Psychiatric symptoms and syndromes transcending diagnostic boundaries in Indian multiplex families: The cohort of ADBS study

•Pattern of occurrence of psychiatric symptoms and syndromes in members of multiplex families was studied.•The participants had high familial prevalence with a third of all first-degree relatives being affected.•Similar diagnoses aggregate within families, but 62% of families had members with other...

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Published in:Psychiatry research 2021-02, Vol.296, p.113647-113647, Article 113647
Main Authors: Sreeraj, Vanteemar S, Holla, Bharath, Ithal, Dhruva, Nadella, Ravi Kumar, Mahadevan, Jayant, Balachander, Srinivas, Ali, Furkhan, Sheth, Sweta, Narayanaswamy, Janardhanan C, Venkatasubramanian, Ganesan, John, John P, Varghese, Mathew, Benegal, Vivek, Jain, Sanjeev, Reddy, YC Janardhan, Viswanath, Biju
Format: Article
Language:English
Subjects:
Biomarkers
cross-cutting symptoms
Genetics
Prevalence
Psychiatric disorders
Relatives
Transdiagnosis
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Summary:•Pattern of occurrence of psychiatric symptoms and syndromes in members of multiplex families was studied.•The participants had high familial prevalence with a third of all first-degree relatives being affected.•Similar diagnoses aggregate within families, but 62% of families had members with other syndromes•Considerable heterogeneity of psychiatric syndromes, as well as sub-threshold symptoms were seen in multiplex families. Syndromes of schizophrenia, bipolar disorder, obsessive-compulsive disorder, substance use disorders and Alzheimer's dementia are highly heritable. About 10-20% of subjects have another affected first degree relative (FDR), and thus represent a ‘greater’ genetic susceptibility. We screened 3583 families to identify 481 families with multiple affected members, assessed 1406 individuals in person, and collected information systematically about other relatives. Within the selected families, a third of all FDRs were affected with serious mental illness. Although similar diagnoses aggregated within families, 62% of the families also had members with other syndromes. Moreover, 15% of affected individuals met criteria for co-occurrence of two or more syndromes, across their lifetime. Using dimensional assessments, we detected a range of symptom clusters in both affected and unaffected individuals, and across diagnostic categories. Our findings suggest that in multiplex families, there is considerable heterogeneity of clinical syndromes, as well as sub-threshold symptoms. These families would help provide an opportunity for further research using both genetic analyses and biomarkers.
ISSN:0165-1781
1872-7123
DOI:10.1016/j.psychres.2020.113647