Further evidence of association between two NET single-nucleotide polymorphisms with ADHD

被引:41
|
作者
Kim, J. W. [1 ]
Biederman, J.
McGrath, C. L. [1 ]
Doyle, A. E.
Mick, E.
Fagerness, J. [1 ]
Purcell, S. [1 ]
Smoller, J. W. [1 ]
Sklar, P. [1 ]
Faraone, S. V. [2 ]
机构
[1] Harvard Univ, Massachusetts Gen Hosp, Ctr Human Genet Res, Psychiat & Neurodev Genet Unit,Med Sch, Boston, MA 02114 USA
[2] SUNY Upstate Med Univ, Dept Psychiat, Syracuse, NY USA
关键词
ADHD; NET; association; SNP; replication;
D O I
10.1038/sj.mp.4002090
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The norepinephrine transporter (NET) gene is an attractive candidate gene for attention-deficit hyperactivity disorder (ADHD). Noradrenergic systems are critical to higher brain functions such as attention and executive function, which are defective in ADHD. The clinical efficacy of medications that target NET also supports its role in the etiology of ADHD. Here, we have applied a dense mapping strategy to capture all genetic variations within the NET gene in a large number of ADHD families (474 trios). As a result, we found association of the same alleles from two single-nucleotide polymorphisms (rs3785143 and rs11568324) previously identified in another large-scale ADHD genetic study (International Multisite ADHD Geneproject). Furthermore, the effect sizes were consistent across both studies. This is the first time that identical alleles of NET from different studies were implicated, and thus our report provides further evidence that the NET gene is involved in the etiology of ADHD.
引用
收藏
页码:624 / 630
页数:7
相关论文
共 50 条
  • [21] Association between single-nucleotide polymorphisms within candidate genes and fertility in Landrace and Duroc pigs
    Tremoen, Nina Hardnes
    Van Son, Maren
    Andersen-Ranberg, Ina
    Grindflek, Eli
    Myromslien, Froydis Deinboll
    Gaustad, Ann Helen
    Vage, Dag Inge
    [J]. ACTA VETERINARIA SCANDINAVICA, 2019, 61 (01)
  • [22] No evidence of linkage or association between the norepinephrine transporter (NET) gene polymorphisms and ADHD in the Irish population
    McEvoy, B
    Hawi, Z
    Fitzgerald, M
    Gill, M
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 2002, 114 (06): : 665 - 666
  • [23] Linkage and association analyses of microsatellites and single-nucleotide polymorphisms in nuclear families
    Lin, J
    Liu, KY
    [J]. BMC GENETICS, 2005, 6 (Suppl 1)
  • [24] Exploratory study on Association of Single-Nucleotide Polymorphisms with Hydromorphone Analgesia in ED
    Xia, Shujun
    Persaud, Shaun
    Birnbaum, Adrienne
    [J]. AMERICAN JOURNAL OF EMERGENCY MEDICINE, 2015, 33 (03): : 444 - 447
  • [25] Shifting paradigm of association studies: Value of rare single-nucleotide polymorphisms
    Gorlov, Ivan P.
    Gorlova, Olga Y.
    Sunyaev, Shamil R.
    Spitz, Margaret R.
    Amos, Christopher I.
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2008, 82 (01) : 100 - 112
  • [26] Association and haplotype analaysis of 90 single-nucleotide polymorphisms in mood disorders
    Maron, E
    Koks, S
    Nikopensius, T
    Altmäe, S
    Heinaste, E
    Vabrit, K
    Tammekivi, V
    Hallast, P
    Koido, K
    Kurg, A
    Shlik, J
    Vasar, V
    Metspalu, A
    Vasar, E
    [J]. EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2005, 15 : S55 - S56
  • [27] First Evidence of Genetic Association Between the MIF-173G/C Single-Nucleotide Polymorphisms and Polycystic Ovary Syndrome
    Li, Chao
    Qiao, Binglong
    Zhan, Ying
    Qi, Weihong
    Chen, Zi-Jiang
    [J]. AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 2011, 66 (05) : 416 - 422
  • [28] Picking single-nucleotide polymorphisms in forests
    Daniel F Schwarz
    Silke Szymczak
    Andreas Ziegler
    Inke R König
    [J]. BMC Proceedings, 1 (Suppl 1)
  • [29] Single-nucleotide polymorphisms and glaucoma severity
    Bunce, C
    Hitchings, RA
    Bhattacharyya, S
    Lehmann, OJ
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 72 (06) : 1593 - 1594
  • [30] Association of IL4 Single-Nucleotide Polymorphisms With Febrile Seizures
    Zare-shahabadi, Ameneh
    Soltani, Samaneh
    Ashrafi, Mahmoud Reza
    Shahrokhi, Amin
    Zoghi, Samaneh
    Pourakbari, Babak
    Zamani, Gholam Reza
    Mohammadi, Mahmoud
    Rezaei, Nima
    [J]. JOURNAL OF CHILD NEUROLOGY, 2015, 30 (04) : 423 - 428