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Published in: BMC Medical Genetics 1/2009

Open Access 01-12-2009 | Research article

Mitochondrial DNA haplogroup T is associated with coronary artery disease and diabetic retinopathy: a case control study

Authors: Barbara Kofler, Edith E Mueller, Waltraud Eder, Olaf Stanger, Richard Maier, Martin Weger, Anton Haas, Robert Winker, Otto Schmut, Bernhard Paulweber, Bernhard Iglseder, Wilfried Renner, Martina Wiesbauer, Irene Aigner, Danijela Santic, Franz A Zimmermann, Johannes A Mayr, Wolfgang Sperl

Published in: BMC Medical Genetics | Issue 1/2009

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Abstract

Background

There is strong and consistent evidence that oxidative stress is crucially involved in the development of atherosclerotic vascular disease. Overproduction of reactive oxygen species (ROS) in mitochondria is an unifying mechanism that underlies micro- and macrovascular atherosclerotic disease. Given the central role of mitochondria in energy and ROS production, mitochondrial DNA (mtDNA) is an obvious candidate for genetic susceptibility studies on atherosclerotic processes. We therefore examined the association between mtDNA haplogroups and coronary artery disease (CAD) as well as diabetic retinopathy.

Methods

This study of Middle European Caucasians included patients with angiographically documented CAD (n = 487), subjects with type 2 diabetes mellitus with (n = 149) or without (n = 78) diabetic retinopathy and control subjects without clinical manifestations of atherosclerotic disease (n = 1527). MtDNA haplotyping was performed using multiplex PCR and subsequent multiplex primer extension analysis for determination of the major European haplogroups. Haplogroup frequencies of patients were compared to those of control subjects without clinical manifestations of atherosclerotic disease.

Results

Haplogroup T was significantly more prevalent among patients with CAD than among control subjects (14.8% vs 8.3%; p = 0.002). In patients with type 2 diabetes, the presence of diabetic retinopathy was also significantly associated with a higher prevalence of haplogroup T (12.1% vs 5.1%; p = 0.046).

Conclusion

Our data indicate that the mtDNA haplogroup T is associated with CAD and diabetic retinopathy in Middle European Caucasian populations.
Literature
1.
go back to reference Gutierrez J, Ballinger SW, Darley-Usmar VM, Landar A: Free radicals, mitochondria, and oxidized lipids: the emerging role in signal transduction in vascular cells. Circ Res. 2006, 99: 924-932. 10.1161/01.RES.0000248212.86638.e9.CrossRefPubMed Gutierrez J, Ballinger SW, Darley-Usmar VM, Landar A: Free radicals, mitochondria, and oxidized lipids: the emerging role in signal transduction in vascular cells. Circ Res. 2006, 99: 924-932. 10.1161/01.RES.0000248212.86638.e9.CrossRefPubMed
2.
go back to reference DiMauro S, Schon EA: Mitochondrial respiratory-chain diseases. N Engl J Med. 2003, 348: 2656-2668. 10.1056/NEJMra022567.CrossRefPubMed DiMauro S, Schon EA: Mitochondrial respiratory-chain diseases. N Engl J Med. 2003, 348: 2656-2668. 10.1056/NEJMra022567.CrossRefPubMed
3.
go back to reference Wallace DC: A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine. Annu Rev Genet. 2005, 39: 359-407. 10.1146/annurev.genet.39.110304.095751.CrossRefPubMedPubMedCentral Wallace DC: A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine. Annu Rev Genet. 2005, 39: 359-407. 10.1146/annurev.genet.39.110304.095751.CrossRefPubMedPubMedCentral
4.
go back to reference Torroni A, Petrozzi M, D'Urbano L, Sellitto D, Zeviani M, Carrara F, Carducci C, Leuzzi V, Carelli V, Barboni P, De Negri A, Scozzari R: Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484. Am J Hum Genet. 1997, 60: 1107-1121.PubMedPubMedCentral Torroni A, Petrozzi M, D'Urbano L, Sellitto D, Zeviani M, Carrara F, Carducci C, Leuzzi V, Carelli V, Barboni P, De Negri A, Scozzari R: Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484. Am J Hum Genet. 1997, 60: 1107-1121.PubMedPubMedCentral
5.
go back to reference Ruiz-Pesini E, Lapena AC, Diez-Sanchez C, Perez-Martos 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. 10.1086/303040.CrossRefPubMedPubMedCentral Ruiz-Pesini E, Lapena AC, Diez-Sanchez C, Perez-Martos 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. 10.1086/303040.CrossRefPubMedPubMedCentral
6.
go back to reference Esposito LA, Melov S, Panov A, Cottrell BA, Wallace DC: Mitochondrial disease in mouse results in increased oxidative stress. Proc Natl Acad Sci USA. 1999, 96: 4820-4825. 10.1073/pnas.96.9.4820.CrossRefPubMedPubMedCentral Esposito LA, Melov S, Panov A, Cottrell BA, Wallace DC: Mitochondrial disease in mouse results in increased oxidative stress. Proc Natl Acad Sci USA. 1999, 96: 4820-4825. 10.1073/pnas.96.9.4820.CrossRefPubMedPubMedCentral
7.
go back to reference Rose G, Passarino G, Carrieri G, Altomare K, Greco V, Bertolini S, Bonafe M, Franceschi C, De Benedictis G: Paradoxes in longevity: sequence analysis of mtDNA haplogroup J in centenarians. Eur J Hum Genet. 2001, 9: 701-707. 10.1038/sj.ejhg.5200703.CrossRefPubMed Rose G, Passarino G, Carrieri G, Altomare K, Greco V, Bertolini S, Bonafe M, Franceschi C, De Benedictis G: Paradoxes in longevity: sequence analysis of mtDNA haplogroup J in centenarians. Eur J Hum Genet. 2001, 9: 701-707. 10.1038/sj.ejhg.5200703.CrossRefPubMed
8.
go back to reference Darvishi K, Sharma S, Bhat AK, Rai E, Bamezai RN: Mitochondrial DNA G10398A polymorphism imparts maternal Haplogroup N a risk for breast and esophageal cancer. Cancer Lett. 2007, 249: 249-255. 10.1016/j.canlet.2006.09.005.CrossRefPubMed Darvishi K, Sharma S, Bhat AK, Rai E, Bamezai RN: Mitochondrial DNA G10398A polymorphism imparts maternal Haplogroup N a risk for breast and esophageal cancer. Cancer Lett. 2007, 249: 249-255. 10.1016/j.canlet.2006.09.005.CrossRefPubMed
9.
go back to reference Pyle A, Foltynie T, Tiangyou W, Lambert C, Keers SM, Allcock LM, Davison J, Lewis SJ, Perry RH, Barker R, Burn DJ, Chinnery PF: Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PD. Ann Neurol. 2005, 57: 564-567. 10.1002/ana.20417.CrossRefPubMed Pyle A, Foltynie T, Tiangyou W, Lambert C, Keers SM, Allcock LM, Davison J, Lewis SJ, Perry RH, Barker R, Burn DJ, Chinnery PF: Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PD. Ann Neurol. 2005, 57: 564-567. 10.1002/ana.20417.CrossRefPubMed
10.
go back to reference Aiello LP, Avery RL, Arrigg PG, Keyt BA, Jampel HD, Shah ST, Pasquale LR, Thieme H, Iwamoto MA, Park JE, et al: Vascular endothelial growth factor in ocular fluid of patients with diabetic retinopathy and other retinal disorders. N Engl J Med. 1994, 331: 1480-1487. 10.1056/NEJM199412013312203.CrossRefPubMed Aiello LP, Avery RL, Arrigg PG, Keyt BA, Jampel HD, Shah ST, Pasquale LR, Thieme H, Iwamoto MA, Park JE, et al: Vascular endothelial growth factor in ocular fluid of patients with diabetic retinopathy and other retinal disorders. N Engl J Med. 1994, 331: 1480-1487. 10.1056/NEJM199412013312203.CrossRefPubMed
11.
go back to reference Aiello LP, Gardner TW, King GL, Blankenship G, Cavallerano JD, Ferris FL, Klein R: Diabetic retinopathy. Diabetes Care. 1998, 21: 143-156.CrossRefPubMed Aiello LP, Gardner TW, King GL, Blankenship G, Cavallerano JD, Ferris FL, Klein R: Diabetic retinopathy. Diabetes Care. 1998, 21: 143-156.CrossRefPubMed
12.
go back to reference Norgaz T, Hobikoglu G, Aksu H, Guveli A, Aksoy S, Ozer O, Bolca O, Narin A: Retinopathy is related to the angiographically detected severity and extent of coronary artery disease in patients with type 2 diabetes mellitus. Int Heart J. 2005, 46: 639-646. 10.1536/ihj.46.639.CrossRefPubMed Norgaz T, Hobikoglu G, Aksu H, Guveli A, Aksoy S, Ozer O, Bolca O, Narin A: Retinopathy is related to the angiographically detected severity and extent of coronary artery disease in patients with type 2 diabetes mellitus. Int Heart J. 2005, 46: 639-646. 10.1536/ihj.46.639.CrossRefPubMed
13.
go back to reference Wong TY, Klein R, Sharrett AR, Manolio TA, Hubbard LD, Marino EK, Kuller L, Burke G, Tracy RP, Polak JF, Gottdiener JS, Siscovick DS: The prevalence and risk factors of retinal microvascular abnormalities in older persons: The Cardiovascular Health Study. Ophthalmology. 2003, 110: 658-666. 10.1016/S0161-6420(02)01931-0.CrossRefPubMed Wong TY, Klein R, Sharrett AR, Manolio TA, Hubbard LD, Marino EK, Kuller L, Burke G, Tracy RP, Polak JF, Gottdiener JS, Siscovick DS: The prevalence and risk factors of retinal microvascular abnormalities in older persons: The Cardiovascular Health Study. Ophthalmology. 2003, 110: 658-666. 10.1016/S0161-6420(02)01931-0.CrossRefPubMed
14.
go back to reference Brownlee M: The pathobiology of diabetic complications: a unifying mechanism. Diabetes. 2005, 54: 1615-1625. 10.2337/diabetes.54.6.1615.CrossRefPubMed Brownlee M: The pathobiology of diabetic complications: a unifying mechanism. Diabetes. 2005, 54: 1615-1625. 10.2337/diabetes.54.6.1615.CrossRefPubMed
15.
go back to reference Madamanchi NR, Runge MS: Mitochondrial dysfunction in atherosclerosis. Circ Res. 2007, 100: 460-473. 10.1161/01.RES.0000258450.44413.96.CrossRefPubMed Madamanchi NR, Runge MS: Mitochondrial dysfunction in atherosclerosis. Circ Res. 2007, 100: 460-473. 10.1161/01.RES.0000258450.44413.96.CrossRefPubMed
16.
go back to reference Weitgasser R, Galvan G, Malaimare L, Derflinger I, Hedegger M, Lang J, Iglseder B, Ladurner G, Paulweber B: Cholesteryl ester transfer protein TaqIB polymorphism and its relation to parameters of the insulin resistance syndrome in an Austrian cohort. Biomed Pharmacother. 2004, 58: 619-627. 10.1016/j.biopha.2004.09.010.CrossRefPubMed Weitgasser R, Galvan G, Malaimare L, Derflinger I, Hedegger M, Lang J, Iglseder B, Ladurner G, Paulweber B: Cholesteryl ester transfer protein TaqIB polymorphism and its relation to parameters of the insulin resistance syndrome in an Austrian cohort. Biomed Pharmacother. 2004, 58: 619-627. 10.1016/j.biopha.2004.09.010.CrossRefPubMed
17.
go back to reference Wiesbauer M, Meierhofer D, Mayr JA, Sperl W, Paulweber B, Kofler B: Multiplex primer extension analysis for rapid detection of major European mitochondrial haplogroups. Electrophoresis. 2006, 27: 3864-3868. 10.1002/elps.200600086.CrossRefPubMed Wiesbauer M, Meierhofer D, Mayr JA, Sperl W, Paulweber B, Kofler B: Multiplex primer extension analysis for rapid detection of major European mitochondrial haplogroups. Electrophoresis. 2006, 27: 3864-3868. 10.1002/elps.200600086.CrossRefPubMed
18.
go back to reference Malyarchuk BA, Grzybowski T, Derenko MV, Czarny J, Drobnic K, Miscicka-Sliwka D: Mitochondrial DNA variability in Bosnians and Slovenians. Ann Hum Genet. 2003, 67: 412-425. 10.1046/j.1469-1809.2003.00042.x.CrossRefPubMed Malyarchuk BA, Grzybowski T, Derenko MV, Czarny J, Drobnic K, Miscicka-Sliwka D: Mitochondrial DNA variability in Bosnians and Slovenians. Ann Hum Genet. 2003, 67: 412-425. 10.1046/j.1469-1809.2003.00042.x.CrossRefPubMed
19.
go back to reference Monsalve M, Borniquel S, Valle I, Lamas S: Mitochondrial dysfunction in human pathologies. Front Biosci. 2007, 12: 1131-1153. 10.2741/2132.CrossRefPubMed Monsalve M, Borniquel S, Valle I, Lamas S: Mitochondrial dysfunction in human pathologies. Front Biosci. 2007, 12: 1131-1153. 10.2741/2132.CrossRefPubMed
20.
go back to reference Tan AL, Forbes JM, Cooper ME: AGE, RAGE, and ROS in diabetic nephropathy. Semin Nephrol. 2007, 27: 130-143. 10.1016/j.semnephrol.2007.01.006.CrossRefPubMed Tan AL, Forbes JM, Cooper ME: AGE, RAGE, and ROS in diabetic nephropathy. Semin Nephrol. 2007, 27: 130-143. 10.1016/j.semnephrol.2007.01.006.CrossRefPubMed
21.
go back to reference Schleicher E, Friess U: Oxidative stress, AGE, and atherosclerosis. Kidney Int Suppl. 2007, S17-26. 10.1038/sj.ki.5002382. Schleicher E, Friess U: Oxidative stress, AGE, and atherosclerosis. Kidney Int Suppl. 2007, S17-26. 10.1038/sj.ki.5002382.
22.
go back to reference Raule N, Sevini F, Santoro A, Altilia S, Franceschi C: Association studies on human mitochondrial DNA: methodological aspects and results in the most common age-related diseases. Mitochondrion. 2007, 7: 29-38. 10.1016/j.mito.2006.11.013.CrossRefPubMed Raule N, Sevini F, Santoro A, Altilia S, Franceschi C: Association studies on human mitochondrial DNA: methodological aspects and results in the most common age-related diseases. Mitochondrion. 2007, 7: 29-38. 10.1016/j.mito.2006.11.013.CrossRefPubMed
23.
go back to reference Duval C, Cantero AV, Auge N, Mabile L, Thiers JC, Negre-Salvayre A, Salvayre R: Proliferation and wound healing of vascular cells trigger the generation of extracellular reactive oxygen species and LDL oxidation. Free Radic Biol Med. 2003, 35: 1589-1598. 10.1016/j.freeradbiomed.2003.09.008.CrossRefPubMed Duval C, Cantero AV, Auge N, Mabile L, Thiers JC, Negre-Salvayre A, Salvayre R: Proliferation and wound healing of vascular cells trigger the generation of extracellular reactive oxygen species and LDL oxidation. Free Radic Biol Med. 2003, 35: 1589-1598. 10.1016/j.freeradbiomed.2003.09.008.CrossRefPubMed
24.
go back to reference Kopprasch S, Pietzsch J, Graessler J: Validation of different chemilumigenic substrates for detecting extracellular generation of reactive oxygen species by phagocytes and endothelial cells. Luminescence. 2003, 18: 268-273. 10.1002/bio.737.CrossRefPubMed Kopprasch S, Pietzsch J, Graessler J: Validation of different chemilumigenic substrates for detecting extracellular generation of reactive oxygen species by phagocytes and endothelial cells. Luminescence. 2003, 18: 268-273. 10.1002/bio.737.CrossRefPubMed
25.
go back to reference Kalman B: Role of mitochondria in multiple sclerosis. Curr Neurol Neurosci Rep. 2006, 6: 244-252. 10.1007/s11910-006-0012-0.CrossRefPubMed Kalman B: Role of mitochondria in multiple sclerosis. Curr Neurol Neurosci Rep. 2006, 6: 244-252. 10.1007/s11910-006-0012-0.CrossRefPubMed
26.
go back to reference Pike DA: Phylogenetic networks for human mtDNA haplogroup T. J of Genetic Genealogy. 2006, 2: 1-11. Pike DA: Phylogenetic networks for human mtDNA haplogroup T. J of Genetic Genealogy. 2006, 2: 1-11.
27.
go back to reference Amo T, Yadava N, Oh R, Nicholls DG, Brand MD: Experimental assessment of bioenergetic differences caused by the common European mitochondrial DNA haplogroups H and T. Gene. 2008, 411: 69-76. 10.1016/j.gene.2008.01.007.CrossRefPubMedPubMedCentral Amo T, Yadava N, Oh R, Nicholls DG, Brand MD: Experimental assessment of bioenergetic differences caused by the common European mitochondrial DNA haplogroups H and T. Gene. 2008, 411: 69-76. 10.1016/j.gene.2008.01.007.CrossRefPubMedPubMedCentral
28.
go back to reference Chinnery PF, Mowbray C, Patel SK, Elson JL, Sampson M, Hitman GA, McCarthy MI, Hattersley AT, Walker M: Mitochondrial DNA haplogroups and type 2 diabetes: a study of 897 cases and 1010 controls. J Med Genet. 2007, 44: e80-10.1136/jmg.2007.048876.CrossRefPubMedPubMedCentral Chinnery PF, Mowbray C, Patel SK, Elson JL, Sampson M, Hitman GA, McCarthy MI, Hattersley AT, Walker M: Mitochondrial DNA haplogroups and type 2 diabetes: a study of 897 cases and 1010 controls. J Med Genet. 2007, 44: e80-10.1136/jmg.2007.048876.CrossRefPubMedPubMedCentral
29.
go back to reference Takagi K, Yamada Y, Gong JS, Sone T, Yokota M, Tanaka M: Association of a 5178C-->A (Leu237Met) polymorphism in the mitochondrial DNA with a low prevalence of myocardial infarction in Japanese individuals. Atherosclerosis. 2004, 175: 281-286. 10.1016/j.atherosclerosis.2004.03.008.CrossRefPubMed Takagi K, Yamada Y, Gong JS, Sone T, Yokota M, Tanaka M: Association of a 5178C-->A (Leu237Met) polymorphism in the mitochondrial DNA with a low prevalence of myocardial infarction in Japanese individuals. Atherosclerosis. 2004, 175: 281-286. 10.1016/j.atherosclerosis.2004.03.008.CrossRefPubMed
30.
go back to reference Nishigaki Y, Yamada Y, Fuku N, Matsuo H, Segawa T, Watanabe S, Kato K, Yokoi K, Yamaguchi S, Nozawa Y, Tanaka M: Mitochondrial haplogroup N9b is protective against myocardial infarction in Japanese males. Hum Genet. 2007, 120: 827-836. 10.1007/s00439-006-0269-z.CrossRefPubMed Nishigaki Y, Yamada Y, Fuku N, Matsuo H, Segawa T, Watanabe S, Kato K, Yokoi K, Yamaguchi S, Nozawa Y, Tanaka M: Mitochondrial haplogroup N9b is protective against myocardial infarction in Japanese males. Hum Genet. 2007, 120: 827-836. 10.1007/s00439-006-0269-z.CrossRefPubMed
31.
go back to reference Benn M, Schwartz M, Nordestgaard BG, Tybjaerg-Hansen A: Mitochondrial haplogroups: ischemic cardiovascular disease, other diseases, mortality, and longevity in the general population. Circulation. 2008, 117: 2492-2501. 10.1161/CIRCULATIONAHA.107.756809.CrossRefPubMed Benn M, Schwartz M, Nordestgaard BG, Tybjaerg-Hansen A: Mitochondrial haplogroups: ischemic cardiovascular disease, other diseases, mortality, and longevity in the general population. Circulation. 2008, 117: 2492-2501. 10.1161/CIRCULATIONAHA.107.756809.CrossRefPubMed
32.
go back to reference Lenzen MJ, Boersma E, Bertrand ME, Maier W, Moris C, Piscione F, Sechtem U, Stahle E, Widimsky P, de Jaegere P, Scholte op Reimer WJ, Mercado N, Wijns W: Management and outcome of patients with established coronary artery disease: the Euro Heart Survey on coronary revascularization. Eur Heart J. 2005, 26: 1169-1179. 10.1093/eurheartj/ehi238.CrossRefPubMed Lenzen MJ, Boersma E, Bertrand ME, Maier W, Moris C, Piscione F, Sechtem U, Stahle E, Widimsky P, de Jaegere P, Scholte op Reimer WJ, Mercado N, Wijns W: Management and outcome of patients with established coronary artery disease: the Euro Heart Survey on coronary revascularization. Eur Heart J. 2005, 26: 1169-1179. 10.1093/eurheartj/ehi238.CrossRefPubMed
33.
go back to reference Do D, West JA, Morise A, Atwood E, Froelicher V: A consensus approach to diagnosing coronary artery disease based on clinical and exercise test data. Chest. 1997, 111: 1742-1749. 10.1378/chest.111.6.1742.CrossRefPubMed Do D, West JA, Morise A, Atwood E, Froelicher V: A consensus approach to diagnosing coronary artery disease based on clinical and exercise test data. Chest. 1997, 111: 1742-1749. 10.1378/chest.111.6.1742.CrossRefPubMed
Metadata
Title
Mitochondrial DNA haplogroup T is associated with coronary artery disease and diabetic retinopathy: a case control study
Authors
Barbara Kofler
Edith E Mueller
Waltraud Eder
Olaf Stanger
Richard Maier
Martin Weger
Anton Haas
Robert Winker
Otto Schmut
Bernhard Paulweber
Bernhard Iglseder
Wilfried Renner
Martina Wiesbauer
Irene Aigner
Danijela Santic
Franz A Zimmermann
Johannes A Mayr
Wolfgang Sperl
Publication date
01-12-2009
Publisher
BioMed Central
Published in
BMC Medical Genetics / Issue 1/2009
Electronic ISSN: 1471-2350
DOI
https://doi.org/10.1186/1471-2350-10-35

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