This study was an in-depth exploration of unique data from a nationally representative sample of adults living in the United States to identify biomarkers associated with musculoskeletal pain.
We performed secondary analyses of 2003–2004 NHANES data. After a first screening of 187 markers, analyses of 31 biomarkers were conducted on participants aged ≥20 years identified in all counties using the 2000 Census Bureau data (n = 4,742). To assess the association of each biomarker with each pain outcome (acute, subacute and chronic low back, neck, and shoulder pain), analyses were carried out using multivariable logistic regression with adjustments for sex, age and body mass index. Biomarkers were considered as continuous variables and categorized at the median of their distributions.
Pain at any site for ≥24 hours during the past month was reported by 1,214 participants. Of these, 779 mentioned that the pain had lasted for ≥3 months (“chronic pain”). α-carotene, ascorbic acid, β-carotene, mercury and total protein had a statistically significant, inverse association with ≥2 chronic pain sites. Acrylamide, alkaline phosphatase, cadmium, cotinine, glycidamide, homocysteine, retinol, triglycerides and white blood cell count were positively associated with ≥2 chronic pain sites. Few biological markers were associated with acute and subacute pain.
This study identified some biomarkers that were strongly and consistently associated with musculoskeletal pain. These results raise new hypotheses and could have tremendous implications for advancing knowledge in the field. Research on musculoskeletal pain needs to put more effort on the biological dimension of the biopsychosocial model of pain.
Citation: Djade CD, Diorio C, Laurin D, Dionne CE (2022) An exploratory identification of biological markers of chronic musculoskeletal pain in the low back, neck, and shoulders. PLoS ONE 17(4): e0266999. https://doi.org/10.1371/journal.pone.0266999
Editor: Bing Xue, Institute for Advanced Sustainability Studies, GERMANY
Received: February 2, 2021; Accepted: March 31, 2022; Published: April 15, 2022
Copyright: © 2022 Djade et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: Data from NHANES 2003-204 are available on Centers for Disease Control and Prevention website. https://wwwn-cdc-gov.acces.bibl.ulaval.ca/nchs/nhanes/continuousnhanes/default.aspx?BeginYear=2003.
Funding: The author(s) received no specific funding for this work.
Competing interests: The authors have declared that no competing interests exist.
Musculoskeletal pain, particularly at the lower back, is one of the main sources of disability-adjusted life years in several countries [1, 2]. Low back pain is a major cause of work absence worldwide  and generates one of the heaviest burdens of disease . Our current understanding of musculoskeletal pain is based on the biopsychosocial model of pain that has led to much progress in the past 30 years . However, while a lot of research interest has been directed toward psychosocial determinants, it seems that the “bio” part of the model has been mistreated, as the studies that have been conducted on these specific potential determinants targeted mostly mechanical and clinical variables.
In recent years, research on musculoskeletal pain has shown that work exposures are explaining only a limited fraction of the problem, that children, teenagers and adults, and not only workers in their fifties, suffer from musculoskeletal pain, and that most interventions are useless and do not alter the natural history of the disease . In fact, we have made much progress on excluding potential determinants and interventions, but much less advances on identifying actual ones. Although designing new interventions against musculoskeletal pain and conducting randomized controlled trials on such interventions are useful, the design of efficient interventions would have much better chances if based on a specific understanding of the disease. Musculoskeletal epidemiology still has to identify major determinants of musculoskeletal pain beyond socio-economic deprivation, cigarette smoking, psychological distress, obesity and some specific job exposures (e.g. manual material handling and job’s physical and psychological demands).
A biomarker is a characteristic that can be objectively measured and evaluated as an indicator of normal biological processes, pathogenic processes or pharmacological responses to a therapeutic intervention . In other applications of epidemiology, some biomarkers have been identified that have major clinical and research utility. Because the onerous costs of measuring biomarkers coupled with the numerous candidates considerably limit the opportunity of research, it is possible that we have not yet identified all biological determinants of musculoskeletal pain. Biomarkers of inflammation, vitamins, and pesticides, for example, could lead us to a better understanding of the pathogenic pathways to musculoskeletal pain. We thus conducted this study as a stringent exploration of biomarkers of musculoskeletal pain using very unique data from the National Health and Nutrition Examination Surveys (NHANES). These data document a wide range of biomarkers on a large representative sample of the US population, and as such offer a rare opportunity to study multiple biological variables with high statistical power.
Materials and methods
Source of data
Conducted by the National Center for Health Statistics (NCHS) of the Centers for Disease Control and Prevention (CDC), NHANES is a periodic cross-sectional program designed to assess the health and nutritional status of the population of the United States. The sample is representative of the resident civilian non-institutionalized U.S. population . We used NHANES 2003–2004 survey data because it still is the most recent examination that included questions related to pain.
NHANES data collection took place throughout the year and included a household interview and an examination conducted in a Mobile Examination Center (MEC)  which occurred within two weeks after the interview. The examination consisted of several questionnaires, and included physical measurements such as blood pressure, dental examination, and collection of blood, hair and urine specimens for laboratory testing .
Identification and recruitment of participants
NHANES sample is representative of the non-institutionalized civilian population residing in the 50 U.S. states and the District of Columbia . Participants were identified from Primary Sampling Units (PSU) in all counties using the 2000 Census Bureau data. Clusters of households were selected, each person in a selected household was screened for demographic characteristics, and one or more persons per household were chosen for the sample. The analysis was restricted to participants aged ≥20 years (n = 5,041). In this age group, 4,742 (94.1%) answered the questions about miscellaneous pain. Fig 1 shows the details of participation.
The outcomes for this study were retrieved from the “Miscellaneous Pain” questionnaire. These dichotomous variables indicated, during the past month, whether or not participants had pain that had lasted for ≥24 hours on a given anatomical site. We selected three anatomical sites: the lower back, neck and shoulder, which are sites most commonly affected by musculoskeletal pain. This definition of pain included acute (duration ≤1 month), subacute (between 1 and 3 months), and “chronic” (i.e. persistent for ≥3 months) episodes [11, 12]. The three sites were chosen because they are the most common; the idea is not to show the mechanism that causes pain, but the fact that a biomarker is associated with several pain sites supports the importance of this biomarker in musculoskeletal pain. Because the physiological processes of a musculoskeletal injury vary by duration, we performed analyses stratified by the duration of pain, with a main focus on chronic pain, since it is responsible for the largest part of the burden of musculoskeletal pain .
The laboratory components of NHANES 2003–2004 included the collection of various biological and environmental samples. The data collection and reporting systems are integrated within the main NHANES survey database. While the complete blood count analyses were performed in the MEC laboratory, most of the laboratory analyses were conducted off site. Biomarkers documented included bone formation markers, markers of inflammation, metals, vitamins, pesticides, and other environmental markers, among others (see S3 Appendix for complete list). Laboratory procedures used by NHANES were applied according to recognized and valid methods . To avoid over-dispersion, biomarkers with more than 30% missing data were not included in the analyses for the current study.
• Other independent variables.
The other independent variables considered were taken from the NHANES 2003–2004 demographic variables list. Sex was indicated as female or male. Age was that at the time of the interview. Body mass index (BMI) was calculated from measures taken during the interview, as weight in kilograms divided by height in meters squared and partitioned into four categories: [15, 16].
The general background descriptive characteristics of the participants were computed in terms of frequency and percentage for categorical variables and means (standard deviations—SD) for continuous ones. Biomarkers were characterized by median and interquartile range. To assess the association of each biomarker with each of the three pain outcomes according to the combination of duration and anatomical site, two analyses were carried out. Bivariate and multivariable logistic regressions were performed to produce respectively crude prevalence odds ratios (OR) and adjusted OR (aOR) for sex, age and BMI. Due to the numerous biomarkers measured in NHANES, and considering the exploratory nature of the study, we first ran the bivariate analyses using all biomarkers as continuous variables and dichotomized at the median of the distribution and retained only those that were statistically associated with pain on at least two anatomical sites (all durations) for the subsequent analyses. With biomarkers considered continuously, the estimates were computed for the increase of one unit. All estimates were weighted, and variances corrected by considering strata and PSU . Sensitivity analyses were conducted to assess the impacts on the conclusions of using each biomarker categorized into quartiles.
All analyses were conducted using SAS 9.4 (SAS Institute Inc., Cary, NC, USA) survey procedures with weight, stratum and cluster provided by NHANES . Statistical significance was fixed at a 0.05 threshold. In agreement with Rothman and Rubin, we did not adjust for multiple comparisons [19, 20]
Table 1 presents selected characteristics of the 4,742 study participants and the prevalence of pain outcomes. Overall, 52% of participants were females and the mean age was 46.4 years (SD: 0.5). The vast majority was composed of non-Hispanic whites (72.1%), married, or living as married (63.6%) and currently working (60.7%). The proportion of participants who had a high school diploma as the highest level of formal education was 58.3% and 33.3% reported an annual family income of 55,000 USD or more. Almost half (49.2%) of participants were nonsmokers, 21.4% reported daily smoking, 31.7% were obese and 17.7% had more than one comorbidity. Over 25% (n = 1,214) of participants reported pain in at least one musculoskeletal site that had lasted ≥24 hours during the past month: 36.6% at the lower back, 26.4% at the neck, and 24.5% at the shoulder. Among them, 779 (64.2%) mentioned that the pain had lasted ≥3 months (“chronic pain”) .
Table 2 presents the median and interquartile range of the biomarkers retained following the preliminary analyses (i.e. all the biomarkers that were statistically associated with at least two pain sites—all durations—when considered as continuous variables or dichotomized at the median of the distribution in bivariate logistic regression). These biomarkers are subdivided into groups of 1) vitamins and urinary markers, 2) cadmium, lead and total mercury, 3) blood count, marker of inflammation, cotinine and homocysteine, and 4) standard biochemicals. Biomarkers belonging to the groups of brominated flame retardants, metals in urine, organophosphorus insecticides, pesticides environmental in urine, pesticides—organochlorine metabolites, phthalates, phytoestrogens and polyfluoroalkyl chemicals were not statistically associated with any two of the three musculoskeletal pain sites considered. Because crude and adjusted models provided similar results, only those from adjusted models are presented.
Table 3 presents aORs for each biomarker retained in the first analysis step (continuous or dichotomized distribution) with the three chronic pain sites (n = 4,307). Only those remaining associated with at least two chronic pain sites after the second analysis step (dichotomized at the median or continuously) are described below.
- Vitamins and urinary markers
In this group of biomarkers, only six were associated with two (α-carotene, β-carotene, and ascorbic acid (vitamin C)) or three (acrylamide, glycidamide and retinol (vitamin A)) chronic pain sites. Among these, inverse associations were observed for median levels: α-carotene with chronic low back pain (aOR: 0.6; 95%CI: 0.4–0.8) and chronic shoulder pain (aOR: 0.4; 95%CI: 0.3–0.6); β-carotene with chronic low back pain (aOR: 0.5; 95%CI: 0.4–0.8) and chronic shoulder pain (aOR: 0.6; 95%CI: 0.4–1.0); and ascorbic acid with chronic neck pain (aOR: 0.7; 95%CI: 0.6–0.9) and chronic shoulder pain (aOR: 0.6; 95%CI: 0.4–0.9). Median levels of albumin and α-tocopherol (vitamin E) were positively associated with only one site of chronic pain.
- Cadmium, lead and total mercury
Two of these biomarkers were associated with the outcomes: positive associations were observed between cadmium levels and chronic low back pain (aOR: 1.5; 95%CI: 1.2–1.8), chronic shoulder pain (aOR: 1.5; 95%CI: 1.2–1.8), and chronic neck pain (aOR: 1.4; 95%CI: 1.1–1.7), and inverse associations were observed between median levels of total mercury and chronic low back pain (aOR: 0.6; 95%CI: 0.5–0.9), chronic neck pain (aOR: 0.7; 95%CI: 0.6–0.9) and chronic shoulder pain (aOR: 0.6; 95%CI: 0.4–0.9). Levels of lead were associated with only one chronic pain site.
- Blood count, marker of inflammation, cotinine and homocysteine
When treated as continuous variables, levels of cotinine and white blood cell count were positively associated with all three sites of chronic pain. Homocysteine levels were positively associated with two chronic pain sites, while median levels of platelet count, and C-reactive protein were associated with only one chronic pain site.
- Standard biochemicals
Biomarkers of standard biochemistry profiles such as phosphorus, sodium, total calcium, and uric acid were not statistically associated with any pain site. Bicarbonate, chloride, lactate dehydrogenase, potassium, cholesterol (direct-HDL and total), gamma glutamyl transferase and globulin were statistically associated with only one site, whereas alkaline phosphatase and total protein levels were associated with two sites. Median levels of triglycerides were positively associated with low back pain (aOR: 1.7; 95%CI: 1.2–2.5) and neck pain (aOR: 1.6; 95%CI: 1.1–2.4).
In separate analyses on acute and subacute pain, very few biomarkers were statistically associated with the outcomes; more importantly, the aOR was rarely far from 1.0. Only white blood cell count (aOR: 1.9, 95%CI: 1.0–3.7), alkaline phosphatase (aOR: 0.5, 95%CI: 0.3–0.9) and gamma glutamyl transferase (aOR: 2.5, 95%CI: 1.2–5.3) were statistically associated with acute neck pain (Table 4 in S1 Appendix). For subacute pain, β-carotene (aOR: 0.2, 95%CI: 0.1–0.4) and total mercury (aOR: 0.3, 95%CI: 0.1–0.8) were associated with shoulder pain, total cholesterol (aOR: 3.1, 95%CI: 1.1–8.4) and gamma glutamyl transferase (aOR: 4.1, 95%CI: 1.2–13.8) were associated with neck pain, and bicarbonate (aOR: 0.3, 95%CI: 0.1–0.8) was associated with low back pain (Table 5 in S2 Appendix). For both acute and subacute pain, no biomarkers were statistically associated with two or three sites.
Results were similar when biomarkers were categorized based on quartiles: almost all the variables associated with at least two pain sites in the main analyses retained their statistical significance.
This study used unique data to explore the associations of numerous biomarkers with self-reported musculoskeletal pain on three anatomical sites. The determinants of musculoskeletal pain are undoubtedly biopsychosocial, but very few studies have examined other potential biological determinants than clinical and mechanical ones. Our study thus makes an original contribution by providing the first report examining the relationship of several dozens of biomarkers with musculoskeletal pain. Only a few positive and inverse associations between biomarkers and chronic musculoskeletal pain syndromes were identified.
The literature on biomarkers of musculoskeletal pain is quite scarce. A recent systematic review found moderate evidence for a direct association between pro-inflammatory biomarkers, tumor necrosis factor alpha (TNF-α), C-reactive protein, interleukin-6, and nonspecific low back pain . Although this evidence is important, the investigators only looked at one site of musculoskeletal pain with a limited number of biomarkers. While their conclusion on C-reactive protein being statistically associated with low back pain is consistent with our findings, we used very stringent criteria to retain biomarkers, including a statistically significant association with at least two pain sites, and C-reactive protein did not qualify (although it was significant for low back pain). This approach was chosen to allow the identification of only the most prominent markers among many, but in so doing, could have resulted in missing ones.
Croft et al. , Natvig et al. , and Thomas et al.  found that musculoskeletal pain at one site is often accompanied by pain at other sites. Our finding of a few biomarkers being associated with chronic pain in at least two sites is consistent with the hypothesis of a systemic mechanism for chronic musculoskeletal pain.
Some authors have noted significant associations between specific vitamins and fibromyalgia . In other studies, although unclear for α-carotene , while plasma levels of provitamin A, β-carotene, were inversely associated with higher risk of fracture , other associations were direct; for instance, increased risk of fracture at high serum concentrations of retinol (s-retinol) has been observed in epidemiologic studies [28, 29]. More recently, cumulative dose of isotretinoin, a vitamin A derivative used to treat acne, has been associated with low back pain . Ascorbic acid (vitamin C) for its part, is essential for the activity of some enzymes (proline hydroxylase and lysine hydroxylase) that are necessary to maintain stable collagen helixes that characterize healthy connective tissues . In a previous report, suboptimal serum ascorbic acid concentrations were found to be independently associated with the prevalence of neck pain, low back pain, and low back pain with pain below knee in the past three months, self-reported diagnosis of arthritis/rheumatism and related functional limitations .
Exposure to environmental cadmium poses many public health problems, as it is a highly toxic substance that can cause important adverse health effects [33–35]. At high doses, cadmium is known to cause the so-called itai-itai disease whose dominant symptom is back pain . Like isotretinoin , cadmium is also known to be positively associated with homocysteine [38, 39], alkaline phosphatase , white blood cell count , triglycerides and monocyte elevation , HDL-cholesterol [43–45] and total protein reduction [44, 46]. Triglycerides are positively associated with retinol and α-tocopherol but negatively associated with β-carotene , which is partly consistent with our findings. Chronic mercury exposure has devastating effects on the human body , although mercury has been used for long time for its medicinal properties, including as a diuretic, antibacterial agent and laxative . Our results showing a protective association between mercury and chronic pain may be spurious, as observed in some studies , or it may represent a proxy for fish consumption as in others . Actually, 99% of participants showed mercury levels much below 20 μg/L, which is considered normal.
Cotinine is a marker of smoking that is preferred to nicotine because of its longer half-life . The association of smoking with musculoskeletal pain is very consistent and follows a dose-response gradient. This relationship is not explained by vitamin C deficiency among smokers . Acrylamide, a marker that has been classified as a probable carcinogen, can be ingested, inhaled (in tobacco smoke) or absorbed . It is formed in high amounts in many types of food prepared at high temperature. It has also been shown to cause progressive peripheral neuropathy . Our results that cotinine, acrylamide and its metabolite glycidamide , and cadmium—all cigarette smoke derivatives—being positively associated with chronic musculoskeletal pain, are compatible with the hypothesis placing them as mediators of the positive association between smoking and musculoskeletal pain; this hypothesis will need to be tested in future work.
While our study was exploratory, the fact that most associations identified were with chronic musculoskeletal pain and not with acute or subacute syndromes is interesting and again, would support the hypothesis of systemic mechanisms for chronic musculoskeletal pain.
The NHANES survey included a large national sample that was representative of the non-institutionalized population, which suggests that a selection bias is unlikely to have affected our results. Also, NHANES offered specific laboratory information on almost 200 biomarkers, using rigorous quality control and measurement instruments that provided high-quality data, a rare opportunity. The large number of participants provided high statistical power and precise estimates. We used a conservative and systemic approach to diminish chance findings.
Among the study limitations, its cross-sectional design does not allow to conclude to causal associations. Also, because musculoskeletal pain was self-reported, it is possible that our measures of outcomes suffered from non-differential misclassification due to recall bias. However, since the reference period was short, such a recall bias is probably limited. The definitions of musculoskeletal pain often differ between studies; we used definitions similar to those published by Dionne et al.  and Griffith et al.  that are widely used. These definitions require that participants had experienced pain during the past four weeks. Such definitions minimize recall bias since the focus is not on pain duration and the measurement instruments have been validated. Non-differential misclassification of the biomarkers is also to be expected, since each biomarker has a different threshold of exposure. Given the number of markers examined and the exploratory nature of our study, we could not use specific threshold for each marker. While the fact that most associations were found with chronic pain supports biological plausibility, the smaller sample sizes in the acute and subacute groups and the consequent limited statistical power could have prevented us to identify important associations in these subgroups. Finally, residual confounding is likely, given the same basic adjustments we have made in all regression models. Future studies on individual markers will be able to identify specific confounders and adjust for them, an enterprise that was impossible here given the numerous markers examined. Again, in interpreting the results of this study, it is thus important to keep its exploratory nature in mind.
In these exploratory stringent analyses of a very unique set of data, we found strong and consistent associations between some biomarkers and chronic musculoskeletal pain in the low back, shoulder, and neck. Acrylamide, glycidamide, α-carotene, β-carotene, cadmium, cotinine, mercury, retinol (vitamin A), triglycerides, white blood cell, homocysteine, alkaline phosphatase, total protein and ascorbic acid (vitamin C) had the strongest and more consistent associations with chronic musculoskeletal pain. As knowledge on the determinants of musculoskeletal pain is still very limited, these results could have tremendous implications in the field by opening new avenues of research. Research on musculoskeletal pain needs to put more effort on the biological dimension of the biopsychosocial model of pain.
S1 Appendix. Table 4. Results of multivariable analyses of the associations between biomarkers retained and the three acute pain sites studied (n = 3,834).
S2 Appendix. Table 5. Results of multivariable analyses of the associations between biomarkers retained and the three subacute pain sites studied (n = 3,658).
S3 Appendix. List of specific biomarkers considered in NHANES 2003–2004.
Thanks to Pierre-Hugues Carmichael and Myrto Mondor for statistical support. CD Djade holds scholarships from La Fondation CHU de Québec and the Centre d’excellence sur le vieillissement de Québec (CEVQ) du Centre de recherche en santé durable VITAM.
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