Clinical Chemistry
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
QUICK SEARCH:   [advanced]


     

Clinical Chemistry 45: 1200-1205, 1999;
This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Web of Science (22)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by de Valk-de Roo, G. W.
Right arrow Articles by Netelenbos, C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by de Valk-de Roo, G. W.
Right arrow Articles by Netelenbos, C.
Related Collections
Right arrow Clinical Immunology
Right arrow Nutrition
Right arrow Evidence Based Laboratory Medicine and Test Utilization
Right arrow Hemostasis and Thrombosis
Right arrow Proteomics and Protein Markers
Right arrow Lipids, Lipoproteins, and Cardiovascular Risk Factors
Right arrow Endocrinology and Metabolism
(Clinical Chemistry. 1999;45:1200-1205.)
© 1999 American Association for Clinical Chemistry, Inc.

Articles

Plasma Homocysteine Is Weakly Correlated with Plasma Endothelin and von Willebrand Factor but not with Endothelium-dependent Vasodilatation in Healthy Postmenopausal Women

Gerdien W. de Valk-de Roo1, Coen D.A. Stehouwer2, Jan Lambert2, Casper G. Schalkwijk4, Marius J. van der Mooren3, Cornelis Kluft5 and Coen Netelenbos1,a

1 Department of Endocrinology, Research Institute for Endocrinology, Reproduction and Metabolism; Departments of
2 Internal Medicine and
3 Obstetrics and Gynaecology, Institute for Cardiovascular Research-Vrije Universiteit; and
4 Department of Clinical Chemistry, University Hospital Vrije Universiteit Amsterdam, De Boelelaan 1117, Postbus 7057, 1007 MB Amsterdam, The Netherlands.

5 The Gaubius Laboratory, TNO-PG, Postbus 2215, 2301 CE Leiden, The Netherlands.
a Author for correspondence. Fax 31-20-4440502; e-mail C.Netelen{at}azvu.nl


   Abstract
Top
 Abstract
Introduction
 Subjects and Methods
 Results
 Discussion
 References
 
Background: Hyperhomocysteinemia is an independent cardiovascular risk factor, possibly through the induction of endothelial dysfunction. The postmenopausal state is associated with increased plasma homocysteine. We examined whether increased homocysteine is associated with impaired endothelial function.

Methods: Sixty-three hysterectomized but otherwise healthy postmenopausal women (54.8 ± 3.5 years) participated in this study. Fasting total plasma homocysteine (tHcy) was measured as free plus protein-bound homocysteine. Endothelial function was assessed by measuring plasma concentrations of the endothelium-derived proteins endothelin (ET), von Willebrand factor (vWF), and plasminogen activator inhibitor type 1 (PAI-1) as well as brachial artery flow-mediated, endothelium-dependent vasodilatation (FMD).

Results: Plasma tHcy was 9.6 ± 2.5 µmol/L. After adjustment for possible confounders, a 1 µmol/L increase in tHcy was associated with an increase in ET of 0.08 ng/L (P = 0.045) and an increase in vWF of 4.2% (P = 0.05). No statistically significant association was present between tHcy and PAI-1 or FMD.

Conclusions: Increased fasting homocysteine in postmenopausal women may impair some aspects of endothelial function. It is of clinical interest to study whether homocysteine lowering can improve endothelial function and thus cardiovascular morbidity and mortality in postmenopausal women.© 1999 American Association for Clinical Chemistry


   Introduction
Top
 Abstract
 Introduction
Subjects and Methods
 Results
 Discussion
 References
 
Hyperhomocysteinemia is an independent risk factor for atherosclerosis and thromboembolic disease. These associations are not limited to severe hyperhomocysteinemia, such as that related to homozygous cystathionine-ß-synthase deficiency; they are also observed when fasting or postmethionine concentrations are moderately increased (1)(2)(3). Increased total homocysteine (tHcy)1 is thought to confer a graded risk of atherothrombotic disease and may be attributed to commonly occurring genetic and acquired factors such as the C677T mutation in the methylenetetrahydrofolate reductase gene, impaired renal function, inadequate folic acid and/or vitamin B6 and B12 intake, and the use of certain medications. Sex steroids also affect the tHcy concentration (4). The tHcy concentration is higher in men than in women (5)(6). Low tHcy concentrations are present during pregnancy, a state characterized by high concentrations of endogenous estrogens (7), as well as in premenopausal compared with postmenopausal women (8). In addition, in postmenopausal women, administration of hormone replacement therapy has been reported to lower homocysteine (9)(10)(11). It may, therefore, be hypothesized that a menopause-associated increase in homocysteine contributes to the postmenopausal increase in cardiovascular risk.

Homocysteine may promote atherothrombogenesis by a variety of mechanisms. Homocysteine affects the balance between coagulation and fibrinolysis, in which the endothelium plays a key role (12). It adversely affects the production of endothelium-derived nitric oxide, and it induces proliferation of vascular smooth muscle cells (12)(13)(14). However, it is not known whether tHcy modulates endothelial function in postmenopausal women. We therefore examined, in a population of healthy postmenopausal women, whether an increased tHcy concentration was associated with impaired endothelial function. As estimates of endothelial function, we assessed the endothelium-derived regulatory proteins, endothelin (ET), von Willebrand factor (vWF), and plasminogen activator inhibitor type 1 (PAI-1) as well as the brachial artery flow-mediated, endothelium-dependent vasodilatation (FMD). High plasma concentrations of ET, vWF, and PAI-1 are associated with a poor cardiovascular outcome (15)(16)(17)(18)(19)(20).


   Subjects and Methods
Top
 Abstract
 Introduction
 Subjects and Methods
Results
 Discussion
 References
 
subjects
We recruited 68 healthy, postmenopausal women, ages 40–60 years. All subjects had undergone a hysterectomy and were screened for a long-term follow-up study on estrogen monotherapy. Hysterectomy had been performed because of a benign endometrial abnormality (n = 54), uterine prolapse (n = 9), and/or a benign ovarian abnormality (n = 5). Postmenopausal status was defined as serum estradiol <=73 pmol/L and follicle-stimulating hormone (FSH) >=40 IU/L. Exclusion criteria were a history of breast carcinoma and/or recent thromboembolism, evidence of liver disease (serum bilirubin >34 µmol/L, alanine aminotransferase >100 U/L, and/or alkaline phosphatase >300 U/L) and/or renal dysfunction (serum creatinine >180 µmol/L), diabetes mellitus requiring pharmacological therapy, use of lipid-lowering drugs and/or anticonvulsives, and use of sex steroids and/or corticosteroids more recently than 6 months before the start of the study. Five subjects were subsequently excluded because of lack of sufficient plasma for tHcy measurement (n = 4) or because of rheumatoid arthritis (n = 1). All subjects gave informed consent, and the protocol was approved by the local ethics committee. Subject characteristics are summarized in Table 1 .


View this table:
[in this window]
[in a new window]
  		Table 1. Characteristics of the 63 healthy, postmenopausal women.

general procedures
In all subjects, we assessed current smoking status (yes/no), alcohol use (units per week), and blood pressure. Blood pressure (mean of four readings) was measured on the left arm after 10 min of rest, using an automated device (BP-8800; Colin). Hypertension was defined as a systolic blood pressure >=160 mmHg and/or a diastolic blood pressure >=95 mmHg and/or the use of antihypertensive drugs. As indexes of body composition, we assessed the body mass index (BMI; kg/m2) and the waist-to-hip ratio (WHR; waist circumference divided by hip circumference). Blood samples were collected between 0830 and 1130 in the morning after an overnight fast. Plasma and serum samples, prepared from the blood samples, were then either used directly (to determine serum estradiol, FSH, lipids, and glucose) or stored at -70 °C until analysis (for the determination of serum insulin and plasma tHcy, ET, vWF, PAI-1, and C-reactive protein).

tHcy AND ENDOTHELIUM-DERIVED REGULATORY PROTEINS
Plasma concentrations of tHcy, ET, vWF, and PAI-1 were assayed in a single run. Fasting plasma tHcy was measured as free plus protein-bound homocysteine by HPLC with fluorescence detection (21). The intraassay CV was 2%; the lower limit of detection was 0.5 µmol/L. Plasma immunoreactive ET was measured by RIA (Nichols Institute) after extraction on Sep-Pak C18 cartridges (Waters). The intraassay CV was 10%. The lower limit of detection of the assay, defined as the lowest single value that could be distinguished from zero at the 99% confidence limit, was 2 ng/L. Cross-reactivity with ET-1 was 100%, with ET-2 was 67%, with ET-3 was 84%, and with "big" ET-1 was 2.6%. vWF antigen was measured by a peroxidase ELISA (22), using rabbit anti-vWF antigen IgG in the coating buffer and peroxidase-conjugated rabbit anti-vWF antigen IgG (Dako). o-Phenylenediamine (Sigma Chemical Co.) was used as substrate. The intraassay CV was 2.3%. vWF concentrations were expressed as percentages of normal pooled plasma, the antigenic concentration of which is defined as 100%. We used a carefully standardized procedure (23) for samples to be used for determination of the antigenic concentrations of PAI-1. The plasma PAI-1 concentration was determined by ELISA (Innotest PAI-1; Innogenetics). The intraassay CV was <10%; the detection limit was 2.5 µg/L.

other laboratory variables
Serum estradiol was measured using a RIA (Double Antibody; Diagnostic Products). The intra- and interassay CVs were both 5.9%; the lower limit of detection was 5 pmol/L. Serum FSH was measured using a microparticle enzyme immunoassay (IMx; Abbott Laboratories). The intra- and interassay CVs were 2.4% and 9.6%, respectively. Serum total cholesterol, HDL-cholesterol, and triglyceride concentrations were measured with enzymatic methods (Boehringer Mannheim). LDL-cholesterol was calculated by the Friedewald formula. Serum glucose was measured by a routine method. Finally, the serum insulin and C-reactive protein plasma concentrations were measured, both assayed in a single analytical run. The serum insulin was measured by a RIA (Biosource Diagnostics). The intraassay CV was 5%. The C-reactive protein plasmaconcentration was measured using an in-house ELISA, with rabbit anti-CRP (Dako) as the capture and tagging antibodies. The intraassay CV was <10%; the detection limit was 0.01 mg/L.

endothelium-(in)dependent vasodilatation
Measurements of FMD were performed after the subjects had refrained from smoking and from the use of caffeine-containing beverages for at least 4 h. We used a vessel wall movement detector system (Wall Track System; Neurodata), which consists of an ultrasound imager (Ultramark IV; ATL) connected to a data acquisition and processing unit. In M-mode (motion-mode), in which the vessel wall distension is repeatedly registered during a period of 5–6 s, the arterial diameter can be obtained with an accuracy of 0.1–0.2 mm. The baseline end-diastolic brachial artery diameter was measured after 15 min of rest in the supine position. Reactive hyperemia was induced by the release of a blood pressure tourniquet that had been inflated around the forearm for 4 min at a pressure of 100 mmHg above the systolic blood pressure. The brachial artery diameter was again measured between 45 and 60 s after the release of the cuff. After a period of 15 min, a second baseline measurement was performed. Endothelium-independent vasodilatation was measured 5 min after sublingual administration of 0.4 mg of nitroglycerin (NTG). Endothelium-(in)dependent vasodilatation was expressed as the percentage of increase of the arterial diameter from baseline. In our hands, the CVs for the measurements of baseline diameter and endothelium-dependent and -independent vasodilatation were 4.6%, 5.5%, and 7.7%, respectively (24).

statistical analysis
Data are presented as mean (SD) and range. In cases of skewed distribution, the geometric mean is presented. Pearson correlation analysis was used to describe the relationship between endothelium-(in)dependent vasodilatation and endothelium-derived regulatory proteins on the one hand and tHcy on the other. To study whether tHcy was independently associated with endothelial function parameters, we constructed univariate and multivariate models. Univariate analyses were used to study the relationship between the dependent variables (ET, vWF, PAI-1, FMD, and NTG-induced vasodilatation) and possible determinants thereof: tHcy, age, serum estradiol and FSH concentrations, smoking habits, alcohol use, variables of the insulin resistance syndrome (plasma concentrations of glucose and insulin, serum lipids, blood pressure, BMI, and WHR), and as an estimate of low-grade inflammatory state, the C-reactive protein concentration. For variables with a skewed distribution, the logarithmically transformed data were used. Variables that had a P value <0.15 in the univariate analyses were entered into a multivariate model. The residuals were checked for gaus-sian distribution and constancy of variance. All testing was two-tailed with 0.05 as the level of significance.


   Results
Top
 Abstract
 Introduction
 Subjects and Methods
 Results
Discussion
 References
 
The characteristics of the participants are shown in Table 1Up . The mean tHcy plasma concentration was 9.6 ± 2.5 µmol/L. Ten subjects (16%) had a tHcy concentration >=12 µmol/L, the cutoff value used in the European Concerted Action Project (1) to define an increased fasting tHcy concentration.

As Fig. 1 shows, tHcy was associated with ET (r = 0.25; P = 0.04) and tended to be associated with vWF (r = 0.22; P = 0.08) but was not associated with PAI-1, FMD, or NTG-induced vasodilatation (r = 0.17, -0.10, and -0.05, respectively). ET was associated with vWF (r = 0.30; P = 0.02); neither ET nor vWF were associated with PAI-1; FMD tended to be associated with NTG-induced vasodilatation (r = 0.23; P = 0.07). No association existed between the endothelium-derived regulatory proteins and endothelium-(in)dependent vasodilatation.



View larger version (12K):
[in this window]
[in a new window]
  		Figure 1. Relationship between the dependent variables ET (top), vWF (middle), and FMD (bottom), and the fasting tHcy concentration.

Univariate regression coefficients: r = 0.25, P = 0.04 for ET; r = 0.22, P = 0.08 for vWF; and r = -0.10, P = 0.45 for FMD.

Adjustment for possible confounders did not affect the association between the tHcy and ET plasma concentrations nor between the tHcy and vWF plasma concentra-tions (Table 2 A). A 5 µmol/L increase in tHcy was thus associated with an increase in ET of 0.4 ng/L (95% confidence interval, 0.01–0.85) and an increase in vWF of 20.8% (95% confidence interval, -0.2% to 41.8%).


View this table:
[in this window]
[in a new window]
  		Table 2. Multivariate regression analysis.1

PAI-1 was significantly associated with the BMI and WHR (both r = 0.49) and with the concentrations of insulin (r = 0.49), glucose (r = 0.26), serum total cholesterol (r = 0.43), triglycerides (r = 0.54), estradiol (r = 0.31), and FSH (r = -0.26), and C-reactive protein (r = 0.31) but not with tHcy. Substitution of the tissue-type plasminogen activator antigen concentration or the tissue-type plasminogen activator/PAI-1 ratio for the PAI-1 concentrations gave very similar results (data not shown).


   Discussion
Top
 Abstract
 Introduction
 Subjects and Methods
 Results
 Discussion
References
 
This is the first study that evaluates the association between increased tHcy and endothelial function parameters in healthy postmenopausal women. We found an independent, although rather weak, association between fasting plasma tHcy and ET as well as between fasting tHcy and vWF. A 5 µmol/L increase in plasma tHcy (1 SD in most populations) was associated with an increase of ~15–20% of these potential markers of endothelial dysfunction, which may not be trivial. No association existed between the fasting tHcy concentration on the one hand and the PAI-1 concentration or endothelium-dependent vasodilatation on the other hand.

Experimental evidence suggests that the propensity toward atherothrombosis associated with hyperhomocysteinemia results from endothelial dysfunction and injury followed by platelet activation and thrombus formation (14). There are no direct methods of measuring endothelial function in humans. Estimates of different types of endothelial (dys)function, however, may be obtained indirectly by measurement of plasma concentrations of endothelium-derived regulatory proteins and endothelium-dependent vasodilatation (25). In this study, we found a significant association between tHcy and ET that remained unchanged after adjustment for other vascular risk factors. A weak but independent association existed between tHcy and vWF.

The endothelins are a family of peptides that possess characteristically sustained vasoconstrictor properties (26). ET-1 is the predominant isoform and is produced mainly by endothelial cells. vWF is also produced mainly by endothelial cells and functions as a carrier protein for factor VIII procoagulant protein; it also enhances platelet adhesion to exposed extracellular matrix. PAI-1, on the other hand, is produced not only by endothelial cells, but also by adipocytes, hepatocytes, and vascular smooth muscle cells. By complex formation with tissue-type plasminogen activator, it functions as an essential antagonist of fibrinolysis. Increased concentrations of ET, vWF, and PAI-1 are present in diseases that involve the endothelium, such as atherosclerosis (27)(28), diabetic angiopathy (25), and vasculitis (29). Moreover, prospective studies have found increased concentrations of ET, vWF, and PAI-1 to be associated with an adverse cardiovascular outcome (15)(16)(17)(18)(19)(20).

Our results contrast somewhat with a recently published case-control study that found no difference in the plasma concentrations of endothelium-derived regulatory proteins between healthy subjects with and without mild hyperhomocysteinemia. In patients with peripheral arterial occlusive disease, however, that study did find higher vWF concentrations in hyperhomocysteinemic than in normohomocysteinemic subjects (30). Moreover, in hyperhomocysteinemic patients with peripheral arterial occlusive disease, 1 year of treatment with pyridoxine plus folic acid was associated not only with a decrease in tHcy but also a decrease in plasma vWF (31). Both studies were performed in young adults (<56 years) and defined hyperhomocysteinemia by an abnormal postmethionine tHcy concentration, which was not necessarily accompanied by an increased fasting tHcy concentrations. Taken together, these data and the present study suggest that increased tHcy concentrations may be a determinant of impaired endothelial function as reflected by increased ET and vWF.

We did not find any relationship between fasting tHcy and FMD of the brachial artery. Hyperemia-induced FMD is largely NO-mediated (32)(33). Most studies to date have suggested an adverse effect of homocysteine on NO activity and/or endothelium-dependent vasodilatation (12)(13)(34)(35)(36). Whether these studies are relevant to our results is not clear. Results of in vitro and animal studies (35)(36) cannot readily be extrapolated to the human situation. The studies performed in humans investigated subjects with either substantially higher tHcy concentrations (13)(34) than in our study or, as in the study by Tawakol et al. (12), investigated elderly subjects, many of whom had additional cardiovascular risk factors. In healthy siblings of patients with premature atherothrombotic disease, Lambert et al. (37) found FMD to be inversely associated with postmethionine tHcy concentrations but not with fasting tHcy concentrations.

There is increasing evidence that homocysteine-induced vascular dysfunction is mediated through oxidative mechanisms. Autooxidation of homocysteine generates several potent reactive oxygen species that may impair endothelial function (38). Whether homocysteine-induced oxidant stress is associated with increased synthesis of ET and vWF needs further investigation. Alternatively, tHcy may reduce NO-mediated inhibition of ET generation by reducing the bioavailability of NO. The latter, however, appears less likely because we did not find any relationship between the tHcy concentration and FMD, which is largely NO-mediated.

We performed a cross-sectional analysis. Therefore, it is obvious that we must interpret the results of our study with caution. Furthermore, we assessed only the fasting and not the postmethionine homocysteine concentration. However, both the fasting and postload tHcy concentrations are strong and independent predictors of vascular disease (1).

In summary, in a well-defined group of hysterectomized, but otherwise healthy, postmenopausal women, we demonstrated an independent, although rather weak, association between the fasting tHcy concentration and the plasma ET and vWF concentrations. We did not find a relationship between tHcy and endothelium-dependent vasodilatation. Our findings suggest that during postmenopause, which is associated with a rise in tHcy, an increased fasting homocysteine concentration may impair endothelial function to some extent. It is of clinical interest to study whether lowering the homocysteine concentration can improve endothelial function and thus reduce cardiovascular morbidity and mortality in postmenopausal women.


   Acknowledgments
 
Financial support for this study was supplied by the University Hospital Vrije Universiteit Amsterdam, The Netherlands and Eli Lilly Research Laboratories, Indianapolis, IN. We thank all patients and subjects who participated in this study. We thank A. Nicolaas-Merkus for coordinating the study, A. Kok for coordinating the laboratory procedures, P. Meijer for technical assistance and quality assurance, and M. Steyn for performance of the brachial artery measurements.


   Footnotes
 
From the project "Ageing Women":

1 Nonstandard abbreviations: tHcy, total plasma homocysteine; ET, endothelin; vWF, von Willebrand factor; PAI-1, plasminogen activator inhibitor type 1; FMD, flow-mediated, endothelium-dependent vasodilatation; FSH, follicle-stimulating hormone; BMI, body mass index; WHR, waist-to-hip ratio; and NTG, nitroglycerin.


   References
Top
 Abstract
 Introduction
 Subjects and Methods
 Results
 Discussion
 References
 

  1. Graham IM, Daly LE, Refsum HM, Robinson K, Brattstrom LE, Ueland PM, et al. Plasma homocysteine as a risk factor for vascular disease. The European Concerted Action Project. JAMA 1997;277:1775-1781. [Abstract/Free Full Text]
  2. den Heijer M, Koster T, Blom HJ, Bos GM, Briet E, Reitsma PH, et al. Hyperhomocysteinemia as a risk factor for deep-vein thrombosis. N Engl J Med 1996;334:759-762. [Abstract/Free Full Text]
  3. Boushey CJ, Beresford SAA, Omenn GS, Motulski AG. A quantitative assessment of plasma homocysteine as a risk factor for cardiovascular disease. Probably benefits of increasing folic acid intakes. JAMA 1995;274:1049-1057. [Abstract/Free Full Text]
  4. Giltay EJ, Hoogeveen EK, Elbers JM, Gooren LJ, Asscheman H, Stehouwer CD. Effects of sex steroids on plasma total homocysteine levels: a study in transsexual males and females. J Clin Endocrinol Metab 1998;83:550-553. [Abstract/Free Full Text]
  5. Nygard O, Vollset SE, Refsum H, Stensvold I, Tverdal A, Nordrehaug JE, et al. Total plasma homocysteine and cardiovascular risk profile. The Hordaland Homocysteine Study. JAMA 1995;274:1526-1533. [Abstract/Free Full Text]
  6. Blom HJ, Boers GH, van den Elzen JP, van Roessel JJ, Trijbels JM, Tangerman A. Differences between premenopausal women and young men in the transamination pathway of methionine catabolism, and the protection against vascular disease. Eur J Clin Investig 1988;18:633-638. [Web of Science][Medline] [Order article via Infotrieve]
  7. Andersson A, Hultberg B, Brattström L, Isaksson A. Decreased serum homocysteine in pregnancy. Eur J Clin Chem Clin Biochem 1992;30:377-379. [Web of Science][Medline] [Order article via Infotrieve]
  8. Wouters MGAJ, Moorrees MTEC, Van der Mooren MJ, Blom HJ, Boers FGHJ, Schellekens LA, et al. Plasma homocysteine and postmenopausal status. Eur J Clin Investig 1995;25:801-805. [Web of Science][Medline] [Order article via Infotrieve]
  9. Mijatovic V, Netelenbos C, van der Mooren MJ, de Valk-de Roo GW, Jakobs C, Kenemans P. Randomized, double-blind, placebo-controlled study of the effects of raloxifene and conjugated equine estrogen on plasma homocysteine levels in healthy postmenopausal women. Fertil Steril 1998;70:1085-1089. [Web of Science][Medline] [Order article via Infotrieve]
  10. Mijatovic V, Kenemans P, Jakobs C, van Baal WM, Peters-Muller ERA, van der Mooren MJ. A randomized controlled study of the effects of 17ß-oestradiol-dydrogesterone on plasma homocysteine in postmenopausal women. Obstet Gynecol 1998;91:432-436. [Web of Science][Medline] [Order article via Infotrieve]
  11. van der Mooren MJ, Demacker PNM, Blom HJ, De Rijke YB, Rolland R. The effects of sequential three monthly hormone replacement therapy on several cardiovascular risk estimators in postmenopausal women. Fertil Steril 1997;67:67-73. [Web of Science][Medline] [Order article via Infotrieve]
  12. Tawakol A, Omland T, Gerhard M, Wu JT, Creager MA. Hyperhomocyst(e)inemia is associated with impaired endothelium-dependent vasodilation in humans. Circulation 1997;95:1119-1121. [Abstract/Free Full Text]
  13. Woo KS, Chook P, Lolin YI, Cheung ASP, Chan LT, Sun YY, et al. Hyperhomocyst(e)inemia is a risk factor for arterial endothelial dysfunction in humans. Circulation 1997;96:2542-2544. [Abstract/Free Full Text]
  14. Welch GN, Loscalzo J. Homocysteine and atherothrombosis [Review]. N Engl J Med 1998;338:1042-1050. [Free Full Text]
  15. Thögersen AM, Jansson J, Boman K, Nilsson TK, Weinehall L, Huhtasaari F, et al. High plasminogen activator inhibitor and tissue plasminogen activator levels in plasma precede a first acute myocardial infarction in both men and women. Circulation 1998;98:2241-2247. [Abstract/Free Full Text]
  16. Blann AD, Miller JP, McCollum CN. von Willebrand factor and soluble E-selectin in the prediction of cardiovascular disease progression in hyperlipidaemia. Atherosclerosis 1997;132:151-156. [Web of Science][Medline] [Order article via Infotrieve]
  17. Juhan-Vague I, Pyke SDM, Alessi MC, Jespersen J, Haverkate F, Thompson SG. Fibrinolytic factors and the risk of myocardial infarction or sudden death in patients with angina pectoris. Circulation 1996;94:2057-2063. [Abstract/Free Full Text]
  18. Thompson SG, Kienast J, Pyke SD, Haverkate F, van de Loo JC. Hemostatic factors and the risk of myocardial infarction or sudden death in patients with angina pectoris. European Concerted Action on Thrombosis and Disabilities Angina Pectoris Study Group. N Engl J Med 1995;332:635-641. [Abstract/Free Full Text]
  19. Omland T, Lie RT, Aakvaag A, Aarsland T, Dickstein K. Plasma endothelin determination as a prognostic indicator of 1 year mortality after acute myocardial infarction. Circulation 1994;89:1573-1579. [Abstract/Free Full Text]
  20. Jansson JH, Nilsson TK, Johnson O. von Willebrand factor in plasma: a novel risk factor for recurrent myocardial infarction and death. Br Heart J 1991;66:351-355. [Abstract/Free Full Text]
  21. Ubbink JB, Vermaak WJH, Bissbort S. Rapid high performance liquid chromatographic assay for total homocysteine levels in human serum. J Chromatogr 1991;565:441-446. [Web of Science][Medline] [Order article via Infotrieve]
  22. Cejka J. Enzyme immunoassay for factor VIII related-antigen. Clin Chem 1982;28:1356-1358. [Abstract/Free Full Text]
  23. Kluft C, Meijer P. Update 1996: blood collection and handling procedures for assessment of plasminogen activators and inhibitors (Leiden Fibrinolysis Workshop). Fibrinolysis 1996;10:171-179. [Web of Science]
  24. Lambert J, Aarsen M, Donker AJM, Stehouwer CDA. Endothelium-dependent and -independent vasodilatation of large arteries in normoalbuminuric insulin-dependent diabetes mellitus. Arterioscler Thromb Vasc Biol 1996;16:705-711. [Abstract/Free Full Text]
  25. Stehouwer CDA, Lambert J, Donker AJM, Hinsbergh VWM. Endothelial dysfunction and pathogenesis of diabetic angiopathy. Cardiovasc Res 1997;34:55-68. [Abstract/Free Full Text]
  26. Yanagisawa M, Kurihawa H, Kimura S, Tomobe Y, Kobayashi M, Mitsui Y, et al. A novel potent vasoconstrictor peptide produced by vascular endothelial cells. Nature 1988;:411-415. [Abstract/Free Full Text]
  27. Cortellaro M, Cofrancesco E, Boschetti C, Mussoni L, Donati MB, Cardillo M, et al. Increased fibrin turnover and high PAI-1 activity as predictors of ischemic events in atherosclerotic patients. A case-control study. Arterioscler Thromb 1993;13:1412-1417.
  28. Lerman A, Edwards BS, Hallett JW, Heublein DM, Sandberg SM, Burnett JC, Jr. Circulating and tissue endothelin immunoreactivity in advanced atherosclerosis. N Engl J Med 1991;325:997-1001. [Abstract]
  29. Savage CO, Pottinger BE, Gaskin G, Lockwood CM, Pusey CD, Pearson JD. Vascular damage in Wegener's granulomatosis and microscopic polyarteritis: presence of anti-endothelial cell antibodies and their relation to anti-neutrophil cytoplasm antibodies. Clin Exp Immunol 1991;85:14-19. [Web of Science][Medline] [Order article via Infotrieve]
  30. de Jong SC, Stehouwer CDA, van den Berg M, Vischer UM, Rauwerda JA, Emeis JJ. Endothelial marker proteins in hyperhomocysteinemia. Thromb Haemost 1997;78:1332-1337. [Web of Science][Medline] [Order article via Infotrieve]
  31. van den Berg M, Boers GHJ, Franken DG, Blom HJ, van Kamp GJ, Jakobs C, et al. Hyperhomocysteinemia and endothelial dysfunction in young patients with peripheral arterial occlusive disease. Eur J Clin Investig 1995;25:176-181. [Web of Science][Medline] [Order article via Infotrieve]
  32. Meredith IT, Currie KE, Anderson TJ, Roddy MA, Ganz P, Creager MA. Postischemic vasodilation in human forearm is dependent on endothelium-derived nitric oxide. Am J Physiol 1996;270:H1435-H1440. [Abstract/Free Full Text]
  33. Joannides R, Haefeli WE, Linder L, Ricahrd V, Bakkali EH, Thuillez C, et al. Nitric oxide is responsible for flow-dependent dilatation of human peripheral conduit arteries in vivo. Circulation 1995;91:1314-1319. [Abstract/Free Full Text]
  34. Celermajer DS, Sorensen K, Ryalls M, Robinson J, Thomas O, Leonard JV, et al. Impaired endothelial function occurs in the systemic arteries of children with homozygous homocystinuria but not in their heterozygous parents. J Am Coll Cardiol 1993;22:854-858. [Abstract]
  35. Lentz SR, Sobey CG, Piegors DJ, Bhopatkar MY, Faraci FM, Malinov MR, et al. Vascular dysfunction in monkeys with diet-induced hyperhomocyst(e)inemia. J Clin Investig 1996;98:24-29. [Web of Science][Medline] [Order article via Infotrieve]
  36. Stamler JS, Osborne JA, Jaraki O, Rabbani LE, Mullins M, Singel D, et al. Adverse vascular effects of homocysteine are modulated by endothelium-derived relaxing factor and related oxides of nitrogen. J Clin Investig 1993;91:308-318.
  37. Lambert J, van den Berg M, Steyn M, Rauwerda JA, Donker AJM, Stehouwer CDA. Familial hyperhomocysteinaemia and endothelium-dependent vasodilation and arterial distensibility of large arteries. Cardiovasc Res 1999;in press..
  38. Loscalzo J. The oxidant stress of hyperhomocyst(e)inemia [Editorial]. J Clin Investig 1996;98:5-7. [Web of Science][Medline] [Order article via Infotrieve]



The following articles in journals at HighWire Press have cited this article:


Home page
 J. Am. Coll. Nutr.Home page
D. Tousoulis, C. Antoniades, K. Marinou, C. Vasiliadou, G. Bouras, E. Stefanadi, G. Latsios, G. Siasos, K. Toutouzas, and C. Stefanadis
Methionine-Loading Rapidly Impairs Endothelial Function, by Mechanisms Independent of Endothelin-1: Evidence for an Association of Fasting Total Homocysteine with Plasma Endothelin-1 Levels
J. Am. Coll. Nutr., June 1, 2008; 27(3): 379 - 386.
[Abstract] [Full Text] [PDF]

Home page
 Am. J. Physiol. Heart Circ. Physiol.Home page
J. D. Symons, J. C. Rutledge, U. Simonsen, and R. A. Pattathu
Vascular dysfunction produced by hyperhomocysteinemia is more severe in the presence of low folate
Am J Physiol Heart Circ Physiol, January 1, 2006; 290(1): H181 - H191.
[Abstract] [Full Text] [PDF]

Home page
 Arterioscler. Thromb. Vasc. Bio.Home page
A.M.W. Spijkerman, Y.M. Smulders, P.J. Kostense, R.M.A. Henry, A. Becker, T. Teerlink, C. Jakobs, J.M. Dekker, G. Nijpels, R.J. Heine, et al.
S-Adenosylmethionine and 5-Methyltetrahydrofolate Are Associated With Endothelial Function After Controlling for Confounding by Homocysteine: The Hoorn Study
Arterioscler Thromb Vasc Biol, April 1, 2005; 25(4): 778 - 784.
[Abstract] [Full Text] [PDF]

Home page
 Eur Heart JHome page
M. L. Bots, J. Westerink, T. J. Rabelink, and E. J.P. de Koning
Assessment of flow-mediated vasodilatation (FMD) of the brachial artery: effects of technical aspects of the FMD measurement on the FMD response
Eur. Heart J., February 2, 2005; 26(4): 363 - 368.
[Abstract] [Full Text] [PDF]

Home page
 Ann Rheum DisHome page
M C Lodder, W F Lems, H J Ader, A E Marthinsen, S C C M van Coeverden, P Lips, J C Netelenbos, B A C Dijkmans, and J C Roos
Reproducibility of bone mineral density measurement in daily practice
Ann Rheum Dis, March 1, 2004; 63(3): 285 - 289.
[Abstract] [Full Text] [PDF]

Home page
 LupusHome page
P R J Ames, A Margarita, J D. Alves, C Tommasino, L Iannaccone, and V Brancaccio
Anticardiolipin antibody titre and plasma homocysteine level independently predict intima media thickness of carotid arteries in subjects with idiopathic antiphospholipid antibodies
Lupus, April 1, 2002; 11(4): 208 - 214.
[Abstract] [PDF]

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Web of Science (22)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by de Valk-de Roo, G. W.
Right arrow Articles by Netelenbos, C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by de Valk-de Roo, G. W.
Right arrow Articles by Netelenbos, C.
Related Collections
Right arrow Clinical Immunology
Right arrow Nutrition
Right arrow Evidence Based Laboratory Medicine and Test Utilization
Right arrow Hemostasis and Thrombosis
Right arrow Proteomics and Protein Markers
Right arrow Lipids, Lipoproteins, and Cardiovascular Risk Factors
Right arrow Endocrinology and Metabolism

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS