Reduction in daily hydrocortisone dose improves bone health in primary adrenal insufficiency

ObjectiveIndividuals with primary adrenal insufficiency (PAI) or congenital adrenal hyperplasia (CAH) receive life-long glucocorticoid (GC) replacement therapy. Current daily GC doses are still higher than the reported adrenal cortisol production rate. This GC excess could result in long-term morbid...

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Published inEuropean Journal of Endocrinology Vol. 174; no. 4; pp. 531 - 538
Main Authors Schulz, Julia, Frey, Kathrin R, Cooper, Mark S, Zopf, Kathrin, Ventz, Manfred, Diederich, Sven, Quinkler, Marcus
Format Journal Article
LanguageEnglish
Published England Bioscientifica Ltd 01.04.2016
Oxford University Press (OUP)
Subjects
Online AccessGet full text
ISSN0804-4643
1479-683X
DOI10.1530/EJE-15-1096

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Abstract ObjectiveIndividuals with primary adrenal insufficiency (PAI) or congenital adrenal hyperplasia (CAH) receive life-long glucocorticoid (GC) replacement therapy. Current daily GC doses are still higher than the reported adrenal cortisol production rate. This GC excess could result in long-term morbidities such as osteoporosis. No prospective trials have investigated the long-term effect of GC dose changes in PAI and CAH patients.MethodsThis is a prospective and longitudinal study including 57 subjects with PAI (42 women) and 33 with CAH (21 women). Bone mineral density (BMD) was measured by dual energy X-ray absorptiometry at baseline and after 2 years. Subjects were divided into three groups (similar baseline characteristics) depending on changes in daily hydrocortisone equivalent dose (group 1: unchanged 25.2±8.2 mg (mean±s.d., n=50); group 2: increased 18.7±10.3 to 25.9±12.0 mg (n=13); group 3: decreased 30.8±8.5 to 21.4±7.2 mg (n=27)).ResultsSubjects in group 1 showed normal lumbar and femoral Z-scores which were unchanged over time. Group 2 subjects showed a significant decrease in femoral neck Z-scores over time (−0.15±1.1 to −0.37±1.0 (P<0.05)), whereas group 3 subjects showed a significant increase in lumbar spine and hip Z-scores (L1–L4: −0.93±1.2 to –0.65±1.5 (P<0.05); total hip: −0.40±1.0 to −0.28±1.0 (P<0.05)). No changes in BMI over time were seen within any group. Reduction in GC dose did not increase the risk of adrenal crisis.ConclusionThis study demonstrates for the first time that cautious reduction in hydrocortisone equivalent doses leads to increases in BMD, whereas dose increments reduced BMD. These data emphasize the need for the lowest possible GC replacement dose in AI patients to maintain health and avoid long-term adverse effects.
AbstractList ObjectiveIndividuals with primary adrenal insufficiency (PAI) or congenital adrenal hyperplasia (CAH) receive life-long glucocorticoid (GC) replacement therapy. Current daily GC doses are still higher than the reported adrenal cortisol production rate. This GC excess could result in long-term morbidities such as osteoporosis. No prospective trials have investigated the long-term effect of GC dose changes in PAI and CAH patients.MethodsThis is a prospective and longitudinal study including 57 subjects with PAI (42 women) and 33 with CAH (21 women). Bone mineral density (BMD) was measured by dual energy X-ray absorptiometry at baseline and after 2 years. Subjects were divided into three groups (similar baseline characteristics) depending on changes in daily hydrocortisone equivalent dose (group 1: unchanged 25.2±8.2 mg (mean±s.d., n=50); group 2: increased 18.7±10.3 to 25.9±12.0 mg (n=13); group 3: decreased 30.8±8.5 to 21.4±7.2 mg (n=27)).ResultsSubjects in group 1 showed normal lumbar and femoral Z-scores which were unchanged over time. Group 2 subjects showed a significant decrease in femoral neck Z-scores over time (−0.15±1.1 to −0.37±1.0 (P<0.05)), whereas group 3 subjects showed a significant increase in lumbar spine and hip Z-scores (L1–L4: −0.93±1.2 to –0.65±1.5 (P<0.05); total hip: −0.40±1.0 to −0.28±1.0 (P<0.05)). No changes in BMI over time were seen within any group. Reduction in GC dose did not increase the risk of adrenal crisis.ConclusionThis study demonstrates for the first time that cautious reduction in hydrocortisone equivalent doses leads to increases in BMD, whereas dose increments reduced BMD. These data emphasize the need for the lowest possible GC replacement dose in AI patients to maintain health and avoid long-term adverse effects.
Individuals with primary adrenal insufficiency (PAI) or congenital adrenal hyperplasia (CAH) receive life-long glucocorticoid (GC) replacement therapy. Current daily GC doses are still higher than the reported adrenal cortisol production rate. This GC excess could result in long-term morbidities such as osteoporosis. No prospective trials have investigated the long-term effect of GC dose changes in PAI and CAH patients. This is a prospective and longitudinal study including 57 subjects with PAI (42 women) and 33 with CAH (21 women). Bone mineral density (BMD) was measured by dual energy X-ray absorptiometry at baseline and after 2 years. Subjects were divided into three groups (similar baseline characteristics) depending on changes in daily hydrocortisone equivalent dose (group 1: unchanged 25.2±8.2  mg (mean±S.D., n=50); group 2: increased 18.7±10.3 to 25.9±12.0  mg (n=13); group 3: decreased 30.8±8.5 to 21.4±7.2  mg (n=27)). Subjects in group 1 showed normal lumbar and femoral Z-scores which were unchanged over time. Group 2 subjects showed a significant decrease in femoral neck Z-scores over time (-0.15±1.1 to -0.37±1.0 (P<0.05)), whereas group 3 subjects showed a significant increase in lumbar spine and hip Z-scores (L1-L4: -0.93±1.2 to -0.65±1.5 (P<0.05); total hip: -0.40±1.0 to -0.28±1.0 (P<0.05)). No changes in BMI over time were seen within any group. Reduction in GC dose did not increase the risk of adrenal crisis. This study demonstrates for the first time that cautious reduction in hydrocortisone equivalent doses leads to increases in BMD, whereas dose increments reduced BMD. These data emphasize the need for the lowest possible GC replacement dose in AI patients to maintain health and avoid long-term adverse effects.
Author Zopf, Kathrin
Quinkler, Marcus
Frey, Kathrin R
Schulz, Julia
Ventz, Manfred
Cooper, Mark S
Diederich, Sven
Author_xml – sequence: 1
  givenname: Julia
  surname: Schulz
  fullname: Schulz, Julia
– sequence: 2
  givenname: Kathrin R
  surname: Frey
  fullname: Frey, Kathrin R
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  givenname: Mark S
  surname: Cooper
  fullname: Cooper, Mark S
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  givenname: Kathrin
  surname: Zopf
  fullname: Zopf, Kathrin
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  givenname: Manfred
  surname: Ventz
  fullname: Ventz, Manfred
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  givenname: Sven
  surname: Diederich
  fullname: Diederich, Sven
– sequence: 7
  givenname: Marcus
  surname: Quinkler
  fullname: Quinkler, Marcus
  email: marcus.quinkler@t-online.de
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https://www.ncbi.nlm.nih.gov/pubmed/26811406$$D View this record in MEDLINE/PubMed
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Snippet ObjectiveIndividuals with primary adrenal insufficiency (PAI) or congenital adrenal hyperplasia (CAH) receive life-long glucocorticoid (GC) replacement...
Individuals with primary adrenal insufficiency (PAI) or congenital adrenal hyperplasia (CAH) receive life-long glucocorticoid (GC) replacement therapy. Current...
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StartPage 531
SubjectTerms Addison Disease
Addison Disease - diagnostic imaging
Addison Disease - drug therapy
Addison Disease - metabolism
Adrenal Hyperplasia, Congenital
Adrenal Hyperplasia, Congenital - diagnostic imaging
Adrenal Hyperplasia, Congenital - drug therapy
Adrenal Hyperplasia, Congenital - metabolism
Adult
Bone and Bones
Bone and Bones - drug effects
Bone and Bones - metabolism
Bone Density
Bone Density - drug effects
Clinical Study
Dose-Response Relationship, Drug
Down-Regulation
Drug Administration Schedule
Female
Glucocorticoids
Glucocorticoids - administration & dosage
Glucocorticoids - adverse effects
Humans
Hydrocortisone
Hydrocortisone - blood
Longitudinal Studies
Male
Middle Aged
Radiography
Title Reduction in daily hydrocortisone dose improves bone health in primary adrenal insufficiency
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https://cir.nii.ac.jp/crid/1870583643204562560
https://www.ncbi.nlm.nih.gov/pubmed/26811406
Volume 174
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