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15 July 2020: Clinical Research

Association Between Ghrelin Gene Polymorphism and Cerebral Infarction

Li Chen 1ABE , Hua Zhao 1BCF , Jing Shen 2DF , Xiaoyu Ji 3ACG*

DOI: 10.12659/MSM.924539

Med Sci Monit 2020; 26:e924539

Table 3 Analysis of polymorphisms at ghrelin gene loci rs26312, rs26802, and rs27647.

LocusGenotypeControl groupDisease groupχ2P
Dominant modelrs26312GG+GA162 (0.810)151 (0.755)2.810.381
AA38 (0.190)49 (0.245)
rs26802TT+TG152 (0.760)140 (0.700)1.510.583
GG48 (0.240)60 (0.300)
rs27647CC+CT155 (0.775)171 (0.855)7.450.023
TT45 (0.225)29 (0.145)
Recessive modelrs26312GG49 (0.245)42 (0.210)2.140.401
GA+AA151 (0.755)158 (0.790)
rs26802TT61 (0.305)38 (0.190)6.340.033
TG+GG139 (0.695)162 (0.810)
rs27647CC50 (0.250)35 (0.175)2.340.451
CT+TT150 (0.750)165 (0.825)
Heterozygous modelrs26312GG49 (0.245)42 (0.210)1.930.485
GA113 (0.565)109 (0.545)
rs26802TT61 (0.305)38 (0.190)3.950.058
TG91 (0.455)102 (0.510)
rs27647CC50 (0.250)35 (0.175)8.340.007
CT105 (0.525)136 (0.680)
Homozygous modelrs26312GG49 (0.245)42 (0.210)2.740.331
AA38 (0.190)49 (0.245)
rs26802TT61 (0.305)38 (0.190)2.380.351
GG48 (0.240)60 (0.300)
rs27647CC50 (0.250)35 (0.175)3.010.134
TT45 (0.225)29 (0.145)

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Medical Science Monitor eISSN: 1643-3750
Medical Science Monitor eISSN: 1643-3750