Evidence map›Paper›PMID 27472737›Full record

ArticleMedicine2016

Improving risk assessment and familial aggregation of age at onset in schizophrenia using minor physical anomalies and craniofacial measures.

I-Ning Tsai, Jin-Jia Lin, Ming-Kun Lu, Hung-Pin Tan, Fong-Lin Jang, Shu-Ting Gan, Sheng-Hsiang Lin

Abstract read
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Article in Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

I-Ning TsaiInstitute of Clinical Medicine, College of Medicine, National Cheng Kung University Department of Psychiatry, Chimei Medical Center Department of Health, Jianan Mental Hospital Department of Applied Life Science and Health, Chia Nan University of Pharmacy and Science Department of Psychiatry, Kaohsiung Veterans General Hospital Tainan Branch Department of Acupressure Technology, Chung Hwa University of Medical Technology Department of Environmental and Occupational Health, College of Medicine, National Cheng Kung University Biostatistics Consulting Center, National Cheng Kung University Hospital, Tainan, Taiwan.
Jin-Jia Lin
Ming-Kun Lu
Hung-Pin Tan
Fong-Lin Jang
Shu-Ting Gan
Sheng-Hsiang Lin

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Age at onset is the most important feature of schizophrenia that could indicate its origin. Minor physical anomalies (MPAs) characterize potential marker indices of disturbances in early neurodevelopment. However, the association between MPAs and age at onset of schizophrenia is still unclear. We aimed to compare risk assessment and familial aggregation in patients with early-onset schizophrenia (EOS) and adult-onset schizophrenia (AOS) with MPAs and craniofacial measures.We estimated the risk assessment of MPAs among patients with EOS (n = 68), patients with AOS (n = 183), nonpsychotic relatives (n = 147), and healthy controls (n = 241) using 3 data-mining algorithms. In addition, we assessed the magnitude of familial aggregation of MPAs with respect to the age at onset of schizophrenia.The performance of EOS was superior to that of AOS, with discrimination accuracies of 89% and 76%, respectively. Combined MPA scores as the risk assessment were significantly higher in all schizophrenia subgroups and the nonpsychotic relatives of EOS patients than in the healthy controls. The recurrence risk ratio for familial aggregation of the MPA scores of EOS families (odds ratio 9.27) was substantially higher than that of AOS families (odds ratio 2.47).The results highlight that EOS improves risk assessment and has a severe magnitude of familial aggregation of MPAs. These findings indicate that EOS might result from a stronger genetic susceptibility to neurodevelopmental deficits.

Indexed as

CephalometryRisk AssessmentAdolescentAdultAge of OnsetCongenital AbnormalitiesFemaleGenetic MarkersGenetic Predisposition to DiseaseGenetic TestingHumansMaleNeurodevelopmental DisordersSchizophreniaTaiwanYoung AdultGenetic Markers

Identifiers

PMID27472737
PMCPMC5265874

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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.