P50 sensory gating in multiplex schizophrenia families from a Pacific island isolate.
P50 sensory gating in multiplex schizophrenia families from a Pacific island isolate.
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来自太平洋岛屿分离株的多重精神分裂症家族中的 P50 感觉门控。
DOI:
10.1176/appi.ajp.159.12.2007
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发表时间:
2002
期刊:
影响因子:
--
通讯作者:
Myles-Worsley,Marina
中科院分区:
文献类型:
--
作者:
Myles-Worsley,Marina
OBJECTIVEMultiplex schizophrenia families from Palau, Micronesia, were assessed with P50 sensory gating to 1) test for replication of the association between this inhibitory neurobiological trait and familial schizophrenia in non-Caucasian subjects and 2) evaluate the ability of the P50 trait to serve as an endophenotype in a genetic linkage study of these families.METHODA paired-stimulus auditory event- related potential paradigm was used to examine P50 sensory gating in 85 schizophrenia patients (56 medicated with typical antipsychotics and 29 unmedicated), 83 of their first-degree relatives (46 parents and 37 siblings), and 29 normal comparison subjects.RESULTSAuditory sensory gating as measured by the P50 ratio was similarly impaired in medicated and unmedicated schizophrenia patients compared to the normal subjects, and medication dose had no significant effect on any P50 variable. This impairment extended to first-degree relatives, who also showed significantly higher P50 ratios than the normal subjects. Abnormal P50 ratios were found in 64.7% of the schizophrenia patients and 51.8% of their first-degree relatives but only 10.3% of the normal subjects.CONCLUSIONSP50 sensory gating deficits were confirmed in Palauan schizophrenia families. Rates of abnormal P50 sensory gating in relatives versus normal subjects resulted in a risk ratio of 5.0. Impairment was independent of medication effects, indicating that the P50 paradigm measures a stable neurobiological trait unaffected by treatment with typical antipsychotics. These results suggest that this trait can fulfill the major criteria for an endophenotype for genetic liability to schizophrenia in these multiply affected Palauan families.
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影响因子:
--
作者:
C. Siegel;M. Waldo;G. Mizner;L. Adler;R. Freedman
通讯作者:
C. Siegel;M. Waldo;G. Mizner;L. Adler;R. Freedman
DOI:
10.1176/ajp.149.4.488
发表时间:
1992-04
期刊:
The American journal of psychiatry
影响因子:
--
作者:
L. Judd;L. Mcadams;Byron Budnick;D. Braff
通讯作者:
L. Judd;L. Mcadams;Byron Budnick;D. Braff
影响因子:
17.7
作者:
Light, GA;Geyer, MA;Braff, DL
通讯作者:
Braff, DL
DOI:
10.1176/ajp.152.9.1286
发表时间:
1995
期刊:
The American journal of psychiatry.
影响因子:
--
作者:
Faraone,SV;Kremen,WS;Lyons,MJ;Pepple,JR;Seidman,LJ;Tsuang,MT
通讯作者:
Tsuang,MT
影响因子:
9.8
作者:
Almasy, L;Blangero, J
通讯作者:
Blangero, J