Abstract
Purpose
Individuals with cerebral palsy (CP) are at increased risk for frailty and chronic disease due to factors experienced throughout the lifespan, such as excessive sedentary behaviors and malnutrition. However, little is known about noncommunicable diseases (NCDs) and multimorbidity profiles in young adults with CP. The study objective was to compare NCD and multimorbidity profiles between young adults with and without CP.
Methods
A clinic-based sample of adults (18–30 years) with (n=452) and without (n=448) CP was examined at the University of Michigan Medical Center. The prevalence and predictors of 13 NCDs were evaluated, including existing diagnoses or historical record of musculoskeletal, cardiometabolic, and pulmonary morbidities. The level of motor impairment was determined by the Gross Motor Function Classification System (GMFCS) and stratified by less vs more severe motor impairment (GMFCS I–III vs IV–V). Logistic regression was used to determine the odds of NCD morbidity and multimorbidity in adults with CP compared to adults without CP, and for GMFCS IV–V compared to GMFCS I–III in those with CP, after adjusting for age, sex, body mass index, and smoking.
Results
Adults with CP had a higher prevalence of osteopenia, osteoporosis, hypertension, myocardial infarction, hyperlipidemia, asthma, and multimorbidity compared to adults without CP, and higher odds of musculoskeletal (odds ratio [OR]: 6.97) and cardiometabolic morbidity (OR: 1.98), and multimorbidity (OR: 2.67). Adults with CP with GMFCS levels IV–V had a higher prevalence of osteopenia/osteoporosis, osteoarthritis, hypertension, other cardiovascular conditions, pulmonary embolism, and multimorbidity, and higher odds of musculoskeletal (OR: 3.41), cardiometabolic (OR: 2.05), pulmonary morbidity (OR: 1.42), and multimorbidity (OR: 3.45) compared to GMFCS I–III.
Conclusion
Young adults with CP have a higher prevalence of chronic NCDs and multimorbidity compared to young adults without CP, which is pronounced in those with more severe motor impairment. These findings reiterate the importance of early screening for prevention of NCDs in CP.
Keywords: cerebral palsy, noncommunicable disease, multimorbidity, osteoporosis, osteoarthritis, cardiovascular disease, diabetes, pulmonary disease
Introduction
Cerebral palsy (CP) results from damage to or malformation of the infant brain and is the most common physical disability in childhood.1 Children with CP present with impaired neuromuscular function,2–4 low levels of physical activity,5–7 poor cardiorespiratory fitness,8 underdeveloped musculoskeletal tissue,5,6 and a high degree of fat of total body9 and musculoskeletal5,6 depots, which are largely governed by the extent of motor impairment.5,6 Mobility decrements are common in children with CP as they transition into and throughout adulthood.10–12 Consequently, individuals with CP may be at a heightened risk for developing chronic, noncommunicable diseases (NCDs) at younger ages compared to the general population.
There has been a considerable shift in the global burden of disease, with the prevalence of NCDs now outranking injuries and communicable, maternal, neonatal, and nutritional disorders combined.13 The burden of NCDs has been climbing with estimated costs of $7 trillion US dollars by 2030.14 The adult CP population is steadily growing due to increases in survival rate15 and prevalence16 of CP in recent decades. Indeed, CP represents a significant lifetime disability for individuals, their families, and caregivers. CP is associated with increased prevalence of cardiometabolic mortality17 and morbidity,18,19 greatly reducing life expectancy,20 all of which may develop or be accelerated by the presence of impairments and/or the aging process.18,19 There is, thus, strong rationale for approaching health care delivery for persons with CP within the context of a life course health development model.21 However, the framework that encompasses clinical care for patients with CP has been largely confined to issues that arise during childhood and adolescence, with little to no focus on understanding life course health development.
A comprehensive understanding of the primary and resulting sequela associated with aging in those with CP is lacking, especially in the early adult years. Better understanding these changes in health through the lifespan will help to guide future, target-specific preventive efforts in rehabilitation research and clinical practice to mitigate the exaggerated chronic conditions observed in patients with CP.19 The primary objective of this study was to examine the NCD profiles and risk factors in young adults with CP compared to young adults without CP. We hypothesized that young adults with CP would have a higher prevalence of NCDs compared to those without CP, and that risk factors would include obesity and greater motor impairments.
Patients and methods
Patient identification
A cohort query tool (Data Direct: https://datadirect.med.umich.edu) was used to identify patients who had clinical appointments at the University of Michigan Medical Center, as previously described.19 Briefly, we annotated the dataset using the Electronic Medical Records Search Engine (EMERSE) software. The EMERSE software is hosted behind the University of Michigan Medical Center firewall in a computing environment certified for storing protected health information. Access to EMERSE is limited to authorized personnel who have patient data access privileges or, among those using it for research, have provided evidence of training in responsible research practices and proof of valid institutional review board (IRB) approvals, including demonstration of a need to review identifiable patient information.22 At each login, users must complete a brief attestation form to document their intent of use. Audit trail logs are kept for each use session. The principal investigators (Peterson and Hurvitz) take full responsibility for de-identifying patient records and maintaining patient data confidentiality. The University of Michigan IRB approved this retrospective study, and patient consent to review their medical record was waived by the IRB because the nature of this study involved no more than minimal risk to the subjects; the waiver did not adversely affect the rights and welfare of the subjects; the research could not practicably (ie, feasibly) be carried out without the waiver.
This internally developed web application provides an interface for searching electronic medical records with a bundle of word iterations and phrases for variables of interest.22 Adults between 18 and 30 years of age, with a confirmed diagnosis of CP or no known neurological disorders (controls), who had an encounter with University of Michigan Medicine between 01/01/2011 and 07/31/2017 (6.5-year period), were considered for this study. Among individuals with CP, the distribution of affected limbs (ie, quadriplegic, hemiplegic, diplegic) was obtained from medical records. The level of motor impairment was classified according to the Gross Motor Function Classification System (GMFCS). GMFCS ranks motor impairment with GMFCS I/II reflecting gross motor independence, GMFCS III reflecting the use of assistive walking devices, and GMFCS IV–V reflecting wheelchair use for most to all mobility. We stratified GMFCS into two categories, GMFCS I–III and GMFCS IV–V, to reflect lesser and greater motor impairment, respectively.
Noncommunicable diseases
Clinical data were included for existing diagnosis or historical record of various NCDs and were grouped into three categories, including 1) musculoskeletal morbidity: osteopenia and osteoporosis, osteoarthritis, and rheumatoid arthritis; 2) cardiometabolic morbidity: stroke, hypertension, other cardiovascular problems (eg, heart valve disorders, peripheral artery disease, aortic aneurysm, heart failure), coronary artery disease, impaired glucose tolerance or type 2 diabetes, myocardial infarction, and hyperlipidemia (total cholesterol >240 mg/dL and/or triglyceride >200 mg/dL); and 3) pulmonary morbidity: asthma, pulmonary embolism, and emphysema. These conditions were chosen because of their potential impact on physical function and in accordance with the guidance from the literature relating to older adults and adults with disabilities.23,24
In addition to using the EMERSE, certain variables required additional data collection. For blood pressure, the most recent measurement was used to determine hypertension status (present vs absent) based on the Eighth Joint National Committee:25 systolic blood pressure ≥140 mmHg and/or diastolic blood pressure ≥90 mmHg. A clinical history of stroke and/or other cardiovascular problems (eg, heart valve disorders, peripheral artery disease, aortic aneurysm, heart failure) was included if it occurred at 18 years or older. Musculoskeletal, cardiometabolic, and pulmonary morbidities were defined on the basis of presence of at least one of the aforementioned chronic NCDs within each respective category. A morbidity score was created by summing the number of individual NCDs. Multimorbidity was defined as the presence of having at least two of the aforementioned NCDs.
Covariates
Demographic data, including race, age, and sex, were collected using the EMERSE software. Body mass index (BMI) was calculated by dividing body mass by height squared (kg/m2). BMI was separated into underweight (<18.5), normal weight (18.5–24.9), overweight (25.0–29.9), and obese (≥30.0) categories. Smoking status was categorized as never vs current, occasional, or previous smoker.
Statistical analyses
Descriptive characteristics are provided as mean, standard deviation, and percentages. Participant demographics and NCD prevalence were compared between groups (young adults with vs without CP) and between the level of motor impairment for those with CP (GMFCS I–III vs IV–V) using two-sample t-tests and chi-square (χ2) tests for continuous and categorical measures, respectively. Multiple logistic regression was used to determine the odds of NCD morbidity categories (musculoskeletal, cardiometabolic, and pulmonary) and multimorbidity, after adjusting for age, sex, race, BMI, and smoking status. The primary exposure of CP was included as a dichotomous indicator variable in all models. Data were analyzed using SAS software version 9.3 (SAS institute, Cary, NC, USA) with 2-sided 95% confidence intervals to determine significance.
Results
Descriptive characteristics
Descriptive characteristics of the study participants with (n=452) and without (n=448) CP are presented in Table 1. There were no group differences in age, sex, or obesity prevalence. However, there were group differences in race, underweight, normal weight, and overweight measures, and adults with CP had a lower prevalence of smoking status compared to adults without CP.
Table 1.
Descriptive characteristics and NCD prevalence of young adults with and without CP
| Without CP n=448 | With CP n=452 | p-value | |
|---|---|---|---|
| Descriptive characteristics | |||
| Age (years), mean ± SD | 23.7±2.8 | 23.6±3.4 | 0.74 |
| Male, % | 40.0 | 43.4 | 0.23 |
| Race/ethnicity, % | |||
| Non-Hispanic White | 73.7 | 81.2 | 0.01 |
| Non-Hispanic Black | 7.0 | 11.6 | 0.02 |
| Hispanic or Mexican American | 4.1 | 2.7 | 0.23 |
| Unknown/other race | 15.2 | 4.4 | <0.001 |
| BMI category, % | |||
| Underweight (BMI<18.5) | 0.3 | 24.3 | <0.001 |
| Normal weight (BMI 18.5–24.9) | 52.2 | 41.2 | 0.03 |
| Overweight (BMI 25–29.9) | 31.6 | 18.1 | 0.01 |
| Obese (BMI≥30) | 15.9 | 16.4 | 0.87 |
| Smoking status, % | 19.3 | 7.1 | <0.001 |
| Chronic NCD and multimorbidity prevalence, % | |||
| Musculoskeletal morbidity | 7.5 | 44.9 | <0.001 |
| Osteopenia/osteoporosis | 2.3 | 43.6 | <0.001 |
| Osteoarthritis | 4.1 | 5.4 | 0.37 |
| Rheumatoid arthritis | 1.8 | 0.4 | 0.05 |
| Cardiometabolic morbidity | 8.4 | 20.6 | <0.001 |
| Stroke | 0.0 | 0.0 | n/a |
| Hypertension | 3.2 | 11.8 | <0.001 |
| Other heart problems | 4.1 | 5.3 | 0.38 |
| Coronary artery disease | 0.0 | 0.2 | 0.32 |
| Diabetes | 1.4 | 2.2 | 0.33 |
| Myocardial infarction | 0.0 | 2.0 | 0.01 |
| Hyperlipidemia | 1.1 | 3.0 | 0.04 |
| Pulmonary morbidity | 22.2 | 27.9 | 0.04 |
| Asthma | 21.4 | 27.0 | 0.03 |
| Pulmonary embolism | 0.9 | 1.8 | 0.25 |
| Emphysema | 0.0 | 1.0 | 0.05 |
| Multimorbidity | 7.2 | 24.3 | <0.001 |
Abbreviations: BMI, body mass index; CP, cerebral palsy; NCD, noncommunicable disease; n/a, not applicable.
Of the young adults with CP, 231 (51%) were classified as GMFCS I–III and 221 (49%) as GMFCS IV–V (Table 2). There were no group differences in sex or race distribution. However, there were group differences in age, underweight, overweight, smoking status (GMFCS IV–V lower prevalence), and distribution of affected limbs in young adults with CP. A summary of morbidity score prevalence by CP status and GMFCS categories is depicted in Figure 1.
Table 2.
Descriptive characteristics of young adults with cerebral palsy based on motor impairment assessed using the GMFCS
| GMFCS I–III n=231 | GMFCS IV–V n=221 | Difference p-value | |
|---|---|---|---|
| Descriptive characteristics | |||
| Age (years), mean ± SD | 23.0±3.2 | 24.3±3.5 | 0.01 |
| Male, % | 39.4 | 47.5 | 0.08 |
| Race/ethnicity, % | |||
| Non-Hispanic White | 84.4 | 77.9 | 0.09 |
| Non-Hispanic Black | 9.6 | 14.0 | 0.14 |
| Hispanic or Mexican American | 1.7 | 3.6 | 0.21 |
| Unknown/other race | 4.3 | 4.5 | 0.56 |
| BMI category, % | |||
| Underweight (BMI<18.5) | 10.8 | 38.5 | <0.001 |
| Normal weight (BMI 18.5–24.9) | 43.7 | 38.4 0.26 | |
| Overweight (BMI 25–29.9) | 22.9 | 13.1 | 0.01 |
| Obese (BMI≥30) | 22.6 | 10.0 | <0.001 |
| Smoking status, % | 10.4 | 3.8 | 0.01 |
| Distribution, % | |||
| Quadriplegia | 17.1 | 93.6 | <0.001 |
| Hemiplegia | 38.7 | 1.9 | <0.001 |
| Diplegia | 44.2 | 4.5 | <0.001 |
| Chronic NCD and multimorbidity prevalence, % | |||
| Musculoskeletal morbidity | 31.2 | 59.3 | <0.001 |
| Osteopenia/osteoporosis | 29.1 | 58.6 | <0.001 |
| Osteoarthritis | 3.1 | 7.7 | 0.02 |
| Rheumatoid arthritis | 0.0 | 0.9 | 0.14 |
| Cardiometabolic morbidity | 15.2 | 26.2 | <0.01 |
| Stroke | 0.0 | 0.0 | n/a |
| Hypertension | 9.1 | 15.0 | 0.04 |
| Other heart problems | 2.1 | 8.6 | 0.01 |
| Coronary artery disease | 0.0 | 0.5 | 0.31 |
| Diabetes | 1.7 | 2.7 | 0.47 |
| Myocardial infarction | 1.3 | 2.3 | 0.43 |
| Hyperlipidemia | 2.2 | 3.2 | 0.51 |
| Pulmonary morbidity | 25.5 | 30.3 | 0.26 |
| Asthma | 24.8 | 28.6 | 0.36 |
| Pulmonary embolism | 0.4 | 3.5 | 0.02 |
| Emphysema | 0.4 | 0.5 | 0.96 |
| Multimorbidity | 15.2 | 33.9 | <0.001 |
Abbreviations: BMI, body mass index; GMFCS, Gross Motor Function Classification System; NCD, noncommunicable disease.
Figure 1.
Prevalence of morbidity score for adults with CP vs without CP, as well as for adults with CP with GMFCS levels I–III vs IV–V.
Note: Significant differences between adults with and without CP (*), and between GMFCS levels I–III vs IV–V (#); p<0.05.
Abbreviations: CP, cerebral palsy; GMFCS, Gross Motor Function Classification System.
Musculoskeletal morbidity
Adults with CP had a higher prevalence of osteopenia/osteoporosis compared to those without CP (Table 1). Adults with CP had a higher odds of musculoskeletal morbidity compared to those without CP (Table 3). Greater age, being underweight, and smoking status were all significantly associated with musculoskeletal morbidity.
Table 3.
Multiple logistic regression models for predictors of musculoskeletal, cardiometabolic, and pulmonary morbidities
| Model predictor(s) | Odds ratio | 95% CI | p-value | ||
|---|---|---|---|---|---|
| Musculoskeletal morbidity | Cerebral palsy | Unadjusted | 10.10 | 6.77–15.1 | <0.001 |
| Adjusted | 6.97 | 4.46–10.89 | <0.001 | ||
| Age (years) | 1.09 | 1.03–1.14 | <0.001 | ||
| Sex (Ref: women) | 0.88 | 0.62–1.26 | 0.48 | ||
| Race (Ref: Non-Hispanic White) | 0.86 | 0.72–1.02 | 0.08 | ||
| BMI category (Ref: normal weight [BMI 18.5–24.9]) | |||||
| Underweight (BMI<18.5) | 1.68 | 1.03–2.74 | 0.04 | ||
| Overweight (BMI 25–29.9) | 0.95 | 0.59–1.52 | 0.82 | ||
| Obese (BMI≥30) | 1.04 | 0.62–1.73 | 0.89 | ||
| Smoking status (Ref: never smoked) | 2.17 | 1.10–4.25 | 0.03 | ||
| Cardiometabolic morbidity | Cerebral palsy | Unadjusted | 2.84 | 1.89–4.26 | <0.001 |
| Adjusted | 1.98 | 1.26–3.13 | <0.01 | ||
| Age (years) | 1.05 | 0.99–1.11 | 0.14 | ||
| Sex (Ref: women) | 1.11 | 0.75–1.64 | 0.61 | ||
| Race (Ref: Non-Hispanic White) | 1.01 | 0.84–1.20 | 0.96 | ||
| BMI category (Ref: normal weight [BMI 18.5–24.9]) | |||||
| Underweight (BMI<18.5) | 1.30 | 0.74–2.30 | 0.37 | ||
| Overweight (BMI 25–29.9) | 0.65 | 0.36–1.15 | 0.13 | ||
| Obese (BMI≥30) | 1.78 | 1.06–2.98 | 0.02 | ||
| Smoking status (Ref: never smoked) | 1.16 | 0.61–2.22 | 0.65 | ||
| Pulmonary morbidity | Cerebral palsy | Unadjusted | 1.36 | 1.01–1.84 | 0.04 |
| Adjusted | 1.11 | 0.78–1.58 | 0.56 | ||
| Age (years) | 0.97 | 0.92–1.02 | 0.17 | ||
| Sex (Ref: women) | 1.25 | 0.90–1.72 | 0.18 | ||
| Race (Ref: Non-Hispanic White) | 1.08 | 0.95–1.2 | 0.22 | ||
| BMI category (Ref: normal weight [BMI 18.5–24.9]) | |||||
| Underweight (BMI<18.5) | 1.15 | 0.69–1.93 | 0.58 | ||
| Overweight (BMI 25–29.9) | 1.06 | 0.71–1.59 | 0.78 | ||
| Obese (BMI≥30) | 1.26 | 0.79–2.00 | 0.32 | ||
| Smoking status (Ref: never smoked) | 1.42 | 1.02–1.97 | 0.04 |
Abbreviations: BMI, body mass index; Ref, reference.
Of the adults with CP, those with GMFCS IV–V had a higher prevalence of osteopenia/osteoporosis and osteoarthritis compared to those with GMFCS I–III (Table 2). Moreover, a higher prevalence of musculoskeletal morbidity was found for individuals with GMFCS levels IV–V (59.3%) as compared to those with GMFCS levels I–III (31.2%), as well as higher odds of musculoskeletal morbidity (odds ratio [OR]: 3.41; 95% CI: 2.18–5.35). Greater age (OR: 1.10; 95% CI: 1.04–1.16) and underweight status (OR: 1.52; 95% CI: 1.02–1.27) were both associated with musculoskeletal morbidity in individuals with CP.
Cardiometabolic morbidity
Adults with CP had a higher prevalence of hypertension, myocardial infarction, and hyperlipidemia compared to those without CP (Table 1). Adults with CP had a higher odds of cardiometabolic morbidity compared to those without CP (Table 3), and only obesity was significantly associated with cardiometabolic morbidity.
Of the adults with CP, those with GMFCS IV–V had a higher prevalence of hypertension and other cardiovascular problems compared to those with GMFCS I–III (Table 2). Moreover, a higher prevalence of cardiometabolic morbidity was found for individuals with GMFCS levels IV–V (26.2%) compared to GMFCS levels I–III (15.2%), as well as higher odds of cardiometabolic morbidity (OR: 2.05; 95% CI: 1.20–3.50). Only obesity (OR: 1.85; 95% CI: 1.01–3.41) was significantly associated with cardiometabolic morbidity in individuals with CP.
Pulmonary morbidity
Adults with CP had a higher prevalence of asthma compared to those without CP (Table 1). There were no group differences in the odds of pulmonary morbidity (Table 3), and only smoking status was significantly associated with pulmonary morbidity.
Of the adults with CP, those with GMFCS IV–V had a higher prevalence of pulmonary embolism compared to those with GMFCS I–III (Table 2). No difference in prevalence of pulmonary morbidity was found for individuals with GMFCS levels IV–V compared to GMFCS levels I–III; however, individuals with GMFCS levels IV–V had higher odds of pulmonary morbidity (OR: 1.42; 95% CI: 1.02–1.80).
Multimorbidity
Adults with CP had a higher prevalence of multimorbidity compared to those without CP (Table 1), as well as a higher odds of multimorbidity compared to those without CP (Table 4). Underweight, obesity, and smoking status were all significantly associated with multimorbidity.
Table 4.
Multiple logistic regression models for independent predictors of multimorbidity
| Model predictor(s) | Odds ratio | 95% CI | p-value | ||
|---|---|---|---|---|---|
| Multimorbiditya | Cerebral palsy | Unadjusted | 4.12 | 2.71–6.26 | <0.001 |
| Adjusted | 2.67 | 1.69–4.23 | <0.001 | ||
| Age (years) | 1.00 | 0.94–1.05 | 0.94 | ||
| Sex (Ref: women) | 1.14 | 0.77–1.68 | 0.51 | ||
| Race (Ref: Non-Hispanic White) | 0.94 | 0.78–1.13 | 0.50 | ||
| BMI category (Ref: normal weight [BMI 18.5–24.9]) | |||||
| Underweight (BMI<18.5) | 1.95 | 1.14–3.33 | 0.01 | ||
| Overweight (BMI 25–29.9) | 1.15 | 0.68–1.94 | 0.61 | ||
| Obese (BMI≥30) | 2.04 | 1.20–3.47 | 0.01 | ||
| Smoking status (Ref: never smoked) | 1.92 | 1.02–3.61 | 0.04 |
Note:
≥2 musculoskeletal, cardiometabolic, and pulmonary morbidities.
Abbreviations: BMI, body mass index; Ref, reference.
Of the adults with CP, adults with GMFCS IV–V had a higher prevalence of multimorbidity compared to those with GMFCS I–III (Table 2). There was also a higher odds of multimorbidity among those with GMFCS levels IV–V compared to GMFCS levels I–III (OR: 3.45; 95% CI: 2.04–5.83). Only obesity (OR: 1.83; 95% CI: 1.01–1.20) was significantly associated with multimorbidity in individuals with CP.
Discussion
The principal findings of this study are that young adults with CP have a higher prevalence of NCDs relating to musculoskeletal, cardiometabolic, and pulmonary systems compared to the general population of young adults without CP. Age, being underweight or obese, smoking, and the level of motor impairment were each independently associated with higher odds of many NCDs and multimorbidity in young adults with CP.
Over the past few decades, global disease burden has shifted from premature death to years lived with disabilities, and from communicable diseases to NCDs.13 Nearly 40% of global NCD-related deaths occur before the age of 70 years.26 Given the increased survival rate15 and a marginally increasing prevalence of CP16 throughout the past several decades, there is an expanding adult CP population that is at risk for premature NCD-related deaths. In the current study, young adults with CP had a higher prevalence of multiple NCDs and a multimorbidity prevalence of nearly 25%. By middle age (40–60 years), adults with CP have a multimorbidity prevalence of nearly 60%,19 which is 1.5–2.9 times higher than the general population of middle-age adults.27 Collectively, these data highlight a CP-specific NCD burden that is unique from the general population.
Musculoskeletal morbidity
The finding that young adults with CP have a high prevalence of musculoskeletal morbidities is clinically important, but not surprising. Children with CP have an underdeveloped musculoskeletal system,5,6 with deficits presenting as early as 2 years old.28 Mobility deficits are observed as children with CP age into and throughout their adult years10–12 leading to a progressive loss of mechanical loading, which is an essential stimulus for musculoskeletal growth and maintenance. Mobility deficits are also associated with musculoskeletal pain,10,12 which is inversely related to physical activity levels in those with CP.29 We found age to be a significant risk factor for musculoskeletal morbidity in the current study, suggesting a worsening of musculoskeletal morbidity prevalence in those with CP even within a young and narrow age range.
Cardiometabolic morbidity
The progressive loss of function in persons with CP may help to explain why the risk for cardiometabolic morbidities is higher in young adults with CP.30,31 The prevalence of hypertension and hyperlipidemia in young adults with CP in the current study was 11.8% and 3%, respectively. Ryan et al32 showed that children and adolescents with CP, aged 6–17 years, had a 10.5% prevalence of hypertension, with age being significantly and positively associated with blood pressure. Moreover, van der Slot et al33 reported a higher prevalence of hypertension of 25.6% in those with CP between the ages of 25 and 45 years, while we have previously reported prevalences up to 50% in 40–60-year-olds for prehypertension and hypertension.19 Ryan et al34 found a prevalence of hyperlipidemia of 27.3% in adults with CP aged 18–65 years, while 9% were taking medication for dyslipidemia and another 9% for hypertension. Although the frequency reporting myocardial infarction was low in the CP cohort (2%) and absent in the adults without CP in the current study, the difference is still clinically meaningful given the young age of study participants. These findings suggest an early cardiovascular risk phenotype among individuals with CP, which provides insight as to why adults with CP have a substantially higher cardiovascular mortality rates compared to the general population.17 Taken together, the window to prevent cardiovascular complications in those with CP occurs prior to reaching adulthood.
Somewhat surprisingly, we did not see a difference in the prevalence of impaired glucose tolerance or type 2 diabetes, which is consistent with another study in adults with CP that found normal fasting glucose levels.34 However, a glucose challenge, such as a glucose tolerance test, may be more indicative of glucose handling, and has not been exclusively studied in those with CP. Elder et al35 reported that adults with spinal cord injury, a comparative reference population often used to better understand pathologies observed in CP,36,37 saw no differences in fasting glucose or insulin levels compared to individuals without CP. However, after administering a glucose load, both glucose and insulin levels were significantly elevated compared to individuals without CP, suggesting impaired glucose handling. Given the hallmark altered musculoskeletal5,6,38 and functional profiles5–7 in CP, both of which are associated with insulin resistance,30,31,35 it is curious as to why glucose dysregulation is not a prevalent complication in those with CP. This phenomenon requires further investigation; and yet, it may be a direct result of poor clinical screening for metabolic diseases in this population.
Pulmonary morbidity
Children with CP have poor cardiorespiratory fitness, which is associated with an increased cardiometabolic disease risk.8 In addition, the low cardiorespiratory capacity in children with CP39 is linked to lower chest mobility during respiration.40 It is of interest whether functional limitations in CP lead to pulmonary dysfunction and morbidity, or if pulmonary dysfunction and morbidity are drivers of the functional loss with age and subsequent increased risk for developing NCDs. Future research is needed to better understand the causal pathways leading to pulmonary dysfunction and morbidity in the context of disability severity.
The finding that modifiable risk factors, such as weight status and smoking status, are associated with NCDs and multimorbidity prevalence is consistent with our previous study in middle-age adults with CP.19 While there are known associations between NCDs and being underweight,41 being obese,42 and using tobacco,14 there are weight management and smoking cessation programs that may help to mitigate the high prevalence of NCDs observed in the adult CP population. Not surprisingly, motor impairment was also significantly associated with NCDs and multimorbidity in the current study. In general, adults with CP have lower levels of physical activity. However, the degree of physical activity restriction is inversely related to increasing levels of motor impairment.43 Poor diet or malnutrition, tobacco use, and physical inactivity are the three most common modifiable risk factors associated with NCD-related premature death.14 These three modifiable risk factors are associated with NCDs and multimorbidity in the entire cohort of young adults with and without CP. Interestingly, young adults with CP had a fewer number of risk factors associated with musculoskeletal morbidity, pulmonary morbidity, and multimorbidity, but similar strength of associations, compared with the combined sample of young adults with and without CP. This may suggest that those with CP have a unique set of risk factors for developing or accelerating NCDs compared with the general population. Future initiatives are needed to develop programs with goals specific to assist persons with CP and caregivers for maintaining a healthy body composition, abstinence from tobacco use, and improving sleep, nutrition, and physical activity levels.44
Strength and limitations
The study has several strengths. To date, this is the largest study in young adults with CP, which also includes a control group within the same age range. The recent initiatives in CP-specific surveillance programs have helped to identify a disease burden that is accelerated in the CP population by middle age.19 This has prompted the investigation of evaluating the NCD profiles in a younger cohort of adults with CP to help identify the window of disease clustering. Another strength of the current study is that all data were pulled from the same site (hospital system at the University of Michigan) and within a relatively narrow time period. This is important to consider because different global regions and time periods are associated with heterogeneous development of communicable diseases and NCDs.13
Several limitations must also be discussed. First, due to the design, we were unable to determine a cause and effect among exposures and outcomes. Second, we were limited to identifying NCDs using medical records that yielded a dichotomous coding for NCDs rather than a graded scale. Therefore, the severity of conditions was not accessible, which could have provided further insight into the NCD profiles of young adults with CP (eg, bone mineral density or T-scores for osteopenia and osteoporosis). Another limitation is the accuracy of the medical charts. If the NCD was not diagnosed on their medical chart, the participant was considered to not have that NCD. However, screening for NCDs in young adults with CP is not a common clinical practice in the United States. Therefore, our estimates may actually be underrepresenting the true extent of the NCD risk in young adults with CP.
Conclusion
Young adults with CP have a high prevalence of NCDs and multimorbidity, particularly for the musculoskeletal and cardiometabolic systems. Modifiable risk factors, such as underweight, obesity, and smoking status, were associated with NCDs and multimorbidity. This is an important finding because adults with CP are not expected to have such a disease burden at a young age, and clinical screening has been inadequate. Our findings highlight the importance of clinical screening for NCD clustering in persons with CP as early as adolescence or young adulthood, and may prompt early behavioral interventions for NCD prevention in this population.
Acknowledgments
We thank Rachael V Torres, University of Delaware, for critically reviewing the later versions of this manuscript. Mark D Peterson is funded by the National Institutes of Health (NIH) (1KO1 HD074706) and the National Institute on Disability, Independent Living, and Rehabilitation Research (NIDILRR) (90IF0102-01).
Footnotes
Author contributions
EA Hurvitz and MD Peterson had full access to all of the data in the study and take full responsibility for the integrity of the data and the accuracy of the data analyses. DG Whitney, EA Hurvitz, JM Ryan, and MD Peterson contributed to the concept and design. EA Hurvitz, ZP French, EC Ellenberg, and MD Peterson contributed to acquisition of data. All authors contributed to drafting of the manuscript. MD Peterson contributed to statistical analysis, and study supervision. All authors contributed to the interpretation of data. EA Hurvitz, MJ Devlin, MS Caird, ZP French, EC Ellenberg, and MD Peterson contributed to administrative, technical, or material support. All authors contributed to critical revision of the manuscript for important intellectual content. All authors provided final approval of the manuscript version to be published, and have agreed to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.
Disclosure
The authors report no conflicts of interest in this work.
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