Mitochondria in the pathogenesis of lipodystrophy induced by anti-HIV antiretroviral drugs: actors or bystanders?
Corresponding Author
Andrea Cossarizza
Department of Biomedical Sciences, University of Modena and Reggio Emilia School of Medicine, Modena, Italy
Chair of Immunology, Department of Biomedical Sciences, Section of General Pathology, University of Modena and Reggio Emilia, School of Medicine, via Campi, 287. 41100 - Modena, Italy.Search for more papers by this authorCristina Mussini
Infectious Diseases Clinics, Azienda Policlinico, University Hospital, Modena, Italy
Search for more papers by this authorAlessandra Viganò
Chair of Pediatrics, University of Milan, Ospedale Sacco, Milan, Italy
Search for more papers by this authorCorresponding Author
Andrea Cossarizza
Department of Biomedical Sciences, University of Modena and Reggio Emilia School of Medicine, Modena, Italy
Chair of Immunology, Department of Biomedical Sciences, Section of General Pathology, University of Modena and Reggio Emilia, School of Medicine, via Campi, 287. 41100 - Modena, Italy.Search for more papers by this authorCristina Mussini
Infectious Diseases Clinics, Azienda Policlinico, University Hospital, Modena, Italy
Search for more papers by this authorAlessandra Viganò
Chair of Pediatrics, University of Milan, Ospedale Sacco, Milan, Italy
Search for more papers by this authorAbstract
Effective therapies are now available that can stop the progression of HIV infection and significantly delay the onset of AIDS. The “highly active antiretroviral therapy” (HAART) is a combination of potent antiretroviral drugs such as viral protease inhibitors or nucleoside-analogue reverse-transcriptase inhibitors, that has a variety of serious side effects, including lipodystrophy, a pathology characterized by accumulation of visceral fat, breast adiposity, cervical fat-pads, hyperlipidemia, insulin resistance as well as fat wasting in face and limbs. There is still an open debate that concerns the precise responsibility of HAART as well as metabolic pathways and mechanisms that are involved in the onset of lipodystrophy. The similarities with multiple symmetric lipomatosis (MSL), in which mitochondria impairment plays a crucial role, lead to the hypothesis that drug-induced damages to mitochondrial DNA are able to alter mitochondria functionality to an extent that is similar to what occurs in MSL. In addition, several evidences indicate that HAART is also linked to a deregulated production of tumour necrosis factor-α, which uses mitochondria as intracellular targets. In this paper, we review data concerning the role of mitochondria in the pathogenesis of lipodystrophy, and advance a unifying hypothesis involving either direct or indirect effects of the drugs employed during HAART. BioEssays 23:1070–1080, 2001. © 2001 John Wiley & Sons, Inc.
References
- 1 Viraben R, Aquilina C. Indinavir-associated lipodystrophy. AIDS 1998; 12: F37–39.
- 2 Carr A, Samaras K, Burton S, Law M, Freund J, Chisholm DJ, Cooper DA. A syndrome of peripheral lipodystrophy, hyperlipidaemia and insulin resistance in patients receiving HIV protease inhibitors. AIDS 1998; 12: F51–58.
- 3 Carr A, Samaras K, Chisholm DJ, Cooper DA. Pathogenesis of HIV-1-protease inhibitor-associated peripheral lipodystrophy, hyperlipidaemia, and insulin resistance. Lancet 1998; 351: 1181–1183.
- 4 Carr A. HIV protease inhibitor-related lipodystrophy syndrome. Clin Inf Dis 2000; 30: S135–142.
- 5 Klopstock T, Naumann M, Seibel P, Shalke B, Reiners K, Reichmann H. Mitochondrial DNA mutations in multiple symmetric lipomatosis. Mol Cell Biol 1997; 174: 271–275.
- 6
Munoz-Malaga A,
Bautista J,
Salazar JA,
Aguilera I,
Garcia R,
Chinchon I,
Segura MD,
Campos Y,
Arenas J.
Lipomatosis, proximal myopathy, and the mitochondrial 8344 mutation. A lipid storage myopathy?
Muscle Nerve
2000;
23:
538–542.
10.1002/(SICI)1097-4598(200004)23:4<538::AID-MUS12>3.0.CO;2-T CAS PubMed Web of Science® Google Scholar
- 7 Becker Wegerich P, Steuber M, Olbrisch R, Ruzicka T, Auburger G, Hofhaus G. Defects of mitochondrial respiratory chain in multiple symmetric lipomatosis. Arch Dermatol Res 1998; 290: 652–655.
- 8 Brinkman K, Smeitink JA, Romijn JA, Reiss P. Mitochondrial toxicity induced by nucleoside-analogue reverse-transcriptase inhibitors is a key factor in the pathogenesis of antiretroviral-therapy-related lipodystrophy. Lancet 1999; 354: 1112–1115.
- 9 Lo JC, Mulligan K, Tai VW, Algren H, Schambelan M. “Buffalo hump” in men with HIV-1 infection. Lancet 1998; 351: 867–870.
- 10 Safrin S, Grunfeld C. Fat distribution and metabolic changes inpatients with HIV infection. AIDS 1999; 13: 2493–2505.
- 11 Kotler DP. Fat redistribution and metabolic abnormalities. In: JP Phair, E King, editors. Medscape HIV/AIDS Annual Update 2000 Medscape, New York: 2000. pp 135–149.
- 12 Babl FE, Regan AM, Pelton SI. Abnormal body-fat distribution in HIV-1-infected children on antiretrovirals. Lancet 1999; 353: 1243–1244.
- 13 Jaquet D, Lévine M, Ortega-Rodriguez E, Faye A, Polak M, Vilmer E, Lévy-Marchal C. Clinical and metabolic presentation of the lipodystrophic syndrome in HIV-infected children. AIDS 2000; 14: 2123–2138.
- 14 Arpadi SM, Cuff PA, Horlick MB, Kotler DP, Wang J. Changes in regional body fat and serum triglycerids and cholesterol in HIV-infected children. Antiviral Therapy 2000; 5: (Suppl. 5). 14–21.
- 15 Viganò A, Mora S, Bricalli D, Sala N, Renzetti F, Chiumello G, Principi N, Brambilla P. 2001. HAART-associated changes in body fat distribution and bone mineral loss are detectable in HIV-infected children even in the absence of clinical evidence of lipodystrophy. In 8th Conference on Retroviruses and Opportunistic Infections, Abstract p 239, Chicago, IL (USA).
- 16 Carr A, Samaras K, Thorisdottir A, Kaufmann GR, Chisholm DJ, Cooper DA. Diagnosis, prediction, and natural course of HIV-1 protease-inhibitor-associated lipodystrophy, hyperlipidaemia, and diabetes mellitus: a cohort study. Lancet 1999; 353: 2093–2099.
- 17 Saint Marc T, Partisani M, Poizot Martin I, Bruno F, Rouviere O, Lang JM, Gastaut JA, Touraine JL. A syndrome of peripheral fat wasting (lipodystrophy) in patients receiving long-term nucleoside analogue therapy. AIDS 1999; 13: 1659–1667.
- 18 Behrens G, Dejam A, Schmidt H, Balks HJ, Brabant G, Korner T, Stoll M, Schmidt RE. Impaired glucose tolerance, beta cell function and lipid metabolism in HIV patients under treatment with protease inhibitors. AIDS 1999; 13: F63–70.
- 19
Ferri KF,
Kroemer G.
Mitochondria - the suicide organelle.
Bioessays
2001;
23:
111–115.
10.1002/1521-1878(200102)23:2<111::AID-BIES1016>3.0.CO;2-Y CAS PubMed Web of Science® Google Scholar
- 20 Richter C, Schweizer M, Cossarizza A, Franceschi C. Control of apoptosis by the cellular ATP level. FEBS Lett 1996; 378: 107–110.
- 21 Skulachev VP. Mitochondria in the programmed cell death phenomena; a principle of biology: “It is better to dye than to ne wrong”. IUBMB Life 2000; 49: 365–373.
- 22 Patterson S, Spahr CS, Dayugas E, Susin SA, Irinopoulos T, Koehler C, Kroemer G. Mass spectrometric identification of proteins released from mitochondria undergoing permeability transition. Cell Death Diff 2000; 7: 137–144.
- 23 Susin SA, Zamzami N, Castedo M, Daugas E, Wang HG, Geley S, Fassy F, Reed JC, Kroemer G. The central executioner of apoptosis: multiple connections between protease activation and mitochondria in Fas/APO-1/CD95- and ceramide-induced apoptosis. J Exp Med 1997; 186: 25–37.
- 24 Salvioli S, Barbi C, Dobrucki J, Troiano L, Moretti L, Pinti M, Pedrazzi J, Pazienza TL, Bobyleva V, Franceschi C, Cossarizza A. Opposite role of changes in mitochondrial membrane potential (Dy) in different apoptotic processes. FEBS Lett 2000; 469: 186–190.
- 25 Flomenbaum M, Soeiro R, Udem SA, Kress Y, Factor SM. Proliferative membranopathy and human immunodeficiency virus in AIDS hearts. J AIDS 1989; 2: 129–135.
- 26 Dalakas MC, Illa I, Pezeshkpour GH, Laukaitis JP, Cohen B, Griffin JL. Mitochondrial myopathy caused by long-term zidovudine therapy. New Engl J Med 1990; 322: 1098–1105.
- 27 Pezeshkpour G, Illa I, Dalakas MC. Ultrastructural characteristics and DNA immunocytochemistry in human immunodeficiency virus and zidovudine-associated myopathies. Hum Pathol 1991; 22: 1281–1288.
- 28 Arnaudo E, Dalakas M, Shanske S, Moraes CT, DiMauro S, Schon EA. Depletion of muscle mitochondrial DNA in AIDS patients with zidovudine-induced myopathy. Lancet 1991; 337: 508–510.
- 29 Lewis W, Gonzalez B, Chomyn A, Papoian T. Zidovudine induces molecular, biochemical, and ultrastructural changes in rat skeletal muscle mitochondria. J Clin Invest 1992; 89: 1354–1360.
- 30 Chen SC, Barker SM, Mitchell DH, Stevens SM, O' Neill P, Cunningham AL. Concurrent zidovudine-induced myopathy and hepatoxicity in patients treated for human immunodeficiency virus (HIV) infection. Pathology 1992; 24: 109–111.
- 31 Del Llano AM, Amiero-Puig JP, Kraiselburd EN, Kessler MJ, Malaga CA, Lavergne JA. The combined assessment of cellular apoptosis, mitochondrial function and proliferative response to pokeweed mitogen has prognostic value in SIV infection. J Med Primatol 1993; 22: 194–200.
- 32 Somasundaran M, Zapp ML, Beattie LK, Pang L, Byron KS, Bassell GJ, Sullivan JL, Singer RH. Localization of HIV RNA in mitochondria of infected cells: potential role in J Cell Biol 1994; 126: 1353–1360.
- 33 Gherardi RK, Florea Strat A, Fromont G, Poron F, Sabourin JC, Authier J. Cytokine expression in the muscle of HIV-infected patients: evidence for interleukin-1 alpha accumulation in mitochondria of AZT fibers. Ann Neur 1994; 36: 752–758.
- 34 Agarwal RP, Olivero OA. Genotoxicity and mitochondrial damage in human lymphocytic cells chronically exposed to 3′-azido-2′, 3′-dideoxythymidine. Mutat Res 1997; 390: 223–231.
- 35 Bialkowska A, Bialkowski K, Gerschenson M, Diwan BA, Jones AB, Olivero OA, Poirier MC, Anderson LM, Kasprzak KS, Sipowicz MA. Oxidative DNA damage in fetal tissues after transplacental exposure to 3′-azido-3′-deoxythymidine (AZT). Carcinogenesis 2000; 21: 1059–1062.
- 36 Hayakawa M, Ogawa T, Sugiyama S, Tanaka M, Ozawa T. Massive conversion of guanosine to 8-hydroxy-guanosine in mouse liver mitochondrial DNA by administration of azidothymidine. Biochem Biophys Res Commun 1991; 176: 87–93.
- 37 Chariot P, Drogou I, de Lacroix Szmania I, Eliezer Vanerot MC, Chazaud B, Lombes A, Schaeffer A, Zafrani ES. Zidovudine-induced mitochondrial disorder with massive liver steatosis, myopathy, lactic acidosis, and mitochondrial DNA depletion. J Hepatol 1999; 30: 156–160.
- 38 Radovanovic J, Todorovic V, Boricic I, Jankovic Hladni M, Korac A. Comparative ultrastructural studies on mitochondrial pathology in the liver of AIDS patients: clusters of mitochondria, protuberances, “minimitochondria,” vacuoles, and virus-like particles. Ultrastruct Pathol 1999; 23: 19–24.
- 39 Pan Zhou XR, Cui L, Zhou XJ, Sommadossi JP, Darley Usmar VM. Differential effects of antiretroviral nucleoside analogs on mitochondrial function in HepG2 cells. Antimicrob Agents Chemother 2000; 44: 496–503.
- 40 Cui L, Locatelli L, Xie MY, Sommadossi JP. Effect of nucleoside analogs on neurite regeneration and mitochondrial DNA synthesis in PC-12 cells. J Pharmacol Exp Therapeut 1997; 280: 1228–1234.
- 41 Faraj A, Fowler DA, Bridges EG, Sommadossi JP. Effects of 2′,3′-dideoxynucleosides on proliferation and differentiation of human pluripotent progenitors in liquid culture and their effects on mitochondrial DNA synthesis. Antimicrob Agents Chemother 1994; 38: 924–930.
- 42 Medina DJ, Tsai CH, Hsiung GD, Cheng YC. Comparison of mitochondrial morphology, mitochondrial DNA content, and cell viability in cultured cells treated with three anti-human immunodeficiency virus dideoxynucleosides. Antimicrob Agents Chemother 1994; 38: 1824–1828.
- 43 Rossi L, Serafini S, Schiavano GF, Casabianca A, Vallanti G, Chiarantini L, Magnani M. Metabolism, mitochondrial uptake and toxicity of 2′, 3′-dideoxycytidine. Biochem J 1999; 344: 915–920.
- 44 Foli A, Benvenuto F, Piccinini G, Bareggi A, Cossarizza A, Lisziewicz J, Lori F. Direct analysis of mitochondrial toxicity of antiretroviral drugs. AIDS 2001; (in press).
- 45 Cossarizza A, Mussini C, Mongiardo N, Borghi V, Sabbatini A, De Rienzo B, Franceschi C. Mitochondria alterations and dramatic tendency to apoptosis in peripheral blood lymphocytes during acute HIV syndrome. AIDS 1997; 11: 19–26.
- 46 Jacotot E, Ravagnan L, Loeffler M, Ferri KF, Vieira HL, Zamzami N, Costantini P, Druillennec S, Hoebeke J, Briand JP, Irinopoulou T, Daugas E, Susin SA, Cointe D, Xie ZH, Reed JC, Roques BP, Kroemer G. The HIV-1 viral protein R induces apoptosis via a direct effect on the mitochondrial permeability transition pore. J Exp Med 2000; 191: 33–46.
- 47 Kowal RC, Herz J, Goldstein JL, Esser V, Brown MS. Low density lipoprotein receptor-related protein mediates uptake of cholesteryl esters derived from apoprotein E-enriched lipoproteins. Proc Natl Acad Sci USA 1989; 86: 5810–5814.
- 48 Tontonoz P, Hu E, Spiegelman BM. Stimulation of adipogenesis in fibroblasts by PPAR gamma 2, a lipid-activated transcription factor. Cell 1994; 79: 1147–1156.
- 49 Tontonoz P, Singer S, Forman BM, Sarraf P, Fletcher JA, Fletcher CD, Brun RP, Mueller E, Altiok S, Oppenheim H, Evans RM, Spiegelman BM. Terminal differentiation of human liposarcoma cells induced by ligands for peroxisome proliferator-activated receptor gamma and the retinoid X receptor. Proc Natl Acad Sci USA 1997; 94: 237–241.
- 50 Adams M, Montague CT, Prins JB, Holder JC, Smith SA, Sanders L, Digby JE, Sewter CP, Lazar MA, Chatterjee VK, O'Rahilly S. Activators of peroxisome proliferator-activated receptor gamma have depot-specific effects on human preadipocyte differentiation. J Clin Invest 1997; 100: 3149–3153.
- 51 Wentworth JM, Burris TP, Chatterjee VK. HIV protease inhibitors block human preadipocyte differentiation, but not via the PPARgamma/RXR heterodimer. J Endocrinol 2000; 164: R7–R10.
- 52 Izuta S, Saneyoshi M, Sakurai T, Suzuki M, Kojima K, Yoshida S. The 5′-triphosphates of 3′-azido-3′-deoxythymidine and 2′, 3′-dideoxynucleosides inhibit DNA polymerase gamma by different mechanisms. Biochem Biophys Res Commun 1991; 179: 776–783.
- 53 Martin JL, Brown CE, Matthews-Davis N, Reardon JE. Effects of antiviral nucleoside analogs on human DNA polymerases and mitochondrial DNA synthesis. Antimicrob Agents Chemother 1994; 38: 2743–2749.
- 54 Brinkman K, Kakuda TN. Mitochondrial toxicity of nucleoside analogue reverse transcriptase inhibitors: a looming obstacle for long-term antiretroviral therapy? Curr Opin Infect Dis 2000; 13: 5–11.
- 55 Barile M, Valenti D, Hobbs GA, Abruzzese MF, Keibaugh SA, Passarella S, Quagliariello E, Simpson MV. Mechanism of toxicity of 3′-azido-3′-deoxythymidine: its interaction with adenylate kinase. Biochem Pharmacol 1994; 48: 1405–1412.
- 56 Barile M, Valenti D, Passarella S, Quagliariello E. 3′-Azido-3′-deoxythymidine uptake into isolated rat liver mitochondria and impairment of ADP/ATP translocator. Biochem Pharmacol 1997; 53: 913–920.
- 57 Nusbaum NJ, Joseph PE. AZT incorporation into mitochondria: study in a human myeloid cell line. DNA Cell Biol 1996; 15: 363–366.
- 58 Masini A, Scotti C, Calligaro A, Cazzalini O, Stivala LA, Bianchi L, Giovannini F, Ceccarelli D, Muscatello U, Tomasi A, Vannini V. Zidovudine-induced experimental myopathy: dual mechanism of mitochondrial damage. J Neurol Sci 1999; 166: 131–140.
- 59 Moyle G. Mitochondrial toxicity hypothesis for lipoatrophy: a refutation. AIDS 2001; 15: 413–414.
- 60 Schulze-Osthoff K, Bakker AC, Vanhaesebroeck B, Beyaert R, Jacob WA, Fiers W. Cytotoxic activity of tumor necrosis factor is mediated by early damage of mitochondrial function. Evidence for the involvement of mitochondrial radical generation. J Biol Chem 1992; 267: 5317–5323.
- 61 Cossarizza A, Franceschi C, Monti D, Salvioli S, Bellesia E, Rivabene R, Biondo L, Rainaldi G, Tinari A, Malorni W. Protective effect of N-acetylcysteine in Tumor Necrosis Factor α-induced apoptosis in U937 cells: the role of mitochondria. Exp Cell Res 1995; 220: 232–240.
- 62 Ledru E, Christeff N, Patey O, de Truchis P, Melchior JC, Gougeon ML. Alteration of tumor necrosis factor-alpha T-cell homeostasis following potent antiretroviral therapy: contribution to the development of human immunodeficiency virus-associated lipodystrophy syndrome. Blood 2000; 95: 3191–3198.
- 63 Beutler B, Cerami A. The biology of cachectin/TNF - a primary mediator of the host response. Annu Rev Immunol 1989; 7: 625–655.
- 64 Zhou YT, Wang ZW, Higa M, Newgard CB, Unger RH. Reversing adipocyte differentiation: implications for treatment of obesity. Proc. Natl Acad Sci USA 1999; 96: 2391–2395.
- 65 Hotamisligil GS, Murray DL, Choy LN, Spiegelman BM. Tumor necrosis factor alpha inhibits signaling from the insulin recpetor. Proc Natl Acad Sci USA 1994; 91: 4854–4858.
- 66 Sethi JK, Hotamisligil GS. The role of TNF alpha in adipocyte metabolism. Semin Cell Dev Biol 1999; 10: 19–29.
- 67 Torti FM, Torti SV, Larrick JW, Ringold GM. Modulation of adipocyte differentiation by tumor necrosis factor and transforming growth factor beta. J Cell Biol 1989; 108: 1105–1113.
- 68 Reid TR, Torti FM, Ringold GM. Evidence for two mechanisms by which tumor necrosis factor kills cells. J Biol Chem 1989; 264: 4583–4589.
- 69 Petruschke T, Hauner H. Tumor necrosis factor-alpha prevents the differentiation of human adipocyte precursor cells and causes delipidation of newly developed fat cells. J Clin Endocr Metab 1993; 76: 742–747.
- 70 Xing H, Northrop JP, Grove JR, Kilpatrick KE, Su JL, Ringold GM. TNF alpha-mediated inhibition and reversal of adipocyte differentiation is accompanied by suppressed expression of PPARgamma without effects on Pref-1 expression. Endocrinology 1997; 138: 2776–2783.
- 71 Prins JB, Niesler CU, Winterford CM, Bright NA, Siddle K, O'Rahilly S, Walker NI, Cameron DP. Tumor necrosis factor-alpha induces apoptosis of human adipose cells. Diabetes 1997; 46: 1939–1944.
- 72 Niesler CU, Siddle K, Prins JB. Human preadipocytes display a depot-specific susceptibility to apoptosis. Diabetes 1998; 47: 1365–1368.
- 73 Domingo P, Matias-Guiu X, Pujol RM, Francia E, Lagarda E, Sambeat MA, Vazquez G. Subcutaneous adipocyte apoptosis in HIV-1 protease inhibitor-associated lipodystrophy. AIDS 1999; 13: 2261–2267.
- 74 Shikuma C, Hu N, Milne C, Yost F, Shimizu S, Shiramizu B. Analysis of subcutaneous adipose tissue mitochondrial DNA from individuals with HAART-associated lipodystrophy. In: 8th Conference on Retroviruses and Opportunistic Infections, Abstract p 244, Chicago, IL, USA: 2001.
- 75 Khoo SH, Pepper L, Snowden N, Hajeer AH, Vallely P, Wilkins EG, Mandal BK, Ollier WE. Tumour necrosis factor c2 microsatellite allele is associated with the rate of HIV disease progression. AIDS 1997; 15: 423–428.
- 76 Brinkman BM, Keet IP, Miedema F, Verweij CL, Klein MR. Polymorphisms within the human tumor necrosis factor-alpha promoter region in human immunodeficiency virus type 1-seropositive persons. J Infect Dis 1997; 175: 188–190.
- 77 Day CP, Grove J, Daly AK, Stewart MW, Avery PJ, Walker M. Tumour necrosis factor-alpha gene promoter polymorphism and decreased insulin resistance. Diabetologia 1998; 41: 430–434.
- 78 Hoffmeyer S, Burk O, von Richter O, Arnold HP, Brockmoller J, Johne A, Cascorbi I, Gerloff T, Roots I, Eichelbaum M, Brinkmann U. Functional polymorphisms of the human multidrug-resistance gene: multiple sequence variations and correlation of one allele with P-glycoprotein expression and activity in vivo. Proc Natl Acad Sci USA 2000; 97: 3473–3478.
- 79 Aalto Setala K, Palomaki H, Miettinen H, Vuorio A, Kuusi T, Raininko R, Salonen O, Kaste M, Kontula K. Genetic risk factors and ischaemic cerebrovascular disease: role of common variation of the genes encoding apolipoproteins and angiotensin-converting enzyme. Ann Med 1998; 30: 224–233.
- 80 Huang QR, Morris D, Manolios N. Identification and characterization of polymorphisms in the promoter region of the human Apo-1/Fas (CD95) gene. Mol Immunol 1997; 34: 577–582.
- 81 van den Ouweland JM, Maechler P, Wollheim CB, Attardi G, Maassen JA. Functional and morphological abnormalities of mitochondria harbouring the tRNA(Leu)(UUR) mutation in mitochondrial DNA derived from patients with maternally inherited diabetes and deafness (MIDD) and progressive kidney disease. Diabetologia 1999; 42: 485–492.
- 82 Torroni A, Schurr TG, Cabell MF, Brown MD, Neel JV, Larsen M, Smith DG, Vullo CM, Wallace DC. Asian affinities and continental radiation of the four founding Native American mtDNAs. Am J Hum Genet 1993; 53: 563–590.
- 83 De Benedictis G, Rose G, Carrieri G, De Luca M, Falcone E, Passarino G, Bonafè M, Monti D, Baggio G, Bertolini S, Mari D, Mattace R, Franceschi C. Mitochondrial DNA inherited variants are associated with successful aging and longevity in humans. FASEB J 1999; 13: 1532–1536.
- 84 Hofmann S, Bezold R, Jaksch M, Obermaier Kusser B, Mertens S, Kaufhold P, Rabl W, Hecker W, Gerbitz KD. Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinct mitochondrial DNA haplotypes. Genomics 1997; 39: 8–18.
- 85 Ruiz Pesini E, Lapena AC, Diez Sanchez C, Martos Perez A, Montoya J, Alvarez E, Diaz M, Urries A, Montoro L, Lopez Perez MJ, Enriquez JA. Human mtDNA haplogroups associated with high or reduced spermatozoa motility. Am J Hum Genet 2000; 67: 682–696.