Sickle cell disease is a global prototype for integrative research and healthcare
PMCID: PMC9744540
PMID:
Abstract
Abstract Differences in health outcomes and treatment responses within and between global populations have been well documented. There is growing recognition of the need to move beyond simple inventories and descriptions of these differences and our linear explanations for them, and gain a better understanding of the multifaceted systems and networks underlying them in order to develop more precise and effective remedies. Typical targets for such integrative research have been common multifactorial diseases. We propose sickle cell disease, one of the most common monogenic diseases, as an ideal candidate for elucidating the complexity of the influences of endogenous and exogenous factors on disease pathophysiology, phenotypic diversity, and variations in responses to treatments at both the individual and population levels. We provide data‐informed representations of diverse contributors to sickle cell disease complications that could guide innovative efforts to advance scientific knowledge, clinical practice, and policy formulation related to the disease; help improve outcomes for people worldwide with sickle cell disease; and inform approaches to studying and addressing other diseases. Sickle cell disease, one of the most common monogenic diseases with global reach, illustrates the complexity of the influences of endogenous and exogenous factors on disease pathophysiology, phenotypic diversity, and variations in responses to treatments. Multiple domains of influence comprise intricate networks that interact with one another over the life course at both the individual and population levels. These biological, psychological, clinical, behavioral, sociocultural, structural, and environmental variables interact to produce episodes of clinical disease and changing experience of disability and resilience. Data from both clinical records and affected individuals suggest conceptual models that can in turn be tested statistically. Other monogenic disorders could also serve to model and decode more common and etiologically complicated health conditions, advancing global efforts to improve and sustain health.
Full Text
The moral imperative to improve health and eliminate health inequities and disparities calls for fundamental changes in how disease and individual and population health differences are investigated and addressed.
Integrative (holistic) research and global health are recurring themes in this discourse and in the burgeoning shift toward transdisciplinary, translational, and transformational science.
,
The United States (US) Precision Medicine Initiative (PMI) and other similar country‐ and continent‐wide biomedical efforts have emerged from this shift, heralding a potential global revolution in research and healthcare.
,
,
However, the capacity of these initiatives to effectively facilitate optimal health, disease prevention, and health equity will be largely dependent on their commitment to and embodiment of the integrative guiding frameworks they espouse.
Advances in biology (eg, genomics) are providing new insights into the molecular and other endogenous contributors to health and the etiology, course, and treatment of disease, while epidemiological and health disparities research have been shedding light on social and other exogenous dimensions. For example, observed differences in health and disease indicators within and between countries and populations have been attributed to factors such as genetic variation, geographical location, cultural and psychosocial influences, behaviors, and unequal distributions of power, income, goods, and services.
,
,
,
,
Any breakdown in health represents a nonlinear phenomenon; therefore, it is critical to view the disease process not solely as a collection of individual risk factors, but to model it as a network of relationships with properties not attributable to individual components.
Despite increased recognition of the need for more integrative approaches to biomedical research, a substantial portion of research (including some claiming to be integrative) is still guided by linear, reductionist heuristics. Furthermore, most of the published studies and emerging initiatives on genotype‐environment interactions (broadly defined) and multi‐level systems science instinctively focus on multifactorial or so‐called complex diseases and traits. It has long been acknowledged that despite their monogenic etiology, classical Mendelian diseases, such as cystic fibrosis, phenylketonuria, hemochromatosis, G6PD deficiency, and the hemoglobinopathies are also complex, generally having variable phenotypic expression due to interactions among an array of genetic and non‐genetic factors.
,
Nonetheless, these disorders traditionally have not been targets for systematic genotype‐environment investigations. Monogenic conditions are poised to bring new dimensions to the study of disease complexity over the life course and to our understanding of health differences at the individual, family, and population levels. They provide a unique opportunity to identify diverse modifiers of risk and resilience as they have uniform etiology, detailed phenotyping of affected individuals, and familial clustering.
Naturally, they are also prime candidates for novel genetic tools and technologies such as gene therapy and somatic cell genome editing (eg, CRISPR) that are accelerating the quest for cures.
Overall, monogenic disorders could serve to model and decode more common and etiologically complicated health conditions, advancing global efforts to improve and sustain health.
Sickle cell disease (SCD) is the first disease whose genetic etiology was defined, and is one of the most common severe monogenic diseases in humans. SCD refers to a group of recessively inherited blood disorders characterized by the predominance of sickle hemoglobin (HbS), the result of a single nucleotide change in the structural gene for the beta unit of hemoglobin (HBB).
,
The HbS variant is considered to have originated in Africa and subsequently increased rapidly in frequency as a result of the substantial protection from severe malarial infection that it provides to heterozygote carriers (sickle cell trait; SCT).
,
The clinical manifestations of SCD result from increased red cell hemolysis, vaso‐occlusion, and accompanying physiologic changes that lead to acute complications, including acute painful episodes (vaso‐occlusive crises; VOC), susceptibility to infection, acute chest syndrome, and stroke, along with chronic pain and organ damage to the spleen, kidneys, brain, and lungs.
These and other complications extend across the life spectrum and reduce life expectancy of people living with SCD by about 30 years compared to their healthy peers.
,
,
SCD affects approximately 20 million people worldwide and is most prevalent in parts of Africa, the Caribbean, the Mediterranean basin, the Middle East, India, and South and Central America.
,
Notwithstanding the diverse populations affected, in some countries, such as the US, Brazil, and Turkey, SCD has long been misconstrued as a “black disease” or a disease of racially marginalized groups, and this racialized notion of the disease is a key element of its distinctive biocultural story.
,
,
Globally, more than 300 000 babies are born annually with SCD, of which at least 75% are in Africa.
SCD remains a leading source of mortality, morbidity, and health disparity, and has been designated as a major global health problem and priority by the World Health Organization (WHO) and United Nations (UN).
,
Recent major national and global initiatives aimed at providing new financial and other resources for monitoring, researching, treating, and curing SCD demonstrate increasing attention to the disease.
,
,
,
The frequency and severity of SCD complications vary markedly between patients and at different ages. Both genetic and non‐genetic factors are known to influence SCD severity.
,
,
,
For example, high fetal hemoglobin (HbF) levels have long been associated with less severity
; HbF levels are under genetic control and are amenable to therapeutic manipulation in SCD.
Similarly, co‐inheritance of α‐thalassemia is protective against some SCD‐related complications, such as hemolysis and stroke.
,
,
However, most of the viable clinical expression remains unexplained by the genetic markers that have been examined. Indeed, availability of appropriate medical care, as in industrialized countries, usually mitigates morbidity and facilitates longer survival of people with SCD.
In countries with less resources, on the other hand, morbidity is high and survival is low due to the combined effect of inadequate care and often severe clinical complications,
compounded by other factors such as malnutrition, poverty, and exposure to pathogens.
,
Studies have also found that pain severity is associated with exposures to a variety of climate factors, including temperature fluctuation, wind speed, humidity, and high altitudes, as well as acute air influences such as air pollutants.
,
,
Although these social and environmental influences on SCD complications are known, the exact mechanisms and pathways through which they influence clinical variability and phenotype are not well understood. Yet, there is limited research on the roles of these and other exogenous factors in SCD outcomes and even less published empirical research on the joint impacts of endogenous and exogenous factors. Major knowledge gaps also exist concerning the characteristics and effects of some dimensions of biology such as the microbiome and epigenome.
The scientific and social histories of SCD, coupled with its substantial individual and population variability, have led to the identification of SCD as an ideal model for elucidating mechanisms by which diverse endogenous and exogenous factors combine to influence health, disease, and health disparities.
,
,
Along with spurring new pharmacological, genomic, and other cellular‐ or molecular‐level interventions, adequately resourced and well‐designed integrative SCD research could identify structural, social, environmental, and behavioral targets for prediction, prevention, treatment, and management of SCD complications that are more practical, safe, accessible, and affordable. Integrative SCD research could also complement and inform existing and emerging curative efforts such as bone marrow transplantation, gene therapy, and somatic cell genome editing.
We created an illustration that depicts the confluence of biological, psychological, clinical, behavioral, sociocultural, structural, and environmental factors/domains and SCD outcomes (physician‐ and patient‐reported) in a global context (Figure 1). This theoretical framework is guided by the Identity Networks, Genome, and Affect as Modulators of Health (INGAM) model,
an integrative data‐driven model that attempts to clarify the degree of interdependence between social ecology and genomic processes. The INGAM model draws on principles from nonlinear dynamics, delineating major lines of bifurcation, in an effort to operationalize a multifactorial approach to health and illness. It facilitates understanding of not only the distal factors contributing to health conditions, but also the proximal mechanisms by which disease occurs or health can be restored and maintained. Consequently, INGAM opens the door for the exploration of more effective preventive and treatment measures, or for engineering new ways of delivering care to individuals and communities facing a number of daunting health problems.
Figure 1 posits that the potential causal influence of a given factor, or node, in the system is sensitive to the state of the other nodes in the system. This sensitivity may, for example, take the form of mediating effects, multiplicative (interactive) effects, or feedback loops. For each of the seven “antecedent” domains in the framework, there are selected examples of variables linked in the extant literature to one or more of the SCD outcomes or to some measure of disease severity.
,
,
Furthermore, variables in some of the “antecedent” domains, such as psychological and behavioral, can themselves be outcomes of the SCD experience. This reinforces the fluidity and complexity of the associations among and within the domains.
Focusing on pain, the most common complication of SCD, we constructed a preliminary conceptual model (Figure 2) from our theoretical framework. Factors influencing SCD pain were synthesized from the literature and organized into 4 domain clusters: (1) Biological/Clinical,
,
,
,
,
,
,
,
,
,
,
(2) Structural/Environmental,
,
,
,
,
,
,
(3) Psychosocial,
,
and (4) Behavioral.
,
,
Double‐headed arrows connecting the clusters indicate that all factors may display inter‐cluster relations. Although not displayed, factors within a cluster may also interact with one another. For example, nutritional deficiency, though classified as a behavioral attribute, is highly interlinked with structural/environmental factors such as residential area and socioeconomic status, biological/clinical factors such as genetics, and other behavioral factors such as drug use. Conceptualizations and frameworks of SCD tend to emphasize genetic and clinical contributors to various disease complications, including pain. Although genetic and genomic factors can influence the manifestation and experience of pain, a myriad external factors can modify or interact with an individual's genomic or clinical attributes, confer protection against impending pain episodes, or influence the severity and intensity of pain. While understanding an individual's biological or clinical history may grant clinicians some understanding of the physiological processes underlying pain episodes, it fails to capture the multidimensional nature of SCD. Subsequently, pharmacological treatment of pain may be a process to be included in a multifactorial management design that takes into account a patient's socioeconomic status, residential area, and mental health. Factors in Figure 2represented by solid colored arrows represent known contributors to pain or those that increase the likelihood of worsening pain. Dashed colored lines signify known mediators which lessen/prevent pain or confer protective effects. The mechanisms through which these factors act are also not well known and merit further research. LSD1 inhibitors
and BCL11A silencing
are included as examples of potential therapeutic mechanisms. A variety of protective factors, including HbF, coping mechanisms, and some behavioral factors may be critical targets for integrative research and interventions.
Understanding how factors converge and precipitate or influence SCD complications longitudinally is critical in modeling the complexity of SCD and the processes through which phenotypic variations in outcomes such as pain are expressed.
Temporal modeling of gene‐environment interactions in disease trajectory can be accomplished with tools such as observational data, medical records, and genomic/transcriptomic analysis.
,
,
For SCD pain, modeling could be done through the creation of a “health timeline” (Figure 3), in which intensity, duration, and frequency of stressors and protective factors (see Figure 2) are measured and observed for an individual experiencing a recorded pain outcome. In this conceptual timeline, factors that occur before a pain episode would be classified as precipitating factors, whereas factors that occur during an episode would be considered associative. The frequency and duration of factor co‐occurrence as they correlate with pain events would provide an innovative method of quantifying the nature of co‐factor associations as well as factor/outcome relationships.
Our initial plan included applying accepted techniques for data harmonization.
,
After obtaining institutional research ethics approvals and retrieving the data, it was clear that there would be substantial barriers to achieving our aim of modeling relationships and making meaningful comparisons across sites. For example, datasets from two sites captured information from each separate clinic visit, while data from the other site were aggregated across clinic visits with only one summary value per patient for a given variable. Thus, we could not adequately compare all sites with respect to temporal associations among variables. There were also problems regarding poor standardization of variable names within the dataset at one site.
Ultimately, we elected to abandon any across‐site integration and instead conduct a few simple, largely descriptive analyses within each dataset. We judged that the data from Jamaica were in a condition most amenable to a reliable statistical analysis. Using these data, we estimated the associations between a set of environmental variables and pain episodes using a multivariable logistic regression model. The Huber‐White sandwich estimator was used to account for multiple visits per person (ie, within‐person clustering). Complete data for the variables under study were available from 4404 adults collected from 35 431 clinic visits over 5 years. The subsample had a mean age of 38 years, 55% of whom were women. We found that younger age, colder atmospheric temperature, higher rainfall, lower environmental zinc, and greater poverty were associated with a higher probability of a pain episode. There was no evidence that these associations differed across hemoglobin genotypes. Neither sex, urban vs rural location, elevation, nor geographic distance from a clinic exhibited any appreciable evidence of an association with the probability of a pain episode. Although several of the positive findings corroborate those from previous studies and have important implications for pain prevention and management,
,
,
we caution that all of the pilot study findings (positive and negative) should only be interpreted as preliminary.
The pilot study confirms the importance and urgency of efforts to streamline policies and procedures for informed consent and the storage, sharing, and use of genomic and other types of data. Our initial work also underscores the need for comprehensive, valid, and sustainable standardization of SCD vocabulary and phenotyping. The SCD Ontology (SCDO) developed by an international group of SCD experts is a promising mechanism for meeting this need.
Tools such as the SCDO are essential for large cohort studies and surveillance systems, whether utilizing secondary data or collecting primary data to avert some of the challenges with data harmonization. Experts in computational and statistical data sciences who can skillfully apply and generate novel tools and algorithms for high‐dimensional modeling and data analysis are vital to the interdisciplinary research teams needed to implement this potentially transformative work.
From evolution to genome editing, SCD is preeminent in research on both the origins and eradication of human disease.
,
,
Whether the first molecular disease becomes the first to have an approved molecular cure from CRISPR remains to be seen. In the meantime, we must continue to scale up efforts to develop new tools and techniques for reducing and preventing complications in the millions of people worldwide suffering from SCD, most of whom are unlikely to have immediate access to high‐tech cures when they become available. We note that with SCD unmet needs are prevalent, even in European and North American countries.
Large national and multinational integrative studies are needed to better understand SCD globally and catalyze the development, translation, and implementation of locally‐appropriate interventions and policies. International organizations such as the WHO are best positioned to incentivize countries to adopt this integrated approach to SCD as a complex disease, just as the WHO urged countries in 2006 to develop and implement national programs for the management of SCD and countries in turn established clinical care guidelines for SCD.
,
,
,
,
The recent SCD report from the US National Academies of Sciences, Engineering, and Medicine could serve as a comprehensive roadmap for the WHO and other organizations seeking to encourage or fund ecological SCD research that will accelerate improved health and healthcare at local, national, and global levels.
Although this work is challenging and requires ample resources, it will yield tremendous rewards for human knowledge and wellbeing far beyond SCD.
Sections
"[{\"pmc\": \"PMC9744540\", \"pmid\": \"\", \"reference_ids\": [\"ggn210037-bib-0001\", \"ggn210037-bib-0001\", \"ggn210037-bib-0002\", \"ggn210037-bib-0002\", \"ggn210037-bib-0003\", \"ggn210037-bib-0004\"], \"section\": \"INTRODUCTION\", \"text\": \"The moral imperative to improve health and eliminate health inequities and disparities calls for fundamental changes in how disease and individual and population health differences are investigated and addressed.\\n Integrative (holistic) research and global health are recurring themes in this discourse and in the burgeoning shift toward transdisciplinary, translational, and transformational science.\\n, \\n The United States (US) Precision Medicine Initiative (PMI) and other similar country\\u2010 and continent\\u2010wide biomedical efforts have emerged from this shift, heralding a potential global revolution in research and healthcare.\\n, \\n, \\n However, the capacity of these initiatives to effectively facilitate optimal health, disease prevention, and health equity will be largely dependent on their commitment to and embodiment of the integrative guiding frameworks they espouse.\"}, {\"pmc\": \"PMC9744540\", \"pmid\": \"\", \"reference_ids\": [\"ggn210037-bib-0002\", \"ggn210037-bib-0005\", \"ggn210037-bib-0006\", \"ggn210037-bib-0007\", \"ggn210037-bib-0008\"], \"section\": \"INTRODUCTION\", \"text\": \"Advances in biology (eg, genomics) are providing new insights into the molecular and other endogenous contributors to health and the etiology, course, and treatment of disease, while epidemiological and health disparities research have been shedding light on social and other exogenous dimensions. For example, observed differences in health and disease indicators within and between countries and populations have been attributed to factors such as genetic variation, geographical location, cultural and psychosocial influences, behaviors, and unequal distributions of power, income, goods, and services.\\n, \\n, \\n, \\n, \\n Any breakdown in health represents a nonlinear phenomenon; therefore, it is critical to view the disease process not solely as a collection of individual risk factors, but to model it as a network of relationships with properties not attributable to individual components.\"}, {\"pmc\": \"PMC9744540\", \"pmid\": \"\", \"reference_ids\": [\"ggn210037-bib-0009\", \"ggn210037-bib-0010\", \"ggn210037-bib-0009\", \"ggn210037-bib-0011\"], \"section\": \"INTRODUCTION\", \"text\": \"Despite increased recognition of the need for more integrative approaches to biomedical research, a substantial portion of research (including some claiming to be integrative) is still guided by linear, reductionist heuristics. Furthermore, most of the published studies and emerging initiatives on genotype\\u2010environment interactions (broadly defined) and multi\\u2010level systems science instinctively focus on multifactorial or so\\u2010called complex diseases and traits. It has long been acknowledged that despite their monogenic etiology, classical Mendelian diseases, such as cystic fibrosis, phenylketonuria, hemochromatosis, G6PD deficiency, and the hemoglobinopathies are also complex, generally having variable phenotypic expression due to interactions among an array of genetic and non\\u2010genetic factors.\\n, \\n Nonetheless, these disorders traditionally have not been targets for systematic genotype\\u2010environment investigations. Monogenic conditions are poised to bring new dimensions to the study of disease complexity over the life course and to our understanding of health differences at the individual, family, and population levels. They provide a unique opportunity to identify diverse modifiers of risk and resilience as they have uniform etiology, detailed phenotyping of affected individuals, and familial clustering.\\n Naturally, they are also prime candidates for novel genetic tools and technologies such as gene therapy and somatic cell genome editing (eg, CRISPR) that are accelerating the quest for cures.\\n Overall, monogenic disorders could serve to model and decode more common and etiologically complicated health conditions, advancing global efforts to improve and sustain health.\"}, {\"pmc\": \"PMC9744540\", \"pmid\": \"\", \"reference_ids\": [\"ggn210037-bib-0012\", \"ggn210037-bib-0013\", \"ggn210037-bib-0013\", \"ggn210037-bib-0014\", \"ggn210037-bib-0012\", \"ggn210037-bib-0013\", \"ggn210037-bib-0015\", \"ggn210037-bib-0016\"], \"section\": \"THE CASE OF SICKLE CELL DISEASE\", \"text\": \"Sickle cell disease (SCD) is the first disease whose genetic etiology was defined, and is one of the most common severe monogenic diseases in humans. SCD refers to a group of recessively inherited blood disorders characterized by the predominance of sickle hemoglobin (HbS), the result of a single nucleotide change in the structural gene for the beta unit of hemoglobin (HBB).\\n, \\n The HbS variant is considered to have originated in Africa and subsequently increased rapidly in frequency as a result of the substantial protection from severe malarial infection that it provides to heterozygote carriers (sickle cell trait; SCT).\\n, \\n The clinical manifestations of SCD result from increased red cell hemolysis, vaso\\u2010occlusion, and accompanying physiologic changes that lead to acute complications, including acute painful episodes (vaso\\u2010occlusive crises; VOC), susceptibility to infection, acute chest syndrome, and stroke, along with chronic pain and organ damage to the spleen, kidneys, brain, and lungs.\\n These and other complications extend across the life spectrum and reduce life expectancy of people living with SCD by about 30\\u2009years compared to their healthy peers.\\n, \\n, \\n\\n\"}, {\"pmc\": \"PMC9744540\", \"pmid\": \"\", \"reference_ids\": [\"ggn210037-bib-0013\", \"ggn210037-bib-0017\", \"ggn210037-bib-0018\", \"ggn210037-bib-0019\", \"ggn210037-bib-0020\", \"ggn210037-bib-0013\", \"ggn210037-bib-0021\", \"ggn210037-bib-0022\", \"ggn210037-bib-0011\", \"ggn210037-bib-0023\", \"ggn210037-bib-0024\", \"ggn210037-bib-0025\"], \"section\": \"THE CASE OF SICKLE CELL DISEASE\", \"text\": \"SCD affects approximately 20 million people worldwide and is most prevalent in parts of Africa, the Caribbean, the Mediterranean basin, the Middle East, India, and South and Central America.\\n, \\n Notwithstanding the diverse populations affected, in some countries, such as the US, Brazil, and Turkey, SCD has long been misconstrued as a \\u201cblack disease\\u201d or a disease of racially marginalized groups, and this racialized notion of the disease is a key element of its distinctive biocultural story.\\n, \\n, \\n Globally, more than 300\\u2009000 babies are born annually with SCD, of which at least 75% are in Africa.\\n SCD remains a leading source of mortality, morbidity, and health disparity, and has been designated as a major global health problem and priority by the World Health Organization (WHO) and United Nations (UN).\\n, \\n Recent major national and global initiatives aimed at providing new financial and other resources for monitoring, researching, treating, and curing SCD demonstrate increasing attention to the disease.\\n, \\n, \\n, \\n\\n\"}, {\"pmc\": \"PMC9744540\", \"pmid\": \"\", \"reference_ids\": [\"ggn210037-bib-0010\", \"ggn210037-bib-0013\", \"ggn210037-bib-0026\", \"ggn210037-bib-0027\", \"ggn210037-bib-0011\", \"ggn210037-bib-0028\", \"ggn210037-bib-0011\", \"ggn210037-bib-0013\", \"ggn210037-bib-0028\", \"ggn210037-bib-0029\", \"ggn210037-bib-0030\", \"ggn210037-bib-0013\", \"ggn210037-bib-0031\", \"ggn210037-bib-0031\", \"ggn210037-bib-0032\", \"ggn210037-bib-0033\"], \"section\": \"THE CASE OF SICKLE CELL DISEASE\", \"text\": \"The frequency and severity of SCD complications vary markedly between patients and at different ages. Both genetic and non\\u2010genetic factors are known to influence SCD severity.\\n, \\n, \\n, \\n For example, high fetal hemoglobin (HbF) levels have long been associated with less severity\\n; HbF levels are under genetic control and are amenable to therapeutic manipulation in SCD.\\n Similarly, co\\u2010inheritance of \\u03b1\\u2010thalassemia is protective against some SCD\\u2010related complications, such as hemolysis and stroke.\\n, \\n, \\n However, most of the viable clinical expression remains unexplained by the genetic markers that have been examined. Indeed, availability of appropriate medical care, as in industrialized countries, usually mitigates morbidity and facilitates longer survival of people with SCD.\\n In countries with less resources, on the other hand, morbidity is high and survival is low due to the combined effect of inadequate care and often severe clinical complications,\\n compounded by other factors such as malnutrition, poverty, and exposure to pathogens.\\n, \\n Studies have also found that pain severity is associated with exposures to a variety of climate factors, including temperature fluctuation, wind speed, humidity, and high altitudes, as well as acute air influences such as air pollutants.\\n, \\n, \\n Although these social and environmental influences on SCD complications are known, the exact mechanisms and pathways through which they influence clinical variability and phenotype are not well understood. Yet, there is limited research on the roles of these and other exogenous factors in SCD outcomes and even less published empirical research on the joint impacts of endogenous and exogenous factors. Major knowledge gaps also exist concerning the characteristics and effects of some dimensions of biology such as the microbiome and epigenome.\"}, {\"pmc\": \"PMC9744540\", \"pmid\": \"\", \"reference_ids\": [\"ggn210037-bib-0010\", \"ggn210037-bib-0026\", \"ggn210037-bib-0027\"], \"section\": \"THE CASE OF SICKLE CELL DISEASE\", \"text\": \"The scientific and social histories of SCD, coupled with its substantial individual and population variability, have led to the identification of SCD as an ideal model for elucidating mechanisms by which diverse endogenous and exogenous factors combine to influence health, disease, and health disparities.\\n, \\n, \\n Along with spurring new pharmacological, genomic, and other cellular\\u2010 or molecular\\u2010level interventions, adequately resourced and well\\u2010designed integrative SCD research could identify structural, social, environmental, and behavioral targets for prediction, prevention, treatment, and management of SCD complications that are more practical, safe, accessible, and affordable. Integrative SCD research could also complement and inform existing and emerging curative efforts such as bone marrow transplantation, gene therapy, and somatic cell genome editing.\"}, {\"pmc\": \"PMC9744540\", \"pmid\": \"\", \"reference_ids\": [\"ggn210037-fig-0001\", \"ggn210037-bib-0026\", \"ggn210037-bib-0026\"], \"section\": \"ADVANCING INTEGRATIVE SICKLE CELL DISEASE RESEARCH\", \"text\": \"We created an illustration that depicts the confluence of biological, psychological, clinical, behavioral, sociocultural, structural, and environmental factors/domains and SCD outcomes (physician\\u2010 and patient\\u2010reported) in a global context (Figure 1). This theoretical framework is guided by the Identity Networks, Genome, and Affect as Modulators of Health (INGAM) model,\\n an integrative data\\u2010driven model that attempts to clarify the degree of interdependence between social ecology and genomic processes. The INGAM model draws on principles from nonlinear dynamics, delineating major lines of bifurcation, in an effort to operationalize a multifactorial approach to health and illness. It facilitates understanding of not only the distal factors contributing to health conditions, but also the proximal mechanisms by which disease occurs or health can be restored and maintained. Consequently, INGAM opens the door for the exploration of more effective preventive and treatment measures, or for engineering new ways of delivering care to individuals and communities facing a number of daunting health problems.\\n\\n\"}, {\"pmc\": \"PMC9744540\", \"pmid\": \"\", \"reference_ids\": [\"ggn210037-fig-0001\", \"ggn210037-bib-0013\", \"ggn210037-bib-0034\", \"ggn210037-bib-0035\"], \"section\": \"ADVANCING INTEGRATIVE SICKLE CELL DISEASE RESEARCH\", \"text\": \"Figure 1 posits that the potential causal influence of a given factor, or node, in the system is sensitive to the state of the other nodes in the system. This sensitivity may, for example, take the form of mediating effects, multiplicative (interactive) effects, or feedback loops. For each of the seven \\u201cantecedent\\u201d domains in the framework, there are selected examples of variables linked in the extant literature to one or more of the SCD outcomes or to some measure of disease severity.\\n, \\n, \\n Furthermore, variables in some of the \\u201cantecedent\\u201d domains, such as psychological and behavioral, can themselves be outcomes of the SCD experience. This reinforces the fluidity and complexity of the associations among and within the domains.\"}, {\"pmc\": \"PMC9744540\", \"pmid\": \"\", \"reference_ids\": [\"ggn210037-fig-0002\", \"ggn210037-bib-0012\", \"ggn210037-bib-0013\", \"ggn210037-bib-0028\", \"ggn210037-bib-0029\", \"ggn210037-bib-0030\", \"ggn210037-bib-0034\", \"ggn210037-bib-0035\", \"ggn210037-bib-0036\", \"ggn210037-bib-0037\", \"ggn210037-bib-0038\", \"ggn210037-bib-0039\", \"ggn210037-bib-0013\", \"ggn210037-bib-0027\", \"ggn210037-bib-0031\", \"ggn210037-bib-0032\", \"ggn210037-bib-0033\", \"ggn210037-bib-0040\", \"ggn210037-bib-0041\", \"ggn210037-bib-0042\", \"ggn210037-bib-0043\", \"ggn210037-bib-0044\", \"ggn210037-bib-0045\", \"ggn210037-bib-0046\", \"ggn210037-fig-0002\", \"ggn210037-bib-0034\", \"ggn210037-bib-0039\"], \"section\": \"ADVANCING INTEGRATIVE SICKLE CELL DISEASE RESEARCH\", \"text\": \"Focusing on pain, the most common complication of SCD, we constructed a preliminary conceptual model (Figure 2) from our theoretical framework. Factors influencing SCD pain were synthesized from the literature and organized into 4 domain clusters: (1) Biological/Clinical,\\n, \\n, \\n, \\n, \\n, \\n, \\n, \\n, \\n, \\n, \\n (2) Structural/Environmental,\\n, \\n, \\n, \\n, \\n, \\n, \\n (3) Psychosocial,\\n, \\n and (4) Behavioral.\\n, \\n, \\n Double\\u2010headed arrows connecting the clusters indicate that all factors may display inter\\u2010cluster relations. Although not displayed, factors within a cluster may also interact with one another. For example, nutritional deficiency, though classified as a behavioral attribute, is highly interlinked with structural/environmental factors such as residential area and socioeconomic status, biological/clinical factors such as genetics, and other behavioral factors such as drug use. Conceptualizations and frameworks of SCD tend to emphasize genetic and clinical contributors to various disease complications, including pain. Although genetic and genomic factors can influence the manifestation and experience of pain, a myriad external factors can modify or interact with an individual's genomic or clinical attributes, confer protection against impending pain episodes, or influence the severity and intensity of pain. While understanding an individual's biological or clinical history may grant clinicians some understanding of the physiological processes underlying pain episodes, it fails to capture the multidimensional nature of SCD. Subsequently, pharmacological treatment of pain may be a process to be included in a multifactorial management design that takes into account a patient's socioeconomic status, residential area, and mental health. Factors in Figure 2represented by solid colored arrows represent known contributors to pain or those that increase the likelihood of worsening pain. Dashed colored lines signify known mediators which lessen/prevent pain or confer protective effects. The mechanisms through which these factors act are also not well known and merit further research. LSD1 inhibitors\\n and BCL11A silencing\\n are included as examples of potential therapeutic mechanisms. A variety of protective factors, including HbF, coping mechanisms, and some behavioral factors may be critical targets for integrative research and interventions.\"}, {\"pmc\": \"PMC9744540\", \"pmid\": \"\", \"reference_ids\": [\"ggn210037-bib-0047\", \"ggn210037-bib-0047\", \"ggn210037-bib-0048\", \"ggn210037-bib-0049\", \"ggn210037-fig-0003\", \"ggn210037-fig-0002\"], \"section\": \"ADVANCING INTEGRATIVE SICKLE CELL DISEASE RESEARCH\", \"text\": \"Understanding how factors converge and precipitate or influence SCD complications longitudinally is critical in modeling the complexity of SCD and the processes through which phenotypic variations in outcomes such as pain are expressed.\\n Temporal modeling of gene\\u2010environment interactions in disease trajectory can be accomplished with tools such as observational data, medical records, and genomic/transcriptomic analysis.\\n, \\n, \\n For SCD pain, modeling could be done through the creation of a \\u201chealth timeline\\u201d (Figure 3), in which intensity, duration, and frequency of stressors and protective factors (see Figure 2) are measured and observed for an individual experiencing a recorded pain outcome. In this conceptual timeline, factors that occur before a pain episode would be classified as precipitating factors, whereas factors that occur during an episode would be considered associative. The frequency and duration of factor co\\u2010occurrence as they correlate with pain events would provide an innovative method of quantifying the nature of co\\u2010factor associations as well as factor/outcome relationships.\"}, {\"pmc\": \"PMC9744540\", \"pmid\": \"\", \"reference_ids\": [\"ggn210037-bib-0050\", \"ggn210037-bib-0051\"], \"section\": \"ADVANCING INTEGRATIVE SICKLE CELL DISEASE RESEARCH\", \"text\": \"Our initial plan included applying accepted techniques for data harmonization.\\n, \\n After obtaining institutional research ethics approvals and retrieving the data, it was clear that there would be substantial barriers to achieving our aim of modeling relationships and making meaningful comparisons across sites. For example, datasets from two sites captured information from each separate clinic visit, while data from the other site were aggregated across clinic visits with only one summary value per patient for a given variable. Thus, we could not adequately compare all sites with respect to temporal associations among variables. There were also problems regarding poor standardization of variable names within the dataset at one site.\"}, {\"pmc\": \"PMC9744540\", \"pmid\": \"\", \"reference_ids\": [\"ggn210037-bib-0031\", \"ggn210037-bib-0032\", \"ggn210037-bib-0033\"], \"section\": \"ADVANCING INTEGRATIVE SICKLE CELL DISEASE RESEARCH\", \"text\": \"Ultimately, we elected to abandon any across\\u2010site integration and instead conduct a few simple, largely descriptive analyses within each dataset. We judged that the data from Jamaica were in a condition most amenable to a reliable statistical analysis. Using these data, we estimated the associations between a set of environmental variables and pain episodes using a multivariable logistic regression model. The Huber\\u2010White sandwich estimator was used to account for multiple visits per person (ie, within\\u2010person clustering). Complete data for the variables under study were available from 4404 adults collected from 35\\u2009431 clinic visits over 5\\u2009years. The subsample had a mean age of 38\\u2009years, 55% of whom were women. We found that younger age, colder atmospheric temperature, higher rainfall, lower environmental zinc, and greater poverty were associated with a higher probability of a pain episode. There was no evidence that these associations differed across hemoglobin genotypes. Neither sex, urban vs rural location, elevation, nor geographic distance from a clinic exhibited any appreciable evidence of an association with the probability of a pain episode. Although several of the positive findings corroborate those from previous studies and have important implications for pain prevention and management,\\n, \\n, \\n we caution that all of the pilot study findings (positive and negative) should only be interpreted as preliminary.\"}, {\"pmc\": \"PMC9744540\", \"pmid\": \"\", \"reference_ids\": [\"ggn210037-bib-0052\"], \"section\": \"ADVANCING INTEGRATIVE SICKLE CELL DISEASE RESEARCH\", \"text\": \"The pilot study confirms the importance and urgency of efforts to streamline policies and procedures for informed consent and the storage, sharing, and use of genomic and other types of data. Our initial work also underscores the need for comprehensive, valid, and sustainable standardization of SCD vocabulary and phenotyping. The SCD Ontology (SCDO) developed by an international group of SCD experts is a promising mechanism for meeting this need.\\n Tools such as the SCDO are essential for large cohort studies and surveillance systems, whether utilizing secondary data or collecting primary data to avert some of the challenges with data harmonization. Experts in computational and statistical data sciences who can skillfully apply and generate novel tools and algorithms for high\\u2010dimensional modeling and data analysis are vital to the interdisciplinary research teams needed to implement this potentially transformative work.\"}, {\"pmc\": \"PMC9744540\", \"pmid\": \"\", \"reference_ids\": [\"ggn210037-bib-0011\", \"ggn210037-bib-0014\", \"ggn210037-bib-0053\"], \"section\": \"CONCLUSION\", \"text\": \"From evolution to genome editing, SCD is preeminent in research on both the origins and eradication of human disease.\\n, \\n, \\n Whether the first molecular disease becomes the first to have an approved molecular cure from CRISPR remains to be seen. In the meantime, we must continue to scale up efforts to develop new tools and techniques for reducing and preventing complications in the millions of people worldwide suffering from SCD, most of whom are unlikely to have immediate access to high\\u2010tech cures when they become available. We note that with SCD unmet needs are prevalent, even in European and North American countries.\"}, {\"pmc\": \"PMC9744540\", \"pmid\": \"\", \"reference_ids\": [\"ggn210037-bib-0021\", \"ggn210037-bib-0054\", \"ggn210037-bib-0055\", \"ggn210037-bib-0056\", \"ggn210037-bib-0057\", \"ggn210037-bib-0058\"], \"section\": \"CONCLUSION\", \"text\": \"Large national and multinational integrative studies are needed to better understand SCD globally and catalyze the development, translation, and implementation of locally\\u2010appropriate interventions and policies. International organizations such as the WHO are best positioned to incentivize countries to adopt this integrated approach to SCD as a complex disease, just as the WHO urged countries in 2006 to develop and implement national programs for the management of SCD and countries in turn established clinical care guidelines for SCD.\\n, \\n, \\n, \\n, \\n The recent SCD report from the US National Academies of Sciences, Engineering, and Medicine could serve as a comprehensive roadmap for the WHO and other organizations seeking to encourage or fund ecological SCD research that will accelerate improved health and healthcare at local, national, and global levels.\\n Although this work is challenging and requires ample resources, it will yield tremendous rewards for human knowledge and wellbeing far beyond SCD.\"}]"
Metadata
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