), also DDF was negatively correlated with vitality (<italic>r</italic>&#x2009;=&#x2009;&#x2212;028; <italic>p</italic>&#x2009;=&#x2009;0.02) and mental health (<italic>r</italic>&#x2009;=&#x2009;&#x2212;0.32; <italic>p</italic>&#x2009;=&#x2009;0.01) and positively associated with depressive symptoms (<italic>r</italic>&#x2009;=&#x2009;0.26; <italic>p</italic>&#x2009;=&#x2009;0.04). Additionally, anxiety (somatic and psychic) was positively correlated with depressive symptoms (<italic>r</italic>&#x2009;=&#x2009;0.61; <italic>p</italic>&#x2009;&#x003C;&#x2009;0.001). Only in the group of patients with SAA, the alexithymia total score was associated with anxiety (<italic>r</italic>&#x2009;=&#x2009;0.36; <italic>p</italic>&#x2009;=&#x2009;0.04), while DDF was correlated with depressive symptoms (<italic>r</italic>&#x2009;=&#x2009;0.42; <italic>p</italic>&#x2009;=&#x2009;0.01).</p>
<p>Finally, at multiple regression analysis which considered alexithymia as the dependent variable, and age, age at diagnosis, anxiety and depression as explanatory variables, only anxiety was significantly and independently associated with alexithymia in the SAA group (<italic>&#x03B2;</italic>&#x2009;=&#x2009;0.4375; SE&#x2009;=&#x2009;0.198; <italic>p</italic>&#x2009;=&#x2009;0.03).</p>
</sec>
</sec>
<sec sec-type="discussion" id="sec12">
<label>3</label>
<title>Discussion</title>
<p>This research highlights that patients with a history of severe allergic diseases, including SAA and HVA, show moderate anxiety levels, mild depressive symptoms, conceivable alexithymia and low perceived HR-QoL. The main results of this study indicate that the group of patients with SAA showed low HR-QoL in both physical and emotional dimensions. In line with this statement, empirical evidence underlined that the experience of living with SAA significantly impacts physical and emotional functioning, determining limitations in completing daily activities (<xref ref-type="bibr" rid="ref40">McDonald et al., 2018</xref>), decrease in work performance (<xref ref-type="bibr" rid="ref24">Hiles et al., 2018</xref>), and difficulty in managing leisure time and social activities (<xref ref-type="bibr" rid="ref16">Dockrell et al., 2007</xref>).</p>
<p>Regarding differences between patients with SAA and with HVA, the first group reported lower results in all dimensions of the SF-36, except for vitality, limitations due to emotional role, and mental health. Both groups reported low-to-medium scores in these dimensions, highlighting the potential negative impact of these chronic conditions on patients&#x2019; psychological well-being. Concerning these results, we hypothesized that, if on the one hand the invalidating respiratory symptoms of SAA, most of all shortness of breath, may cause significant impairment in all dimensions of perceived HR-QoL, on the other hand, anaphylaxis experienced by patients with HVA can lead to uncertainty and fear of experiencing a new hypersensitivity reaction, with negative effects on psychological dimensions of HR-QoL in the long term. <xref ref-type="bibr" rid="ref64">Tal et al. (2020)</xref>, analyzing 44 patients with a history of anaphylaxis due to a Hymenoptera sting, highlighted a major susceptibility to symptoms of post-traumatic stress disorders in patients with local reactions, demonstrating that severe hypersensitivity reactions could compromise psychological health.</p>
<p>In the present study, no differences were found between the two disease groups for anxiety levels and alexithymia. However, patients with SAA presented more depressive symptoms than patients with HVA. Numerous evidence suggests comorbidity between asthma and depression (<xref ref-type="bibr" rid="ref76">Zielinski et al., 2000</xref>; <xref ref-type="bibr" rid="ref19">Gao et al., 2015</xref>; <xref ref-type="bibr" rid="ref35">Lu et al., 2018</xref>). Meta-analysis of <xref ref-type="bibr" rid="ref29">Jiang et al. (2014)</xref> highlighted that patients with depression are more likely to present in comorbidity asthma (3.17 times more) than healthy subjects. Similarly, patients with asthma are more likely to have depression as a comorbidity (1.52 times more). According to <xref ref-type="bibr" rid="ref42">Medina-Rodriguez et al. (2018)</xref>, patients with major depressive disorder present immune system alterations with significant changes in plasma cytokine levels. Therefore, the inflammatory response might represent a common pathway between allergic diseases such as asthma and mental disorders (<xref ref-type="bibr" rid="ref29">Jiang et al., 2014</xref>; <xref ref-type="bibr" rid="ref35">Lu et al., 2018</xref>).</p>
<p>Regarding the association between clinical psychological features and levels of HR-QoL, depression and anxiety, both somatic and psychic, were related to low HR-QoL, while higher levels of alexithymia were associated with reduced vitality and social function dimensions, in both groups. These findings confirmed the relevance of accurate psycho-diagnostic assessment to detect the presence of clinically significant features in both SAA and HVA patients (<xref ref-type="bibr" rid="ref12">Conversano and Di Giuseppe, 2021</xref>; <xref ref-type="bibr" rid="ref1">Adelmeyer et al., 2021</xref>; <xref ref-type="bibr" rid="ref17">Esmaeel and Aly, 2019</xref>). A multidisciplinary clinical approach, both medical and psychological, could allow early detection of at-risk situations or identification of cases in which a mental disorder is already concluded, to ensure the most suitable patient-tailored treatment (<xref ref-type="bibr" rid="ref36">Majellano et al., 2019</xref>; <xref ref-type="bibr" rid="ref13">Cooley et al., 2022</xref>).</p>
<p>Furthermore, it would be appropriate to give indications on the correct risk management at work of subjects highly exposed to hymenoptera stings, both in the case of workers suffering from occupational asthma and for those with HVA. The risk of being affected by the exposure to environmental factors can be the cause of suffering among outdoor workers with the consequent development of depression and anxiety. In the coming researches it could be relevant to study further populations of outdoor workers in relation to what has emerged from our findings to provide guidelines on the management and prevention of such sufferings (<xref ref-type="bibr" rid="ref54">Ru&#x00EB;ff et al., 2023</xref>).</p>
<p>Depression, anxiety, and alexithymia have been associated with adverse health outcomes in several chronic conditions; regarding asthma, in the United States, <xref ref-type="bibr" rid="ref31">Lin et al. (2022)</xref> highlighted that 14.16% of patients with asthma showed comorbidity with depression and the co-occurrence of asthma and depression was associated with major death risk than in asthmatic patients without depression. The presence of anxiety and/or depression in comorbidity with asthma was associated with poorer asthma control (<xref ref-type="bibr" rid="ref61">Stubbs et al., 2022</xref>), higher corticosteroid dosage (<xref ref-type="bibr" rid="ref41">McLoughlin and McDonald, 2021</xref>), greater frequency of exacerbation (<xref ref-type="bibr" rid="ref75">Zhang et al., 2016</xref>) and greater healthcare use (<xref ref-type="bibr" rid="ref55">Sastre et al., 2018</xref>). Regarding the correlation of HVA with depression and anxiety, <xref ref-type="bibr" rid="ref56">Schaarschmidt et al. (2018)</xref>, analysing 55 patients with HVA, found that 14.5% showed clinically significant levels of anxiety, while 5.5% had definite depressive disorder. <xref ref-type="bibr" rid="ref58">Schoeben et al. (2020)</xref> suggested that female patients with HVA had higher anxiety symptoms than male patients. Despite such empirical evidence, there is a lack of knowledge regarding the risk of depression and anxiety in patients with HVA and the impact of these variables on HR-QoL. Therefore, future research should analyse, also through longitudinal designs, the association between psychological factors and HVA, with particular attention to patients who have experienced a severe anaphylactic reaction. The latter, due to the risk of death from anaphylaxis, could develop strong anxiety in outdoor environments, limit social activities and experience low perceived HR-QoL, with negative effects on global psychophysical well-being (<xref ref-type="bibr" rid="ref25">H&#x00F6;fer et al., 2023</xref>; <xref ref-type="bibr" rid="ref48">Nowak et al., 2015</xref>).</p>
<p>Regarding alexithymia, in the present study, 38% of participants showed a clinically significant score of TAS-20. Alexithymic patients showed greater depressive symptoms, anxiety, both psychic and somatic, and a lower perception of HR-QoL for the dimension vitality, social functioning, and mental health than non-alexithymic patients. From a qualitative perspective, these findings support the hypothesis that alexithymia is linked to precise medical domains (<xref ref-type="bibr" rid="ref67">Tesio et al., 2018</xref>; <xref ref-type="bibr" rid="ref15">Di Giuseppe and Conversano, 2022</xref>), as in the case of dermatological (<xref ref-type="bibr" rid="ref26">Holmes et al., 2022</xref>; <xref ref-type="bibr" rid="ref46">Namdar and Kurtoglu, 2021</xref>), gastrointestinal (<xref ref-type="bibr" rid="ref18">Fuchs et al., 2023</xref>; <xref ref-type="bibr" rid="ref37">Martino et al., 2020</xref>, <xref ref-type="bibr" rid="ref39">2023</xref>; <xref ref-type="bibr" rid="ref30">Kano et al., 2018</xref>) and respiratory diseases (<xref ref-type="bibr" rid="ref60">Silvestro et al., 2023</xref>; <xref ref-type="bibr" rid="ref52">Ricciardi et al., 2023</xref>), as in the present study which considered also patients with a history HVA. Although in the present study, it was not possible to consider causal associations between alexithymia and the other variables, the results allow us to observe how the difficulty in identifying and recognizing feelings and the external event oriented-thinking style may negatively impact the course of chronic illnesses. Alexithymia could alter patients&#x2019; ability to distinguish kinaesthetic sensations related to emotional arousal from symptoms of severe hypersensitivity reactions, negatively affecting the ability to self-manage chronic conditions (<xref ref-type="bibr" rid="ref7">Baiardini et al., 2011</xref>).</p>
<p>Finally, we acknowledge that the present study has some limitations, as the number of participants was low and moreover, that the group with HVA was mostly of men; these factors limit the possibility of generalizing our results to a broader context. The cross-sectional design does not allow us to establish a cause-effect association among clinical psychological features and dimensions of perceived HR-QoL, and because of the lack of studies, the psychological characteristics of patients with HVA should be further investigated. Nevertheless, our findings may contribute to a better understanding of the psychological complexity of patients with hypersensitivity reactions, allowing a greater awareness of how anxiety, depressive symptoms, and alexithymia can influence the clinical characteristics of severe allergic diseases.</p>
</sec>
<sec sec-type="conclusions" id="sec13">
<label>4</label>
<title>Conclusion</title>
<p>The present study highlights that patients with SAA showed lower perceived HR-QoL and greater depressive symptoms than patients with HVA. Patients with HVA reported moderate-low levels of vitality, limitations due to emotional role, and mental health, as well as patients with SAA. Overall, clinically significant levels of alexithymia were associated with higher depressive symptoms and lower vitality and mental health. Therefore, clinicians and psychologists could apply a multidisciplinary approach, considering the body&#x2013;mind complex, to early detect clinical psychological features such as depression, anxiety, and alexithymia, and to reach a timely diagnosis and accurate therapeutic support in clinical settings, targeting a higher perceived HR-QoL.</p>
</sec>
</body>
<back>
<sec sec-type="data-availability" id="sec14">
<title>Data availability statement</title>
<p>The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.</p>
</sec>
<sec sec-type="ethics-statement" id="sec15">
<title>Ethics statement</title>
<p>The studies involving humans were approved by Ethical Committee, &#x201C;Gaetano Martino&#x201D; University Hospital of Messina, Italy. The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study.</p>
</sec>
<sec sec-type="author-contributions" id="sec16">
<title>Author contributions</title>
<p>LR: Writing &#x2013; original draft, Conceptualization. OS: Writing &#x2013; original draft, Investigation. GM: Writing &#x2013; review &#x0026; editing, Writing &#x2013; original draft, Methodology, Investigation, Formal analysis, Data curation, Conceptualization. AC: Writing &#x2013; original draft, Software, Methodology, Investigation, Formal analysis. CV: Writing &#x2013; original draft, Formal analysis, Data curation. TL-J: Writing &#x2013; original draft, Supervision. PS: Writing &#x2013; original draft, Supervision. DS: Writing &#x2013; original draft, Supervision. SG: Writing &#x2013; original draft, Project administration, Supervision. GP: Writing &#x2013; original draft, Project administration. CG: Writing &#x2013; review &#x0026; editing, Writing &#x2013; original draft, Supervision.</p>
</sec>
<sec sec-type="funding-information" id="sec17">
<title>Funding</title>
<p>The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.</p>
</sec>
<sec sec-type="COI-statement" id="sec18">
<title>Conflict of interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
<p>The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.</p>
</sec>
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<title>Publisher&#x2019;s note</title>
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<sec sec-type="supplementary-material" id="sec20">
<title>Supplementary material</title>
<p>The Supplementary material for this article can be found online at: <ext-link xlink:href="https://www.frontiersin.org/articles/10.3389/fpsyg.2024.1394954/full#supplementary-material" ext-link-type="uri">https://www.frontiersin.org/articles/10.3389/fpsyg.2024.1394954/full#supplementary-material</ext-link></p>
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