Abstract
Background
Aortic abdominal calcification (AAC) is associated with spine-related conditions, such as lower back pain and reduced bone mineral density. Similar to peripheral vascular disease, AAC possibly reduces blood flow to the lumbar posterior paraspinal muscles (PPM) which may lead to atrophy and increased fatty infiltration.
Methods
Imaging of patients with lower back pain was analyzed. AAC was assessed on lateral lumbar radiographs according to the Kauppila classification. The cross-sectional area of the PPM was measured on a T2-weighted axial MRI sequence and the functional cross-sectional area (fCSA) and fatty infiltration (FI) were calculated with custom software. The association of AAC and FI as well as AAC and fCSA was assessed by multivariable linear regression, adjusted for age, sex, body mass index (BMI), diabetes, and smoking.
Results
Two hundred and thirty patients (47.8% female) with a median age of 60 years (IQR 48–68) were analyzed. In patients, without AAC the median FI of the PPM was 33.3% (IQR 29.1–37.6%), compared to 44.6% (IQR 38.5–54.3%) in patients with AAC (p < 0.001). In the multivariable linear regression, both fCSA and FI of the PPM were significantly and independently associated with the degree of AAC (p = 0.037 and p = 0.015, respectively).
Conclusions
This is the first study to demonstrate a significant and independent association between AAC and PPM morphology. The results of this study improve our understanding of the interaction between AAC and spinal musculature, with AAC being a reason for atrophy of the PPM.
Similar content being viewed by others
Data availability
The datasets generated and analyzed during the current study are available from the corresponding author upon reasonable request.
References
Boukhris R, Becker KL (1972) Calcification of the aorta and osteoporosis. A roentgenographic study. JAMA 219(10):1307–1311
Kauppila LI et al (1997) Disc degeneration/back pain and calcification of the abdominal aorta. A 25-year follow-up study in Framingham. Spine (Phila Pa 1976) 22(14): 1642–1647; discussion 1648–1649.
Estublier C, Chapurlat R, Szulc P (2015) Association of severe disc degeneration with all-cause mortality and abdominal aortic calcification assessed prospectively in older men: findings of a single-center prospective study of osteoporosis in men. Arthritis Rheumatol 67(5):1295–1304
Kauppila LI (2009) Atherosclerosis and disc degeneration/low-back pain—a systematic review. Eur J Vasc Endovasc Surg 37(6):661–670
Sakaura H et al (2019) Abdominal aortic calcification is a significant poor prognostic factor for clinical outcomes after decompressive laminotomy for lumbar spinal canal stenosis. Global Spine J 9(7):724–728
Sakaura H et al (2021) Does atherosclerosis have negative impacts on early adjacent segment degeneration after posterior lumbar interbody fusion? Global Spine J 11(5):674–678
Szulc P (2016) Abdominal aortic calcification: a reappraisal of epidemiological and pathophysiological data. Bone 84:25–37
Sfyri P, Matsakas A (2017) Crossroads between peripheral atherosclerosis, western-type diet and skeletal muscle pathophysiology: emphasis on apolipoprotein E deficiency and peripheral arterial disease. J Biomed Sci 24(1):42
Cholewicki J, McGill SM (1996) Mechanical stability of the in vivo lumbar spine: implications for injury and chronic low back pain. Clin Biomech (Bristol, Avon) 11(1):1–15
Panjabi MM (1992) The stabilizing system of the spine. Part I. Function, dysfunction, adaptation, and enhancement. J Spinal Disord 5(4):383–389; discussion 397.
Cramer GD (2014) Chapter 7—the lumbar region. In: Cramer GD, Darby SA (eds) Clinical anatomy of the spine, spinal cord, and ans, 3rd edn. Mosby, Saint Louis, pp 246–311
Hamrick MW, McGee-Lawrence ME, Frechette DM (2016) Fatty infiltration of skeletal muscle: mechanisms and comparisons with bone marrow adiposity. Front Endocrinol (Lausanne) 7:69
Ranger TA et al (2019) Paraspinal muscle cross-sectional area predicts low back disability but not pain intensity. Spine J 19(5):862–868
Noonan AM, Brown SHM (2021) Paraspinal muscle pathophysiology associated with low back pain and spine degenerative disorders. JOR Spine 4(3):e1171
Shi L et al (2022) Correlation between the fatty infiltration of paraspinal muscles and disc degeneration and the underlying mechanism. BMC Musculoskelet Disord 23(1):509
McDermott MM et al (2020) Skeletal muscle pathology in peripheral artery disease: a brief review. Arterioscler Thromb Vasc Biol 40(11):2577–2585
Cuschieri S (2019) The STROBE guidelines. Saudi J Anaesth 13(Suppl 1):S31–S34
Faron A et al (2019) Quantification of fat and skeletal muscle tissue at abdominal computed tomography: associations between single-slice measurements and total compartment volumes. Abdom Radiol (NY) 44(5):1907–1916
Chiapparelli E et al (2022) The association between lumbar paraspinal muscle functional cross-sectional area on MRI and regional volumetric bone mineral density measured by quantitative computed tomography. Osteoporos Int 33(12):2537–2545
Kauppila LI et al (1997) New indices to classify location, severity and progression of calcific lesions in the abdominal aorta: a 25-year follow-up study. Atherosclerosis 132(2):245–250
Koo TK, Li MY (2016) A guideline of selecting and reporting intraclass correlation coefficients for reliability research. J Chiropr Med 15(2):155–163
Kang S et al (2021) The effects of paraspinal muscle volume on physiological load on the lumbar vertebral column: a finite-element study. Spine (Phila Pa 1976) 46(19): E1015–E1021.
Lim WS et al (2022) Singapore clinical practice guidelines for sarcopenia: screening, diagnosis, management and prevention. J Frailty Aging 11(4):348–369
Li S et al (2020) Relationship of volumetric bone mineral density by quantitative computed tomography with abdominal aortic calcification. Bone 133:115226
Mandelli F et al (2021) Assessing fatty infiltration of paraspinal muscles in patients with lumbar spinal stenosis: goutallier classification and quantitative MRI measurements. Front Neurol 12:656487
Funding
The authors report no conflicts of interest concerning the materials or methods used in this study or the findings specified in this paper.
Author information
Authors and Affiliations
Contributions
LS: conceptualization, methodology, statistical analysis, investigation, writing-original draft, visualization, MM: conceptualization, methodology, writing—review& editing, TC: investigation, writing—review & editing, ST: writing—review & editing, GCW: writing—review & editing, JZ: formal analysis, investigation, validation, writing—review& editing, HH: writing—review & editing, PS: investigation, writing—review, AA: investigation, data curation, writing—review& editing, EC: investigation, data curation, writing—review& editing, KA: investigation, data curation, writing—review& editing, M.M.: investigation, data curation, writing—review & editing, JS: data curation, writing—review& editing, project administration, ET: methodology; writing—review& editing, JAC: methodology, project administration, writing—review& editing, AAS: project administration, writing—review& editing, FPC: project administration, writing—review& editing, APH: project administration, writing—review& editing; supervision, conceptualization, methodology.
Corresponding author
Ethics declarations
Conflict of interest
The authors declare that there is no conflict of interest concerning materials or methods used in this study or the findings specified in this paper.
Disclosure
Dr. Sama reports royalties from Ortho Development, Corp.; private investments for Vestia Ventures MiRUS Investment, LLC, ISPH II, LLC, ISPH 3, LLC, and VBros Venture Partners X Centinel Spine; consulting fee from Clariance, Inc., Kuros Biosciences AG, and Medical Device Business Service, Inc.; speaking and teaching arrangements of DePuy Synthes Products, Inc.; membership of the scientific advisory board of Clariance, Inc., and Kuros Biosciences AG; and trips/travel of Medical Device Business research support from Spinal Kinetics, Inc., outside the submitted work. Dr. Cammisa reports royalties from NuVasive, Inc.; private investments for 4WEB Medical/4WEB, Inc., Bonovo Orthopedics, Inc., Healthpoint Capital Partners, LP, ISPH II, LLC, ISPH 3 Holdings, LLC, Ivy Healthcare Capital Partners, LLC, Medical Device Partners II, LLC, Medical Device Partners III, LLC, Orthobond Corporation, Spine Biopharma, LLC, Synexis, LLC, Tissue Differentiation Intelligence, LLC, VBVP VI, LLC, VBVP X, LLC (Centinel) and Woven Orthopedics Technologies; consulting fees from 4WEB Medical/4WEB, Inc., DePuy Synthes Spine, NuVasive, Inc., Spine Biopharma, LLC, and Synexis, LLC; membership of scientific advisory board/other offices of Healthpoint Capital Partners, LP, Medical Device Partners III, LLC, Orthobond Corporation, Spine Biopharma, LLC, Synexis, LLC, and Woven Orthopedic Technologies; and research support from 4WEB Medical/4WEB, Inc., Mallinckrodt Pharmaceuticals, Camber Spine, and Centinel Spine, outside the submitted work. Dr. Girardi reports royalties from Lanx, Inc., and Ortho Development Corp.; private investments for Centinel Spine, and BCMID; stock ownership of Healthpoint Capital Partners, LP; and consulting fees from NuVasive, Inc., and DePuy Synthes Spine, outside the submitted work. Dr. Hughes reports research support from NuVasive, Inc. and Kuros Biosciences AG; and fellowship support from NuVasive, Inc. and Kuros Biosciences AG, outside the submitted work.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
The work was performed at Hospital for Special Surgery, New York City, NY, USA. The institutional review board of Hospital for Special Surgery approved this study.
Rights and permissions
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Schönnagel, L., Muellner, M., Caffard, T. et al. Abdominal aortic calcification is independently associated with increased atrophy and fatty infiltration of the lumbar paraspinal muscles: a retrospective cross-sectional study. Eur Spine J 32, 3002–3008 (2023). https://doi.org/10.1007/s00586-023-07783-5
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00586-023-07783-5