Supplementation with a Salmon Bone Complex (CalGo®) Preserves Femoral Neck BMD and Attenuates Lumbar Spine Loss: A 24-Month Randomized, Placebo-Controlled Trial

<b>Background/Objectives</b>: Osteopenia is common in postmenopausal women and predisposes to osteoporosis and fracture, representing a population at risk of bone loss but without indication for pharmacologic therapy. Conventional calcium salts offer modest, often transient gains in bone mineral density (BMD). We evaluated whether CalGo<sup>®</sup>, a salmon bone complex containing microcrystalline hydroxyapatite within a collagen-rich matrix, preserves BMD versus placebo in post-menopausal women with osteopenia. <b>Methods</b>: In a 24-month, randomized, double-blind, placebo-controlled trial, 80 women (50-80 years) with dual-energy X-ray absorptiometry (DXA)-confirmed femoral-neck osteopenia were assigned to CalGo<sup>®</sup> (2 g/day) or placebo. The prespecified primary endpoint was 24-month change in femoral-neck BMD (g/cm<sup>2</sup>) analyzed by linear regression (unadjusted and baseline-adjusted). Secondary endpoints included lumbar spine and distal radius BMD, serum P1NP and β-CTX-I, health-related quality of life, and safety. <b>Results</b>: The primary analysis included participants with 24-month DXA (CalGo<sup>®</sup><i>n</i> = 29; placebo <i>n</i> = 30). Femoral-neck BMD was maintained with CalGo<sup>®</sup> (+0.003 g/cm<sup>2</sup>; +0.4%) but declined with placebo (-0.017 g/cm<sup>2</sup>; -2.4%), yielding a significant baseline-adjusted between-group difference of +0.019 g/cm<sup>2</sup> (95% confidence interval (CI) 0.001-0.038; <i>p</i> = 0.044). Lumbar-spine loss was attenuated with CalGo<sup>®</sup> (-0.005 g/cm<sup>2</sup>; -0.3%) versus placebo (-0.028 g/cm<sup>2</sup>; -3.4%); the adjusted difference favored CalGo<sup>®</sup> (+0.026 g/cm<sup>2</sup>; <i>p</i> = 0.058). In exploratory responder analysis, ≥1% lumbar-spine gain was more likely with CalGo<sup>®</sup> (32.5% vs. 11.4%; OR 3.61; <i>p</i> = 0.043). No treatment effects were observed at the distal radius, in P1NP or β-CTX-I, or in EQ-5D-3L/EQ-VAS. CalGo<sup>®</sup> was well tolerated with no hepatic or renal safety signals. <b>Conclusions</b>: CalGo<sup>®</sup> maintained femoral-neck bone mineral density and reduced lumbar-spine loss over 24 months in osteopenic women, with good tolerability. These findings support its potential role as a nutritional approach for maintaining bone health.

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Journal
Biomedicines
Published
2025-10-25
DOI
https://doi.org/10.3390/biomedicines13112616
Primary Topic
Hip and Femur Fractures
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article
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article

Supplementation with a Salmon Bone Complex (CalGo®) Preserves Femoral Neck BMD and Attenuates Lumbar Spine Loss: A 24-Month Randomized, Placebo-Controlled Trial

Erland Hermansen, Crawford Currie, Tommy Frøseth Aae, Christian Bjerknes et al.
Biomedicines
Hip and Femur Fractures
article

Supplementation with a Salmon Bone Complex (CalGo®) Preserves Femoral Neck BMD and Attenuates Lumbar Spine Loss: A 24-Month Randomized, Placebo-Controlled Trial

Erland Hermansen, Crawford Currie, Tommy Frøseth Aae, Christian Bjerknes, Bomi Framroze, Tor Åge Myklebust, Anne Rørvik Standal
article en

Abstract

<b>Background/Objectives</b>: Osteopenia is common in postmenopausal women and predisposes to osteoporosis and fracture, representing a population at risk of bone loss but without indication for pharmacologic therapy. Conventional calcium salts offer modest, often transient gains in bone mineral density (BMD). We evaluated whether CalGo<sup>®</sup>, a salmon bone complex containing microcrystalline hydroxyapatite within a collagen-rich matrix, preserves BMD versus placebo in post-menopausal women with osteopenia. <b>Methods</b>: In a 24-month, randomized, double-blind, placebo-controlled trial, 80 women (50-80 years) with dual-energy X-ray absorptiometry (DXA)-confirmed femoral-neck osteopenia were assigned to CalGo<sup>®</sup> (2 g/day) or placebo. The prespecified primary endpoint was 24-month change in femoral-neck BMD (g/cm<sup>2</sup>) analyzed by linear regression (unadjusted and baseline-adjusted). Secondary endpoints included lumbar spine and distal radius BMD, serum P1NP and β-CTX-I, health-related quality of life, and safety. <b>Results</b>: The primary analysis included participants with 24-month DXA (CalGo<sup>®</sup><i>n</i> = 29; placebo <i>n</i> = 30). Femoral-neck BMD was maintained with CalGo<sup>®</sup> (+0.003 g/cm<sup>2</sup>; +0.4%) but declined with placebo (-0.017 g/cm<sup>2</sup>; -2.4%), yielding a significant baseline-adjusted between-group difference of +0.019 g/cm<sup>2</sup> (95% confidence interval (CI) 0.001-0.038; <i>p</i> = 0.044). Lumbar-spine loss was attenuated with CalGo<sup>®</sup> (-0.005 g/cm<sup>2</sup>; -0.3%) versus placebo (-0.028 g/cm<sup>2</sup>; -3.4%); the adjusted difference favored CalGo<sup>®</sup> (+0.026 g/cm<sup>2</sup>; <i>p</i> = 0.058). In exploratory responder analysis, ≥1% lumbar-spine gain was more likely with CalGo<sup>®</sup> (32.5% vs. 11.4%; OR 3.61; <i>p</i> = 0.043). No treatment effects were observed at the distal radius, in P1NP or β-CTX-I, or in EQ-5D-3L/EQ-VAS. CalGo<sup>®</sup> was well tolerated with no hepatic or renal safety signals. <b>Conclusions</b>: CalGo<sup>®</sup> maintained femoral-neck bone mineral density and reduced lumbar-spine loss over 24 months in osteopenic women, with good tolerability. These findings support its potential role as a nutritional approach for maintaining bone health.

BiomedicinesVol. 13(11)
Norwegian University of Science and Technology (NO), Ålesund Hospital (NO), Cancer Registry of Norway (NO)
Norges Forskningsråd
Openalex Percentile: Top 51%
Hip and Femur Fractures
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