Association between telomere length with alcohol use disorder and internalizing/externalizing comorbidities in a Brazilian male sample

IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Helena Ferreira Moura , Jaqueline Bohrer Schuch , Felipe Ornell , Cibele Edom Bandeira , Raffael Massuda , Claiton Henrique Dotto Bau , Eugenio Horácio Grevet , Felix H.P. Kessler , Lisia von Diemen
{"title":"Association between telomere length with alcohol use disorder and internalizing/externalizing comorbidities in a Brazilian male sample","authors":"Helena Ferreira Moura ,&nbsp;Jaqueline Bohrer Schuch ,&nbsp;Felipe Ornell ,&nbsp;Cibele Edom Bandeira ,&nbsp;Raffael Massuda ,&nbsp;Claiton Henrique Dotto Bau ,&nbsp;Eugenio Horácio Grevet ,&nbsp;Felix H.P. Kessler ,&nbsp;Lisia von Diemen","doi":"10.1016/j.alcohol.2024.04.004","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>Shortening telomere length (TL) is an important ageing marker associated with substance use disorder (SUD). However, the influence of psychiatric and clinical comorbidities and alcohol-related outcomes has not been much explored in the context of TL in individuals with alcohol use disorder (AUD) and may be a source of heterogeneity in AUD studies. Therefore, our aim was to investigate the influence of AUD, alcohol-related outcomes, and common psychiatric comorbidities on TL in men with AUD and healthy controls (HC).</p></div><div><h3>Methods</h3><p>Men with AUD (n = 108, mean age = 52.4, SD = 8.6) were recruited in a detoxification unit, and HC (n = 80, mean age = 50.04, SD = 9.1) from the blood bank, both located in Brazil. HC had no current or lifetime diagnosis of any substance use disorder. Psychiatric comorbidities were assessed using SCID-I. TL ratio was measured in triplicates using quantitative multiplex PCR.</p></div><div><h3>Results</h3><p>Telomere length did not differ between individuals with AUD and HC (p = 0.073) or was associated with AUD-related outcomes, trauma, or clinical comorbidities. Individuals with externalizing disorders had longer TL when comparing with those with internalizing disorders (p = 0.018) or without comorbidity (p = 0.018).</p></div><div><h3>Conclusion</h3><p>Our findings indicate that TL was influenced by the presence of psychiatric comorbidity rather than case or control status. These results were adjusted for potential confounders, such as age.</p></div>","PeriodicalId":7712,"journal":{"name":"Alcohol","volume":"119 ","pages":"Pages 1-5"},"PeriodicalIF":2.5000,"publicationDate":"2024-04-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Alcohol","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0741832924000624","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

Abstract

Background

Shortening telomere length (TL) is an important ageing marker associated with substance use disorder (SUD). However, the influence of psychiatric and clinical comorbidities and alcohol-related outcomes has not been much explored in the context of TL in individuals with alcohol use disorder (AUD) and may be a source of heterogeneity in AUD studies. Therefore, our aim was to investigate the influence of AUD, alcohol-related outcomes, and common psychiatric comorbidities on TL in men with AUD and healthy controls (HC).

Methods

Men with AUD (n = 108, mean age = 52.4, SD = 8.6) were recruited in a detoxification unit, and HC (n = 80, mean age = 50.04, SD = 9.1) from the blood bank, both located in Brazil. HC had no current or lifetime diagnosis of any substance use disorder. Psychiatric comorbidities were assessed using SCID-I. TL ratio was measured in triplicates using quantitative multiplex PCR.

Results

Telomere length did not differ between individuals with AUD and HC (p = 0.073) or was associated with AUD-related outcomes, trauma, or clinical comorbidities. Individuals with externalizing disorders had longer TL when comparing with those with internalizing disorders (p = 0.018) or without comorbidity (p = 0.018).

Conclusion

Our findings indicate that TL was influenced by the presence of psychiatric comorbidity rather than case or control status. These results were adjusted for potential confounders, such as age.

巴西男性样本中端粒长度与酒精使用障碍和内化/外化合并症之间的关系。
背景端粒长度(TL)缩短是与药物使用障碍(SUD)相关的一个重要衰老标志。然而,在酒精使用障碍(AUD)患者端粒长度的背景下,精神和临床合并症以及酒精相关结果的影响尚未得到广泛探讨,这可能是AUD研究中异质性的一个来源。因此,我们的目的是调查 AUD、酒精相关结果和常见精神疾病合并症对 AUD 男性患者和健康对照组(HC)TL 的影响。方法在巴西的一家戒毒单位招募 AUD 男性患者(n = 108,平均年龄 = 52.4,SD = 8.6),并从血库招募 HC 患者(n = 80,平均年龄 = 50.04,SD = 9.1)。HC 目前或终生未被诊断患有任何药物使用障碍。精神合并症使用 SCID-I 进行评估。采用定量多重 PCR 方法测量了三重的 TL 比值。结果单核细胞长度在 AUD 患者和 HC 患者之间没有差异(p = 0.073),也与 AUD 相关结果、创伤或临床合并症无关。结论我们的研究结果表明,骨髓长度受精神疾病合并症的影响,而不是受病例或对照身份的影响。这些结果已对潜在的混杂因素(如年龄)进行了调整。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Alcohol
Alcohol 医学-毒理学
CiteScore
4.60
自引率
4.30%
发文量
74
审稿时长
15.6 weeks
期刊介绍: Alcohol is an international, peer-reviewed journal that is devoted to publishing multi-disciplinary biomedical research on all aspects of the actions or effects of alcohol on the nervous system or on other organ systems. Emphasis is given to studies into the causes and consequences of alcohol abuse and alcoholism, and biomedical aspects of diagnosis, etiology, treatment or prevention of alcohol-related health effects. Intended for both research scientists and practicing clinicians, the journal publishes original research on the neurobiological, neurobehavioral, and pathophysiological processes associated with alcohol drinking, alcohol abuse, alcohol-seeking behavior, tolerance, dependence, withdrawal, protracted abstinence, and relapse. In addition, the journal reports studies on the effects alcohol on brain mechanisms of neuroplasticity over the life span, biological factors associated with adolescent alcohol abuse, pharmacotherapeutic strategies in the treatment of alcoholism, biological and biochemical markers of alcohol abuse and alcoholism, pathological effects of uncontrolled drinking, biomedical and molecular factors in the effects on liver, immune system, and other organ systems, and biomedical aspects of fetal alcohol spectrum disorder including mechanisms of damage, diagnosis and early detection, treatment, and prevention. Articles are published from all levels of biomedical inquiry, including the following: molecular and cellular studies of alcohol''s actions in vitro and in vivo; animal model studies of genetic, pharmacological, behavioral, developmental or pathophysiological aspects of alcohol; human studies of genetic, behavioral, cognitive, neuroimaging, or pathological aspects of alcohol drinking; clinical studies of diagnosis (including dual diagnosis), treatment, prevention, and epidemiology. The journal will publish 9 issues per year; the accepted abbreviation for Alcohol for bibliographic citation is Alcohol.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信