eISSN: 1896-9151
ISSN: 1734-1922
Archives of Medical Science
Current issue Archive Special issues Subscription
SCImago Journal & Country Rank

vol. 2

Pulmonary artery pressure in association with serum parathormone in maintenance hemodialysis patients

Hamid Nasri

Arch Med Sci 2006; 2, 1: 32-35
Online publish date: 2006/03/23
Article file
- Pulmonary artery.pdf  [0.06 MB]
Get citation
JabRef, Mendeley
Papers, Reference Manager, RefWorks, Zotero
Cardiovascular disease (CVD) remains the main cause of morbidity and mortality in patients with end-stage renal disease (ESRD) [1, 2]. Left ventricular hypertrophy (LVH), interstitial myocardial fibrosis, arteriolar wall thickening and coronary artery calcification are hallmarks of this disorder [3, 4]. Although traditional risk factors such as diabetes mellitus, hypertension, dyslipidemia and advanced age, are prevalent in ESRD patients, they may not be sufficient by themselves to account for the high prevalence of CVD in patients with this condition [1]. Thus the search for other non-traditional risk factors that may be involved in the pathogenesis of uremic CVD has been an area of intense study [1, 5]. There is growing evidence to suggest that abnormalities in serum parathyroid hormone (PTH) levels are resulting in vascular and visceral calcification leading to an increased risk of cardiovascular morbidity and mortality in these patients [6, 7]. Secondary hyperparathyroidism is often found to be an independent risk factor for uremic calcification. Serum PTH contributes to cardiovascular complications in many ways [6, 8]. It has a permissive role in arteriolar wall thickening, myocardial interstitial fibrosis [9] promoting hyperlipidemia and hypertension [10-12]. It was suggested that the abnormalities in right ventricular function in patients with end-stage renal disease (ESRD) are in largely due to pulmonary hypertension (PH) which may develop secondary to ESRD [13, 14]. There are several potential explanations for the development of PH in patients with ESRD, hormonal and metabolic derangement associated with ESRD might lead to pulmonary arterial vasoconstriction and an increase of the pulmonary vascular resistance [13, 7]. The parathyroid hormone is known to enhance the entry of calcium into many cells, chronic exposure to excess blood levels of PTH is associated with increased calcium content of many tissues [4, 7, 13]. Cardiovascular cells (cardiomyocytes and smooth muscle cells) are target cells for the parathyroid hormone [7, 15]. In addition to the cardiovascular effects of secondary hyperparathyroidism (SHPTH), it has been shown that high serum parathormone is associated with an increased incidence of hypertension [7, 16]. Therefore, it is possible that SHPTH in hemodialysis patients may also have some effects to increase the pulmonary artery pressure. Studies concerning the effect of high serum PTH on the pulmonary artery systolic pressure (PAP) increment are scarce and controversial, we therefore aimed to consider the association of serum parathormone with PAP in ESRD patients who are undergoing regular hemodialysis treatment.

Material and methods
This is a cross-sectional study conducted on patients with end-stage renal disease undergoing maintenance hemodialysis treatment through an arteriovenous fistula which was created on the hand, and with acetate basis dialysate and polysulfone membranes. The study was carried-out in the hemodialysis section of Hajar Medical Educational & Therapeutic Center of Shahrekord University of Medical Sciences in Shahrekord of Iran. Blood samples were collected after an overnight fast. In all patients serum intact parathormone (iPTH) was determined by the radio-immuno assay (RIA) method using DSL-8000 kits of the USA (normal range of values is 10-65 pg/ml). The patients were under hemodialysis (HD) for two or three times per week. Exclusion criteria were past history of chronic obstructive lung disease (COPD), multiple lung infections, cigarette smoking, history of cough, allergy, asthma, using drugs affects pulmonary function or structure, chest wall or parenchymal lung disease, previous pulmonary embolism, systemic lupus erythmatosous, left-to-right shunt, and significant mitral or aortic valve disease and also any other past history of lung disease and also any lung abnormality on the chest x-ray. According to the severity of secondary hyperparathyroidism, each patient being treated for secondary hyperparathyroidism (SHPTH) was given oral active vitamin D3 (Rocaltrol), calcium carbonate capsule, and Rena-Gel tablets at various doses. After their hemodialysis session, the patients were subjected to two-dimensional and doppler echocardiographic studies. Systolic right ventricular (or pulmonary artery) pressure was calculated using the Bernoulli equation (p=4 v2, where p is the pressure drop [mmHg] and v is the velocity of blood flow [m/sec]), the pressure in the RV can be calculated by RV pressure = RA pressure + (4 x [TR jet velocity]2) [17, 18]. All echocardiographic studies were done by a single cardiologist. Pulmonary hypertension (PH) was defined as a systolic PAP greater than or equal to 35 mmHg [14, 17, 18]. Duration and doses of hemodialysis treatment were calculated from patient’s records and the duration of each hemodialysis session was four hours. For 3 years before the study, the polysulfone membranes had been used in our hemodialysis center. For the statistical analysis descriptive data are expressed as mean ±SD. A comparison between groups was considered using the students’ t test. For correlations the partial correlation test was used. All statistical analysis was performed using the SPSS (version 11.5.00). The statistical analysis was considered significant when p<0.05.

The total patients were 102 (F=46, M=56) under hemodialysis due to end-stage renal disease (ESRD) consisting of 73 non diabetic hemodialysis patients (F=33, M=40), and 29 diabetic hemodialysis patients (F=13, M=16). Table I shows the mean ±SD of age, the length of the time patients had been on hemodialysis, dialysis dosage and serum values of iPTH. The mean ±SD of age of total patients were 51±17.6 years. The length of the time patients had been on hemodialysis were 17.8±29 months. Mean ±SD of serum iPTH of total patients were 338±306 pg/ml. Mean ±SD of iPTH of diabetic group and nondiabetic group were 272±237 pg/ml and 364±327 pg/ml respectively. Mean ±SD of pulmonary artery systolic pressure (PAP) of total HD patients, diabetic HD group and non diabetic hemodialysis were 41.5±12.6, 45±9.8 and 40±18 mmHg respectively. In this study no significant difference of serum iPTH between diabetics and nondiabetic hemodialysis patients was found (p NS). A significant positive correlation of PAP with dosage (r=0.36, p=0.001) and duration of hemodialysis (r=0.35, p<0.001) (data adjusted for ages of patients for two above correlations) were seen. A significant positive correlation of pulmonary artery systolic pressure with serum intact parathormone (iPTH) in hemodialysis patients was found (r=0.20, p=0.040; Figure 1) (data adjusted for ages of patients).

In this study, significant positive correlations of PAP with hemodialysis duration and dosage were seen, also a significant positive correlation of pulmonary artery systolic pressure with serum intact parathormone was found, too. Studies regarding the prevalence and the predictors of pulmonary hypertension (PH) in patients with end-stage renal failure undergoing regular hemodialysis are quite scarce. Yigla et al. in a study on 58 patients with ESRD receiving long-term hemodialysis and on control groups of 5 patients receiving peritoneal dialysis (PD) and 12 predialysis patients, found a 39.7% of pulmonary hypertension in patients who where under hemodialysis, (mean ±SD =44±7 mmHg; range, 37 to 65 mmHg) [14]. Amin et al. in a study on 51 patients (28 men and 23 women) with end-stage renal disease, who were receiving regular hemodialysis PH was detected in 15 patients (29%), this study showed women had a higher prevalence of PH (48% vs 14%), moreover in this study there were no significant differences between patients with PH and those without PH with regard to age, duration of dialysis, serum calcium, phosphorus, alkaline phosphatase, parathyroid hormone (PTH) or the prevalence of an abnormal (99m)Tc diphosphate lung scan result (60% vs 73%, respectively). They showed that 29% of patients with ESRD receiving regular hemodialysis have PH and the presence of PH was not related to the level of PTH or the severity of other metabolic abnormalities, also there was no relation between PH and the presence or the severity of pulmonary artery calcification. They also found that PH is detected more frequently in women. Their study does not support a role for secondary hyperparathyroidism as one of the etiologies of PH in patients with ESRD [19]. Yigla also in an another study evaluated the role of pulmonary calcification in the pathogenesis of PH in patients with ESRD who receiving chronic HD therapy by an A-V access. To consider the correlation between pulmonary calcification expressed by lung uptake of 99mTc-MDP and PH, selected 36 men and 13 women with a mean age of 61.7±13.2 years receiving HD therapy for 38.2±43 months. Yigla concluded that pulmonary calcification has no role in the pathogenesis of PH among ESRD patients undergoing hemodialysis therapy [20]. Our study is in agreement with previous two studies in which ESRD patients under regular hemodialysis had pulmonary hypertension. In contrast to the Amin’s study, only our female diabetic hemodialysis patients had PAP more than male diabetic patients. In contrast to the above mentioned studies we could show a significant positive correlation of serum iPTH with pulmonary artery pressure. The influence of high serum parathormone hormone concentration on pulmonary pressure may be through an increasing calcium content of the smooth muscle cells of the artery [4, 7, 13]. Previously we shown that high serum parathormone is associated with an increased incidence of systemic hypertension in stable hemodialysis patients [7]. Indeed, the parathyroid hormone is known to enhance the entry of calcium into many cells, chronic exposure to excess blood levels of PTH is associated with increased calcium content of many tissues [4, 7, 13].

In conclusion, a positive association of high serum parathormone and pulmonary artery pressure is very important because pulmonary hypertension is a disease with poor prognosis and implies the need for a better control of secondary hyperparathyroidism in hemodialysis patientsm through controlling of hyperphosphatemia.
We would like to thank Dr. B. Amra, Pulmonologist, and Associate professor of Isfahan University of Medical Sciences for his very useful comments and from Dr. F. Roghani cardiologist of our hospital for cardiac graphies.

1. Yao Q, Pecoits-Filho R, Lindholm B, Stenvinkel P. Traditional and non-traditional risk factors as contributors to atherosclerotic cardiovascular disease in end-stage renal disease. Scand J Urol Nephrol 2004; 38: 405-16. 2. Baradaran A. Nasri H. Effect of anemia on left ventricular hypertrophy and ejection fraction in maintenance hemodialysis patients. J Biol Sci (Faisalabad) 2005; 8: 1623-7. 3. Urso S, Garozzo M, Milone F, Battaglia G. Cardiovascular risk markers in hemodialysis patients. Int J Artif Organs 2004; 27: 1083-90. 4. Nasri H, Baradaran A, Naderi AS. Close association between parathyroid hormone and left ventricular function and structure in end-stage renal failure patients under maintenance hemodialysis. Acta Med Austriaca 2004; 31: 67-72. 5. Nasri H, Baradaran A. B-mode ultrasonography of carotid and femoral arteries for calcified plaques in chronic renal failure, hemodialysis and kidney transplant patients. Hong Kong Journal of Nephrology 2004; 6, 2. 6. Nasri H. Baradaran A. Long-lasting advanced primary hyperparathyroidism associated with end-stage renal failure in a diabetic patient. Acta Med Iran 42; 461-6. 7. Baradaran A. Nasri H. Correlation of serum parathormone with hypertension in chronic renal failure patients treated with hemodialysis. Saudi Journal of Renal Disease and Transplatation 2005; 16: 288-92. 8. Geoffrey AB, Friedrich KP. Re-evaluation of risks associated with hyperphosphataemia and hyperparathyroidism in dialysis patients: recommendations for a change in management. Am J Kid Dis 2000; 35: 1226-37. 9. Wessels S, Amman K, Tornig J, Ritz E. Cardiovascular structural changes in uremia: Implications for cardiovascular function. Semin Dial 1999; 12: 288-92. 10. Foley RN, Parfrey PS, Sarnak MJ. Clinical epidemiology of cardiovascular disease in chronic renal disease. Am J Kidney Dis 1998; 32 (5 Suppl 3): S112-9. 11. Nishizawa Y, Shoji T, Kawagishi T, Morii H. Atherosclerosis in uremia: possible roles of hyperparathyroidism and intermediate density lipoprotein accumulation. Kidney Int Suppl 1997; 62: S90-2. 12. Nasri H, Baradaran A. Strong inverse association of serum parathormone with plasma HCO3 in female hemodialysis patients. Pakistan Journal of Nutrition 2005; 6: 409-13. 13. Yigla M, Nakhoul F, Sabag A, Tov N, Gorevich B, et al. Pulmonary hypertension in patients with end-stage renal disease. Chest 2003; 123: 1577-82. 14. Nasri H, Shirani S, Baradaran A. Pulmonary artery pressure in maintenance hemodialysis patients. Pakistan Journal of Biological Sciences 2006; 9: 107-10. 15. Schluter KD, Piper HM. Cardiovascular actions of parathyroid hormone and parathyroid hormone-related peptide. Cardiovasc Res 1998; 37: 34-41. 16. Chadwick DR, Harrison BJ, Chan P, Chong L, Peachell P. Vasoactive and proliferative effects of parathyroid hormone and parathyroid hormone-related peptide on human vascular smooth muscle. Br J Surg 2000; 87: 1529-33. 17. Chazova IE, Kolos IP, Dzemeshkevich SL, Samko AN, Lepilin MG, et al. Staroverov II. Prolonged pulmonary artery pressure monitoring in patients with pulmonary hypertension. Kardiologiia 2002; 42: 42-6. 18. Marangoni S, Quadri A, Dotti A, Scalvini S, Volterrani M, et al. Noninvasive assessment of pulmonary hypertension: a simultaneous echo-Doppler hemodynamic study. Cardiology 1988; 75: 401-8. 19. Amin M, Fawzy A, Hamid MA, Elhendy A. Pulmonary hypertension in patients with chronic renal failure: role of parathyroid hormone and pulmonary artery calcifications. Chest 2003; 124: 2093-7. 20. Yigla M, Keidar Z, Safadi I, Tov N, Reisner SA, et al. Pulmonary calcification in hemodialysis patients: correlation with pulmonary artery pressure values. Kidney Int 2004; 66: 806-10.
Copyright: © 2006 Termedia & Banach. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
Quick links
© 2021 Termedia Sp. z o.o. All rights reserved.
Developed by Bentus.
PayU - płatności internetowe