Research output: Contribution to journal › Article › peer-review
Causal Associations Between Carnitine-Related Metabolites and Spinal Pain : A Bidirectional Mendelian Randomization Study. / Chiu, Abby Pei Ting; Elgaeva, Elizaveta; Arendt-Nielsen, Lars et al.
In: European Journal of Pain, Vol. 30, No. 9, 28.09.2026.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Causal Associations Between Carnitine-Related Metabolites and Spinal Pain
T2 - A Bidirectional Mendelian Randomization Study
AU - Chiu, Abby Pei Ting
AU - Elgaeva, Elizaveta
AU - Arendt-Nielsen, Lars
AU - Curatolo, Michele
AU - Suri, Pradeep
N1 - Chiu, A. P.-T., E. Elgaeva, L. Arendt-Nielsen, M. Curatolo, and P. Suri. 2026. “ Causal Associations Between Carnitine-Related Metabolites and Spinal Pain: A Bidirectional Mendelian Randomization Study.” European Journal of Pain 30, no. 9: e70407. https://doi.org/10.1002/ejp.70407. P.S. is supported by the Clinical, Learning, Evidence, And Research(CLEAR) Center, at the University of Washington, which is fundedby NIAMS/NIH P30AR072572. The work of E.E. was supportedby the budget project of the Institute of Cytology and Genetics №FWNR-2026- 0023.
PY - 2026/9/28
Y1 - 2026/9/28
N2 - Background: Spinal pain is the leading cause of disability worldwide. Previous studies have suggested the therapeutic effects of acetyl-L-carnitine (ALC) and L-carnitine (LC) supplementation in specific chronic pain conditions, but not others. Mendelian randomization (MR) is an analytical approach using genetic variants for estimating causal associations. This bidirectional MR study aimed to examine the potential causal associations of ALC and LC on spinal pain (forward), and vice versa (reverse). Methods: To obtain genetic instrumental variables, we used summary statistics from large publicly available genome-wide association analyses datasets, with sample sizes between 6128 and 1,028,947 participants, for ALC, LC and spinal pain. We conducted MR analyses of potential causal associations using inverse-variance weighted analysis and Causal Analysis Using Summary Effect. Results: There were no statistically significant causal associations between ALC and spinal pain or LC and spinal pain in either forward or reverse directions. Results from secondary analyses were consistent with the primary analyses. Conclusions: Although some prior evidence supports the effectiveness of ALC and LC supplementation in improving pain intensity in some pain conditions, results from this bidirectional MR study do not suggest causal effects of physiologic levels of ALC or LC on spinal pain, nor causal effects of spinal pain on ALC or LC. Significance: Although some prior evidence supports the effectiveness of acetyl-L-carnitine (ALC) and L-carnitine (LC) supplementation in improving pain intensity in some pain conditions, results from this bidirectional MR study do not suggest causal effects of circulating levels of ALC or LC on spinal pain, nor vice versa.
AB - Background: Spinal pain is the leading cause of disability worldwide. Previous studies have suggested the therapeutic effects of acetyl-L-carnitine (ALC) and L-carnitine (LC) supplementation in specific chronic pain conditions, but not others. Mendelian randomization (MR) is an analytical approach using genetic variants for estimating causal associations. This bidirectional MR study aimed to examine the potential causal associations of ALC and LC on spinal pain (forward), and vice versa (reverse). Methods: To obtain genetic instrumental variables, we used summary statistics from large publicly available genome-wide association analyses datasets, with sample sizes between 6128 and 1,028,947 participants, for ALC, LC and spinal pain. We conducted MR analyses of potential causal associations using inverse-variance weighted analysis and Causal Analysis Using Summary Effect. Results: There were no statistically significant causal associations between ALC and spinal pain or LC and spinal pain in either forward or reverse directions. Results from secondary analyses were consistent with the primary analyses. Conclusions: Although some prior evidence supports the effectiveness of ALC and LC supplementation in improving pain intensity in some pain conditions, results from this bidirectional MR study do not suggest causal effects of physiologic levels of ALC or LC on spinal pain, nor causal effects of spinal pain on ALC or LC. Significance: Although some prior evidence supports the effectiveness of acetyl-L-carnitine (ALC) and L-carnitine (LC) supplementation in improving pain intensity in some pain conditions, results from this bidirectional MR study do not suggest causal effects of circulating levels of ALC or LC on spinal pain, nor vice versa.
KW - L-carnitine
KW - Mendelian randomization
KW - acetyl-L-carnitine
KW - causation
KW - epidemiology
KW - spinal pain
KW - ацетил-L-карнитин
KW - причинно-следственная связь
KW - эпидемиология
KW - L-карнитин
KW - менделевская рандомизация
KW - боль в позвоночнике
UR - https://www.mendeley.com/catalogue/38e18446-fabb-310e-9dac-752164278b09/
UR - https://www.scopus.com/pages/publications/105051950573
U2 - 10.1002/ejp.70407
DO - 10.1002/ejp.70407
M3 - Article
C2 - 42804423
VL - 30
JO - European Journal of Pain
JF - European Journal of Pain
SN - 1532-2149
IS - 9
ER -
ID: 83871139