African Mitochondrial DNA Subhaplogroups and Peripheral Neuropathy during Antiretroviral Therapy

被引:29
作者
Canter, Jeffrey A. [1 ,2 ]
Robbins, Gregory K. [7 ]
Selph, Doug [2 ]
Clifford, David B. [9 ]
Kallianpur, Asha R. [3 ]
Shafer, Robert [8 ]
Levy, Shawn [5 ]
Murdock, Deborah G. [1 ,2 ]
Ritchie, Marylyn D. [1 ,2 ]
Haas, David W. [4 ,6 ]
Hulgan, Todd [4 ]
机构
[1] Vanderbilt Univ, Sch Med, Dept Mol Physiol & Biophys, Nashville, TN 37212 USA
[2] Vanderbilt Univ, Sch Med, Ctr Human Genet Res, Dept Med, Nashville, TN 37212 USA
[3] Vanderbilt Univ, Sch Med, Div Gen Internal Med & Publ Hlth, Nashville, TN 37212 USA
[4] Vanderbilt Univ, Sch Med, Div Infect Dis, Nashville, TN 37212 USA
[5] Vanderbilt Univ, Sch Med, Microarray Shared Resource Facil, Nashville, TN 37212 USA
[6] Vanderbilt Univ, Sch Med, Dept Microbiol & Immunol, Nashville, TN 37212 USA
[7] Harvard Univ, Massachusetts Gen Hosp, Dept Med, Boston, MA 02115 USA
[8] Stanford Univ, Dept Med Infect Dis, Stanford, CA 94305 USA
[9] Washington Univ, Sch Med, Dept Neurol & Med, St Louis, MO USA
关键词
REGION SEQUENCES; HAPLOGROUPS; DISEASE; RISK;
D O I
10.1086/652419
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Susceptibility to peripheral neuropathy during antiretroviral therapy with nucleoside reverse-transcriptase inhibitors was previously associated with a European mitochondrial DNA (mtDNA) haplogroup among non-Hispanic white persons. To determine whether nucleoside reverse-transcriptase inhibitor-associated peripheral neuropathy was related to mtDNA variation in non-Hispanic black persons, we sequenced mtDNA of participants from AIDS Clinical Trials Group study 384. Of 156 non-Hispanic black persons with genomic data, 51 (33%) developed peripheral neuropathy. In a multivariate model, African mtDNA subhaplogroup L1c was an independent predictor of peripheral neuropathy (odds ratio, 3.7 [95% confidence interval, 1.1-12.0]). An African mtDNA subhaplogroup is for the first time implicated in susceptibility to nucleoside reverse-transcriptase inhibitor-associated toxicity.
引用
收藏
页码:1703 / 1707
页数:5
相关论文
共 16 条
[1]   Characterization of human control region sequences of the African American SWGDAM forensic mtDNA data set [J].
Allard, MW ;
Polanskey, D ;
Miller, K ;
Wilson, MR ;
Monson, KL ;
Budowle, B .
FORENSIC SCIENCE INTERNATIONAL, 2005, 148 (2-3) :169-179
[2]  
[Anonymous], 2009, GUID US ANT AG HIV 1
[3]   Peripheral neuropathy and antiretroviral drugs [J].
Dalakas, MC .
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2001, 6 (01) :14-20
[4]   Mitochondrial alterations with mitochondrial DNA depletion in the nerves of AIDS patients with peripheral neuropathy induced by 2′3′-dideoxycytidine (ddC) [J].
Dalakas, MC ;
Semino-Mora, C ;
Leon-Monzon, M .
LABORATORY INVESTIGATION, 2001, 81 (11) :1537-1544
[5]  
Hawkins C, 2007, JAIDS-J ACQ IMM DEF, V45, P304
[6]   Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups [J].
Herrnstadt, C ;
Elson, JL ;
Fahy, E ;
Preston, G ;
Turnbull, DM ;
Anderson, C ;
Ghosh, SS ;
Olefsky, JM ;
Beal, MF ;
Davis, RE ;
Howell, N .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (05) :1152-1171
[7]   Mitochondrial haplogroups and peripheral neuropathy during antiretroviral therapy: an adult AIDS clinical trials group study [J].
Hulgan, T ;
Haas, DW ;
Haines, JL ;
Ritchie, MD ;
Robbins, GK ;
Shafer, RW ;
Clifford, D ;
Kallianpur, AR ;
Summar, M ;
Canter, JA .
AIDS, 2005, 19 (13) :1341-1349
[8]   Modification of the incidence of drug-associated symmetrical peripheral neuropathy by host and disease factors in the HIV outpatient study cohort [J].
Lichtenstein, KA ;
Armon, C ;
Baron, A ;
Moorman, AC ;
Wood, KC ;
Holmberg, SD .
CLINICAL INFECTIOUS DISEASES, 2005, 40 (01) :148-157
[9]   Mitochondrial DNA polymorphisms associated with longevity in a Finnish population [J].
Niemi, AK ;
Hervonen, A ;
Hurme, M ;
Kurhunen, PJ ;
Jylhä, M ;
Majamaa, K .
HUMAN GENETICS, 2003, 112 (01) :29-33
[10]   Comparison of sequential three-drug regimens as initial therapy for HIV-1 infection [J].
Robbins, GK ;
De Gruttola, V ;
Shafer, RW ;
Smeaton, LM ;
Snyder, SW ;
Pettinelli, C ;
Dube, MP ;
Fischl, MA ;
Pollard, RB ;
Delapenha, R ;
Gedeon, L ;
van der Horst, C ;
Murphy, RL ;
Becker, MI ;
D'Aquila, RT ;
Vella, S ;
Merigan, TC ;
Hirsch, MS ;
Nokta, M ;
Johnson, V ;
Morse, G ;
Putnam, B ;
Klebert, M ;
Martinez, A ;
Chiesi, A ;
Tomino, C ;
Deeks, S ;
Testa, M ;
Nevin, T ;
Levin, J ;
French, V ;
Fennell, O ;
Stevens, M ;
Grosso, R ;
Dusak, B ;
Hodder, S ;
Squibb, M ;
Brothers, C ;
Tolson, J ;
Leavitt, R ;
Manion, D ;
Ruiz, N ;
Morrisey, K ;
Quart, B ;
Jennings, C ;
Dascomb, S ;
Cooper, M ;
Murphy, M ;
Blakelock, K ;
Doolan, A .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 349 (24) :2293-2303