Academic Journal

Multiple nonglycemic genomic loci are newly associated with blood level of glycated hemoglobin in East Asians

Λεπτομέρειες βιβλιογραφικής εγγραφής
Τίτλος: Multiple nonglycemic genomic loci are newly associated with blood level of glycated hemoglobin in East Asians
Συγγραφείς: Chen, P, Takeuchi, F, Lee, JY, Li, H, Wu, JY, Liang, J, Long, J, Tabara, Y, Goodarzi, MO, Pereira, MA, Kim, YJ, Go, MJ, Stram, DO, Vithana, E, Khor, CC, Liu, J, Liao, J, Ye, X, Wang, Y, Lu, L, Young, TL, Lee, J, Thai, AC, Cheng, CY, Van Dam, RM, Friedlander, Y, Heng, CK, Koh, WP, Chen, CH, Chang, LC, Pan, WH, Qi, B, Isono, M, Zheng, W, Cai, Q, Gao, Y, Yamamoto, K, Ohnaka, K, Takayanagi, R, Kita, Y, Ueshima, H, Hsiung, CA, Cui, J, Sheu, WHH, Rotter, JI, Chen, YDI, Hsu, C, Okada, Y, Kubo, M, Takahashi, A, Tanaka, T, Van Rooij, FJA, Ganesh, SK, Huang, J, Huang, T, Yuan, J, Hwang, JY, Gross, MD, Assimes, TL, Miki, T, Shu, XO, Qi, L, Chen, YT, Lin, X, Aung, T, Wong, TY, Teo, YY, Kim, BJ, Kato, N, Tai, ES
Στοιχεία εκδότη: American Diabetes Association
Έτος έκδοσης: 2014
Συλλογή: The University of Melbourne: Digital Repository
Περιγραφή: Glycated hemoglobin A1c (HbA1c) is used as a measure of glycemic control and also as a diagnostic criterion for diabetes. To discover novel loci harboring common variants associated with HbA1c in East Asians, we conducted a meta-analysis of 13 genome-wide association studies (GWAS; N = 21,026). We replicated our findings in three additional studies comprising 11,576 individuals of East Asian ancestry. Ten variants showed associations that reached genome-wide significance in the discovery data set, of which nine (four novel variants at TMEM79 [P value = 1.3 × 10(-23)], HBS1L/MYB [8.5 × 10(-15)], MYO9B [9.0 × 10(-12)], and CYBA [1.1 × 10(-8)] as well as five variants at loci that had been previously identified [CDKAL1, G6PC2/ABCB11, GCK, ANK1, and FN3KI]) showed consistent evidence of association in replication data sets. These variants explained 1.76% of the variance in HbA1c. Several of these variants (TMEM79, HBS1L/MYB, CYBA, MYO9B, ANK1, and FN3K) showed no association with either blood glucose or type 2 diabetes. Among individuals with nondiabetic levels of fasting glucose (<7.0 mmol/L) but elevated HbA1c (≥6.5%), 36.1% had HbA1c <6.5% after adjustment for these six variants. Our East Asian GWAS meta-analysis has identified novel variants associated with HbA1c as well as demonstrated that the effects of known variants are largely transferable across ethnic groups. Variants affecting erythrocyte parameters rather than glucose metabolism may be relevant to the use of HbA1c for diagnosing diabetes in these populations.
Τύπος εγγράφου: article in journal/newspaper
Γλώσσα: English
ISSN: 0012-1797
Relation: https://hdl.handle.net/11343/306278
Διαθεσιμότητα: https://hdl.handle.net/11343/306278
Rights: https://creativecommons.org/licenses/by-nc-nd/4.0 ; CC BY-NC-ND
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  Data: American Diabetes Association
– Name: DatePubCY
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  Data: 2014
– Name: Subset
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  Data: The University of Melbourne: Digital Repository
– Name: Abstract
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  Group: Ab
  Data: Glycated hemoglobin A1c (HbA1c) is used as a measure of glycemic control and also as a diagnostic criterion for diabetes. To discover novel loci harboring common variants associated with HbA1c in East Asians, we conducted a meta-analysis of 13 genome-wide association studies (GWAS; N = 21,026). We replicated our findings in three additional studies comprising 11,576 individuals of East Asian ancestry. Ten variants showed associations that reached genome-wide significance in the discovery data set, of which nine (four novel variants at TMEM79 [P value = 1.3 &#215; 10(-23)], HBS1L/MYB [8.5 &#215; 10(-15)], MYO9B [9.0 &#215; 10(-12)], and CYBA [1.1 &#215; 10(-8)] as well as five variants at loci that had been previously identified [CDKAL1, G6PC2/ABCB11, GCK, ANK1, and FN3KI]) showed consistent evidence of association in replication data sets. These variants explained 1.76% of the variance in HbA1c. Several of these variants (TMEM79, HBS1L/MYB, CYBA, MYO9B, ANK1, and FN3K) showed no association with either blood glucose or type 2 diabetes. Among individuals with nondiabetic levels of fasting glucose (&lt;7.0 mmol/L) but elevated HbA1c (≥6.5%), 36.1% had HbA1c &lt;6.5% after adjustment for these six variants. Our East Asian GWAS meta-analysis has identified novel variants associated with HbA1c as well as demonstrated that the effects of known variants are largely transferable across ethnic groups. Variants affecting erythrocyte parameters rather than glucose metabolism may be relevant to the use of HbA1c for diagnosing diabetes in these populations.
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  Data: 0012-1797
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  Data: https://hdl.handle.net/11343/306278
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      – PersonEntity:
          Name:
            NameFull: Sheu, WHH
      – PersonEntity:
          Name:
            NameFull: Rotter, JI
      – PersonEntity:
          Name:
            NameFull: Chen, YDI
      – PersonEntity:
          Name:
            NameFull: Hsu, C
      – PersonEntity:
          Name:
            NameFull: Okada, Y
      – PersonEntity:
          Name:
            NameFull: Kubo, M
      – PersonEntity:
          Name:
            NameFull: Takahashi, A
      – PersonEntity:
          Name:
            NameFull: Tanaka, T
      – PersonEntity:
          Name:
            NameFull: Van Rooij, FJA
      – PersonEntity:
          Name:
            NameFull: Ganesh, SK
      – PersonEntity:
          Name:
            NameFull: Huang, J
      – PersonEntity:
          Name:
            NameFull: Huang, T
      – PersonEntity:
          Name:
            NameFull: Yuan, J
      – PersonEntity:
          Name:
            NameFull: Hwang, JY
      – PersonEntity:
          Name:
            NameFull: Gross, MD
      – PersonEntity:
          Name:
            NameFull: Assimes, TL
      – PersonEntity:
          Name:
            NameFull: Miki, T
      – PersonEntity:
          Name:
            NameFull: Shu, XO
      – PersonEntity:
          Name:
            NameFull: Qi, L
      – PersonEntity:
          Name:
            NameFull: Chen, YT
      – PersonEntity:
          Name:
            NameFull: Lin, X
      – PersonEntity:
          Name:
            NameFull: Aung, T
      – PersonEntity:
          Name:
            NameFull: Wong, TY
      – PersonEntity:
          Name:
            NameFull: Teo, YY
      – PersonEntity:
          Name:
            NameFull: Kim, BJ
      – PersonEntity:
          Name:
            NameFull: Kato, N
      – PersonEntity:
          Name:
            NameFull: Tai, ES
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 01
              M: 01
              Type: published
              Y: 2014
          Identifiers:
            – Type: issn-print
              Value: 00121797
            – Type: issn-locals
              Value: edsbas
            – Type: issn-locals
              Value: edsbas.oa
ResultId 1