Evidence map›Paper›PMID 31325594›Full record

ArticleJournal of the American Academy of Child and Adolescent Psychiatry2020

Borderline Symptoms at Age 12 Signal Risk for Poor Outcomes During the Transition to Adulthood: Findings From a Genetically Sensitive Longitudinal Cohort Study.

Jasmin Wertz, Avshalom Caspi, Antony Ambler, Louise Arseneault, Daniel W Belsky, Andrea Danese, Helen L Fisher, Timothy Matthews, Leah S Richmond-Rakerd, Terrie E Moffitt

Open access · hybridAbstract readTwin Study
In one paragraph

Article in Journal of the American Academy of Child and Adolescent Psychiatry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
11.2field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 90 citations in OpenAlex.

  1. Pooled it
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  9. Psychosocial functioning in personality disorders.Borderline personality disorder and emotion dysregulation · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 4 countries.

Jasmin WertzDuke University, Durham, North Carolina. Electronic address: jasmin.wertz@duke.edu.
Avshalom CaspiDuke University, Durham, North Carolina; Duke University Medical Center, Durham, North Carolina; Social, Genetic & Developmental Psychiatry Center, Institute of Psychiatry, Psychology and Neuroscience, King's College London, United Kingdom.
Antony AmblerSocial, Genetic & Developmental Psychiatry Center, Institute of Psychiatry, Psychology and Neuroscience, King's College London, United Kingdom; Dunedin Multidisciplinary Health and Development Unit, University of Otago, New Zealand.
Louise ArseneaultSocial, Genetic & Developmental Psychiatry Center, Institute of Psychiatry, Psychology and Neuroscience, King's College London, United Kingdom.
Daniel W BelskyColumbia University Mailman School of Public Health, New York.
Andrea DaneseSocial, Genetic & Developmental Psychiatry Center, Institute of Psychiatry, Psychology and Neuroscience, King's College London, United Kingdom; Institute of Psychiatry, Psychology and Neuroscience, King's College London, United Kingdom; National & Specialist CAMHS Clinic for Trauma, Anxiety and Depression, South London & Maudsley NHS Foundation Trust, London, United Kingdom.
Helen L FisherSocial, Genetic & Developmental Psychiatry Center, Institute of Psychiatry, Psychology and Neuroscience, King's College London, United Kingdom.
Timothy MatthewsSocial, Genetic & Developmental Psychiatry Center, Institute of Psychiatry, Psychology and Neuroscience, King's College London, United Kingdom.
Leah S Richmond-RakerdDuke University, Durham, North Carolina; Frank Porter Graham Child Development Institute, University of North Carolina, Chapel Hill.
Terrie E MoffittDuke University, Durham, North Carolina; Duke University Medical Center, Durham, North Carolina; Social, Genetic & Developmental Psychiatry Center, Institute of Psychiatry, Psychology and Neuroscience, King's College London, United Kingdom.
King's College London · GBDuke University · USColumbia University · US

Funding

Human Development: Interdisiplinary Research TrainingT32HD007376 · NICHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BELGER, AYSENIL, PROPPER, CATHI BARBRA · 1988 to 2020
$8.0M
Science CoreP2CHD065563 · NICHD · DUKE UNIVERSITY · PI James Moody · 2015 to 2026
$5.7M
Neuropsychological and genomic signatures of violence exposure in childhoodR01HD077482 · NICHD · DUKE UNIVERSITY · PI CASPI, AVSHALOM · 2013 to 2018
$2.8M
Medical Research Council G1002190NICHD NIH HHS P2C HD065563NICHD NIH HHS R01 HD077482NICHD NIH HHS T32 HD007376
6 · The paper itself

Abstract

objectiveBorderline personality disorder in adolescence remains a controversial construct. We addressed concerns about the prognostic significance of adolescent borderline pathology by testing whether borderline symptoms at age 12 years predict functioning during the transition to adulthood, at age 18 years, in areas critical to life-course development.

methodWe studied members of the Environmental Risk (E-Risk) Longitudinal Twin Study, which tracks the development of a birth cohort of 2,232 British twin children. At age 12, study members' borderline symptoms were measured using mothers' reports. At age 18, study members' personality, psychopathology, functional outcomes, and experiences of victimization were measured using self-reports, coinformant reports, and official records.

resultsAt age 18, study members who had more borderline symptoms at age 12 were more likely to have difficult personalities, to struggle with poor mental health, to experience poor functional outcomes, and to have become victims of violence. Reports of poor outcomes were corroborated by coinformants and official records. Borderline symptoms in study members at 12 years old predicted poor outcomes over and above other behavioral and emotional problems during adolescence. Twin analyses showed that borderline symptoms in 12-year-olds were influenced by familial risk, particularly genetic risk, which accounted for associations with most poor outcomes at age 18.

conclusionBorderline symptoms in 12-year-olds signal risk for pervasive poor functioning during the transition to adulthood. This association is driven by genetic influences, suggesting that borderline symptoms and poor outcomes are manifestations of shared genetic risk.

Indexed as

Borderline Personality DisorderBullyingCrime VictimsAdolescentChildCohort StudiesFemaleHumansLongitudinal StudiesMaleYoung Adultadolescenceborderlinelongitudinalpersonalitytwin

Identifiers

PMID31325594
PMCPMC6980181
OpenAlexW2957115773

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.