|LETTER TO THE EDITOR
|Year : 2014 | Volume
| Issue : 4 | Page : 589-590
Response to review article "Type 1 diabetes and osteoporosis: Review of literature"
Ameya S Joshi, Premlata K Varthakavi, Nikhil M Bhagwat, Manoj D Chadha
Department of Endocrinology, Topiwala National Medical College and BYL Nair Charitable Hospital, Mumbai Central, Mumbai, Maharashtra, India
|Date of Web Publication||25-Jul-2014|
Ameya S Joshi
Department of Endocrinology, College Building, 4th Floor, Topiwala National Medical College and BYL Nair Charitable Hospital,Mumbai Central, Mumbai 400 008, Maharashtra
Source of Support: None, Conflict of Interest: None
|How to cite this article:|
Joshi AS, Varthakavi PK, Bhagwat NM, Chadha MD. Response to review article "Type 1 diabetes and osteoporosis: Review of literature". Indian J Endocr Metab 2014;18:589-90
|How to cite this URL:|
Joshi AS, Varthakavi PK, Bhagwat NM, Chadha MD. Response to review article "Type 1 diabetes and osteoporosis: Review of literature". Indian J Endocr Metab [serial online] 2014 [cited 2021 Jan 16];18:589-90. Available from: https://www.ijem.in/text.asp?2014/18/4/589/137505
We read the review article on type 1 diabetes (T1DM) and osteoporosis with great interest. As the article mentioned our group has the only published literature as regards bone mineral density (BMD) in T1DM in India.  Though our study was conducted at a center in Western India, Mumbai being a cosmopolitan city and referral center for all over India our study population practically had members from most of the states.
Another important aspect that we noted among our study population was that the BMD as well as the bone mineral content was remarkable low in patients with celiac autoimmunity (CA) and T1DM as compared with patients T1DM without CA and we got a significantly high prevalence of CA (12.7%) which matches with reports from other parts of India.  Despite such a high prevalence CA is T1DM, the screening rates for same are poor.
Poor glycemic control and low insulin like growth factor-1 levels (which also is partly glycemic control as well as nutrition dependent) with normal growth hormone levels (basal as well as stimulated when indicated) were also associated with poor BMD in T1DM. This also perhaps explains why we got low BMD in T1DM as compared with control population, a finding not universally replicated across the globe (due to perhaps poor nutrition). It also underlines that measures for improvement of better glycemic control in T1DM such as encouraging more frequent monitoring, subsidizing glucostrips, insulin pumps and glucose monitoring systems and emphasizing the concept of basal and bolus or flex regimens in order to achieve better glycemic control. 
Interpretation of BMD/bone mineral content for bone area in pediatric diseased population especially due to effect on stature and pubertal status is also difficult. The popular Molgaard approach does not consider puberty. The model which we had used was Warner model which gives predictive equations considering the effect of age, sex, puberstatus, and antropometric variables and may be used in diseased population. ,
We would like to reiterate that at least from our study experience timely screening of CA as well as measures to improve glycemic control apart from improving nutrition and physical activity may help in better bone health in T1DM.
| References|| |
|1.||Joshi A, Varthakavi P, Chadha M, Bhagwat N. A study of bone mineral density and its determinants in type 1 diabetes mellitus. J Osteoporos 2013;2013:397814. |
|2.||Mehra NK, Kaur G, Kanga U, Tandon N. Immunogenetics of autoimmune diseases in Asian Indians. Ann N Y Acad Sci 2002;958:333-6. |
|3.||Strotmeyer ES, Cauley JA. Diabetes mellitus, bone mineral density, and fracture risk. Curr Opin Endocrinol Diabetes Obes 2007;14:429-35. |
|4.||Mølgaard C, Thomsen BL, Prentice A, Cole TJ, Michaelsen KF. Whole body bone mineral content in healthy children and adolescents. Arch Dis Child 1997;76:9-15. |
|5.||Warner JT, Cowan FJ, Dunstan FD, Evans WD, Webb DK, Gregory JW. Measured and predicted bone mineral content in healthy boys and girls aged 6-18 years: Adjustment for body size and puberty. Acta Paediatr 1998;87:244-9. |