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Insulin-like growth factor-1 levels in children with Beta-thalassemia minor
Hamdollah Karamifar1, Mehran Karimi, Nargrs Sobhani
1Hematology Research Center, Department of Pediatrics, Nemazee Hospital, Shiraz University of Medical Sciences, Shiraz, Iran, Phone: 00987116265024
Insights
Children with beta-thalassemia minor show lower insulin-like growth factor-1 (IGF-1) levels compared to healthy children. This suggests shared growth failure mechanisms between beta-thalassemia minor and major.
Area of Science:
- Pediatric Endocrinology
- Hematology
- Genetics
Background:
- Growth retardation is a known complication in beta-thalassemia major, attributed to factors like hemochromatosis and hormonal imbalances.
- Insulin-like growth factor-1 (IGF-1) axis disturbances are implicated in growth failure in beta-thalassemia major.
- The specific role of IGF-1 in beta-thalassemia minor remains less understood.
Purpose of the Study:
- To investigate and compare insulin-like growth factor-1 (IGF-1) levels in children with beta-thalassemia minor versus healthy controls.
- To explore potential shared etiologies of growth failure between beta-thalassemia minor and major.
Main Methods:
- A case-control study involving 50 children with beta-thalassemia minor and 50 age- and sex-matched healthy children.
- Data collection included medical history, physical examination, and measurement of IGF-1 levels.
- The study was conducted in Shiraz, Iran, in 2005.
Main Results:
- Children with beta-thalassemia minor exhibited significantly lower IGF-1 levels compared to the healthy control group (P = 0.015).
- This finding indicates a potential link between beta-thalassemia trait and impaired growth factor signaling.
- The results suggest that underlying growth failure mechanisms might be shared between beta-thalassemia minor and major.
Conclusions:
- IGF-1 levels are decreased in children with beta-thalassemia minor, similar to observations in beta-thalassemia major.
- These findings suggest that similar etiologies may contribute to growth disturbances in both conditions.
- Further research is warranted to elucidate the precise mechanisms linking beta-thalassemia trait to altered IGF-1 levels and growth patterns.
Objective:
Growth retardation in children with b-thalassemia major is multifactorial. Some etiologies described for this condition are hemochromatosis, disturbed growth hormone (GH) / insulin growth factor-1 (IGF-1) axis, undernutrition and hypermetabolism. It has also been proven that growth retardation is present in b-thalassemia major children despite regular transfusion and chelation. Our aim was to evaluate the level of IGF-1 in b-thalassemia minor subjects and compare it with that in healthy children.
Methods:
Fifty children aged 6 months to 15 years with b-thalassemia minor (32 males, 18 females) and 50 age- and sex-matched normal healthy children were selected. Medical history was taken and complete physical examination was done in each case; IGF-1 level was checked in all cases. This study was done in Shiraz, southern Iran, during 2005.
Results:
IGF-1 levels were significantly lower in b-thalassemia minor children than normal children (P = 0.015). This result demonstrates that some etiologies of growth failure in b-thalassemia major other than those described to date can exist, which may be shared with b-thalassemia minor in feature or may be transformed by genes that are either expressed or not.
Conclusion:
We conclude that in addition to that observed in b-thalassemia major, IGF-1 level is also decreased in b-thalassemia minor, and these two may have similar etiologies.
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