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  1. Article ; Online: Telomere shortening unrelated to smoking, body weight, physical activity, and alcohol intake: 4,576 general population individuals with repeat measurements 10 years apart.

    Weischer, Maren / Bojesen, Stig E / Nordestgaard, Børge G

    PLoS genetics

    2014  Volume 10, Issue 3, Page(s) e1004191

    Abstract: Cross-sectional studies have associated short telomere length with smoking, body weight, physical activity, and possibly alcohol intake; however, whether these associations are due to confounding is unknown. We tested these hypotheses in 4,576 ... ...

    Abstract Cross-sectional studies have associated short telomere length with smoking, body weight, physical activity, and possibly alcohol intake; however, whether these associations are due to confounding is unknown. We tested these hypotheses in 4,576 individuals from the general population cross-sectionally, and with repeat measurement of relative telomere length 10 years apart. We also tested whether change in telomere length is associated with mortality and morbidity in the general population. Relative telomere length was measured with quantitative polymerase chain reaction. Cross-sectionally at the first examination, short telomere length was associated with increased age (P for trend across quartiles = 3 × 10(-77)), current smoking (P = 8 × 10(-3)), increased body mass index (P = 7 × 10(-14)), physical inactivity (P = 4 × 10(-17)), but not with increased alcohol intake (P = 0.10). At the second examination 10 years later, 56% of participants had lost and 44% gained telomere length with a mean loss of 193 basepairs. Change in leukocyte telomere length during 10 years was associated inversely with baseline telomere length (P<1 × 10(-300)) and age at baseline (P = 1 × 10(-27)), but not with baseline or 10-year inter-observational tobacco consumption, body weight, physical activity, or alcohol intake. Prospectively during a further 10 years follow-up after the second examination, quartiles of telomere length change did not associate with risk of all-cause mortality, cancer, chronic obstructive pulmonary disease, diabetes mellitus, ischemic cerebrovascular disease, or ischemic heart disease. In conclusion, smoking, increased body weight, and physical inactivity were associated with short telomere length cross-sectionally, but not with telomere length change during 10 years observation, and alcohol intake was associated with neither. Also, change in telomere length did not associate prospectively with mortality or morbidity in the general population.
    MeSH term(s) Adult ; Alcohol Drinking/genetics ; Body Mass Index ; Body Weight/genetics ; Female ; Genetics, Population ; Humans ; Leukocytes/cytology ; Male ; Middle Aged ; Motor Activity/genetics ; Risk Factors ; Smoking/genetics ; Telomere/genetics ; Telomere Shortening/genetics
    Language English
    Publishing date 2014-03-13
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2186725-2
    ISSN 1553-7404 ; 1553-7390
    ISSN (online) 1553-7404
    ISSN 1553-7390
    DOI 10.1371/journal.pgen.1004191
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: CHEK2 (∗) 1100delC Mutation and Risk of Prostate Cancer.

    Hale, Victoria / Weischer, Maren / Park, Jong Y

    Prostate cancer

    2014  Volume 2014, Page(s) 294575

    Abstract: Although the causes of prostate cancer are largely unknown, previous studies support the role of genetic factors in the development of prostate cancer. CHEK2 plays a critical role in DNA replication by responding to double-stranded breaks. In this review, ...

    Abstract Although the causes of prostate cancer are largely unknown, previous studies support the role of genetic factors in the development of prostate cancer. CHEK2 plays a critical role in DNA replication by responding to double-stranded breaks. In this review, we provide an overview of the current knowledge of the role of a genetic variant, 1100delC, of CHEK2 on prostate cancer risk and discuss the implication for potential translation of this knowledge into clinical practice. Currently, twelve articles that discussed CHEK2 (∗)1100delC and its association with prostate cancer were identified. Of the twelve prostate cancer studies, five studies had independent data to draw conclusive evidence from. The pooled results of OR and 95% CI were 1.98 (1.23-3.18) for unselected cases and 3.39 (1.78-6.47) for familial cases, indicating that CHEK2 (∗)1100delC mutation is associated with increased risk of prostate cancer. Screening for CHEK2(∗)1100delC should be considered in men with a familial history of prostate cancer.
    Language English
    Publishing date 2014-11-06
    Publishing country Egypt
    Document type Journal Article ; Review
    ZDB-ID 2627965-4
    ISSN 2090-312X ; 2090-3111
    ISSN (online) 2090-312X
    ISSN 2090-3111
    DOI 10.1155/2014/294575
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Response.

    Weischer, Maren / Nordestgaard, Børge G / Bojesen, Stig E

    Journal of the National Cancer Institute

    2013  Volume 105, Issue 15, Page(s) 1157–1158

    MeSH term(s) Female ; Humans ; Leukocytes/pathology ; Male ; Neoplasms/epidemiology ; Neoplasms/genetics ; Telomere/pathology
    Language English
    Publishing date 2013-08-07
    Publishing country United States
    Document type Comment ; Letter
    ZDB-ID 2992-0
    ISSN 1460-2105 ; 0027-8874 ; 0198-0157
    ISSN (online) 1460-2105
    ISSN 0027-8874 ; 0198-0157
    DOI 10.1093/jnci/djt155
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: High tobacco consumption is causally associated with increased all-cause mortality in a general population sample of 55,568 individuals, but not with short telomeres: a Mendelian randomization study.

    Rode, Line / Bojesen, Stig E / Weischer, Maren / Nordestgaard, Børge G

    International journal of epidemiology

    2014  Volume 43, Issue 5, Page(s) 1473–1483

    Abstract: Background: High cumulative tobacco consumption is associated with short telomeres and with increased all-cause mortality. We tested the hypothesis that high tobacco consumption is causally associated with short telomeres and with increased all-cause ... ...

    Abstract Background: High cumulative tobacco consumption is associated with short telomeres and with increased all-cause mortality. We tested the hypothesis that high tobacco consumption is causally associated with short telomeres and with increased all-cause mortality.
    Methods: We studied 55,568 individuals including 32,823 ever smokers from the Danish general population, of whom 3430 died during 10 years of follow-up. All had telomere length measured, detailed information on smoking history, and CHRNA3 rs1051730 genotype, which is associated with tobacco consumption, determined. In a Mendelian randomization study, we conducted observational, genetic, and mediation analyses.
    Results: First, tobacco consumption was 21.1 pack-years in non-carriers, 22.8 in heterozygotes and 24.8 in homozygotes (P-trend<0.001). Second, the observational multivariable adjusted hazard ratio for all-cause mortality was 1.12 [95% confidence interval (CI): 1.09, 1.15] per doubling in tobacco consumption. In Mendelian randomization analysis, the hazard ratio was 1.08 (1.02, 1.14) per minor CHRNA3 allele in ever smokers. Third, in observational analysis telomeres shortened with -13 base pairs (-18, -8) per doubling in tobacco consumption. In Mendelian randomization analysis, the estimate was +3 base pairs (-10, +15) per minor CHRNA3 allele. Finally, individuals with the shortest vs longest telomeres had a multivariable adjusted hazard ratio of 1.30 (1.13, 1.50) for all-cause mortality; however, in mediation analysis short telomeres explained only +0.4% (-3.5%, +4.3%) of the association between high tobacco consumption and increased all-cause mortality.
    Conclusions: High tobacco consumption is causally associated with increased all-cause mortality. High cumulative tobacco consumption is associated with short telomeres observationally, but there is no clear genetic association.
    MeSH term(s) Denmark/epidemiology ; Female ; Follow-Up Studies ; Genotype ; Humans ; Incidence ; Male ; Mendelian Randomization Analysis ; Mortality ; Multivariate Analysis ; Polymorphism, Genetic ; Risk Factors ; Smoking/genetics ; Smoking/mortality ; Telomere/genetics ; Tobacco Use Disorder/genetics ; Tobacco Use Disorder/mortality
    Language English
    Publishing date 2014-10
    Publishing country England
    Document type Journal Article ; Observational Study ; Research Support, Non-U.S. Gov't
    ZDB-ID 187909-1
    ISSN 1464-3685 ; 0300-5771
    ISSN (online) 1464-3685
    ISSN 0300-5771
    DOI 10.1093/ije/dyu119
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Increased body mass index, elevated C-reactive protein, and short telomere length.

    Rode, Line / Nordestgaard, Børge G / Weischer, Maren / Bojesen, Stig E

    The Journal of clinical endocrinology and metabolism

    2014  Volume 99, Issue 9, Page(s) E1671–5

    Abstract: Context: Obesity is associated with short telomere length. The cause of this association is unknown.: Objective: We hypothesized that genetically increased body mass index (BMI) is associated with telomere length shortening and that low-grade ... ...

    Abstract Context: Obesity is associated with short telomere length. The cause of this association is unknown.
    Objective: We hypothesized that genetically increased body mass index (BMI) is associated with telomere length shortening and that low-grade inflammation might contribute through elevated C-reactive protein.
    Setting and design: We studied 45,069 individuals from the Copenhagen General Population Study with measurements of leukocyte telomere length, BMI, and C-reactive protein in a Mendelian randomization study. Using the three obesity-associated polymorphisms FTO rs9939609, MC4R rs17782313, and TMEM18 rs6548238, and the CRP promoter polymorphism rs3091244 in instrumental variable analyses, we estimated the associations between genetically increased BMI and telomere length and between genetically increased C-reactive protein and telomere length.
    Results: In multivariable-adjusted observational analyses, telomere length decreased with seven base pairs (95% confidence interval, -9--5) per unit increase in BMI, and further adjustment for C-reactive protein attenuated this association to -5 base pairs (-8--3). In accordance, instrumental variable analysis showed a non-significant telomere length shortening of six base pairs (-37-25) per unit increase in genetically determined BMI. Furthermore, in observational analyses, telomere length decreased with nine base pairs (-16--2) for a doubling in C-reactive protein, supported by the instrumental variable analyses showing a corresponding genetically determined decrease of 66 base pairs (-124--7).
    Conclusions: High BMI is associated with short telomere length observationally. This might possibly be mediated through elevated C-reactive protein, given that genetically elevated C-reactive protein levels are associated with short telomere length.
    MeSH term(s) Adult ; Aged ; Aged, 80 and over ; Body Mass Index ; C-Reactive Protein/metabolism ; Female ; Humans ; Inflammation/genetics ; Inflammation/immunology ; Inflammation/metabolism ; Male ; Middle Aged ; Multivariate Analysis ; Obesity/genetics ; Obesity/immunology ; Obesity/metabolism ; Polymorphism, Genetic ; Telomere/genetics ; Telomere/immunology ; Telomere/metabolism ; Young Adult
    Chemical Substances C-Reactive Protein (9007-41-4)
    Language English
    Publishing date 2014-09
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 3029-6
    ISSN 1945-7197 ; 0021-972X
    ISSN (online) 1945-7197
    ISSN 0021-972X
    DOI 10.1210/jc.2014-1161
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Genotyping for NOD2 genetic variants and crohn disease: a metaanalysis.

    Yazdanyar, Shiva / Weischer, Maren / Nordestgaard, Børge G

    Clinical chemistry

    2009  Volume 55, Issue 11, Page(s) 1950–1957

    Abstract: Background: Arg702Trp, Gly908Arg, and Leu1007fsinsC variants of the NOD2 gene (nucleotide-binding oligomerization domain containing 2; alias, CARD15) influence the risk of Crohn disease.: Methods: We conducted a systematic review to examine whether ... ...

    Abstract Background: Arg702Trp, Gly908Arg, and Leu1007fsinsC variants of the NOD2 gene (nucleotide-binding oligomerization domain containing 2; alias, CARD15) influence the risk of Crohn disease.
    Methods: We conducted a systematic review to examine whether Arg702Trp, Gly908Arg, and Leu1007fsinsC are equally important risk factors for Crohn disease. In addition, we used studies for which combined information from all genotypes was available to compare risks in simple heterozygotes, compound heterozygotes, and homozygotes. PubMed, EMBASE, and Web of Science were searched. Seventy-five articles (18 727 cases and 17 102 controls) met the inclusion criteria and contributed data to the metaanalyses.
    Results: The odds ratios per allele for Crohn disease were 2.2 (95% CI, 2.0-2.5) for Arg702Trp, 2.6 (2.2-2.9) for Gly908Arg, and 3.8 (3.4-4.3) for Leu1007fsinsC (z-test results: Arg702Trp vs Gly908Arg, P = 0.03; Arg702Trp vs Leu1007fsinsC, P < 0.001; Gly908Arg vs Leu1007fsinsC, P < 0.001). When all 3 genotypes were combined, odds ratios for Crohn disease were 2.4 (95% CI, 2.0-2.8) for simple heterozygotes, 9.0 (6.0-13.5) for compound heterozygotes, and 6.7 (4.1-10.9) for homozygotes, compared with noncarriers (z-test results: simple heterozygotes vs compound heterozygotes, P < 0.001; simple heterozygotes vs homozygotes, P < 0.001; compound heterozygotes vs homozygotes, P = 0.18).
    Conclusions: The per-allele risk of Crohn disease was markedly higher for Leu1007fsinsC than for Arg702Trp and Gly908Arg. Combining all genotypes revealed the risks of Crohn disease for compound heterozygotes and homozygotes to be similar and markedly higher than for simple heterozygotes.
    MeSH term(s) Alleles ; Crohn Disease/diagnosis ; Crohn Disease/genetics ; Genetic Predisposition to Disease ; Genetic Variation ; Genotype ; Humans ; Nod2 Signaling Adaptor Protein/genetics
    Chemical Substances NOD2 protein, human ; Nod2 Signaling Adaptor Protein
    Language English
    Publishing date 2009-08-27
    Publishing country England
    Document type Journal Article ; Meta-Analysis ; Research Support, Non-U.S. Gov't ; Systematic Review
    ZDB-ID 80102-1
    ISSN 1530-8561 ; 0009-9147
    ISSN (online) 1530-8561
    ISSN 0009-9147
    DOI 10.1373/clinchem.2009.127126
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  7. Article ; Online: Short telomere length, lung function and chronic obstructive pulmonary disease in 46,396 individuals.

    Rode, Line / Bojesen, Stig E / Weischer, Maren / Vestbo, Jørgen / Nordestgaard, Børge G

    Thorax

    2013  Volume 68, Issue 5, Page(s) 429–435

    Abstract: Background: A previous case-control study of 100 individuals found that short telomere length was associated with a 28-fold increased risk of chronic obstructive pulmonary disease (COPD).: Objectives: To test the hypothesis that short telomere length ...

    Abstract Background: A previous case-control study of 100 individuals found that short telomere length was associated with a 28-fold increased risk of chronic obstructive pulmonary disease (COPD).
    Objectives: To test the hypothesis that short telomere length is associated with reduced lung function and an increased risk of COPD.
    Methods: Observational study of 46 396 individuals from the Danish general population.
    Measurements: Leucocyte telomere length and spirometry were measured. COPD was defined using either fixed forced expiratory volume in 1 s (FEV₁)/forced vital capacity (FVC) ratio <0.70 as suggested by the Global initiative for chronic Obstructive Lung Disease (GOLD) or FEV₁/FVC below the lower limit of normal (LLN).
    Results: Telomere length decreased significantly with increasing age (p<10(-300)). FEV₁, FVC and FEV1/FVC decreased with decreasing telomere length quartiles (p trend: 5 × 10(-51), 5 × 10(-35) and 6 × 10(-137), respectively), but the associations attenuated after age and multivariable adjustment. The risk of COPD increased with decreasing telomere length quartile (p trend: p=7 × 10(-92) for GOLD; p=8 × 10(-44) for FEV₁/FVC below LLN), but associations also attenuated after adjustment. Unadjusted and multivariable adjusted OR for shortest versus longest telomere length quartiles were 2.06 (95% CI 1.91 to 2.22) and 1.15 (95% CI 1.06 to 1.25) for GOLD and 1.73 (95% CI 1.60 to 1.88) and 1.19 (95% CI 1.09 to 1.30) for FEV₁/FVC below LLN, respectively. Per 1000 base pairs decrease in telomere length, the multivariable adjusted OR was 1.07 (95% CI 1.03 to 1.10) for GOLD and 1.07 (95% CI 1.03 to 1.11) for FEV₁/FVC below LLN.
    Conclusions: Short telomere length is associated with decreased lung function and with increased risk of COPD, but the associations are markedly attenuated after adjustment. Our data support a modest correlation between telomere length and the lung function indices examined.
    MeSH term(s) Adult ; Aged ; DNA/analysis ; Denmark/epidemiology ; Female ; Forced Expiratory Volume/genetics ; Humans ; Male ; Middle Aged ; Polymerase Chain Reaction ; Prevalence ; Pulmonary Disease, Chronic Obstructive/epidemiology ; Pulmonary Disease, Chronic Obstructive/genetics ; Pulmonary Disease, Chronic Obstructive/physiopathology ; Retrospective Studies ; Telomere ; Vital Capacity/genetics
    Chemical Substances DNA (9007-49-2)
    Language English
    Publishing date 2013-05
    Publishing country England
    Document type Comparative Study ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 204353-1
    ISSN 1468-3296 ; 0040-6376
    ISSN (online) 1468-3296
    ISSN 0040-6376
    DOI 10.1136/thoraxjnl-2012-202544
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  8. Article: Calcineurin inhibitors and rapamycin: cancer protection or promotion?

    Weischer, Maren / Röcken, Martin / Berneburg, Mark

    Experimental dermatology

    2007  Volume 16, Issue 5, Page(s) 385–393

    Abstract: Since the introduction of cyclosporin A (CsA) in the early 1980s, the use of immunosuppressants has markedly increased. Already established drugs have proved effective in the treatment of a wide range of diseases outside transplantation medicine and new ... ...

    Abstract Since the introduction of cyclosporin A (CsA) in the early 1980s, the use of immunosuppressants has markedly increased. Already established drugs have proved effective in the treatment of a wide range of diseases outside transplantation medicine and new immunosuppressants have been developed for more specific indications such as psoriasis and atopic dermatitis. Patients in transplantation medicine as well as in dermatology have benefited significantly from systemic and topical application of both new and established drugs. But are these drugs without risks? Cancer-protecting effects have been reported for some of the available immunosuppressants. Conversely, other publications and the issue of a black box warning by the US Food and Drug Administration have increased concerns about cancer-promoting effects. Knowledge of the specific effects as well as adverse effects is paramount to ensure an application that is safe and beneficial for the patient. Here we review the mechanisms of action and therapeutic potential, and critically review recent literature with respect to possible carcinogenic side effects of systemic and topical CsA, tacrolimus, pimecrolimus and rapamycin.
    MeSH term(s) Calcineurin Inhibitors ; Carcinogens/toxicity ; Cyclosporine/adverse effects ; Cyclosporine/pharmacology ; DNA Repair ; Humans ; Immunosuppressive Agents/adverse effects ; Immunosuppressive Agents/pharmacology ; Models, Biological ; Neoplasms/etiology ; Neoplasms/prevention & control ; Protein Kinases/drug effects ; Sirolimus/adverse effects ; Sirolimus/pharmacology ; TOR Serine-Threonine Kinases ; Tacrolimus/adverse effects ; Tacrolimus/analogs & derivatives ; Tacrolimus/pharmacology ; Ultraviolet Rays/adverse effects
    Chemical Substances Calcineurin Inhibitors ; Carcinogens ; Immunosuppressive Agents ; pimecrolimus (7KYV510875) ; Cyclosporine (83HN0GTJ6D) ; Protein Kinases (EC 2.7.-) ; MTOR protein, human (EC 2.7.1.1) ; TOR Serine-Threonine Kinases (EC 2.7.1.1) ; Sirolimus (W36ZG6FT64) ; Tacrolimus (WM0HAQ4WNM)
    Language English
    Publishing date 2007-05
    Publishing country Denmark
    Document type Journal Article ; Review
    ZDB-ID 1130936-2
    ISSN 1600-0625 ; 0906-6705
    ISSN (online) 1600-0625
    ISSN 0906-6705
    DOI 10.1111/j.1600-0625.2007.00555.x
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  9. Article ; Online: Short telomere length, cancer survival, and cancer risk in 47102 individuals.

    Weischer, Maren / Nordestgaard, Børge G / Cawthon, Richard M / Freiberg, Jacob J / Tybjærg-Hansen, Anne / Bojesen, Stig E

    Journal of the National Cancer Institute

    2013  Volume 105, Issue 7, Page(s) 459–468

    Abstract: Background: Recent meta-analyses have suggested that short telomere length was associated with increased risk of cancer. We therefore tested the hypotheses that short telomere length was associated with increased risk of cancer and with increased risk ... ...

    Abstract Background: Recent meta-analyses have suggested that short telomere length was associated with increased risk of cancer. We therefore tested the hypotheses that short telomere length was associated with increased risk of cancer and with increased risk of early death after cancer.
    Methods: We measured leukocyte telomere length in a prospective study of 47 102 Danish general population participants from the Copenhagen City Heart Study and the Copenhagen General Population Study. Participants were followed for up to 20 years for cancer diagnosis and death. Follow-up was 100% complete. All statistical tests were two-sided.
    Results: Telomere length decreased linearly with increasing age (P <.001). During follow-up, we observed 3142 first cancers and, among these individuals, 1730 deaths. Decreasing quartiles of telomere length were associated with decreasing survival after cancer (log-rank P <.001). Multivariable-adjusted hazard ratios of early death were 1.31 (95% confidence interval [CI] = 1.14 to 1.52) in individuals in the quartile and 1.43 (95% CI = 1.13 to 1.80) in individuals in the decile with the shortest telomeres vs the longest. Unadjusted hazard ratios of cancer risk were 1.74 (95% CI = 1.58 to 1.93) and 2.00 (95% CI = 1.70 to 2.35) in individuals in the quartile and decile with the shortest vs longest telomeres; however, multivariable adjustment changed these hazard ratios to 0.98 (95% CI = 0.88 to 1.08) and 0.95 (95% CI = 0.80 to 1.11), mainly because of age adjustment.
    Conclusions: Short telomere length is associated with reduced survival after cancer but not with cancer risk. The latter contrasts with findings from recent meta-analyses.
    MeSH term(s) Age Factors ; Aged ; Denmark/epidemiology ; Female ; Follow-Up Studies ; Humans ; Incidence ; Leukocytes/pathology ; Linear Models ; Male ; Middle Aged ; Multivariate Analysis ; Neoplasms/epidemiology ; Neoplasms/genetics ; Neoplasms/mortality ; Neoplasms/pathology ; Odds Ratio ; Prospective Studies ; Risk Assessment ; Risk Factors ; Survival Analysis ; Survival Rate ; Telomere/pathology ; Telomere Shortening
    Language English
    Publishing date 2013-04-03
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2992-0
    ISSN 1460-2105 ; 0027-8874 ; 0198-0157
    ISSN (online) 1460-2105
    ISSN 0027-8874 ; 0198-0157
    DOI 10.1093/jnci/djt016
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  10. Article ; Online: Short telomere length, myocardial infarction, ischemic heart disease, and early death.

    Weischer, Maren / Bojesen, Stig E / Cawthon, Richard M / Freiberg, Jacob J / Tybjærg-Hansen, Anne / Nordestgaard, Børge G

    Arteriosclerosis, thrombosis, and vascular biology

    2012  Volume 32, Issue 3, Page(s) 822–829

    Abstract: Objective: We tested the hypothesis that short telomere length is associated with increased risk of myocardial infarction, ischemic heart disease, and early death.: Methods and results: We measured leukocyte telomere length in 2 prospective studies ... ...

    Abstract Objective: We tested the hypothesis that short telomere length is associated with increased risk of myocardial infarction, ischemic heart disease, and early death.
    Methods and results: We measured leukocyte telomere length in 2 prospective studies of 19 838 Danish general population participants from the Copenhagen City Heart Study and the Copenhagen General Population Study. Participants were followed for up to 19 years for incident myocardial infarction (n=929), ischemic heart disease (n=2038), and death (n=4342). Follow-up was 100% complete. Telomere length decreased linearly with increasing age in women and men in both studies (P=7×10(-74) to P=3×10(-125)). Multifactorially adjusted hazard ratios were 1.10 (95% CI 1.01-1.19) for myocardial infarction, 1.06 (1.00-1.11) for ischemic heart disease, and 1.09 (1.05-1.13) for early death per 1000-base pair decrease in telomere length. The multifactorially adjusted hazard ratios for the shortest versus the longest decile of telomere length were 1.49 (1.07-2.07) for myocardial infarction, 1.24 (1.01-1.53) for ischemic heart disease, and 1.25 (1.07-1.46) for early death.
    Conclusion: Short telomere length is associated with only modestly increased risk of myocardial infarction, ischemic heart disease, and early death.
    MeSH term(s) Adult ; Age Factors ; Aged ; Aging/genetics ; Denmark/epidemiology ; Female ; Follow-Up Studies ; Genetic Predisposition to Disease ; Humans ; Male ; Middle Aged ; Myocardial Infarction/genetics ; Myocardial Infarction/mortality ; Myocardial Ischemia/genetics ; Myocardial Ischemia/mortality ; Phenotype ; Proportional Hazards Models ; Prospective Studies ; Real-Time Polymerase Chain Reaction ; Risk Assessment ; Risk Factors ; Telomere Shortening ; Time Factors
    Language English
    Publishing date 2012-03
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1221433-4
    ISSN 1524-4636 ; 1079-5642
    ISSN (online) 1524-4636
    ISSN 1079-5642
    DOI 10.1161/ATVBAHA.111.237271
    Database MEDical Literature Analysis and Retrieval System OnLINE

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