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- W2017485612 abstract "Purpose. To understand the role of polymorphisms in the LEP (rs7799039 and rs2167270) and LEPR (rs1137101 and rs1137100) genes in DTC susceptibility and their effect on leptin levels. Methods. We studied 153 patients with DTC and 234 controls through TaqMan SNP Genotyping and ELISA, comparing these data to the clinicopathological data of patients with DTC. Results. Patients with AA genotype of rs7799039 had higher levels of serum leptin (<mml:math xmlns:mml=http://www.w3.org/1998/Math/MathML id=M1><mml:mn>9.22</mml:mn><mml:mo>±</mml:mo><mml:mn>0.98</mml:mn></mml:math> ng/mL) than those with AG genotype (<mml:math xmlns:mml=http://www.w3.org/1998/Math/MathML id=M2><mml:mn>10.07</mml:mn><mml:mo>±</mml:mo><mml:mn>0.60</mml:mn></mml:math> ng/mL;<mml:math xmlns:mml=http://www.w3.org/1998/Math/MathML id=M3><mml:mi>P</mml:mi><mml:mo>=</mml:mo><mml:mn>0.005</mml:mn></mml:math>). Individuals with AG genotype of rs2167270 also produced higher serum leptin levels (<mml:math xmlns:mml=http://www.w3.org/1998/Math/MathML id=M4><mml:mn>10.05</mml:mn><mml:mo>±</mml:mo><mml:mn>0.59</mml:mn></mml:math> ng/mL) than the subjects with GG genotype (<mml:math xmlns:mml=http://www.w3.org/1998/Math/MathML id=M5><mml:mn>9.52</mml:mn><mml:mo>±</mml:mo><mml:mn>0.79</mml:mn></mml:math> ng/mL;<mml:math xmlns:mml=http://www.w3.org/1998/Math/MathML id=M6><mml:mi>P</mml:mi><mml:mo><</mml:mo><mml:mn>0.05</mml:mn></mml:math>). A multivariate logistic regression adjusted for gender, age, and BMI showed that the AG genotype of rs7799039 was an independent risk for DTC (OR, 11.689;<mml:math xmlns:mml=http://www.w3.org/1998/Math/MathML id=M7><mml:mi>P</mml:mi><mml:mo>=</mml:mo><mml:mn>0.0183</mml:mn></mml:math>; 95% CI, 1.516–90.119). Similarly, AG and GG genotypes of rs1137101 increased the susceptibility to DTC (OR, 3.747;<mml:math xmlns:mml=http://www.w3.org/1998/Math/MathML id=M8><mml:mi>P</mml:mi><mml:mo>=</mml:mo><mml:mn>0.027</mml:mn></mml:math>; 95% CI, 1.161–12.092 and OR, 5.437;<mml:math xmlns:mml=http://www.w3.org/1998/Math/MathML id=M9><mml:mi>P</mml:mi><mml:mo>=</mml:mo><mml:mn>0.013</mml:mn></mml:math>; 95% CI, 1.426–20.729). Conclusions. We demonstrated that rs7799039 and rs2167270 polymorphisms modify the serum leptin concentrations in patients with DTC. Furthermore, polymorphisms rs7799039 and rs1137101 increase the risk of DTC development, although they do not correlate with tumor aggressiveness." @default.
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- W2017485612 date "2015-01-01" @default.
- W2017485612 modified "2023-10-18" @default.
- W2017485612 title "Polymorphism in<i>LEP</i>and<i>LEPR</i>May Modify Leptin Levels and Represent Risk Factors for Thyroid Cancer" @default.
- W2017485612 cites W1565308578 @default.
- W2017485612 cites W1909229464 @default.
- W2017485612 cites W1967715137 @default.
- W2017485612 cites W1976907183 @default.
- W2017485612 cites W1978723415 @default.
- W2017485612 cites W1980614497 @default.
- W2017485612 cites W1984063927 @default.
- W2017485612 cites W1985823120 @default.
- W2017485612 cites W1990088457 @default.
- W2017485612 cites W1995867455 @default.
- W2017485612 cites W1999376821 @default.
- W2017485612 cites W1999734164 @default.
- W2017485612 cites W1999920710 @default.
- W2017485612 cites W2009855338 @default.
- W2017485612 cites W2011607258 @default.
- W2017485612 cites W2017596133 @default.
- W2017485612 cites W2018821331 @default.
- W2017485612 cites W2025222032 @default.
- W2017485612 cites W2031054403 @default.
- W2017485612 cites W2031729449 @default.
- W2017485612 cites W2031870544 @default.
- W2017485612 cites W2035484524 @default.
- W2017485612 cites W2037404553 @default.
- W2017485612 cites W2041951510 @default.
- W2017485612 cites W2042656890 @default.
- W2017485612 cites W2042908502 @default.
- W2017485612 cites W2047870575 @default.
- W2017485612 cites W2047871811 @default.
- W2017485612 cites W2048682872 @default.
- W2017485612 cites W2050019640 @default.
- W2017485612 cites W2059027713 @default.
- W2017485612 cites W2066541334 @default.
- W2017485612 cites W2072700176 @default.
- W2017485612 cites W2072893247 @default.
- W2017485612 cites W2079850803 @default.
- W2017485612 cites W2081132301 @default.
- W2017485612 cites W2087044021 @default.
- W2017485612 cites W2090826082 @default.
- W2017485612 cites W2092165051 @default.
- W2017485612 cites W2104277744 @default.
- W2017485612 cites W2108780640 @default.
- W2017485612 cites W2116542352 @default.
- W2017485612 cites W2119016364 @default.
- W2017485612 cites W2126685041 @default.
- W2017485612 cites W2129038576 @default.
- W2017485612 cites W2129537368 @default.
- W2017485612 cites W2132043021 @default.
- W2017485612 cites W2145781737 @default.
- W2017485612 cites W2153478478 @default.
- W2017485612 cites W2155052327 @default.
- W2017485612 cites W2168184182 @default.
- W2017485612 cites W2248863271 @default.
- W2017485612 cites W2318642820 @default.
- W2017485612 cites W2325815304 @default.
- W2017485612 cites W2334252978 @default.
- W2017485612 cites W2399817020 @default.
- W2017485612 cites W4243637743 @default.
- W2017485612 cites W4255067994 @default.
- W2017485612 cites W4298152758 @default.
- W2017485612 doi "https://doi.org/10.1155/2015/173218" @default.
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