Evidence map›Paper›PMID 41342417›Full record

ArticleJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2026

Lonafarnib clinical trials demonstrate uncoupling of the muscle-bone unit in Hutchinson-Gilford Progeria Syndrome.

Raymond J Kreienkamp, Leslie B Gordon, Rachel Ehrbar, Alicia Pendleton, Daniel J Schiferl, Asya Lyass, Monica E Kleinman, Brian D Snyder, Catherine M Gordon

Abstract read
In one paragraph

Article in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Raymond J KreienkampDepartment of Pediatrics, Division of Endocrinology, Boston Children's Hospital, Boston, MA 02115, United States.ORCID 0000-0002-1683-323X
Leslie B GordonHarvard Medical School, Boston, MA 02115, United States.
Rachel EhrbarDepartment of Mathematics and Statistics, Boston University, Boston, MA 02215, United States.
Alicia PendletonDepartment of Pediatrics, Division of Endocrinology, Boston Children's Hospital, Boston, MA 02115, United States.
Daniel J SchiferlBone Diagnostic LLC, Spring Branch, TX 78070, United States.
Asya LyassDepartment of Mathematics and Statistics, Boston University, Boston, MA 02215, United States.
Monica E KleinmanHarvard Medical School, Boston, MA 02115, United States.
Brian D SnyderHarvard Medical School, Boston, MA 02115, United States.
Catherine M GordonSection on Adolescent Bone Health & Body Composition, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD 20892, United States.ORCID 0000-0001-8988-7186

Funding

Diabetes-Docs: Physician-Scientist Career Development Program (DiabDocs)K12DK133995 · NIDDK · STANFORD UNIVERSITY · PI LINDA A DIMEGLIO, David Matthew Maahs · 2022 to 2026
$16.0M
Research in Development Endocrinology and MetabolismT32DK007699 · NIDDK · CHILDREN'S HOSPITAL BOSTON · PI JOEL N HIRSCHHORN · 1992 to 2026
$7.1M
Adolescent Bone Density & Body Composition SectionZIAHD009023 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI GORDON, CATHERINE · 2024 to 2025
$1.2M
Intramural NIH HHS ZIA HD009023NIDDK NIH HHS K12 DK133995NIDDK NIH HHS T32 DK007699NIH HHSNIH HHS ZIA HD009023Pediatric Endocrine Society Fima Lifshitz Junior Faculty Clinical Research GrantThe Progeria Research Foundation NIDDK K12DK133995The Progeria Research Foundation NIDDK T32DK007699-41The Progeria Research Foundation PRFCLIN2007-01The Progeria Research Foundation PRFCLIN2007-02The Progeria Research Foundation PRFCLIN2009-03
6 · The paper itself

Abstract

Hutchinson-Gilford Progeria Syndrome (HGPS) is a devastating, ultrarare genetic premature aging disease resulting in early atherosclerosis and death during adolescence due to heart failure. Structures of mesenchymal origin, including bone, fat, and muscle, create a progressive skeletal dysplasia, lifelong failure to thrive, and a unique bone phenotype. Characterizing the interaction between muscle and bone has emerged as a powerful tool for defining drivers of bone disease in other conditions but has not been previously explored in HGPS. We examined the "muscle-bone unit" using radial pQCT in youth with HGPS aged 2-18 yr before and after treatment with lonafarnib, a farnesyltransferase inhibitor that extends HGPS lifespan. Untreated radii displayed highly abnormal shapes in 70% of individuals spanning all ages. Compared to controls, HGPS forearm muscle and radial area were lower (p < .001) and grew more slowly (muscle β = 1.4 cm2/yr vs 0.3 cm2/yr in HGPS; radius β = 5.8 mm2/yr vs 0.5 mm2/yr in HGPS). Fat area decreased with age (β = -.2 cm2/yr, p < .001) and muscle area, normalized for either BMI or radial length, was reduced in HGPS (p = .02 and p ≤ .001, respectively). These normalized outcomes were similar to controls at younger ages but diverged as patients aged. Radial architectural changes were present even before changes in muscle area and represent a pattern distinct from the normal aging process and other muscle-wasting pediatric conditions. Lonafarnib therapy did not normalize the muscle-bone phenotype after 24 mo, although some individuals (25%) had partial normalization of radial shape. These results demonstrate that the muscle-bone unit is uncoupled in children with HGPS. Normal muscle mass for body size at younger ages implies that there is an opportunity for early treatment to avoid impending pathology. New strategies are needed to ameliorate this phenotype in HGPS, and this study provides a benchmark for gauging future therapies.

Indexed as

Bone and BonesMuscle, SkeletalPiperidinesProgeriaPyridinesAdolescentChildChild, PreschoolDibenzocycloheptenesFemaleHumansMaleRadiusDibenzocyclohepteneslonafarnibPiperidinesPyridinesagingbone-muscle interactionsbone QCT/microCTdisease and disorders of/related to boneskeletal muscle

Identifiers

PMID41342417
PMCPMC12751024

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.