Intensified treatment of hyperphosphatemia associated with reduction in parathyroid hormone in patients on maintenance hemodialysis. 2018

Lan Chen, and Jin-Xuan He, and Ying-Ying Chen, and Yi-Sheng Ling, and Chun-Hua Lin, and Tian-Jun Guan
a Department of Nephrology , Zhongshan Hospital, Xiamen University , Xiamen , Fujian , China.

BACKGROUND This study investigated the therapeutic effect of intensive phosphorus-lowering therapy on intact-parathyroid hormone (iPTH) levels in hemodialysis patients. METHODS Ninety-five hemodialysis patients with serum phosphorus ≥1.78 mmol/L and iPTH ≥300 pg/dL were apportioned to either the treatment or control group (n = 43 and 52, respectively) based on patient commitment to treatment. The treatment group was given phosphorus-lowering therapies with phosphate binders (lanthanum, sevelamer or/and calcium reagent) combined with dietary phosphate restriction and intensified hemodialysis. The control individuals were given low doses of calcium agents, if serum calcium was <2.54 mmol/L. Percent changes in serum phosphorus and iPTH levels were compared between the two groups. In addition, based on the time required to achieve >20% decrease in serum phosphorus, the patients in the treatment group were further stratified as rapid responders (≤2 months; 27 patients) or slow responders (>2 months; 16 patients) and percent changes in iPTH were compared. RESULTS Serum phosphorus and iPTH levels decreased from baseline in the treatment group (-24.08 ± 1.93% and -9.92 ± 3.70%, respectively) but increased in the control group (22.00 ± 3.63% and 104.21 ± 23.89%; both p < .001). In the rapid responders subgroup, the iPTH decreased (-16.93 ± 3.49%), but in the slow responders subgroup the iPTH increased slightly (0.68 ± 7.37%, p < .05). CONCLUSIONS For these patients on maintenance hemodialysis, intensive treatment of hyperphosphatemia was associated with a decrease in iPTH levels, especially for those who had achieved substantial reduction in serum phosphorus within 2 months.

UI MeSH Term Description Entries
D007676 Kidney Failure, Chronic The end-stage of CHRONIC RENAL INSUFFICIENCY. It is characterized by the severe irreversible kidney damage (as measured by the level of PROTEINURIA) and the reduction in GLOMERULAR FILTRATION RATE to less than 15 ml per min (Kidney Foundation: Kidney Disease Outcome Quality Initiative, 2002). These patients generally require HEMODIALYSIS or KIDNEY TRANSPLANTATION. ESRD,End-Stage Renal Disease,Renal Disease, End-Stage,Renal Failure, Chronic,Renal Failure, End-Stage,Chronic Kidney Failure,End-Stage Kidney Disease,Chronic Renal Failure,Disease, End-Stage Kidney,Disease, End-Stage Renal,End Stage Kidney Disease,End Stage Renal Disease,End-Stage Renal Failure,Kidney Disease, End-Stage,Renal Disease, End Stage,Renal Failure, End Stage
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D010281 Parathyroid Hormone A polypeptide hormone (84 amino acid residues) secreted by the PARATHYROID GLANDS which performs the essential role of maintaining intracellular CALCIUM levels in the body. Parathyroid hormone increases intracellular calcium by promoting the release of CALCIUM from BONE, increases the intestinal absorption of calcium, increases the renal tubular reabsorption of calcium, and increases the renal excretion of phosphates. Natpara,PTH (1-84),PTH(1-34),Parathormone,Parathyrin,Parathyroid Hormone (1-34),Parathyroid Hormone (1-84),Parathyroid Hormone Peptide (1-34),Hormone, Parathyroid
D010710 Phosphates Inorganic salts of phosphoric acid. Inorganic Phosphate,Phosphates, Inorganic,Inorganic Phosphates,Orthophosphate,Phosphate,Phosphate, Inorganic
D011446 Prospective Studies Observation of a population for a sufficient number of persons over a sufficient number of years to generate incidence or mortality rates subsequent to the selection of the study group. Prospective Study,Studies, Prospective,Study, Prospective
D002118 Calcium A basic element found in nearly all tissues. It is a member of the alkaline earth family of metals with the atomic symbol Ca, atomic number 20, and atomic weight 40. Calcium is the most abundant mineral in the body and combines with phosphorus to form calcium phosphate in the bones and teeth. It is essential for the normal functioning of nerves and muscles and plays a role in blood coagulation (as factor IV) and in many enzymatic processes. Coagulation Factor IV,Factor IV,Blood Coagulation Factor IV,Calcium-40,Calcium 40,Factor IV, Coagulation
D002614 Chelating Agents Chemicals that bind to and remove ions from solutions. Many chelating agents function through the formation of COORDINATION COMPLEXES with METALS. Chelating Agent,Chelator,Complexons,Metal Antagonists,Chelators,Metal Chelating Agents,Agent, Chelating,Agents, Chelating,Agents, Metal Chelating,Antagonists, Metal,Chelating Agents, Metal
D005260 Female Females
D006435 Renal Dialysis Therapy for the insufficient cleansing of the BLOOD by the kidneys based on dialysis and including hemodialysis, PERITONEAL DIALYSIS, and HEMODIAFILTRATION. Dialysis, Extracorporeal,Dialysis, Renal,Extracorporeal Dialysis,Hemodialysis,Dialyses, Extracorporeal,Dialyses, Renal,Extracorporeal Dialyses,Hemodialyses,Renal Dialyses

Related Publications

Lan Chen, and Jin-Xuan He, and Ying-Ying Chen, and Yi-Sheng Ling, and Chun-Hua Lin, and Tian-Jun Guan
June 2005, Kidney international. Supplement,
Lan Chen, and Jin-Xuan He, and Ying-Ying Chen, and Yi-Sheng Ling, and Chun-Hua Lin, and Tian-Jun Guan
December 2019, Clinical nutrition ESPEN,
Lan Chen, and Jin-Xuan He, and Ying-Ying Chen, and Yi-Sheng Ling, and Chun-Hua Lin, and Tian-Jun Guan
January 1986, Acta medica Iugoslavica,
Lan Chen, and Jin-Xuan He, and Ying-Ying Chen, and Yi-Sheng Ling, and Chun-Hua Lin, and Tian-Jun Guan
January 1986, Acta medica Iugoslavica,
Lan Chen, and Jin-Xuan He, and Ying-Ying Chen, and Yi-Sheng Ling, and Chun-Hua Lin, and Tian-Jun Guan
January 1985, Przeglad lekarski,
Lan Chen, and Jin-Xuan He, and Ying-Ying Chen, and Yi-Sheng Ling, and Chun-Hua Lin, and Tian-Jun Guan
October 2004, Anesthesia and analgesia,
Lan Chen, and Jin-Xuan He, and Ying-Ying Chen, and Yi-Sheng Ling, and Chun-Hua Lin, and Tian-Jun Guan
January 2010, Jornal brasileiro de nefrologia,
Lan Chen, and Jin-Xuan He, and Ying-Ying Chen, and Yi-Sheng Ling, and Chun-Hua Lin, and Tian-Jun Guan
March 1988, Experimental and clinical endocrinology,
Lan Chen, and Jin-Xuan He, and Ying-Ying Chen, and Yi-Sheng Ling, and Chun-Hua Lin, and Tian-Jun Guan
December 2005, Nephrologie & therapeutique,
Lan Chen, and Jin-Xuan He, and Ying-Ying Chen, and Yi-Sheng Ling, and Chun-Hua Lin, and Tian-Jun Guan
September 2004, Kidney international. Supplement,
Copied contents to your clipboard!