Literature DB >> 33912912

Incidence of complications in 25 adult patients with X-linked hypophosphatemia.

Hajime Kato1, Minae Koga1, Yuka Kinoshita1, Yuki Taniguchi2, Hiroshi Kobayashi2, Seiji Fukumoto3, Masaomi Nangaku1, Noriko Makita1, Nobuaki Ito1.   

Abstract

CONTEXT: Adults with X-linked hypophosphatemia (XLH) present complications other than osteomalacia.
OBJECTIVE: To describe the incidence and severity of comorbidities in adults with XLH.
DESIGN: Observational retrospective study. PATIENTS: A total of 25 adults with XLH with thorough investigations, including spinal computed tomography scans, X-rays of hip/knee joints and Achilles tendons, abdominal ultrasounds and audiograms. MAIN OUTCOME MEASURES: The index of ossification of the anterior/posterior longitudinal ligament and yellow ligament (OA/OP/OY index) and the sum of OA/OP/OY index (OS index) were utilized to evaluate the severity of spinal ligament ossification. The Kellgren-Lawrence (KL) classification was adopted to evaluate the severity of the hip/knee osteophytes.
RESULTS: The participants consisted of 13 male patients and 12 female patients from 21 families, with a median age of 43 (range, 18-72) years. In all, 20 patients (80%) showed spinal ligament ossification. The median OA/OP/OY/OS indices were 2 (0-22), 0 (0-15), 6 (0-13) and 12 (0-41), respectively. Hip/knee osteophytes were reported in 24 (96%) and 17 cases (68%). The median KL grade was 3 in the hip joint and 2 in the knee joint, and 18 cases (72%) developed enthesopathy in the Achilles tendon. Nephrocalcinosis and hearing impairment were observed in 18 (72%) and eight (32%) cases.
CONCLUSION: This study revealed a high prevalence and severity of ectopic ossification and disclosed the incidence of nephrocalcinosis and hearing impairment in adults with XLH. In cases with severe spinal ligament ossification or noticeable osteophytes around the hip/knee joints, undiagnosed XLH should be considered as a possible underlying condition.
© The Author(s) 2021. Published by Oxford University Press on behalf of the Endocrine Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  X-linked hypophosphatemia; enthesopathy; fibroblast growth factor 23; ossification of posterior longitudinal ligament; osteophyte

Year:  2021        PMID: 33912912     DOI: 10.1210/clinem/dgab282

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  4 in total

1.  X-linked hypophosphatemia, obesity and arterial hypertension: data from the XLH21 study.

Authors:  Louisa Bloudeau; Agnès Linglart; Sacha Flammier; Aurélie Portefaix; Aurélia Bertholet-Thomas; Sanaa Eddiry; Anna Barosi; Jean-Pierre Salles; Valérie Porquet-Bordes; Anya Rothenbuhler; Christelle Roger; Justine Bacchetta
Journal:  Pediatr Nephrol       Date:  2022-06-27       Impact factor: 3.714

2.  Identification of ENPP1 Haploinsufficiency in Patients With Diffuse Idiopathic Skeletal Hyperostosis and Early-Onset Osteoporosis.

Authors:  Hajime Kato; Anenya J Ansh; Ethan R Lester; Yuka Kinoshita; Naoko Hidaka; Yoshitomo Hoshino; Minae Koga; Yuki Taniguchi; Taisuke Uchida; Hideki Yamaguchi; Yo Niida; Masamitsu Nakazato; Masaomi Nangaku; Noriko Makita; Toshinari Takamura; Taku Saito; Demetrios T Braddock; Nobuaki Ito
Journal:  J Bone Miner Res       Date:  2022-04-11       Impact factor: 6.390

3.  Lower Limb Deformity and Gait Deviations Among Adolescents and Adults With X-Linked Hypophosphatemia.

Authors:  Gabriel T Mindler; Andreas Kranzl; Alexandra Stauffer; Roland Kocijan; Rudolf Ganger; Christof Radler; Gabriele Haeusler; Adalbert Raimann
Journal:  Front Endocrinol (Lausanne)       Date:  2021-09-27       Impact factor: 5.555

4.  Clinical and genetic characteristics of 29 Chinese patients with X-linked hypophosphatemia.

Authors:  Tian Xu; Xiaohui Tao; Zhenlin Zhang; Hua Yue
Journal:  Front Endocrinol (Lausanne)       Date:  2022-08-19       Impact factor: 6.055

  4 in total

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