scholarly journals The other allele: Exploring the long allele of the serotonin transporter gene as a potential risk factor for psychopathy: A review of the parallels in findings

2011 ◽  
Vol 35 (3) ◽  
pp. 612-620 ◽  
Author(s):  
Andrea L. Glenn
PEDIATRICS ◽  
2001 ◽  
Vol 107 (4) ◽  
pp. 690-692 ◽  
Author(s):  
Naoko Narita ◽  
Masaaki Narita ◽  
Sachio Takashima ◽  
Masahiro Nakayama ◽  
Toshiro Nagai ◽  
...  

Obesity ◽  
2007 ◽  
Vol 15 (2) ◽  
pp. 271-276 ◽  
Author(s):  
Silvia Sookoian ◽  
Carolina Gemma ◽  
Silvia I. García ◽  
Tomas Fernández Gianotti ◽  
Guillermo Dieuzeide ◽  
...  

2011 ◽  
pp. 48-53 ◽  
Author(s):  
Carlos H Escobar ◽  
Jorge Hernán Calderón ◽  
Germán Alberto Moreno

Introduction: Major depression (MD), like other mood disorders, is considered a worldwide endemic pathology, becoming one of the biggest public health problems. The hereditary factors of mood disorders have been studied for many years and different chromosomal regions and genes have been involved in this physiopathological process. Objective: To establish the association between allelic variants of the serotonin transporter gene (5-HTTLPR and VNTR) and MD in a population with this diagnostic in the department of Caldas, Colombia. Materials and methods: A case-control study was conducted with individuals older than 16 years of age born in the department of Caldas. The sample was composed of 59 patients with the MD with family antecedents of the pathology and 59 controls paired by precedence, age, and gender. For the cases and controls selection the Diagnostic Interview for Genetic Studies (DIGS) was used. Using the Hranilovic et al. protocol, the polymorphic regions in the promoter and third intron of the Serotonin Transporter gene was amplified. Results: It was not possible to find association between MD and the genetic or clinical variables. The absence of the short allele of the promoter could act as a protective factor (OR=0.70 CI 95%=0.313 to 1.604), for the development of the pathology in this population, and the presence of at least one copy of the 10 repetition alleles of the third intron could act as a risk factor (OR: 1.25), but the wide confidence interval (CI 95%=0.38 to 2.64) does not permit supporting these conclusions. Discussion: The results obtained in this population do not yield conclusive information related with the etiopathogeny of MD, but do not contradict those obtained in other studies with bigger samples than ours. The broad confidence interval does not support conclusions about the role as a risk factor for the 10 repetition alleles of the intron or the absence of the S allele of the promoter as a protector factor. Further studies with larger population samples may help to clarify these facts.


2007 ◽  
Author(s):  
Tamlin Conner ◽  
Kathleen C. Gunthert ◽  
Stephen Armeli ◽  
Howard Tennen ◽  
Jonathan Covault ◽  
...  

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