Literature DB >> 2823606

Long-term intracaval calcium infusion therapy in end-organ resistance to 1,25-dihydroxyvitamin D.

Y Weisman1, I Bab, D Gazit, Z Spirer, M Jaffe, Z Hochberg.   

Abstract

Two boys aged six and four with the syndrome of hereditary resistance to 1,25-dihydroxyvitamin D3 with rickets alopecia and growth retardation are presented. After unsuccessful therapeutic trials with pharmacologic doses of vitamin D or its active metabolites, the patients were treated by long-term intracaval infusions of calcium through an implantable catheter. A total of 0.5 to 0.9 g of elemental calcium was infused daily for 18 months and the serum calcium concentration was maintained at 9 to 10 mg/dl. Bone pain subsided within one week of treatment. Serum phosphorus, immunoreactive parathyroid hormone, and 1,25-dihydroxyvitamin D concentrations and alkaline phosphatase activity were normalized within four to nine months. Radiographs of the knees and hands revealed progressive healing of rickets with complete resolution after one year of treatment. The patients gained 12 cm and 8 cm per year in height as compared with 3 cm and 2 cm, respectively, in the previous year. A transilial bone biopsy obtained from one patient prior to treatment revealed severe osteomalacia associated with osteitis fibrosa. A follow-up biopsy examined after 12 months of therapy showed almost complete healing of osteomalacia and normal mineralization. These observations indicate the following: (1) Long-term intracaval calcium infusions are an effective mode of therapy for these patients, and (2) When adequate serum calcium and phosphorus concentrations are maintained, healing of rickets and normal growth rate could be achieved even in the absence of a normal 1,25-dihydroxyvitamin D3 receptor-effector system.

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 2823606     DOI: 10.1016/0002-9343(87)90666-8

Source DB:  PubMed          Journal:  Am J Med        ISSN: 0002-9343            Impact factor:   4.965


  11 in total

1.  Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene.

Authors:  Vichit Supornsilchai; Yodporn Hiranras; Suttipong Wacharasindhu; Atchara Mahayosnond; Kanya Suphapeetiporn; Vorasuk Shotelersuk
Journal:  Endocrine       Date:  2011-03-18       Impact factor: 3.633

2.  Intra-atrial calcium infusions, growth, and development in end organ resistance to vitamin D.

Authors:  J P Lin; W S Uttley
Journal:  Arch Dis Child       Date:  1993-12       Impact factor: 3.791

3.  The molecular basis of hereditary 1,25-dihydroxyvitamin D3 resistant rickets in seven related families.

Authors:  P J Malloy; Z Hochberg; D Tiosano; J W Pike; M R Hughes; D Feldman
Journal:  J Clin Invest       Date:  1990-12       Impact factor: 14.808

4.  Hereditary vitamin D resistant rickets caused by a novel mutation in the vitamin D receptor that results in decreased affinity for hormone and cellular hyporesponsiveness.

Authors:  P J Malloy; T R Eccleshall; C Gross; L Van Maldergem; R Bouillon; D Feldman
Journal:  J Clin Invest       Date:  1997-01-15       Impact factor: 14.808

Review 5.  Genetic disorders and defects in vitamin d action.

Authors:  Peter J Malloy; David Feldman
Journal:  Endocrinol Metab Clin North Am       Date:  2010-06       Impact factor: 4.741

Review 6.  Use of calcimimetics in children with normal kidney function.

Authors:  Judith Sebestyen VanSickle; Tarak Srivastava; Uri S Alon
Journal:  Pediatr Nephrol       Date:  2018-03-19       Impact factor: 3.714

Review 7.  Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets.

Authors:  David Feldman; Peter J Malloy
Journal:  Bonekey Rep       Date:  2014-03-05

8.  Vitamin D dependent rickets type II with myelofibrosis and immune dysfunction.

Authors:  M M Walka; S Däumling; H B Hadorn; K Kruse; B H Belohradsky
Journal:  Eur J Pediatr       Date:  1991-07       Impact factor: 3.183

9.  Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor.

Authors:  Peter J Malloy; Jining Wang; Tarak Srivastava; David Feldman
Journal:  Mol Genet Metab       Date:  2010-01       Impact factor: 4.797

10.  Hereditary vitamin D resistant rickets: identification of a novel splice site mutation in the vitamin D receptor gene and successful treatment with oral calcium therapy.

Authors:  Nina S Ma; Peter J Malloy; Pisit Pitukcheewanont; Daina Dreimane; Mitchell E Geffner; David Feldman
Journal:  Bone       Date:  2009-06-10       Impact factor: 4.398

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.