Matches in SemOpenAlex for { <https://semopenalex.org/work/W3048812714> ?p ?o ?g. }
- W3048812714 endingPage "145058" @default.
- W3048812714 startingPage "145058" @default.
- W3048812714 abstract "The nuclear receptors Rev-erb alpha and Rev-erb beta are transcription factors that regulate the function of genes in glucose and lipid metabolism, and they also form a link between circadian rhythm and metabolism. We evaluated the variations in Rev-erb alpha and Rev-erb beta genes together with biochemical parameters as risk factors in type 2 diabetic (T2DM) patients. Molecular analyses of Rev-erb alpha and Rev-erb beta genes were performed on genomic DNA by using next-generation sequencing in 42 T2DM patients (21 obese and 21 non-obese) and 66 healthy controls. We found 26 rare mutations in the study groups, including 13 missense mutations, 9 silent mutations, 3 5′UTR variations, and a 3′UTR variation, of which 9 were novel variations (5 missense and 3 silent and 1 5′UTR). Six common variations were also found in the Rev-erb genes; Rev-erb beta Chr3:24003765 A > G, Rev-erb beta rs924403442 (Chr3:24006717) G > T, Rev-erb alpha Chr17:38253751 T > C, Rev-erb alpha rs72836608 C > A, Rev-erb alpha rs2314339 C > T and Rev-erb alpha rs2102928 C > T. Of these, Rev-erb beta Chr3:24003765 A > G was a novel missense mutation (p.Q197R), while others were identified as intronic variants. T2DM patients with Rev-erb beta rs924403442 T allele had lower body surface area (BSA) than noncarriers (GG genotype) (p = 0.039). Rev-erb alpha rs72836608 A allele and Rev-erb alpha rs2314339 CC genotype were associated with decreased serum HDL-cholesterol levels in T2DM patients (p = 0.025 and p = 0.027, respectively). In our study, different effects of Rev-erbs polymorphisms were found according to gender and presence of obesity. Rev-erb alpha rs72836608 (C > A) and rs2314339 (C > T) and Rev-erb alpha rs2102928 (C > T) were associated with low HDL-C levels in male T2DM patients. In female patients, Rev-erb alpha rs2102928 (C > T) was associated with high microalbuminuria and Rev-erb beta rs9244403442 G > T was associated with low HDL and high BSA values. In addition, Rev-erb alpha Chr17: 38,253,751 (T > C), rs72836608 (C > A), and rs2314339 (C > T) and Rev-erb beta Chr3:24003765 (A > G) were associated with increased serum GGT levels in obese T2DM patients. In non-obese patients, Rev-erbs SNPs had no effect on serum GGT levels. Our findings indicate that variations in the Rev-erb alpha and Rev-erb beta genes can affect metabolic changes in T2DM and these effects may vary depending on gender and obesity." @default.
- W3048812714 created "2020-08-18" @default.
- W3048812714 creator A5000019645 @default.
- W3048812714 creator A5019612804 @default.
- W3048812714 creator A5034543421 @default.
- W3048812714 creator A5045123681 @default.
- W3048812714 creator A5058006139 @default.
- W3048812714 creator A5062190887 @default.
- W3048812714 creator A5066490967 @default.
- W3048812714 creator A5079153497 @default.
- W3048812714 date "2020-12-01" @default.
- W3048812714 modified "2023-10-18" @default.
- W3048812714 title "Determination of genetic changes of Rev-erb beta and Rev-erb alpha genes in Type 2 diabetes mellitus by next-generation sequencing" @default.
- W3048812714 cites W1237751540 @default.
- W3048812714 cites W1509174047 @default.
- W3048812714 cites W1608726413 @default.
- W3048812714 cites W1965921169 @default.
- W3048812714 cites W1975828542 @default.
- W3048812714 cites W1976579158 @default.
- W3048812714 cites W1981321743 @default.
- W3048812714 cites W1986025060 @default.
- W3048812714 cites W1987051340 @default.
- W3048812714 cites W1990356462 @default.
- W3048812714 cites W1991709585 @default.
- W3048812714 cites W2007042885 @default.
- W3048812714 cites W2011072921 @default.
- W3048812714 cites W2019962167 @default.
- W3048812714 cites W2020885061 @default.
- W3048812714 cites W2021990756 @default.
- W3048812714 cites W2023916848 @default.
- W3048812714 cites W2033178220 @default.
- W3048812714 cites W2036061009 @default.
- W3048812714 cites W2044551188 @default.
- W3048812714 cites W2052453572 @default.
- W3048812714 cites W2056265088 @default.
- W3048812714 cites W2058103134 @default.
- W3048812714 cites W2061145694 @default.
- W3048812714 cites W2065660725 @default.
- W3048812714 cites W2075175630 @default.
- W3048812714 cites W2081446679 @default.
- W3048812714 cites W2086590730 @default.
- W3048812714 cites W2087924989 @default.
- W3048812714 cites W2089535377 @default.
- W3048812714 cites W2091379168 @default.
- W3048812714 cites W2093419981 @default.
- W3048812714 cites W2093505571 @default.
- W3048812714 cites W2097456908 @default.
- W3048812714 cites W2101704044 @default.
- W3048812714 cites W2103752249 @default.
- W3048812714 cites W2103970881 @default.
- W3048812714 cites W2104131439 @default.
- W3048812714 cites W2104290916 @default.
- W3048812714 cites W2108836811 @default.
- W3048812714 cites W2110163080 @default.
- W3048812714 cites W2113868760 @default.
- W3048812714 cites W2114108518 @default.
- W3048812714 cites W2115583552 @default.
- W3048812714 cites W2122463654 @default.
- W3048812714 cites W2131660765 @default.
- W3048812714 cites W2134688453 @default.
- W3048812714 cites W2140191267 @default.
- W3048812714 cites W2146589543 @default.
- W3048812714 cites W2147088548 @default.
- W3048812714 cites W2147712103 @default.
- W3048812714 cites W2149886316 @default.
- W3048812714 cites W2156988995 @default.
- W3048812714 cites W2157758348 @default.
- W3048812714 cites W2158365433 @default.
- W3048812714 cites W2158612065 @default.
- W3048812714 cites W2168133698 @default.
- W3048812714 cites W2168558953 @default.
- W3048812714 cites W2225474275 @default.
- W3048812714 cites W2282466811 @default.
- W3048812714 cites W2328983592 @default.
- W3048812714 cites W2613487665 @default.
- W3048812714 cites W2751282522 @default.
- W3048812714 cites W2793051219 @default.
- W3048812714 cites W2793968455 @default.
- W3048812714 cites W3187443279 @default.
- W3048812714 cites W4247053599 @default.
- W3048812714 doi "https://doi.org/10.1016/j.gene.2020.145058" @default.
- W3048812714 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/32798635" @default.
- W3048812714 hasPublicationYear "2020" @default.
- W3048812714 type Work @default.
- W3048812714 sameAs 3048812714 @default.
- W3048812714 citedByCount "7" @default.
- W3048812714 countsByYear W30488127142021 @default.
- W3048812714 countsByYear W30488127142022 @default.
- W3048812714 countsByYear W30488127142023 @default.
- W3048812714 crossrefType "journal-article" @default.
- W3048812714 hasAuthorship W3048812714A5000019645 @default.
- W3048812714 hasAuthorship W3048812714A5019612804 @default.
- W3048812714 hasAuthorship W3048812714A5034543421 @default.
- W3048812714 hasAuthorship W3048812714A5045123681 @default.
- W3048812714 hasAuthorship W3048812714A5058006139 @default.
- W3048812714 hasAuthorship W3048812714A5062190887 @default.
- W3048812714 hasAuthorship W3048812714A5066490967 @default.
- W3048812714 hasAuthorship W3048812714A5079153497 @default.