Hypercalcemia in Patients with Williams-Beuren Syndrome
To evaluate the timing, trajectory, and implications of hypercalcemia in Williams-Beuren syndrome (WBS) through a multicenter retrospective study. Data on plasma calcium levels from 232 subjects with WBS aged 0-67.1 years were compared with that in controls and also with available normative data. As...
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Published in | The Journal of pediatrics Vol. 178; pp. 254 - 260.e4 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
Elsevier Inc
01.11.2016
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ISSN | 0022-3476 1097-6833 1097-6833 |
DOI | 10.1016/j.jpeds.2016.08.027 |
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Abstract | To evaluate the timing, trajectory, and implications of hypercalcemia in Williams-Beuren syndrome (WBS) through a multicenter retrospective study.
Data on plasma calcium levels from 232 subjects with WBS aged 0-67.1 years were compared with that in controls and also with available normative data. Association testing was used to identify relevant comorbidities.
On average, individuals with WBS had higher plasma calcium levels than controls, but 86.7% of values were normal. Nonpediatric laboratories overreport hypercalcemia in small children. When pediatric reference intervals were applied, the occurrence of hypercalcemia dropped by 51% in infants and by 38% in toddlers. Across all ages, 6.1% of the subjects had actionable hypercalcemia. In children, actionable hypercalcemia was seen in those aged 5-25 months. In older individuals, actionable hypercalcemia was often secondary to another disease process. Evidence of dehydration, hypercalciuria, and nephrocalcinosis were common in both groups. Future hypercalcemia could not be reliably predicted by screening calcium levels. A subgroup analysis of 91 subjects found no associations between hypercalcemia and cardiovascular disease, gastrointestinal complaints, or renal anomalies. Analyses of electrogradiography data showed an inverse correlation of calcium concentration with corrected QT interval, but no acute life-threatening events were reported.
Actionable hypercalcemia in patients with WBS occurs infrequently. Although irritability and lethargy were commonly reported, no mortality or acute life-threatening events were associated with hypercalcemia and the only statistically associated morbidities were dehydration, hypercalciuria, and nephrocalcinosis. |
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AbstractList | To evaluate the timing, trajectory, and implications of hypercalcemia in Williams-Beuren syndrome (WBS) through a multicenter retrospective study.
Data on plasma calcium levels from 232 subjects with WBS aged 0-67.1 years were compared with that in controls and also with available normative data. Association testing was used to identify relevant comorbidities.
On average, individuals with WBS had higher plasma calcium levels than controls, but 86.7% of values were normal. Nonpediatric laboratories overreport hypercalcemia in small children. When pediatric reference intervals were applied, the occurrence of hypercalcemia dropped by 51% in infants and by 38% in toddlers. Across all ages, 6.1% of the subjects had actionable hypercalcemia. In children, actionable hypercalcemia was seen in those aged 5-25 months. In older individuals, actionable hypercalcemia was often secondary to another disease process. Evidence of dehydration, hypercalciuria, and nephrocalcinosis were common in both groups. Future hypercalcemia could not be reliably predicted by screening calcium levels. A subgroup analysis of 91 subjects found no associations between hypercalcemia and cardiovascular disease, gastrointestinal complaints, or renal anomalies. Analyses of electrogradiography data showed an inverse correlation of calcium concentration with corrected QT interval, but no acute life-threatening events were reported.
Actionable hypercalcemia in patients with WBS occurs infrequently. Although irritability and lethargy were commonly reported, no mortality or acute life-threatening events were associated with hypercalcemia and the only statistically associated morbidities were dehydration, hypercalciuria, and nephrocalcinosis. Objective To evaluate the timing, trajectory, and implications of hypercalcemia in Williams-Beuren syndrome (WBS) through a multicenter retrospective study. Study design Data on plasma calcium levels from 232 subjects with WBS aged 0-67.1 years were compared with that in controls and also with available normative data. Association testing was used to identify relevant comorbidities. Results On average, individuals with WBS had higher plasma calcium levels than controls, but 86.7% of values were normal. Nonpediatric laboratories overreport hypercalcemia in small children. When pediatric reference intervals were applied, the occurrence of hypercalcemia dropped by 51% in infants and by 38% in toddlers. Across all ages, 6.1% of the subjects had actionable hypercalcemia. In children, actionable hypercalcemia was seen in those aged 5-25 months. In older individuals, actionable hypercalcemia was often secondary to another disease process. Evidence of dehydration, hypercalciuria, and nephrocalcinosis were common in both groups. Future hypercalcemia could not be reliably predicted by screening calcium levels. A subgroup analysis of 91 subjects found no associations between hypercalcemia and cardiovascular disease, gastrointestinal complaints, or renal anomalies. Analyses of electrogradiography data showed an inverse correlation of calcium concentration with corrected QT interval, but no acute life-threatening events were reported. Conclusions Actionable hypercalcemia in patients with WBS occurs infrequently. Although irritability and lethargy were commonly reported, no mortality or acute life-threatening events were associated with hypercalcemia and the only statistically associated morbidities were dehydration, hypercalciuria, and nephrocalcinosis. To evaluate the timing, trajectory, and implications of hypercalcemia in Williams-Beuren syndrome (WBS) through a multicenter retrospective study.OBJECTIVETo evaluate the timing, trajectory, and implications of hypercalcemia in Williams-Beuren syndrome (WBS) through a multicenter retrospective study.Data on plasma calcium levels from 232 subjects with WBS aged 0-67.1 years were compared with that in controls and also with available normative data. Association testing was used to identify relevant comorbidities.STUDY DESIGNData on plasma calcium levels from 232 subjects with WBS aged 0-67.1 years were compared with that in controls and also with available normative data. Association testing was used to identify relevant comorbidities.On average, individuals with WBS had higher plasma calcium levels than controls, but 86.7% of values were normal. Nonpediatric laboratories overreport hypercalcemia in small children. When pediatric reference intervals were applied, the occurrence of hypercalcemia dropped by 51% in infants and by 38% in toddlers. Across all ages, 6.1% of the subjects had actionable hypercalcemia. In children, actionable hypercalcemia was seen in those aged 5-25 months. In older individuals, actionable hypercalcemia was often secondary to another disease process. Evidence of dehydration, hypercalciuria, and nephrocalcinosis were common in both groups. Future hypercalcemia could not be reliably predicted by screening calcium levels. A subgroup analysis of 91 subjects found no associations between hypercalcemia and cardiovascular disease, gastrointestinal complaints, or renal anomalies. Analyses of electrogradiography data showed an inverse correlation of calcium concentration with corrected QT interval, but no acute life-threatening events were reported.RESULTSOn average, individuals with WBS had higher plasma calcium levels than controls, but 86.7% of values were normal. Nonpediatric laboratories overreport hypercalcemia in small children. When pediatric reference intervals were applied, the occurrence of hypercalcemia dropped by 51% in infants and by 38% in toddlers. Across all ages, 6.1% of the subjects had actionable hypercalcemia. In children, actionable hypercalcemia was seen in those aged 5-25 months. In older individuals, actionable hypercalcemia was often secondary to another disease process. Evidence of dehydration, hypercalciuria, and nephrocalcinosis were common in both groups. Future hypercalcemia could not be reliably predicted by screening calcium levels. A subgroup analysis of 91 subjects found no associations between hypercalcemia and cardiovascular disease, gastrointestinal complaints, or renal anomalies. Analyses of electrogradiography data showed an inverse correlation of calcium concentration with corrected QT interval, but no acute life-threatening events were reported.Actionable hypercalcemia in patients with WBS occurs infrequently. Although irritability and lethargy were commonly reported, no mortality or acute life-threatening events were associated with hypercalcemia and the only statistically associated morbidities were dehydration, hypercalciuria, and nephrocalcinosis.CONCLUSIONSActionable hypercalcemia in patients with WBS occurs infrequently. Although irritability and lethargy were commonly reported, no mortality or acute life-threatening events were associated with hypercalcemia and the only statistically associated morbidities were dehydration, hypercalciuria, and nephrocalcinosis. |
Author | Waxler, Jessica L. Elder, Robert W. Brink, Benjamin D. Lugo, Michael Levin, Mark D. Clark, Amy L. Dietzen, Dennis J. Sindhar, Sampat Danback, Joshua R. Yu, Eric Purgert, Carolyn A. Pober, Barbara R. Kozel, Beth A. |
AuthorAffiliation | 6 Harvard Medical School, Boston, MA 4 Massachusetts General Hospital, Boston, MA 5 Section of Cardiology, Departments of Pediatrics and Internal Medicine, Yale University School of Medicine, New Haven, CT 3 Frank H. Netter School of Medicine, Quinnipiac University, North Haven, CT 1 Department of Pediatrics, Washington University School of Medicine, St. Louis, MO 2 National Institutes of Health, National Heart, Lung, and Blood Institute, Bethesda, MD |
AuthorAffiliation_xml | – name: 3 Frank H. Netter School of Medicine, Quinnipiac University, North Haven, CT – name: 4 Massachusetts General Hospital, Boston, MA – name: 6 Harvard Medical School, Boston, MA – name: 5 Section of Cardiology, Departments of Pediatrics and Internal Medicine, Yale University School of Medicine, New Haven, CT – name: 1 Department of Pediatrics, Washington University School of Medicine, St. Louis, MO – name: 2 National Institutes of Health, National Heart, Lung, and Blood Institute, Bethesda, MD |
Author_xml | – sequence: 1 givenname: Sampat surname: Sindhar fullname: Sindhar, Sampat organization: Department of Pediatrics, Washington University School of Medicine, St. Louis, MO – sequence: 2 givenname: Michael surname: Lugo fullname: Lugo, Michael organization: Department of Pediatrics, Washington University School of Medicine, St. Louis, MO – sequence: 3 givenname: Mark D. surname: Levin fullname: Levin, Mark D. organization: National Institutes of Health, National Heart, Lung, and Blood Institute, Bethesda, MD – sequence: 4 givenname: Joshua R. surname: Danback fullname: Danback, Joshua R. organization: Department of Pediatrics, Washington University School of Medicine, St. Louis, MO – sequence: 5 givenname: Benjamin D. surname: Brink fullname: Brink, Benjamin D. organization: Frank H. Netter School of Medicine, Quinnipiac University, North Haven, CT – sequence: 6 givenname: Eric surname: Yu fullname: Yu, Eric organization: Frank H. Netter School of Medicine, Quinnipiac University, North Haven, CT – sequence: 7 givenname: Dennis J. surname: Dietzen fullname: Dietzen, Dennis J. organization: Department of Pediatrics, Washington University School of Medicine, St. Louis, MO – sequence: 8 givenname: Amy L. surname: Clark fullname: Clark, Amy L. organization: Department of Pediatrics, Washington University School of Medicine, St. Louis, MO – sequence: 9 givenname: Carolyn A. surname: Purgert fullname: Purgert, Carolyn A. organization: Department of Pediatrics, Washington University School of Medicine, St. Louis, MO – sequence: 10 givenname: Jessica L. surname: Waxler fullname: Waxler, Jessica L. organization: Massachusetts General Hospital, Boston, MA – sequence: 11 givenname: Robert W. surname: Elder fullname: Elder, Robert W. organization: Section of Cardiology, Departments of Pediatrics and Internal Medicine, Yale University School of Medicine, New Haven, CT – sequence: 12 givenname: Barbara R. surname: Pober fullname: Pober, Barbara R. organization: Frank H. Netter School of Medicine, Quinnipiac University, North Haven, CT – sequence: 13 givenname: Beth A. surname: Kozel fullname: Kozel, Beth A. email: beth.kozel@nih.gov organization: Department of Pediatrics, Washington University School of Medicine, St. Louis, MO |
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Snippet | To evaluate the timing, trajectory, and implications of hypercalcemia in Williams-Beuren syndrome (WBS) through a multicenter retrospective study.
Data on... Objective To evaluate the timing, trajectory, and implications of hypercalcemia in Williams-Beuren syndrome (WBS) through a multicenter retrospective study.... To evaluate the timing, trajectory, and implications of hypercalcemia in Williams-Beuren syndrome (WBS) through a multicenter retrospective study.OBJECTIVETo... |
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SubjectTerms | Adolescent Adult Aged calcium Calcium - blood Child Child, Preschool Female Humans Hypercalcemia - complications Hypercalcemia - epidemiology Infant Male Middle Aged not in the title: QTc pediatric reference intervals Pediatrics Retrospective Studies Williams Syndrome - complications Young Adult |
Title | Hypercalcemia in Patients with Williams-Beuren Syndrome |
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