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Currently used osteoporosis treatments substantially reduce vertebral fracture risk, whereas nonvertebral fracture risk, mainly caused by reduced cortical bone mass, has only moderately been improved by the osteoporosis drugs used, defining an unmet medical need. Because several wingless\u2010type MMTV integration site family members (WNTs) and modulators of WNT activity are major regulators of bone mass, we hypothesized that NOTUM, a secreted WNT lipase, might modulate bone mass\n                    <jats:italic>via<\/jats:italic>\n                    an inhibition of WNT activity. To characterize the possible role of endogenous NOTUM as a physiologic modulator of bone mass, we developed global, cell\u2010specific, and inducible\n                    <jats:italic>Notum<\/jats:italic>\n                    \u2010inactivated mouse models.\n                    <jats:italic>Notum<\/jats:italic>\n                    expression was high in the cortical bone in mice, and conditional\n                    <jats:italic>Notum<\/jats:italic>\n                    inactivation revealed that osteoblast lineage cells are the principal source of NOTUM in the cortical bone. Osteoblast lineage\u2013specific\n                    <jats:italic>Notum<\/jats:italic>\n                    inactivation increased cortical bone thickness\n                    <jats:italic>via<\/jats:italic>\n                    an increased periosteal circumference. Inducible\n                    <jats:italic>Notum<\/jats:italic>\n                    inactivation in adult mice increased cortical bone thickness as a result of increased periosteal bone formation, and silencing of\n                    <jats:italic>Notum<\/jats:italic>\n                    expression in cultured osteoblasts enhanced osteoblast differentiation. Large\u2010scale human genetic analyses identified genetic variants mapping to the\n                    <jats:italic>NOTUM<\/jats:italic>\n                    locus that are strongly associated with bone mineral density (BMD) as estimated with quantitative ultrasound in the heel. Thus, osteoblast\u2010derived NOTUM is an essential local physiologic regulator of cortical bone mass\n                    <jats:italic>via<\/jats:italic>\n                    effects on periosteal bone formation in adult mice, and genetic variants in the\n                    <jats:italic>NOTUM<\/jats:italic>\n                    locus are associated with BMD variation in adult humans. Therapies targeting osteoblast\u2010derived NOTUM may prevent nonvertebral fractures.\u2014Mov\u00e9rare\u2010Skrtic, S., Nilsson, K. H., Henning, P., Funck\u2010Brentano, T., Nethander, M., Rivadeneira, F., Coletto Nunes, G., Koskela, A., Tuukkanen, J., Tuckermann, J., Perret, C., Souza, P. P. C., Lerner, U. H., Ohlsson, C. Osteoblast\u2010derived NOTUM reduces cortical bone mass in mice and the\n                    <jats:italic>NOTUM<\/jats:italic>\n                    locus is associated with bone mineral density in humans. FASEB J. 33, 11163\u201311179 (2019).\n                    <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:href=\"http:\/\/www.fasebj.org\">www.fasebj.org<\/jats:ext-link>\n                  <\/jats:p>","DOI":"10.1096\/fj.201900707r","type":"journal-article","created":{"date-parts":[[2019,7,15]],"date-time":"2019-07-15T21:57:47Z","timestamp":1563227867000},"page":"11163-11179","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":32,"title":["Osteoblast\u2010derived NOTUM reduces cortical bone mass in mice and the\n                    <i>NOTUM<\/i>\n                    locus is associated with bone mineral density in humans"],"prefix":"10.1096","volume":"33","author":[{"given":"Sofia","family":"Mov\u00e9rare-Skrtic","sequence":"first","affiliation":[{"name":"Department of Internal Medicine and Clinical Nutrition Institute of Medicine Centre for Bone and Arthritis Research at the Sahlgrenska Academy University 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