Serum phosphatidylinositol as a biomarker for bipolar disorder liability

Authors

Emma E. M. Knowles
Peter J. Meikle, Baker Heart and Diabetes Institute
Kevin Huynh
Harald H. H. Goring, The University of Texas Rio Grande Valley
Rene L. Olvera
Samuel R. Mathias
Ravi Duggirala, The University of Texas Rio Grande Valley
Laura Almasy, University of Pennsylvania School of Medicine
John Blangero, The University of Texas Rio Grande Valley
Joanne E. Curran, The University of Texas Rio Grande Valley
David C. Glahn, Olin Neuropsychiatry Research Center

Document Type

Article

Publication Date

3-2017

Abstract

Objectives

Individuals with bipolar disorder (BPD) exhibit alterations in their phospholipid levels. It is unclear whether these alterations are a secondary consequence of illness state, or if phospholipids and illness risk overlap genetically. If the latter were true, then phospholipids might provide key insights into the pathophysiology of the illness. Therefore, we rank-ordered phospholipid classes by their genetic overlap with BPD risk in order to establish which class might be most informative in terms of increasing our understanding of illness pathophysiology.

Methods

Analyses were conducted in a sample of 558 individuals, unselected for BPD, from 38 extended pedigrees (average family size=14.79, range=2–82). We calculated a coefficient of relatedness for all family members of nine individuals with BPD in the sample (N=185); this coefficient was set to be zero in unrelated individuals (N=373). Then, under an endophenotype ranking value (ERV) approach, this scalar index was tested against 13 serum-based phospholipid concentrations in order to rank-order lipid classes by their respective overlap with BPD risk.

Results

The phosphatidylinositol class was significantly heritable (h2=0.26, P=6.71 × 10−05). It was the top-ranked class, and was significantly associated with BPD risk after correction for multiple testing (β=−1.18, P=2.10 × 10−03, ERV=0.49).

Conclusions

We identified a peripheral biomarker, serum-based phosphatidylinositol, which exhibits a significant association with BPD risk. Therefore, given that phosphatidylinositol and BPD risk share partially common etiology, it seems that this lipid class warrants further investigation, not only in terms of treatment, but also as a promising diagnostic and risk marker.

Comments

Original published version available at https://doi.org/10.1111/bdi.12468

Recommended Citation

Knowles, E. E., Meikle, P. J., Huynh, K., Göring, H. H., Olvera, R. L., Mathias, S. R., Duggirala, R., Almasy, L., Blangero, J., Curran, J. E., & Glahn, D. C. (2017). Serum phosphatidylinositol as a biomarker for bipolar disorder liability. Bipolar disorders, 19(2), 107–115. https://doi.org/10.1111/bdi.12468

Publication Title

Bipolar disorders

DOI

10.1111/bdi.12468

Academic Level

faculty

Mentor/PI Department

Office of Human Genetics