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  1. Article ; Online: X-Linked Hypophosphatemia: A New Era in Management.

    Dahir, Kathryn / Roberts, Mary Scott / Krolczyk, Stan / Simmons, Jill H

    Journal of the Endocrine Society

    2020  Volume 4, Issue 12, Page(s) bvaa151

    Abstract: X-linked hypophosphatemia (XLH) is a rare, hereditary, progressive musculoskeletal disease that often causes pain and short stature, as well as decreased physical function, mobility, and quality of life. Hypophosphatemia in XLH is caused by loss of ... ...

    Abstract X-linked hypophosphatemia (XLH) is a rare, hereditary, progressive musculoskeletal disease that often causes pain and short stature, as well as decreased physical function, mobility, and quality of life. Hypophosphatemia in XLH is caused by loss of function mutations in the phosphate-regulating endopeptidase homolog X-linked (
    Language English
    Publishing date 2020-10-14
    Publishing country United States
    Document type Journal Article ; Review
    ISSN 2472-1972
    ISSN (online) 2472-1972
    DOI 10.1210/jendso/bvaa151
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Growth abnormalities in pediatric all survivors exposed to lower-dose cranial radiation therapy: the need for continued surveillance.

    Simmons, Jill H

    Pediatric blood & cancer

    2011  Volume 56, Issue 2, Page(s) 173–174

    MeSH term(s) Adolescent ; Child ; Child, Preschool ; Cranial Irradiation/adverse effects ; Growth/radiation effects ; Humans ; Neoplasms/radiotherapy ; Survivors
    Language English
    Publishing date 2011-02
    Publishing country United States
    Document type Comment ; Journal Article ; Review
    ZDB-ID 2131448-2
    ISSN 1545-5017 ; 1545-5009
    ISSN (online) 1545-5017
    ISSN 1545-5009
    DOI 10.1002/pbc.22848
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  3. Article ; Online: Impact of pediatric hypophosphatasia on behavioral health and quality of life.

    Pierpont, Elizabeth I / Simmons, Jill H / Spurlock, Katherine J / Shanley, Ryan / Sarafoglou, Kyriakie M

    Orphanet journal of rare diseases

    2021  Volume 16, Issue 1, Page(s) 80

    Abstract: Background: Hypophosphatasia (HPP) is a rare genetic disorder caused by loss-of-function mutations in the ALPL gene encoding tissue nonspecific alkaline phosphatase. It is characterized by defective bone mineralization associated with low alkaline ... ...

    Abstract Background: Hypophosphatasia (HPP) is a rare genetic disorder caused by loss-of-function mutations in the ALPL gene encoding tissue nonspecific alkaline phosphatase. It is characterized by defective bone mineralization associated with low alkaline phosphatase activity. Clinical features of pediatric HPP are highly variable, and can include premature loss of teeth, musculoskeletal problems, and impaired mobility. The effects of pediatric HPP on sleep, mood, regulation of attention and behavior, and other aspects of behavioral health have not been comprehensively studied.
    Methods: Parents of 30 children with HPP (14 females, 16 males) between the ages of 3 and 16 years (mean age = 8.0 years) enrolled in this cross-sectional survey-based study. Molecular genetic and biochemical testing as well as clinical records were reviewed to verify diagnosis of HPP. The cohort included 15 patients with a more clinically severe presentation of HPP who had received treatment with enzyme replacement therapy (asfotase alfa) and 15 children with less severe HPP who were treatment-naïve. Parents provided information regarding psychopathological comorbidity, emotional and behavioral well-being, and quality of life.
    Results: Clinically significant behavioral health challenges were evident in 67% of children with HPP. The most common behavioral findings included sleep disturbance and symptoms of attention deficit hyperactivity disorder (ADHD), each of which were observed ≥ 50% of individuals. Sleep disturbance, pain interference, poor behavioral regulation, and mood/anxiety symptoms were associated with reduced physical and psychosocial quality of life. Behavioral concerns were evident among children with HPP receiving asfotase alfa treatment as well as among children with clinically less severe disease who had not initiated therapy. Although most children in the cohort (77%) had age-typical development of adaptive skills, emotional and behavioral challenges were associated with weaker adaptive function.
    Conclusions: Children with HPP are at increased risk for ADHD symptoms and other behavioral health challenges. There is likely an under-recognition of these findings in clinical practice.
    MeSH term(s) Adolescent ; Alkaline Phosphatase/therapeutic use ; Child ; Child, Preschool ; Cross-Sectional Studies ; Enzyme Replacement Therapy ; Female ; Humans ; Hypophosphatasia/drug therapy ; Hypophosphatasia/genetics ; Male ; Quality of Life ; Surveys and Questionnaires
    Chemical Substances Alkaline Phosphatase (EC 3.1.3.1)
    Language English
    Publishing date 2021-02-12
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2225857-7
    ISSN 1750-1172 ; 1750-1172
    ISSN (online) 1750-1172
    ISSN 1750-1172
    DOI 10.1186/s13023-021-01722-7
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  4. Article ; Online: Dual X-ray absorptiometry has limited utility in detecting bone pathology in children with hypophosphatasia: A pooled post hoc analysis of asfotase alfa clinical trial data.

    Simmons, Jill H / Rush, Eric T / Petryk, Anna / Zhou, Shanggen / Martos-Moreno, Gabriel Á

    Bone

    2020  Volume 137, Page(s) 115413

    Abstract: Asfotase alfa is an enzyme replacement therapy approved for treatment of patients with pediatric-onset hypophosphatasia (HPP), a rare, inherited, systemic disease causing impaired skeletal mineralization, short stature, and reduced physical function in ... ...

    Abstract Asfotase alfa is an enzyme replacement therapy approved for treatment of patients with pediatric-onset hypophosphatasia (HPP), a rare, inherited, systemic disease causing impaired skeletal mineralization, short stature, and reduced physical function in children. The role of dual X-ray absorptiometry (DXA) in the assessment of children with HPP has been insufficiently explored. This post hoc analysis included pooled DXA data from 2 open-label, multicenter studies in 19 children with HPP. The study population was aged ≥5 to <18 years and had received asfotase alfa for ≤6.6 years at enrollment (male: 79%; median age at enrollment: 10.4 y [range: 5.9-16.7]; treatment duration: 6.3 y [range: 0.1-6.6]. Baseline height Z-scores indicated short stature (median [min, max]: -1.26 [-6.6, 0]); mean [SD]: -2.30 [1.97]), thus requiring height adjustment of DXA Z-scores. At Baseline, few patients had height-adjusted bone mineral density (BMD
    MeSH term(s) Absorptiometry, Photon ; Alkaline Phosphatase ; Bone Density ; Child ; Humans ; Hypophosphatasia/diagnostic imaging ; Hypophosphatasia/drug therapy ; Immunoglobulin G ; Male ; Recombinant Fusion Proteins
    Chemical Substances Immunoglobulin G ; Recombinant Fusion Proteins ; Alkaline Phosphatase (EC 3.1.3.1) ; asfotase alfa (Z633861EIM)
    Language English
    Publishing date 2020-05-14
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 632515-4
    ISSN 1873-2763 ; 8756-3282
    ISSN (online) 1873-2763
    ISSN 8756-3282
    DOI 10.1016/j.bone.2020.115413
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  5. Article ; Online: Failure to thrive, hyponatremia, and hyperkalemia in a neonate.

    Sopfe, Jenna / Simmons, Jill H

    Pediatric annals

    2013  Volume 42, Issue 5, Page(s) 74–79

    Abstract: CME EDUCATIONAL OBJECTIVES: 1.Describe the varying clinical presentations of pseudohypoaldosteronism in the neonatal period.2.Review the physiology of aldosterone production and pathophysiology of pseudohypoaldosteronism.3.Identify treatment options for ... ...

    Abstract CME EDUCATIONAL OBJECTIVES: 1.Describe the varying clinical presentations of pseudohypoaldosteronism in the neonatal period.2.Review the physiology of aldosterone production and pathophysiology of pseudohypoaldosteronism.3.Identify treatment options for pseudohypoaldosteronism when identified in the neonatal period. Pseudohypoaldosteronism type I (PHA1) is a rare disease of mineralocorticoid resistance caused by defects in sodium transport in the distal tubule of the kidney. It presents in the neonate with life-threatening dehydration due to salt wasting, accompanied by hyperkalemia, acidosis, and, frequently, failure to thrive. Patients with PHA1 are often initially diagnosed with congenital adrenal hyperplasia, but their electrolyte abnormalities are resistant to treatment with glucocorticoids and mineralocorticoids. In these patients, an astute clinician will broaden his or her differential, resulting in life-saving treatment.
    MeSH term(s) Aldosterone/physiology ; Diagnosis, Differential ; Failure to Thrive/complications ; Humans ; Hyperkalemia/complications ; Hyponatremia/complications ; Infant, Newborn ; Kidney/physiopathology ; Pseudohypoaldosteronism/diagnosis ; Pseudohypoaldosteronism/physiopathology
    Chemical Substances Aldosterone (4964P6T9RB)
    Language English
    Publishing date 2013-05
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 195430-1
    ISSN 1938-2359 ; 0090-4481
    ISSN (online) 1938-2359
    ISSN 0090-4481
    DOI 10.3928/00904481-20130426-09
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  6. Article ; Online: Burosumab vs conventional therapy in children with X-linked hypophosphatemia: results of the open-label, phase 3 extension period.

    Ward, Leanne M / Högler, Wolfgang / Glorieux, Francis H / Portale, Anthony A / Whyte, Michael P / Munns, Craig F / Nilsson, Ola / Simmons, Jill H / Padidela, Raja / Namba, Noriyuki / Cheong, Hae Il / Sochett, Etienne / Muroya, Koji / Tanaka, Hiroyuki / Pitukcheewanont, Pisit / Gottesman, Gary S / Biggin, Andrew / Perwad, Farzana / Chen, Angel /
    Lawrence Merritt Ii, John / Imel, Erik A

    JBMR plus

    2024  Volume 8, Issue 1, Page(s) ziad001

    Abstract: In a randomized, open-label phase 3 study of 61 children aged 1-12 years old with X-linked hypophosphatemia (XLH) previously treated with conventional therapy, changing to burosumab every 2 weeks (Q2W) for 64 weeks improved the phosphate metabolism, ... ...

    Abstract In a randomized, open-label phase 3 study of 61 children aged 1-12 years old with X-linked hypophosphatemia (XLH) previously treated with conventional therapy, changing to burosumab every 2 weeks (Q2W) for 64 weeks improved the phosphate metabolism, radiographic rickets, and growth compared with conventional therapy. In this open-label extension period (weeks 64-88), 21 children continued burosumab Q2W at the previous dose or crossed over from conventional therapy to burosumab starting at 0.8 mg/kg Q2W with continued clinical radiographic assessments through week 88. Efficacy endpoints and safety observations were summarized descriptively for both groups (burosumab continuation,
    Language English
    Publishing date 2024-01-04
    Publishing country England
    Document type Clinical Trial
    ISSN 2473-4039
    ISSN (online) 2473-4039
    DOI 10.1093/jbmrpl/ziad001
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  7. Article ; Online: Stress, Depression, and Quality of Life Among Caregivers of Children With Osteogenesis Imperfecta.

    Lazow, Margot A / Jaser, Sarah S / Cobry, Erin C / Garganta, Melissa D / Simmons, Jill H

    Journal of pediatric health care : official publication of National Association of Pediatric Nurse Associates & Practitioners

    2019  Volume 33, Issue 4, Page(s) 437–445

    Abstract: Introduction: The purpose of this study was to evaluate stress, depressive symptoms, and quality of life (QOL) among caregivers of children with osteogenesis imperfecta (OI) and to determine if associations exist with patient disease-related ... ...

    Abstract Introduction: The purpose of this study was to evaluate stress, depressive symptoms, and quality of life (QOL) among caregivers of children with osteogenesis imperfecta (OI) and to determine if associations exist with patient disease-related characteristics.
    Methods: Psychosocial outcomes were evaluated in 33 caregivers of 31 patients with OI using the Pediatric Inventory for Parents (assessing stress), PedsQL Family Impact Module (assessing QOL), and Center for Epidemiologic Studies Depression Scale (assessing depressive symptoms).
    Results: Higher levels of patient pain and lower patient physical functioning were significantly associated with both higher caregiver stress and poorer QOL (p < .05). Center for Epidemiologic Studies Depression Scale scores were not associated with patient pain or physical functioning.
    Discussion: Parents caring for children with OI with higher levels of pain and/or lower physical functioning are at higher risk of suffering from increased stress and poorer QOL. Interventions should be developed to screen for and target these at-risk caregiver groups with resources and support.
    MeSH term(s) Adolescent ; Adult ; Caregivers/psychology ; Caregivers/statistics & numerical data ; Child ; Child, Preschool ; Depression/epidemiology ; Depression/etiology ; Female ; Humans ; Male ; Middle Aged ; Osteogenesis Imperfecta/psychology ; Osteogenesis Imperfecta/therapy ; Parents/psychology ; Psychiatric Status Rating Scales ; Quality of Life/psychology ; Stress, Psychological/epidemiology ; Stress, Psychological/etiology ; Surveys and Questionnaires
    Language English
    Publishing date 2019-03-01
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1036356-7
    ISSN 1532-656X ; 0891-5245
    ISSN (online) 1532-656X
    ISSN 0891-5245
    DOI 10.1016/j.pedhc.2018.12.003
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  8. Article ; Online: Comorbidities increase COVID-19 hospitalization in young people with type 1 diabetes.

    Mann, Elizabeth A / Rompicherla, Saketh / Gallagher, Mary Pat / Alonso, Guy Todd / Fogel, Naomi R / Simmons, Jill / Wood, Jamie R / Wong, Jenise C / Noor, Nudrat / Gomez, Patricia / Daniels, Mark / Ebekozien, Osagie

    Pediatric diabetes

    2022  Volume 23, Issue 7, Page(s) 968–975

    Abstract: Objectives: We evaluated COVID-19 outcomes in children and young adults with type 1 diabetes (T1D) to determine if those with comorbidities are more likely to experience severe COVID-19 compared to those without.: Research design and methods: This ... ...

    Abstract Objectives: We evaluated COVID-19 outcomes in children and young adults with type 1 diabetes (T1D) to determine if those with comorbidities are more likely to experience severe COVID-19 compared to those without.
    Research design and methods: This cross-sectional study included questionnaire data on patients <25 years of age with established T1D and laboratory-confirmed COVID-19 from 52 sites across the US between April 2020 and October 2021. We examined patient factors and COVID-19 outcomes between those with and without comorbidities. Multivariate logistic regression analysis examined the odds of hospitalization among groups, adjusting for age, HbA1c, race and ethnicity, insurance type and duration of diabetes.
    Results: Six hundred fifty-one individuals with T1D and COVID-19 were analyzed with mean age 15.8 (SD 4.1) years. At least one comorbidity was present in 31%, and more than one in 10%. Obesity and asthma were the most frequently reported comorbidities, present in 19% and 17%, respectively. Hospitalization occurred in 17% of patients and 52% of hospitalized patients required ICU level care. Patients with at least one comorbidity were almost twice as likely to be hospitalized with COVID-19 than patients with no comorbidities (Odds ratio 2.0, 95% CI: 1.3-3.1). This relationship persisted after adjusting for age, HbA1c, race and ethnicity (minority vs nonminority), insurance type (public vs. private), and duration of diabetes.
    Conclusions: Our findings show that comorbidities increase the risk for hospitalization with COVID-19 in children and young adults highlighting the need for tailored COVID-19 prevention and treatment strategies in T1D.
    MeSH term(s) Adolescent ; COVID-19/epidemiology ; Child ; Comorbidity ; Cross-Sectional Studies ; Diabetes Mellitus, Type 1/complications ; Diabetes Mellitus, Type 1/epidemiology ; Diabetes Mellitus, Type 1/therapy ; Glycated Hemoglobin A ; Hospitalization ; Humans ; SARS-CoV-2 ; Young Adult
    Chemical Substances Glycated Hemoglobin A
    Language English
    Publishing date 2022-08-28
    Publishing country Denmark
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1502504-4
    ISSN 1399-5448 ; 1745-1426 ; 1399-543X
    ISSN (online) 1399-5448
    ISSN 1745-1426 ; 1399-543X
    DOI 10.1111/pedi.13402
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  9. Article ; Online: Phenotypic Profiling in Subjects Heterozygous for 1 of 2 Rare Variants in the Hypophosphatasia Gene (

    Tilden, Daniel R / Sheehan, Jonathan H / Newman, John H / Meiler, Jens / Capra, John A / Ramirez, Andrea / Simmons, Jill / Dahir, Kathryn

    Journal of the Endocrine Society

    2020  Volume 4, Issue 8, Page(s) bvaa084

    Abstract: Context: Hypophosphatasia (HPP) is a syndrome marked by low serum alkaline phosphatase (AlkP) activity as well as musculoskeletal and/or dental disease. While the majority of subjects with HPP carry a pathogenic variant in the : Methods: Through ... ...

    Abstract Context: Hypophosphatasia (HPP) is a syndrome marked by low serum alkaline phosphatase (AlkP) activity as well as musculoskeletal and/or dental disease. While the majority of subjects with HPP carry a pathogenic variant in the
    Methods: Through BioVU, a DNA biobank that pairs individuals' genetic information with their de-identified medical records, we identified subjects with 2 rare variants with distinct reported clinical phenotypes (p.D294A and p.T273M). We then performed a manual review of these subjects' de-identified medical records along with computational modeling of protein structure to construct a genetic, biochemical and clinical phenotype for each subject and variant.
    Results: Twenty subjects with the p.D294A variant and 17 with the p.T273M variant had sufficient data for analysis. Among subjects in our cohort with the p.D294A variant, 6 (30.0%) had both clinical bone disease and serum AlkP activity below 40 IU/L while 4 subjects (23.5%) with the p.T273M variant met the same criteria despite the distinct clinical phenotypes of these variants.
    Conclusions: Given the loose genotype/phenotype correlation in HPP seen in our cohort, clinical context is crucial for the interpretation of genetic test results to guide clinical care in this population. Otherwise, over- or under-diagnosis may occur, resulting in misidentification of those who may benefit from additional screening and perhaps pharmacologic intervention.
    Language English
    Publishing date 2020-06-28
    Publishing country United States
    Document type Journal Article
    ISSN 2472-1972
    ISSN (online) 2472-1972
    DOI 10.1210/jendso/bvaa084
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  10. Article ; Online: Characterization of physical, functional, and cognitive performance in 15 adults with hypophosphatasia.

    Durrough, Christina / Colazo, Juan M / Simmons, Jill / Hu, Jiun-Ruey / Hudson, Margaret / Black, Margo / de Riesthal, Michael / Dahir, Kathryn

    Bone

    2020  Volume 142, Page(s) 115695

    Abstract: Objective: Given the small but growing body of literature related to physical functioning and the scarce data related to fine motor and cognitive functioning in adults with hypophosphatasia (HPP), our objective was to characterize physical, functional, ... ...

    Abstract Objective: Given the small but growing body of literature related to physical functioning and the scarce data related to fine motor and cognitive functioning in adults with hypophosphatasia (HPP), our objective was to characterize physical, functional, and cognitive performance in adults with HPP. A future objective is to utilize this characterization to develop guidelines for evaluation by physical therapists (PT), occupational therapists (OT), and speech-language pathologists (SLP).
    Method: We evaluated physical, functional, and cognitive performance in 15 adults with HPP through standardized assessments of mobility, balance, fine motor control, activities of daily living, cognition, and self-reported measures of health-related quality of life, fatigue, depression, and anxiety. The median age at enrollment was 44 years (range 26-79 years). Among the participants, 11 (73%) were women. Five participants (33%) were on enzyme replacement therapy.
    Results: Compared with the general population, HPP participants traveled shorter distances on the Six-Minute Walk Test (420 m (m) [SD: 132] vs 620 m [SD: 49], p < 0.00005), had slower gait on the 10-Meter Walk Test [HPP men (3.71 ft/s (f/s) [SD: 0.77] vs 4.70 f/s [SD: 0.14], p < 0.00005) and HPP women (3.39 f/s [SD: 0.67] vs 4.56 f/s [SD: 0.09], p < 0.00005)]. HPP participants had decreased upper extremity (UE) dexterity by Nine Hole Peg Test [right UE in HPP men (22.7 s (s) [SD: 2.3] vs 19.0 s [SD: 3.9], p = 0.03), left UE in HPP men (23.3 s [SD: 0.7] vs 19.8 s [SD: 3.7], p = 0.03), right UE in HPP women (19.8 s [SD: 2.0] vs 17.7 s [SD: 3.2], p = 0.01), and left UE in HPP women (21.1 s [SD: 2.5] vs 18.9 s[SD: 3.4], p = 0.02)], and some had abnormally slow bilateral UE reaction times via Dynavision (0.9 s [0.85,0.96], functional speed <1.15 s). On the Short Form-36 (SF36), HPP patients reported worse energy/fatigue (30.4 [SD 22.7] vs 52.2 [SD: 22.4], p = 0.0001), social functioning (54.5 [SD: 34.2] vs 78.8 [SD: 25.5], p = 0.0002), pain (46.1 [SD: 27.3] vs 70.8 [SD: 25.5], p = 0.0001), general health (36.8 [SD: 24.0] vs 57.0 [SD: 21.1], p = 0.0002), and health change i.e. perception of health improvement (32.1 [SD: 15.3] vs 59.1 [SD: 23.1], p < 0.00005) than the general population. Fatigue Severity Scale scores were well above the median for a healthy population (5.21 [SD: 1.8] vs 2.3 [SD: 1.21], p < 0.00005), indicating significant fatigue. HPP participants had significantly higher DASS scores for depression (8.5 [SD: 6.5] vs 5.0 [SD: 7.5], p = 0.02), anxiety (7.9 [SD: 6.7] vs 3.4 [SD: 5.1], p = 0.00009), and stress (14.7 [SD: 12.4] vs 8.1 [SD: 8.4], p = 0.0003) compared to the general population.
    Conclusion: Objective functional assessments demonstrated defects in physical functioning, including decreased ability to walk distances, slow gait speed, and diminished ability to repeatedly rise from a sitting position. In addition, participants self-reported significant limitations due to physical dysfunction. Decreased upper extremity dexterity may indicate problems with activities of daily living and delayed reaction times can have safety implications. Some patients with HPP have increased difficulties with depression, anxiety, and stress. PT, OT, and SLP specialists can aid in establishing baseline assessment of impairment and objective metrics for assessing efficacy of treatment.
    MeSH term(s) Activities of Daily Living ; Adult ; Aged ; Cognition ; Female ; Humans ; Hypophosphatasia ; Male ; Middle Aged ; Quality of Life ; Walking
    Language English
    Publishing date 2020-10-16
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 632515-4
    ISSN 1873-2763 ; 8756-3282
    ISSN (online) 1873-2763
    ISSN 8756-3282
    DOI 10.1016/j.bone.2020.115695
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