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A multivariate Swedish national twin-sibling study in women of major depression, anxiety disorder, fibromyalgia, and irritable bowel syndrome
被引:0
|作者:
Kendler, Kenneth S.
[1
,2
]
Ohlsson, Henrik
[3
]
Neale, Michael
[1
,2
]
van Loo, Hanna
[4
]
Rosmalen, Judith G. M.
[4
,5
]
Sundquist, Jan
[3
,6
,7
]
Sundquist, Kristina
[3
,6
,7
]
机构:
[1] Virginia Commonwealth Univ, Virginia Inst Psychiat & Behav Genet, Richmond, VA 23220 USA
[2] Virginia Commonwealth Univ, Dept Psychiat, Richmond, VA 23220 USA
[3] Lund Univ, Ctr Primary Health Care Res, Malmo, Sweden
[4] Univ Med Ctr Groningen, Dept Psychiat, Groningen, Netherlands
[5] Univ Med Ctr Groningen, Dept Internal Med, Groningen, Netherlands
[6] Univ Clin Primary Care Skane, Malmo, Sweden
[7] Shimane Univ, Ctr Community Based Healthcare Res & Educ CoHRE, Sch Med, Dept Funct Pathol, Matsue, Japan
基金:
美国国家卫生研究院;
瑞典研究理事会;
关键词:
Functional Somatic Disorders;
Internalizing Psychiatric Disorders;
Genetic Risk;
Major Depression;
Anxiety Disorders;
Fibromyalgia;
Irritable Bowel Syndrome;
FUNCTIONAL SOMATIC SYNDROMES;
POPULATION-BASED TWIN;
GENOME-WIDE ANALYSIS;
GENETIC EPIDEMIOLOGY;
METAANALYSIS;
D O I:
10.1017/S0033291725000923
中图分类号:
B849 [应用心理学];
学科分类号:
040203 ;
摘要:
Background Functional Somatic Disorders (FSD) and Internalizing Psychiatric Disorders (IPD) are frequently comorbid and likely share familial/genetic risk factors. Methods We performed a Common Factor Multivariate Analysis of 2 FSDs, Fibromyalgia (FM) and Irritable Bowel Syndrome (IBS), and two IPDs, Major Depression (MD) and Anxiety Disorders (AD), in five kinds of Swedish female-female relative pairs: monozygotic (n = 8,052) dizygotic (n = 7216), full siblings (n = 712,762), half-siblings reared together (n = 23,623), and half-siblings reared apart (n = 53,873). Model fitting was by full information maximum likelihood using OpenMx. Results The best-fit model included genetic, shared environmental, and unique environmental factors. The common factor, similar to 50% heritable with a small shared environmental effect, loaded more strongly on the two IPDs (similar to 0.80) than the 2 FSDs (0.40). Disorder-specific genetic effects were larger for the 2 FSDs (similar to 0.30) than the 2 IPDs (similar to 0.03). Estimated genetic correlations were high for MD and AD (+0.91), moderate between IBS and IPDs (+0.62), and intermediate between FM and MD (+0.54), FM and AD (+0.28), and FM and IBS (+0.38). Shared environmental influences on all disorders were present but small. Conclusions In women, FSDs and IPDs shared a moderate proportion of their genetic risk factors, greater for IBS than for FM. However, the genetic sharing between IBS and FM was less than between MD and AD, suggesting that FSDs do not form a highly genetically coherent group of disorders. The shared environment made a modest contribution to the familial aggregation of FSDs and IPDs.
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