Analyzing leukocyte telomere length in bipolar disorder: Authors’ reply

Our original study adds important information to the evidence base for bipolar disorder (BD) pathology. We show, for the first time, that shorter leukocyte telomere length (LTL) is already present in individuals with the early stages of BD and is comparable to LTL from individuals in the late stages of the disease.¹

This result is at least surprising. We might speculate that, in BD, LTL would be proportional to disease duration. A recent study from our group in patients with schizophrenia (SZ) showed that duration of illness, but not age itself, is related to many markers of aging; these results are consistent with the hypothesis of accelerated aging induced by a pathological state.² Still, SZ is associated with a higher burden of disease. In our recent study, the similar LTL among early-stage and late-stage BD patients could indeed have many other explanations.

First, although hypertension, dyslipidemia, and diabetes mellitus are risk factors for telomere erosion and senescence, and were present in our cohort of BD patients, we chose not to report these data, because we have no information regarding comorbidity duration and its differential impact. Telomeres are naturally shortened during cell division and this process can be accelerated under oxidative, inflammatory or glucocorticoid stress, all of which are present in patients with BD. Importantly, augmented peripheral cell apoptosis, which may be a consequence of augmented turn-over secondary to chronic stress, has been reported in BD. Thus, during chronic stress, cells with shorter telomeres might have already been eliminated, selecting for medium to large telomeres. Second, quantification of telomere length by quantitative PCR (qPCR) provides a measure of the mean LTL present in a given cell population. A major limitation of this technique is its sensitivity, as qPCR does not detect short telomeres. Because short but not average LTL determines pathological phenotypes and drives cell fate, our results must be interpreted with caution.

In addition, LTL is a mosaic trait, and reflects the replicative history of the analyzed tissue. Granulocytes have longer telomeres than any other leukocyte subset and are present in higher numbers in BD patients. LTL from patients with late-stage BD could be enriched in the granulocyte population, leading to overestimation and misinterpretation of the real impact of LTL. Finally, we could also argue that similar LTL could be a consequence of pharmacotherapy. Lithium therapy is associated with neuroprotective properties.³ This effect could explain why euthymic patients in late-stage BD under longer lithium therapy might have similar LTL to early-stage BD patients.

Two recently published reports from our group address telomere shortening and familial traits in BD⁴ and SZ.⁵ Our findings show a significant negative trend for shorter LTL among patients with BD when compared to their healthy siblings, and similar and shorter LTL among patients with SZ and their unaffected siblings. More importantly, in both studies, LTL was shorter in unaffected siblings than in healthy nonrelated controls (HCs). Because HCs and unaffected siblings of BD patients had significant differences in LTL, we might speculate that telomere shortening is not influenced by medication and is indeed a neurobiological change with a clear genetic background. Furthermore, we might consider that genetic background in unaffected siblings could be seen as a susceptibility or vulnerability trait, and that resilience mechanisms may inhibit the appearance of pathological BD. In this study, we indeed failed to address important confounders, such as comorbidities, physical activity, smoking, and lifestyle factors. We also did not include data regarding familial history of major psychiatric disorders, nor did we quantify LTL in participants’ parents.

Both of our studies had cross-sectional designs, thus precluding inference of any causal associations. Prospective epidemiological studies with adequately calculated sample sizes should be designed and conducted in newly diagnosed, therapy-naive BD patients to evaluate specific mechanisms potentially associated with lithium neuroprotection in telomere homeostasis.

References

• ¹
  Barbé-Tuana FM, Parisi MM, Panizzutti BS, Fries GR, Grun LK, Guma FT, et al. Shortened telomere length in bipolar disorder: a comparison of the early and late stages of disease. Rev Bras Psiquiatr. 2016;38:281-6.
• ²
  Czepielewski LS, Massuda R, Panizzutti B, Grun LK, Barbé-Tuana FM, Teixeira AL, et al. Telomere length and CCL11 levels are associated with gray matter volume and episodic memory performance in schizophrenia: evidence of pathological accelerated aging. Schizophr Bull. 2017 Feb 22. doi: 10.1093/schbul/sbx015. [Epub ahead of print]
  » 10.1093/schbul/sbx015
• ³
  Martinsson L, Wei Y, Xu D, Melas PA, Mathé AA, Schalling M, et al. Long-term lithium treatment in bipolar disorder is associated with longer leukocyte telomeres. Transl Psychiatry. 2013;3:e261.
• ⁴
  Vasconcelos-Moreno MP, Fries GR, Gubert C, dos Santos BTMQ, Fijtman A, Sartori J, et al. Telomere length, oxidative stress, inflammation and BDNF levels in siblings of patients with bipolar disorder: implications for accelerated cellular aging. Int J Neuropsychopharmacol. 2017;20:445-54.
• ⁵
  Czepielewski LS, Massuda R, Panizzutti B, da Rosa ED, de Lucena D, Macêdo D, et al. Telomere length in subjects with schizophrenia, their unaffected siblings and healthy controls: evidence of accelerated aging. Schizophr Res. 2016;174:39-42.

Publication Dates

• Publication in this collection
  Sept 2017

History

• Received
  29 May 2017
• Accepted
  29 May 2017