Phenotypic and genetic characteristics of a Dutch cohort of patients with X-linked osteoporosis due to <i>PLS3</i> genetic variants

X-linked osteoporosis, caused by plastin 3 (<i>PLS3</i>) genetic variants, is a rare disease, characterized by low BMD and early-onset fractures, primarily affecting men. Our aim was to further elucidate the phenotypic characteristics, including sex-differences and genotype-phenotype analysis, in individuals with <i>PLS3</i> variants. Our cohort comprises of 28 patients from 11 families, 18 men and 10 women, with a different <i>PLS3</i> variant in each family. Demographic, clinical, and genetic features, imaging and laboratory tests, and treatment details were retrospectively reviewed. Men, (median age 47.0 y), demonstrated low Z-scores of the lumbar spine (-2.8 ± 1.7) and femoral neck (-1.7, IQR: -2.9-0.8). Most women (median age 49.5 y) had normal BMD, two had osteoporosis and one osteopenia. Moreover, men experienced a higher total number of fractures than women (men: 12.0, IQR: 6.7, 18.5, women: 2.0, IQR: 0.7, 5.2). Within one large family (<i>n</i> = 10) there was considerable heterogeneity regarding BMD and fractures, which might be explained by differences in factors like physical exercise (PE) or in (poly) genetic background. Extra-skeletal characteristics such as (mild) blue discoloration of the sclerae (men: 33.3%, women: 30.0%), joint hypermobility (44.4%, 70.0%) and skin hyperlaxity (50.0%, 20.0%) were observed. No relation was found between types and locations of variants and various clinical endpoints in men, using data from our cohort and the literature. Regarding treatment, all men and 40% of women received bone-active therapy, mostly oral bisphosphonates. Adult men demonstrated a 16.6% mean increase in the BMD of the lumbar spine (<i>p</i> = .03), after a median treatment duration of 6 y. In summary, this is so far the largest study of patients with X-linked osteoporosis, including an extensive genotype-phenotype analysis. A potential protective role of increasing weight-bearing PE in osteoporosis severity, as well as effects of penetrance, genetic background, or other environmental or lifestyle factors, need further study.

Authors

Institutions

Publication Details

Journal
JBMR Plus
Published
2025-04-24
DOI
https://doi.org/10.1093/jbmrpl/ziaf046
Citations
1
Primary Topic
Connective tissue disorders research
Type
article
Field-Weighted Citation Impact
1.82
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Phenotypic and genetic characteristics of a Dutch cohort of patients with X-linked osteoporosis due to PLS3 genetic variants

Zografia Zervou, Serwet Demirdas, Hennie T. Brüggenwirth, M. Carola Zillikens
1 citations
JBMR Plus
Connective tissue disorders research
1.82
article

Phenotypic and genetic characteristics of a Dutch cohort of patients with X-linked osteoporosis due to PLS3 genetic variants

Zografia Zervou, Serwet Demirdas, Hennie T. Brüggenwirth, M. Carola Zillikens
article en
1 citations

Abstract

X-linked osteoporosis, caused by plastin 3 (<i>PLS3</i>) genetic variants, is a rare disease, characterized by low BMD and early-onset fractures, primarily affecting men. Our aim was to further elucidate the phenotypic characteristics, including sex-differences and genotype-phenotype analysis, in individuals with <i>PLS3</i> variants. Our cohort comprises of 28 patients from 11 families, 18 men and 10 women, with a different <i>PLS3</i> variant in each family. Demographic, clinical, and genetic features, imaging and laboratory tests, and treatment details were retrospectively reviewed. Men, (median age 47.0 y), demonstrated low Z-scores of the lumbar spine (-2.8 ± 1.7) and femoral neck (-1.7, IQR: -2.9-0.8). Most women (median age 49.5 y) had normal BMD, two had osteoporosis and one osteopenia. Moreover, men experienced a higher total number of fractures than women (men: 12.0, IQR: 6.7, 18.5, women: 2.0, IQR: 0.7, 5.2). Within one large family (<i>n</i> = 10) there was considerable heterogeneity regarding BMD and fractures, which might be explained by differences in factors like physical exercise (PE) or in (poly) genetic background. Extra-skeletal characteristics such as (mild) blue discoloration of the sclerae (men: 33.3%, women: 30.0%), joint hypermobility (44.4%, 70.0%) and skin hyperlaxity (50.0%, 20.0%) were observed. No relation was found between types and locations of variants and various clinical endpoints in men, using data from our cohort and the literature. Regarding treatment, all men and 40% of women received bone-active therapy, mostly oral bisphosphonates. Adult men demonstrated a 16.6% mean increase in the BMD of the lumbar spine (<i>p</i> = .03), after a median treatment duration of 6 y. In summary, this is so far the largest study of patients with X-linked osteoporosis, including an extensive genotype-phenotype analysis. A potential protective role of increasing weight-bearing PE in osteoporosis severity, as well as effects of penetrance, genetic background, or other environmental or lifestyle factors, need further study.

JBMR PlusVol. 9(6)
Erasmus MC (NL)
Openalex Percentile: Top 16%
Connective tissue disorders research
1.82
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.