Subclinical renal abnormalities in young thalassemia major and intermedia patients and its relation to chelation therapy

المؤلفون المشاركون

Adli, Amirah A. M.
Toaima, Dalia N.
Muhammad, Nuha Rafat
Abu al-Suud, Karim Muhammad

المصدر

The Egyptian Journal of Medical Human Genetics

العدد

المجلد 15، العدد 4 (31 أكتوبر/تشرين الأول 2014)، ص ص. 369-377، 9ص.

الناشر

الجمعية المصرية للأمراض الوراثية

تاريخ النشر

2014-10-31

دولة النشر

مصر

عدد الصفحات

9

التخصصات الرئيسية

الطب البشري

الموضوعات

الملخص EN

Background : Limited data are available about renal involvement in thalassemia patients.

Renal dysfunction in these patients seems to be multifactorial attributed mainly to long standing anemia, chronic hypoxia, iron overload and toxicity of iron chelators.

Objective : To assess the frequency of subclinical glomerular and tubular dysfunctions in children and adolescents with b-thalassemia major and intermedia, and to correlate these findings with the degree of iron overload and type of chelation therapy.

Methods : The study included 40 thalassemia major and 20 thalassemia intermedia pediatric patients recruited from the Pediatric hematology clinic, Ain Shams University.

Serum sodium, potassium, phosphorous and creatinine, and urinary sodium, potassium, phosphorous, protein / creatinine ratio and urinary b2 microglobulin were measured.

Fractional excretion of sodium and potassium was calculated.

Results : The mean level of serum creatinine in all patients was within the normal range and comparable in both TM and TI groups (0.17 ± 0.06 and 0.18 ± 0.07 mg / dl, respectively, P > 0.05).

The mean eGFR was higher than normal range in both TM and TI groups (552.65 ±231.73 and 472.15± 272.99 ml / min, respectively).

Mean level of urinary b2 microglobulin was within the normal range (0.13 ± 0.05 and 0.10 ± 0.03 lg / ml) in TM and TI patients, however, it was significantly higher in TM patients (P =0.009).

Urinary b2 microglobulin was positively correlated to both transfusion index and serum ferritin level (P < 0.05).

Tubular reabsorption of phosphorus (TRP) was significantly higher among TM patients (P = 0.037).

The mean height and height percentile were lower in the poorly chelated group (serum ferritin P2500 ng/ml) than the well chelated group.

In addition, the mean serum sodium and urinary protein/creatinine ratio were significantly higher in the poorly chelated group (P < 0.05).

Conclusion : Subclinical renal affection can start earlier in TM patients compared to TI.

Poor chelation is associated with early signs of renal affection.

Periodic renal assessment of those patients is mandatory as they may be affected by hidden renal dysfunction.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Adli, Amirah A. M.& Toaima, Dalia N.& Muhammad, Nuha Rafat& Abu al-Suud, Karim Muhammad. 2014. Subclinical renal abnormalities in young thalassemia major and intermedia patients and its relation to chelation therapy. The Egyptian Journal of Medical Human Genetics،Vol. 15, no. 4, pp.369-377.
https://search.emarefa.net/detail/BIM-422641

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Adli, Amirah A. M.…[et al.]. Subclinical renal abnormalities in young thalassemia major and intermedia patients and its relation to chelation therapy. The Egyptian Journal of Medical Human Genetics Vol. 15, no. 4 (Oct. 2014), pp.369-377.
https://search.emarefa.net/detail/BIM-422641

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Adli, Amirah A. M.& Toaima, Dalia N.& Muhammad, Nuha Rafat& Abu al-Suud, Karim Muhammad. Subclinical renal abnormalities in young thalassemia major and intermedia patients and its relation to chelation therapy. The Egyptian Journal of Medical Human Genetics. 2014. Vol. 15, no. 4, pp.369-377.
https://search.emarefa.net/detail/BIM-422641

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references : p. 376-377

رقم السجل

BIM-422641