BMJ 2005;330:17-18 (1 January), doi:10.1136/bmj.38313.513310.F71 (published 16 December 2004)
Paper
Insulin resistance and depression: cross sectional study
Markku Timonen, acting professor1,
Mauri Laakso, senior lecturer2,
Jari Jokelainen, biostatistician2,
Ulla Rajala, research fellow1,
V Benno Meyer-Rochow, professor3,
Sirkka Keinänen-Kiukaanniemi, professor4
1 Department of Public Health Science and General Practice, University of Oulu, Box 5000, FIN-90014, Finland,
2 Unit of General Practice, Oulu University Hospital, 90029 OYS, Finland,
3 International University Bremen, School of Engineering and Science, D-28725 Bremen, Germany,
4 Oulu Health Centre, Box 8, FIN-90015 City of Oulu, Finland
Correspondence to: M Timonen markku.timonen{at}oulu.fi
Introduction
A recent study found that depression is inversely associated
with insulin resistance, but positively associated with diabetes.
1 Association between insulin resistance and depression is a poorly
studied area and the few earlier findings do not necessarily
support this finding,
1 indicating that patients with serious
depression have insulin resistance assessed by insulin tolerance,
intravenous, or oral glucose tolerance tests.
2 Recently, depression
was found to be associated with greater insulin resistance in
women with polycystic ovary syndrome.
3 Also, more than the normal
rates of depression had already been noted in patients with
clinically manifest diabetes.
2 Since insulin resistance is positively
associated with the development of diabetes,
1 we hypothesisedgiven
that disturbed glucoregulatory functions behind the development
of diabetes might be associated with pathophysiological changes
in depression
2that insulin resistance should be positively
correlated with depressive symptoms. We also investigated whether
depressive symptoms varied with different levels of a disturbed
glucose metabolism.
Participants, methods, and results
We invited all 1008 people born in 1935 and living in the city
of Oulu, Finland, on 1 October 1990 to participate in a study
to assess the prevalence of type 2 diabetes and impaired glucose
tolerance; 831 attended. The follow up of the earlier participants,
on which this study was based (n = 593), was done in 1996-1998;
we excluded patients previously diagnosed as having diabetes,
leaving 491 cases. A detailed description of the data was given
earlier.
4 We defined insulin resistance with the qualitative
insulin sensitivity check index,
4 and we evaluated the severity
of depressive symptoms with Beck's depression inventory 21.
5 We found a negative correlation between the scores (Spearman
correlation coefficient r = -0.13, P = 0.004). The correlation
(see figure on
bmj.com) was most evident in subjects with impaired
glucose tolerance (r = -0.24, P = 0.029;
table). Regarding different
levels of disturbed glucose metabolism, patients with type 2
diabetes and impaired glucose tolerance had higher depression
scores (median 6.0 and 6.0) than those with normal glucose tolerance
(5.0); the difference was statistically significant between
impaired and normal glucose tolerance groups (
table).
View this table:
[in this window]
[in a new window]
|
Medians and interquartile ranges of Beck's depression inventory 21 values in different glucose tolerance categories checked by oral glucose tolerance test in elderly Finns
|
|
| What is already known on this topic
More than normal rates of depression can already be detected in patients with clinically manifest diabetes
The association between insulin resistance and depression is a sparsely studied area, and the few existing findings are contradictory
What this study adds
A positive correlation between insulin resistance and severity of depressive symptoms is present already in subjects with impaired glucose tolerance before the outbreak of type 2 diabetes mellitus
| |
Comment
Insulin resistance (a low qualitative insulin sensitivity check
index) and severity of depressive symptoms (Beck's depression
inventory 21) were positively correlated, particularly in people
with impaired glucose tolerance. Our findings are at variance
with those of Lawlor and colleagues,
1 who suggested that a clinical
diagnosis of diabetes in itself would be an explanation for
their findings regarding diabetic patients. With our database,
clinical diagnoses could not have affected the results, because
we excluded patients previously diagnosed as having diabetes.
Because in our study higher depression scores were already prevalent
in those with impaired glucose tolerance without clinically
manifest diabetes, our findings might be explained biologicallythat
is, by pathophysiological changes behind insulin resistance
and depression.
Insulin resistance could develop as a consequence of an increased release of counter-regulatory hormones associated with depression.2 This, however, is unconfirmed. The strengths of our study were that the qualitative insulin sensitivity check index has shown to be a reliable instrument in screening insulin sensitivity in epidemiological studies.4 Also this was a population based study consisting of a representative sample of one whole age group. A limitation of our study is that the validity of the findings based on self reported Beck's depression inventory scales is inferior to those of structured diagnostic rating scales; thus, it cannot provide specific depression diagnoses. Neither could we test the causal hypothesis, because we did not know the full history of depression in the participants.
This article was posted on bmj.com on 16 December 2004: http://bmj.com/cgi/doi/10.1136/bmj.38313.513310.F7
A figure showing the results is on bmj.com
Contributors: MT conceived the study, reviewed the literature, and wrote the initial and subsequent drafts. SKK helped to conceive the study and revise the initial and subsequent drafts, and was overseer of the research group. JJ designed the statistical analyses, analysed the data, developed the figure, and helped draft the manuscript. ML and UR collected the data and contributed to the study design, interpretation, and revisions of the manuscript. VBMR helped revising the initial draft and contributed to revisions and discussions. MT is guarantor.
Funding: No additional funding.
Competing interests: None declared.
Ethical approval: Ethics Committee of the Faculty of Medicine, University of Oulu, Finland.
References
- Lawlor DA, Smith GD, Ebrahim S. Association of insulin resistance with depression: cross sectional findings from the British Women's Heart and Health Study. BMJ 2003;327: 1383-4.[Free Full Text]
- Musselman DL, Betan E, Larsen H, Phillips LS. Relationship of depression to diabetes types 1 and 2: epidemiology, biology, and treatment. Biol Psychiatry 2003;54: 317-29.[CrossRef][Web of Science][Medline]
- Rasgon NL, Rao RC, Hwang S, Altshuler LL, Elman S, Zuckerbrow-Miller J, et al. Depression in women with polycystic ovary syndrome: clinical and biochemical correlates. J Affect Disord 2003;74: 299-304.[CrossRef][Web of Science][Medline]
- Rajala U, Laakso M, Paivansalo M, Pelkonen O, Suramo I, Keinanen-Kiukaanniemi S. Low insulin sensitivity measured by both quantitative insulin sensitivity check index and homeostasis model assessment method as a risk factor of increased intima-media thickness of the carotid artery. J Clin Endocrinol Metab 2002;87: 5092-7.[Abstract/Free Full Text]
- Beck AT, Ward CH, Mendelson M, Mock J, Erbaugh J. An inventory for measuring depression. Arch Gen Psychiatry 1961;4: 561-71.
(Accepted 16 November 2004)

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