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CORRESPONDENCE
Year : 2015  |  Volume : 142  |  Issue : 6  |  Page : 769

Authors' response


1 Division of Rheumatology, Department of Medicine, Sri Venkateswara Institute of Medical Sciences, Tirupati 517 507, Andhra Pradesh, India
2 Department of Endocrinology, Sri Venkateswara Institute of Medical Sciences, Tirupati 517 507, Andhra Pradesh, India
3 Department of Statistics, Sri Venkateswara University, Tirupati 517 507, Andhra Pradesh, India

Date of Web Publication21-Jan-2016

Correspondence Address:
B S Kumar
Division of Rheumatology, Department of Medicine, Sri Venkateswara Institute of Medical Sciences, Tirupati 517 507, Andhra Pradesh
India
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Source of Support: None, Conflict of Interest: None


PMID: 26831428

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How to cite this article:
Kumar B S, Ravisankar A, Mohan A, Kumar D P, Katyarmal D T, Sachan A, Sarma K. Authors' response . Indian J Med Res 2015;142:769

How to cite this URL:
Kumar B S, Ravisankar A, Mohan A, Kumar D P, Katyarmal D T, Sachan A, Sarma K. Authors' response . Indian J Med Res [serial online] 2015 [cited 2021 Sep 23];142:769. Available from: https://www.ijmr.org.in/text.asp?2015/142/6/769/174576

We thank Mahajan [1] for her comments on our article [2] . The comments, in summary are related to validity of controls, matched analysis, and regarding the term "cross-sectional study".

In our study, the term "cross-sectional study design" was used to identify "cases" i.e. patients with type 2 diabetes millitus (T2DM) who were on treatment with oral hypoglycaemic agents (OHA) for three or more years from among a pool of patients with T2DM. We had studied the patients on one occasion only and did not prospectively follow up these patients in time to study the development of osteoporosis.

The selection of controls for this type of study could have been done in several ways. To test the hypothesis that exposure to OHA affects bone mineral density (BMD) in patients with T2DM, "diseased controls" i.e. patients with T2DM who were not receiving OHA and who were also not using medications that are known to interfere with the calcium metabolism would have been a choice. However, this would have given us an under-estimated odds ratio (OR). For this reason we did not select such "diseased control subjects". Also, it is very difficult to find such "diseased controls" as such patients are uncommonly encountered in present-day routine clinical practice. For this reason we chose "age- and gender-matched healthy control subjects" for comparison, because these control subjects who had no exposure to OHA provided us the right comparison for BMD for a given age and gender. In our study [2] we found no significant difference in BMD in patients with T2DM who were receiving OHA for a period of three years or more compared to healthy control subjects. It would be unlikely that a positive association between OHA use and BMD would be evident by having diseased controls.

Regarding conditional analyses for the matched case-control study, for small numbers with many variables to be controlled, it is very unlikely that matched multivariable analysis will yield clinically meaningful results. Moreover, we could not do stratified analyses for important prognostic variable(s) due to loss of power. Further, stratified analysis has been discouraged for matched case-control studies [3] . We feel that as the simple bi-variate analysis has not shown any positive association, the conditional logistic regression is also unlikely to show any positive association.

 
   References Top

1.
Mahajan A. Selection bias: Selection of controls as a critical issue in the interpretation of results in a case control study. Indian J Med Res 2015; 142 : 768-9.  Back to cited text no. 1
    
2.
Kumar BS, Ravisankar A, Mohan A, Kumar DP, Katyarmal DT, Sachan A, et al. Effect of oral hypoglycaemic agents on bone metabolism in patients with type 2 diabetes mellitus & occurrence of osteoporosis. Indian J Med Res 2015; 141 : 431-7.  Back to cited text no. 2
    
3.
Breslow NE, Day NE. Statistical methods in cancer research, vol. I. The analyses of case control studies, IARC Scientific Publications No.32. Lyon: International Agency for Research on Cancer; 1980.  Back to cited text no. 3
    




 

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