Brown Sandra A, Brumback Ty, Tomlinson Kristin, Cummins Kevin, Thompson Wesley K, Nagel Bonnie J, De Bellis Michael D, Hooper Stephen R, Clark Duncan B, Chung Tammy, Hasler Brant P, Colrain Ian M, Baker Fiona C, Prouty Devin, Pfefferbaum Adolf, Sullivan Edith V, Pohl Kilian M, Rohlfing Torsten, Nichols B Nolan, Chu Weiwei, Tapert Susan F
Department of Psychiatry, University of California, San Diego, La Jolla, California.
Department of Psychology, University of California, San Diego, La Jolla, California.
J Stud Alcohol Drugs. 2015 Nov;76(6):895-908. doi: 10.15288/jsad.2015.76.895.
During adolescence, neurobiological maturation occurs concurrently with social and interpersonal changes, including the initiation of alcohol and other substance use. The National Consortium on Alcohol and NeuroDevelopment in Adolescence (NCANDA) is designed to disentangle the complex relationships between onset, escalation, and desistance of alcohol use and changes in neurocognitive functioning and neuromaturation.
A sample of 831 youth, ages 12-21 years, was recruited at five sites across the United States, oversampling those at risk for alcohol use problems. Most (83%) had limited or no history of alcohol or other drug use, and a smaller portion (17%) exceeded drinking thresholds. A comprehensive assessment of biological development, family background, psychiatric symptomatology, and neuropsychological functioning-in addition to anatomical, diffusion, and functional brain magnetic resonance imaging-was completed at baseline.
The NCANDA sample of youth is nationally representative of sex and racial/ethnic groups. More than 50% have at least one risk characteristic for subsequent heavy drinking (e.g., family history, internalizing or externalizing symptoms). As expected, those who exceeded drinking thresholds (n = 139) differ from those who did not (n = 692) on identified factors associated with early alcohol use and problems.
NCANDA successfully recruited a large sample of adolescents and comprehensively assessed psychosocial functioning across multiple domains. Based on the sample's risk profile, NCANDA is well positioned to capture the transition into drinking and alcohol problems in a large portion of the cohort, as well as to help disentangle the associations between alcohol use, neurobiological maturation, and neurocognitive development and functioning.
在青少年时期,神经生物学成熟与社会和人际变化同时发生,包括开始饮酒及使用其他物质。青少年酒精与神经发育全国联盟(NCANDA)旨在厘清饮酒行为的起始、升级和停止与神经认知功能及神经成熟变化之间的复杂关系。
在美国五个地点招募了831名年龄在12至21岁之间的青少年样本,对有饮酒问题风险的人群进行了过度抽样。大多数(83%)青少年饮酒或使用其他药物的历史有限或没有此类历史,一小部分(17%)超过了饮酒阈值。在基线时完成了对生物发育、家庭背景、精神症状学和神经心理功能的全面评估,此外还进行了解剖学、扩散和功能性脑磁共振成像检查。
NCANDA的青少年样本在性别和种族/族裔群体方面具有全国代表性。超过50%的人至少有一项后续重度饮酒的风险特征(例如家族史、内化或外化症状)。正如预期的那样,饮酒阈值超标的人群(n = 139)在与早期饮酒及问题相关的已确定因素上与未超标的人群(n = 692)存在差异。
NCANDA成功招募了大量青少年样本,并全面评估了多个领域的心理社会功能。基于该样本的风险概况,NCANDA有能力在很大一部分队列中捕捉到向饮酒及酒精问题的转变,同时有助于厘清饮酒、神经生物学成熟以及神经认知发展和功能之间的关联。