Endocrinological and metabolic profile of Gaucher disease patients treated with enzyme replacement therapy

被引:2
|
作者
Kilic, Ayse [1 ,3 ]
Sanli, Merve Emecen [2 ,3 ]
Aktasoglu, Ekin Ozsaydi [3 ]
Gokalp, Sabire [3 ]
Biberoglu, Gursel [3 ]
Inci, Asli [3 ]
Okur, Ilyas [3 ]
Ezgu, Fatih Suheyl [3 ]
Tumer, Leyla [3 ]
机构
[1] Ankara Numune Training & Res Hosp, Dept Inborn Metab Dis, Talatpasa Bulvari 128,Zekai Tahir Burak Ek Binasi, TR-06230 Ankara, Turkiye
[2] Istanbul Medeniyet Univ, Goztepe Educ & Res Hosp, Dept Pediat, Div Inborn Errors Metab, Dr Erkin Cad, TR-34722 Istanbul, Turkiye
[3] Gazi Univ, Dept Pediat, Dept Inborn Metab Dis, Fac Med, Eminiyet Mahallesi,Mevlana Bulvari 29, TR-06560 Yenimahalle Ankara, Turkiye
来源
关键词
Gaucher disease; lysosomal storage diseases; endocrinology; insulin; thyroid; HIGH-DENSITY-LIPOPROTEIN; INSULIN-RESISTANCE; INSIGHTS; CYTOKINES; DISORDER; ALPHA;
D O I
10.1515/jpem-2023-0504
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives Gaucher Disease (GD) is a lysosomal storage disease caused by glucocerebrosidase (GCase) enzyme deficiency. Gaucher cells transformed from the macrophages by progressive sphingolipid accumulation and infiltrate bone marrow, spleen, liver, and other organs. The accumulation of substrate causes inflammation, compromised cellular homeostasis, and disturbed autophagy. It has been hypothesized that this proinflammatory state of GD leads cytokines and chemokines release. As a result of inflammatory process, the cellular dysfunction caused by disruption of cellular signaling, organelle dysfunction, or autoimmune antibodies may affect endocrine profile of GD patients such as hormone levels, lipid profile, and bone mineral density status. Methods A total of 13 patients confirmed to have GD, 12 non-neuronopathic type and one subacute neuronopathic type, were enrolled in our study. Results The median treatment duration in the enzyme therapy was 13.33 years (9-26 years). At least one endocrinological abnormality was detected in blood tests of nine patients. Hyperinsulinism was the most common finding although fasting blood glucose levels HgbA1c levels were normal in all patients. Two patients had osteopenia, and osteoporosis was detected in two patients. Low HDL levels were detected in six patients, but HDL levels below 23 mg/dL associated with disease severity have been detected in two patients who have not receiving enzyme replacement therapy. None of patients had thyroidal dysfunction. Conclusions This study had revealed endocrinological abnormalities in GD patients that have not led any severe morbidity in our patients. However, thyroid hormone abnormalities, insulin resistance, or lipid profile abnormalities may cause unpredictable comorbidities. Endocrinological assessment in GD patients in routine follow-up may prevent possible clinical manifestation in long term as well as can define efficacy of ERT on endocrine abnormalities.
引用
收藏
页码:413 / 418
页数:6
相关论文
共 50 条
  • [41] Enzyme replacement therapy and bony changes in Egyptian paediatric Gaucher disease patients
    El-Beshlawy, A
    Ragab, L
    Youssry, I
    Yakout, K
    El-Kiki, H
    Eid, K
    Mansour, IM
    Abd El-Hamid, S
    Yang, M
    Mistry, PK
    JOURNAL OF INHERITED METABOLIC DISEASE, 2006, 29 (01) : 92 - 98
  • [42] Enzyme replacement therapy with imiglucerase in Taiwanese patients with type I Gaucher disease
    Hsu, CC
    Chien, YH
    Lai, MY
    Hwu, WL
    JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION, 2002, 101 (09) : 627 - 631
  • [43] Velaglucerase alfa enzyme replacement therapy compared with imiglucerase in patients with Gaucher disease
    Ben Turkia, Hadhami
    Gonzalez, Derlis E.
    Barton, Norman W.
    Zimran, Ari
    Kabra, Madhulika
    Lukina, Elena A.
    Giraldo, Pilar
    Kisinovsky, Isaac
    Bavdekar, Ashish
    Ben Dridi, Marie-Francoise
    Gupta, Neerja
    Kishnani, Priya S.
    Sureshkumar, E. K.
    Wang, Nan
    Crombez, Eric
    Bhirangi, Kiran
    Mehta, Atul
    AMERICAN JOURNAL OF HEMATOLOGY, 2013, 88 (03) : 179 - 184
  • [44] Effects of enzyme replacement therapy in thirteen Japanese paediatric patients with Gaucher disease
    Ida, H
    Rennert, OM
    Kobayashi, M
    Eto, Y
    EUROPEAN JOURNAL OF PEDIATRICS, 2001, 160 (01) : 21 - 25
  • [45] Scintigraphic monitoring of enzyme replacement therapy in patients with Gaucher's disease.
    Lorberboym, M
    Pastores, G
    Kim, CK
    Hermann, G
    Glajchen, N
    Machac, J
    JOURNAL OF NUCLEAR MEDICINE, 1996, 37 (05) : 1325 - 1325
  • [46] Osteonecrosis in a patient with Gaucher's disease treated with enzyme replacement
    Lebel, E
    Elstein, D
    Hain, D
    Hadas-Halpern, I
    Zimran, A
    Itzchaki, M
    ISRAEL MEDICAL ASSOCIATION JOURNAL, 2003, 5 (08): : 595 - 596
  • [47] The efficacy of enzyme replacement therapy in patients with chronic neuronopathic Gaucher's disease
    Altarescu, G
    Hill, S
    Wiggs, E
    Jeffries, N
    Kreps, C
    Parker , CC
    Brady, RO
    Barton, NW
    Schiffmann, R
    Bannarjee, TK
    Crutchfield, K
    Frei, K
    McKee, MA
    Moore, DF
    Tournay, A
    JOURNAL OF PEDIATRICS, 2001, 138 (04): : 539 - 547
  • [48] Effects of enzyme replacement therapy in thirteen Japanese paediatric patients with Gaucher disease
    Hiroyuki Ida
    Owen M. Rennert
    Masahisa Kobayashi
    Yoshikatsu Eto
    European Journal of Pediatrics, 2001, 160 : 21 - 25
  • [49] Achievement of the goals of therapy for patients with Gaucher disease on enzyme replacement therapy is higher among earlier-treated patients and is not influenced by disease severity at presentation
    Symeonidis, A.
    Richfield, L.
    Miligan, A.
    Bruce, R.
    Hughes, D.
    Mehta, A.
    HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2007, 92 : 277 - 277
  • [50] Histologic Findings of Femoral Heads From Patients With Gaucher Disease Treated With Enzyme Replacement
    Lebel, Ehud
    Elstein, Deborah
    Peleg, Ariel
    Remus, Constantine
    Zimran, Ari
    Amir, Gail
    AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2013, 140 (01) : 91 - 96