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Proc Natl Acad Sci U S A. 2014 Sep 9;111(36):13010-5. doi: 10.1073/pnas.1323099111. Epub 2014 Aug 25.

Metabolic costs and evolutionary implications of human brain development.

Author information

1
Department of Anthropology, Institute for Policy Research, Northwestern University, Evanston, IL 60208; kuzawa@northwestern.edu.
2
Positron Emission Tomography Center, Children's Hospital of Michigan, Detroit, MI 48201; Department of Pediatrics, Department of Neurology, and.
3
Center for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48201;
4
Department of Neurology, and Center for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48201;
5
Department of Pediatrics.
6
Fishberg Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029;
7
Center for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48201; Institute of Genomic Biology, Department of Molecular and Integrative Physiology, University of Illinois, Urbana, IL 61801;
8
Department of Anthropology, The George Washington University, Washington, DC 20052; and.
9
Department of Anthropology.
10
Department of Psychiatry and Department of Biostatistics, Harvard University and McLean Hospital, Cambridge, MA 02138.

Abstract

The high energetic costs of human brain development have been hypothesized to explain distinctive human traits, including exceptionally slow and protracted preadult growth. Although widely assumed to constrain life-history evolution, the metabolic requirements of the growing human brain are unknown. We combined previously collected PET and MRI data to calculate the human brain's glucose use from birth to adulthood, which we compare with body growth rate. We evaluate the strength of brain-body metabolic trade-offs using the ratios of brain glucose uptake to the body's resting metabolic rate (RMR) and daily energy requirements (DER) expressed in glucose-gram equivalents (glucosermr% and glucoseder%). We find that glucosermr% and glucoseder% do not peak at birth (52.5% and 59.8% of RMR, or 35.4% and 38.7% of DER, for males and females, respectively), when relative brain size is largest, but rather in childhood (66.3% and 65.0% of RMR and 43.3% and 43.8% of DER). Body-weight growth (dw/dt) and both glucosermr% and glucoseder% are strongly, inversely related: soon after birth, increases in brain glucose demand are accompanied by proportionate decreases in dw/dt. Ages of peak brain glucose demand and lowest dw/dt co-occur and subsequent developmental declines in brain metabolism are matched by proportionate increases in dw/dt until puberty. The finding that human brain glucose demands peak during childhood, and evidence that brain metabolism and body growth rate covary inversely across development, support the hypothesis that the high costs of human brain development require compensatory slowing of body growth rate.

KEYWORDS:

anthropology; diabetes; human evolution; neuroimaging; neuronal plasticity

PMID:
25157149
PMCID:
PMC4246958
DOI:
10.1073/pnas.1323099111
[Indexed for MEDLINE]
Free PMC Article
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