Heritability of Alzheimer's disease plasma biomarkers: A nuclear twin family design
Rebecca Z. Rousset, Anouk den Braber, Inge M. W. Verberk, Lynn Boonkamp, David H. Wilson, Lannie Ligthart, Charlotte E. Teunissen, Eco J. C. de GeusAbstract
INTRODUCTION
Alzheimer's disease (AD) is a highly heritable disease (60%–80%). Amyloid beta (Aβ) 42/40, neurofilament light chain (NfL), and glial fibrillary acidic protein (GFAP) are plasma biomarkers for AD. Clinical biomarker research would be served by an understanding of the sources of variance in these markers.
METHODS
Blood concentrations of Aβ42/40, NfL, and GFAP of twins and their families (monozygotic twins: 1574, dizygotic twins: 1266, other: 3657) were analyzed on the Simoa HD‐X. Twin‐family models were used to estimate proportional genetic contributions to the variance in biomarker levels.
RESULTS
Heritability estimates were 16% for Aβ42/40, 42% for NfL, and 60% for GFAP. NfL and GFAP were significantly correlated with each other (0.37) but not with Aβ42/40.
DISCUSSION
The heritability of Aβ42/40 (16%) is lower than the heritability of AD, suggesting strong environmental influences on this biomarker. The lack of correlation between NfL/GFAP and Aβ42/40 indicates these markers may be on different biological pathways.
Highlights
Heritability is found for glial fibrillary acidic protein (60%), neurofilament light chain (42%), and amyloid beta (Aβ) 42/40 (16%) plasma levels. Aβ42/40 plasma levels are sensitive to person‐specific environmental influences.