دورية أكاديمية
Significant association between huntingtin gene mutation and prevalence of hopelessness, depression and anxiety symptoms / ; Ar yra hantingtino geno mutacijos ir dažnesnio depresijos, nevilties ir nerimo simptomų raiškos ryšys?
| العنوان: | Significant association between huntingtin gene mutation and prevalence of hopelessness, depression and anxiety symptoms / ; Ar yra hantingtino geno mutacijos ir dažnesnio depresijos, nevilties ir nerimo simptomų raiškos ryšys? |
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| المؤلفون: | Butėnaitė, Adelė, Strumila, Robertas, Lengvenytė, Aistė, Pakutkaitė, Indrė Kotryna, Morkūnienė, Aušra, Matulevičienė, Aušra, Dlugauskas, Edgaras, Utkus, Algirdas |
| المصدر: | Acta medica Lituanica., Vilnius : Vilniaus universiteto leidykla, 2021, vol. 28, no. 1, p. 43-51. ; ISSN 1392-0138 ; eISSN 2029-4174 |
| سنة النشر: | 2021 |
| المجموعة: | Vilnius University Virtual Library (VU VL) / Vilniaus universitetas virtuali biblioteka |
| مصطلحات موضوعية: | Huntington’s disease, huntingtin, depression, anxiety, hopelessness |
| الوصف: | Background: In Huntington’s disease psychiatric symptoms may manifest prior to motor dysfunction. Such symptoms negatively impact people’s quality of life and can worsen the course of the primary disease. The aim of the present study was to assess and compare depression, anxiety and hopelessness rates in individuals with and without an abnormal expansion of CAG repeats in the huntingtin (HTT) gene and healthy controls. Materials and methods: Study involved 31 individuals referred for genetic testing for Huntington’s disease and a control group of 41. Depressive and anxiety symptoms were assessed using Beck Hopelessness Scale (BHS) and Hospital Anxiety and Depression Scale (HADS). Results between groups were compared using the Mann–Whitney U test. Two-sided Bonferroni corrected p-value was set at ≤0.017. Results: Individuals with HTT gene mutation (“gene mutation positive”, GMP) (N=20) scored higher on the HADS depression subscale (5.90 ± 4.52 vs 1.36 ± 1.91; p ≤ 0.017) than those without HTT gene mutation (“gene mutation negative”, GMN) (N=11). GMP and control groups scored higher than the GMN group on the BHS (5.65 ± 3.91 vs 2.09 ± 1.64 and 5.27 ± 4.11 vs 2.09 ± 1.64, respectively; p ≤ 0.017). No differences in anxiety levels were found. Conclusions: Depressive symptoms and hopelessness were more prevalent in individuals with HTT gene mutation than in individuals who were tested but had no said mutation. Such results emphasise the importance of timely diagnosis and treatment of psychiatric comorbidities in individuals affected by Huntington’s disease. |
| نوع الوثيقة: | article in journal/newspaper |
| وصف الملف: | application/pdf |
| اللغة: | Lithuanian English |
| العلاقة: | https://epublications.vu.lt/object/elaba:89463313/89463313.pdfTest; https://repository.vu.lt/VU:ELABAPDB89463313&prefLang=en_USTest |
| الإتاحة: | https://doi.org/10.15388/Amed.2020.28.1.4Test https://repository.vu.lt/VU:ELABAPDB89463313&prefLang=en_USTest |
| حقوق: | info:eu-repo/semantics/openAccess |
| رقم الانضمام: | edsbas.9A8875CE |
| قاعدة البيانات: | BASE |
| الوصف غير متاح. |