{"title":"Neurological Soft Signs in Type I Bipolar Disorder and Bipolar Spectrum Patients and Their Unaffected First-Degree Relatives: A Cross-Sectional Study.","authors":"Seyed Saeed Sadr, Seyed Mehdi Samimi-Ardestani, Yousef Semnani, Narges Adel, Faezeh Tajari, Nastaran Samani","doi":"10.1002/hsr2.70341","DOIUrl":null,"url":null,"abstract":"<p><strong>Background and aims: </strong>This study aimed to compare neurological soft signs (NSSs) in type 1 bipolar disorder (BD), bipolar spectrum (BS) patients, and their unaffected first-degree relatives.</p><p><strong>Methods: </strong>This descriptive cross-sectional study involved participants referred to the Psychiatric Department of Imam Hossein Hospital. Five groups (<i>n</i> = 25): patients with type 1 BD, patients with BS, unaffected first-degree relatives of the two groups, and a control group were evaluated using the Neurological Evaluation Scale (NES).</p><p><strong>Results: </strong>The analysis revealed that patients with bipolar I disorder had the highest NES scores, with significant group differences (<i>F</i>(4.120) = 10.36, <i>p</i> < 0.001). The Bonferroni correction identified bipolar I patients as the primary source of this difference, while other groups did not significantly differ. ANCOVA showed that age (<i>F</i>(1.123) = 3.92, <i>p</i> = 0.052) and gender (<i>F</i>(1.123) = 0.1, <i>p</i> = 0.75) had no significant influence on NES scores. However, all four NES subsets significantly contributed to the overall score, except for the sensory subset. Differences were significant between bipolar I patients and most other groups, except the BS group, which showed no significant differences from the rest. No correlation was found with age, gender, or age of disease onset.</p><p><strong>Conclusion: </strong>The higher NSS severity in type I BD compared to BS and control groups highlights its potential link to the genetic and neurodevelopmental differences in BD type I. Further research is recommended.</p>","PeriodicalId":36518,"journal":{"name":"Health Science Reports","volume":"8 1","pages":"e70341"},"PeriodicalIF":2.1000,"publicationDate":"2025-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11725529/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Health Science Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/hsr2.70341","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
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Abstract
Background and aims: This study aimed to compare neurological soft signs (NSSs) in type 1 bipolar disorder (BD), bipolar spectrum (BS) patients, and their unaffected first-degree relatives.
Methods: This descriptive cross-sectional study involved participants referred to the Psychiatric Department of Imam Hossein Hospital. Five groups (n = 25): patients with type 1 BD, patients with BS, unaffected first-degree relatives of the two groups, and a control group were evaluated using the Neurological Evaluation Scale (NES).
Results: The analysis revealed that patients with bipolar I disorder had the highest NES scores, with significant group differences (F(4.120) = 10.36, p < 0.001). The Bonferroni correction identified bipolar I patients as the primary source of this difference, while other groups did not significantly differ. ANCOVA showed that age (F(1.123) = 3.92, p = 0.052) and gender (F(1.123) = 0.1, p = 0.75) had no significant influence on NES scores. However, all four NES subsets significantly contributed to the overall score, except for the sensory subset. Differences were significant between bipolar I patients and most other groups, except the BS group, which showed no significant differences from the rest. No correlation was found with age, gender, or age of disease onset.
Conclusion: The higher NSS severity in type I BD compared to BS and control groups highlights its potential link to the genetic and neurodevelopmental differences in BD type I. Further research is recommended.