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Relationship of regional ultraviolet index data with rash and systemic disease activity in youth with childhood-onset systemic lupus: results from the Childhood Arthritis and Rheumatology Research Alliance Registry

Pediatric Rheumatology volume 22, Article number: 54 (2024) Cite this article

Abstract

Objective

To investigate the association between ultraviolet light index (UVI), as a marker for UV exposure, and seasonality with rash and systemic disease activity in youth with childhood-onset systemic lupus (cSLE) from the Childhood Arthritis and Rheumatology Research Alliance (CARRA) Registry.

Methods

We reviewed data on rash and disease activity from Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI-2 K) scores from cSLE CARRA Registry participants with visits between 2010 and 2019 and obtained zipcode level UVI data from the National Oceanic and Atmospheric Administration (NOAA). Our main exposures were UVI and season during the month of visit and one month prior to visit. We used mixed-effects logistic regression models to examine associations between regional UVI (by zipcode)/season and odds of rash and severe SLEDAI-2 K score (≥ 5 vs. 0–4), adjusting for age, sex, race and income.

Results

Among 1222 participants, with a mean of 2.3 visits per participant, 437 visits (15%) had rash and 860 (30%) had SLEDAI-2 K score ≥ 5. There were no associations between UVI during the month prior to visit or the month of the visit and odds of rash or elevated systemic activity. However, fall season was associated with increased odds of rash (OR = 1.59, p = 0.04), but not increased disease activity.

Conclusion

This study found no association between UVI and rash or UVI and disease activity. However, further studies directly measuring UV exposure and accounting for patient-level protective behavioral measures may help to better understand the complex relationship between sun exposure and SLE disease activity.

Introduction

Environmental factors, including sunlight and UV radiation, have been identified as important contributors in the pathogenesis of several autoimmune diseases, among them systemic lupus erythematosus (SLE) [1]. Ultraviolet radiation (UVR) is thought to be a trigger for SLE flares and in particular flares of cutaneous disease or rash. Photosensitive rash is one of the original diagnostic criteria for SLE [2] and skin lesions are found in more than 50% of patients with SLE [3]. Limiting sun exposure is potentially one of the few modifiable risk factors for lupus disease activity, and as such, improving our understanding of this ubiquitous risk factor is of utmost importance.

Seasonal variations in SLE disease activity have been described [4,5,6], however there is conflicting evidence as to whether an association between sun exposure and disease activity exists, even in regard to cutaneous manifestations. In addition, few studies have examined ultraviolet index (UVI) against season to determine whether previously described variations in disease activity are really due to UV exposure versus other possible factors. While most studies that have examined associations between UVR and SLE have been conducted in adults, rash and photosensitivity may be even more prevalent in youth with childhood-onset SLE (cSLE) [7]. Furthermore, even though skin pigmentation alters the risk for UVR-related damage, only a few studies have included diverse populations, demonstrating variation in the prevalence of rash across different ethnic origins, with increased photosensitivity prevalence in people of European ancestry as opposed to people of African ancestry [8,9,10].

The aim of this study was to assess the association between sun UV exposure (quantified by UVI) as well as seasonality with risks of cutaneous and systemic disease activity in a cohort of racially and ethnically diverse youth with childhood-onset lupus enrolled in the Childhood Arthritis and Rheumatology Research Alliance (CARRA) Registry. Based on prior studies, we hypothesized that increased disease activity, especially cutaneous flares, would be associated with elevated UVI.

Methods

Participants

Study participants included all youth aged 0 to 21 years of age with SLE who were enrolled in the Childhood Arthritis and Rheumatology Research Alliance (CARRA) Legacy and New (current) Registry databases. The CARRA SLE Registries comprise data on youth with childhood-onset lupus diagnosed by a pediatric rheumatologist before their 18th birthday and enrolled before the age of 21.

The CARRA Legacy Registry enrolled 1,284 participants with SLE between 2010 and 2015 from 65 participating sites (64 in the US and one in Canada), while the CARRA New Registry enrolled 514 participants with SLE from June 2016 through June 2019 (time of our data request) from 77 participating sites, mostly in the US and Canada. For this analysis, we included only participants residing in the US and with a valid US zip code due to the availability of reliable UVI data, which we obtained from the National Oceanic and Atmospheric Administration (NOAA).

Information obtained from the CARRA Registry database included date of visit, 5-digit zip code at time of visit (to be able to cross reference with UV index database obtained from NOAA). Demographic data was entered by participants or parents including sex, age, race and ethnicity, household income, education (New Registry only). Total and component Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI 2 K) scores were entered by research staff based on clinical visits. Exclusion criteria include incomplete data collection for the variables of participant zip code and date (month, year) of clinic visit, incomplete clinical data such as presence of rash or SLEDAI score.

The study was approved by the Einstein/Montefiore IRB 2018–9819.

Data source

Ultraviolet Index (UVI) data for the month and year of all visits for each participant was obtained from the NOAA for specific zip codes of each patients’ visits. The UVI represents the estimated amount of skin-damaging UV radiation reaching the earth’s surface at solar noon and it is an internationally standardized unit on a linear scale, ranging from 0 to 11+ [11]. A higher number indicates a shorter amount of time to skin erythema. UV calculation considers other elements such as latitude, total column ozone, elevation, earth surface characteristics, cloud cover, and tropospheric aerosol loading (pollutants or dust).

Exposures

The primary exposure was zip code-level UVI from the month and year of the participant’s study visit as well as from the month prior to the study visit, to account for latency (lag) between exposure and onset of symptoms [12]. We also examined seasonality (i.e. spring, summer, fall and winter) as a secondary measure of exposure and examined the association of season with rash and elevated systemic disease activity. For this analysis we used the meteorological definition of season, which defines seasons as beginning at the first day of the month that includes the equinoxes and solstices; for example according to this definition summer begins June 1 and ends August 31 [13].

Outcomes

Rash

The primary outcome was presence of inflammatory rash at the time of the visit defined by the SLEDAI-2 K or SLEDAI rash component. SLEDAI is a global index that evaluates disease activity over the previous 10 days. It includes 24 items with specific manifestations in 9 organ systems: neurological, vascular, musculoskeletal, renal, serosal, mucocutaneous, constitutional, immunological and hematological [14]. The SLEDAI rash score is defined as positive if an SLE-related inflammatory rash is present from up to 10 days prior to the time of visit. On the SLEDAI-2 K (used in the CARRA Registry) this includes new and persistent rash [15].

Elevated systemic disease activity

Definition of active disease in SLE is not standardized, but using SLEDAI activity measure, it is usually defined as increase in score by > 3 for mild/moderate flare and > 10 for severe activity [16]. Since this was difficult to assess using our database, we used SLEDAI score for each visit to assess for disease activity. We used total SLEDAI score ≥ 5 to define elevated systemic disease activity, as studies have defined scores < 5 as low disease activity state [17]. Thus, our secondary outcome was elevated systemic disease activity measured as SLEDAI score 5 or higher.

We excluded patients that were missing zip code information and/or had Canadian residency (n = 174) or those who had missing/unknown information on the outcomes of interest (n = 402) (Fig. 1).

Fig. 1
figure 1

Flowchart of study sample of cSLE participants from the CARRA Registry (Legacy and New)

Full size image

Statistical analysis

We compared socio-demographic characteristics between the two registries using Student t-tests for normally distributed variables and chi-square tests for categorical variables. Statistical significance was determined as p < 0.05 (2-sided). We used mixed-effects logistic regression to examine association between UVI (both as continuous and categorical) and meteorological definition of season (i.e. spring, summer, fall vs. winter) with odds of rash (yes vs. no) as well as SLEDAI score (using ≥ 5 vs. 0–4) in separate logistic regression models. Our main UV exposures were UVI of the month/year of participants’ visits as well as UVI of the month prior to visit date. We used the meteorological cut-off point for UVI to indicate low, medium high and very-high UV exposure [11]. These models use person as random effect to account for repeated measures within the same subject from baseline and follow-up visits. Models were adjusted for potential confounding by sex, age, race/ethnicity, and household income as fixed effects. All analyses were conducted using STATA software version 16.

Results

Participant demographics and clinical characteristics

We examined all available visits (baseline and follow-up) for each Registry participant. We included 740 Legacy Registry participants, accounting for 1703 visits and 482 New Registry participants with a total of 1128 visits for an overall total of 2831 visits. Demographics of participants in the Legacy Registry and the New Registry are shown in Table 1. Overall, most participants were female (84%), 30% identified as Black and 25% as Hispanic, and approximately a third of participants had low household income <$50,000 (n = 394, 32%).

Table 1 Demographic and social characteristics of all participants included in this analysis as well as stratified by registry
Full size table

Participants from Legacy Registry were slightly older at baseline (average age 15.8 ± 3.2) compared to the New Registry (average age 14.4 ± 2.9), but there was no meaningful difference in sex, race/ethnicity, or family income distribution. Information about educational attainment was collected only in the New Registry database (Table 1). Overall, there were 2,831 visits among 1,222 participants (average 2.3 visits/patients), and the frequency of visits was similar in both registries.

Rash

Among all visits included in the analysis, 437 (15%) had reported a rash event (Legacy Registry 249, 15%; New Registry 188, 17%). Table 2 shows associations between UVI and seasonality and odds of rash. There was no association between UVI of the month of the visit (OR = 0.97 CI 0.92–1.04) as well as UVI of the month prior to the visit (OR = 0.99, CI 0.93–1.05) and rash. Similarly we did not see any association when UVI was categorized according to level (low 1–2, moderate 3–5, high 6–7, very high 8–10) [11]. When looking at seasons, fall season was associated with increased odds of rash (OR = 1.61, CI 1.03–2.52, p = 0.04), however there was no association when looking at individual months.

Table 2 Odds of rash by ultraviolet index (UVI) and seasonality among the youth with cSLE from CARRA Registries
Full size table

Elevated systemic disease activity

Among all visits included in the analysis, 860 (30%) had SLEDAI ≥ 5, indicating elevated systemic disease activity; interestingly the proportion of patients reporting a SLEDAI ≥ 5 was lower in Legacy Registry (473, 27%) compared to New Registry (387, 35%).

Unlike some prior studies which showed increased seasonal disease activity [18,19,20], our study did not find an association between UV exposure or season and active disease (Table 3). When looking at UV exposure both during current and previous month, there were no increased odds of active disease (OR = 0.99 CI 0.94–1.04); this remained true when we stratified by UV levels, or when we looked at seasons. Figure 2 shows the monthly distribution of visits with rash and elevated systemic disease activity when compared with mean monthly UVI.

Table 3 Odds of elevated systemic lupus disease activity (SLEDAI ≥ 5) by UVI and season in youth with cSLE from the CARRA Registry
Full size table
Fig. 2
figure 2

Seasonal distribution of systemic lupus disease activity and rash in CARRA Registry cSLE participants

Full size image

Discussion

In this examination of youth with cSLE enrolled in the CARRA Registry, we found that fall season was associated with 30% increased odds of rash when compared to winter. Otherwise, there were no associations between UV exposure at the date of visit as well as UVI of the month prior to each visit and cutaneous or systemic disease activity.

Photosensitivity has long been implicated as one of the environmental risk factors for many autoimmune diseases, and SLE is one of the most described photosensitive autoimmune disease. Photosensitivity was included as one of original ACR diagnostic criteria for SLE, although this criterion proved to be controversial, as being poorly defined and overlapping with other criteria such as malar rash and thus was not included in the most recent 2019 EULAR/ACR classification criteria [21].

Studies have shown multiple mechanisms by which solar irradiation causes tissue damage. These include free radical formation, deregulated apoptosis, activation of plasmacytoid dendritic cells which secrete INF-alpha, upregulation of TNF-alpha and other pro-inflammatory cytokines, all of which have been implicated in SLE pathogenesis [22]. However, epidemiological studies looking at patients with different forms of Lupus Erythematosus (LE) report a wide range of photosensitivity rates (from 27 to 100% for SCLE, 25–90% for discoid lupus, and 43–71% for lupus tumidus) [8], which likely reflect the difficulty in defining and assessing photosensitivity. Studies have shown that patient history corelates poorly with presence of photosensitivity [8], possibly due to the delayed nature of the process. The delay between exposure to UV radiation and onset of rash has been shown in phototesting studies, with studies showing that up to 90% of patients with LE had abnormal reaction to phototesting, however the delay between testing and onset of rash was in the order of days to weeks [23].

It is important to note, however, that phototesting does not correlate well with patients’ and physicians’ subjective assessments of photosensitivity, interjecting doubt as to whether phototesting studies reliably reflect clinical disease flare [12].

When looking at seasonal influence as a possible measure of UV radiation on SLE disease activity the results are conflicting, with some studies showing increased evidence of rashes in summer months [5, 6, 18] while other studies did not show this relationship [4, 19]. A large prospective longitudinal cohort study [5] showed an increase in both photosensitive rash and arthritis activity in the spring and summer months (interestingly, rash only had seasonal variation in white but not African American participants). For systemic disease the evidence is also mixed, with Hopkins Lupus Cohort study [5] showing decreased renalflares in the summer and highest anti-DsDNA levels in winter, while other studies [19, 20] showed higher lupus flare rates in winter months.

Studies have also looked at the relationship between UV radiation and season in other autoimmune diseases. A recent study of youth with Juvenile Dermatomyositis enrolled in the CARRA Registry found no significant association between mean UVI and calcinosis and other measures of disease severity. However, the odds of calcinosis markedly decreased in African American participants and steadily increased in non–African American participants over the range of increasing mean UVI [24]. The seasonal rates of flare in other autoimmune disease have also been described, especially multiple sclerosis, psoriasis, rheumatoid arthritis [25].

The effect of UV radiation on autoimmune disease is not straightforward; while UV (especially UV-B) has been implicated in pathogenesis of photosensitivity, the immunomodulatory beneficial role of UV-A (especially UV-A1) phototherapy has also been described [26]. Another related factor that has been proposed to have a role in SLE pathogenesis is vitamin D, the activation of which is dependent on UV; several studies have found that higher vitamin D levels were associated with lower disease activity scores [27]. In addition, studies of seasonal characteristics of disease must take into account other factors associated with seasonality such as melatonin levels (which have been shown to have an immunomodulatory effect and are lowest in spring), and the role of infections (which are usually more prevalent in cold months). Different studies address some of these factors but not in a consistent way.

The vigilant use of regular sun protection is a common consensus recommendation in most published guidelines on SLE care [28, 29] despite lack of clear evidence. Our study did not find an association between UV exposure and rash or increased disease activity, although this is clearly an area that warrants further study. Multiple studies have emphasized the role of environmental factors in disease onset and activity, and UV radiation is the single most important risk factor identified in in-vitro and clinical studies.

Our study has several limitations. First, the CARRA Registry collects data every 6 months which means disease flares may be missed if they occur between the 6-months data collection visits. Unscheduled visits are included in the Registry at times of changes in medication, which can potentially address this issue partially, however medication changes might be due to flare or medication intolerance; thus not all disease flares are captured in the registry which is an important limitation. We used the SLEDAI category of rash as our primary outcome; while the SLEDAI definition is presence of ‘inflammatory rash’ it is not clear that everyone defines inflammatory rash in similar ways, which is potentially a limitation. We used UVI to infer sun exposure, which is an indirect marker of personal exposure. However, we were lacking information on important individual-level factors such as individual behavior, extent of sun exposure/time spent outdoors, use of sun protective measures such as sunscreen and clothing, levels of vitamin D and presence of infection. In addition, we used UVI to estimate UV radiation exposure, while some investigators argue that UV-B flux, a composite measure of mean UV-B radiation level based on latitude, altitude and cloud cover, better represents ambient exposure [8]. It is important to note that while we adjusted for race/ethnicity in our analyses, this variable represents a social construct that relates to risk associated with racism and structural barriers, not genetic ancestry or phototype. Further studies with characterized phototype may reveal that the relationship between UVR and rash or disease activity may differ across differently melanated skin; this could not be examined in this study with the available Registry data.

Given these important limitations, it is possible that the lack of correlation between UVI and disease activity reflects patients’ adherence to sun avoidance or other individual-level behaviors for which we were lacking information. Though at least with regards to adherence to sun avoidance, it is interesting to note that studies have shown that adequate sunscreen use remains a challenge even in high risk populations such as melanoma patients and their first degree relatives [30]. Other important clinical factors that are not accounted for in this study, such as disease heterogeneity and the possibility that SLE therapies may mitigate some of the dangerous effects of sun exposure in youth with cSLE, should be considered when interpreting these results.

Despite these limitations, this is the largest study to date and first of its kind to evaluate the association between UVR with both rash and systemic disease activity in cSLE. This study leverages a detailed NASA database of regional daily recorded UVI values and the largest database of cSLE participants available;, Patients enrolled in the CARRA Registry are from a diverse geographical distribution which helped provide a more thorough picture for sun exposure.

Conclusion

Sun protection is universally accepted as a major tenet in SLE care, however there are few clinical studies to elucidate the extent and specifics of the relationship between environmental UV exposure and SLE disease, even with regards to cutaneous disease. Even with a large, well phenotyped cohort and the detailed regional UVI data used, this study leaves us with more questions than answers. Further studies that more directly measure sun exposure and account for individual-level risk factors and behaviors (such as time spent outdoors and sun protective measures) are needed to complement larger epidemiologic studies, such as this one, to better understand this relationship and how we should attend to it for prevention of SLE disease activity. In the meantime, without definitive evidence to discount a relationship between UV exposures and SLE outcomes, it is prudent that providers continue to council strongly for practices of sun protection for children with cSLE.

Data availability

Data sources are available through the Childhood Arthritis and Rheumatology Research Alliance Registry (CARRA) and NOAA (National Oceanic and Atmospheric Administration). CARRA Registry data used in this study was made available to the authors through a data use agreement. Data from the CARRA Registry is not publicly available, but available from CARRA by request (carragroup.org).

Abbreviations

ACR:

American College of Rheumatology

CARRA:

Childhood Arthritis and Rheumatology Research Alliance

cSLE:

Childhood-onset systemic lupus erythematosus

DsDNA:

Double-stranded deoxyribonucleic acids

EULAR:

European Alliance of Associations for Rheumatology

INF:

Interferon

NASA:

National Aviation and Space Administration

NOAA:

National Oceanic and Atmospheric Administration

SLE:

Systemic lupus erythematosus

SLEDAI:

Systemic Lupus Erythematosus Disease Activity Index

TNF:

Tumor necrosis factor

UV:

Ultraviolet

UVI:

Ultraviolet index

UVR:

Ultraviolet radiation

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Acknowledgements

The authors would like to acknowledge Craig S. Long for support with obtaining NOAA data, Jessica Neely for support with study design, and Yael Flamand for support in data cleaning. The CARRA Legacy Registry was supported by a grant from National Institute of Arthritis and Musculoskeletal and Skin Diseases of the National Institute of Health under award Number RC2AR058934. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. The CARRA Legacy Registry was also supported by CARRA, Friends of CARRA, the Arthritis Foundation, and the Duke Clinical Research Institute. We would also like to thank all participants and hospital sites that recruited patients for the CARRA Registry. The authors thank the following CARRA Legacy Registry site principal investigators and research coordinators: L. Abramson, E. Anderson, M. Andrew, N. Battle, M. Becker, H. Benham, T. Beukelman, J. Birmingham, P. Blier, A. Brown, H. Brunner, (A) Cabrera, D. Canter, D. Carlton, (B) Caruso, L. Ceracchio, E. Chalom, J. Chang, P. Charpentier, K. Clark, J. Dean, F. Dedeoglu, B. Feldman, P. Ferguson, M. Fox, K. Francis, M. Gervasini, D. Goldsmith, G. Gorton, B. Gottlieb, T. Graham, T. Griffin, H. Grosbein, S. Guppy, H. Haftel, D. Helfrich, G. Higgins, A. Hillard, J.R. Hollister, J. Hsu, A. Hudgins, C. Hung, A. Huttenlocher, N. Ilowite, A. Imlay, L. Imundo, C.J. Inman, J. Jaquith, R. Jerath, L. Jung, P. Kahn, A. Kapedani, D. Kingsbury, K. Klein, M. Klein-Gitelman, A. Kunkel, S. Lapidus, S. Layburn, T. Lehman, C. Lindsley, M. Macgregor-Hannah, M. Malloy, C. Mawhorter, D. McCurdy, K. Mims, N. Moorthy, D. Morus, E. Muscal, M. Natter, J. Olson, K. O’Neil, K. Onel, M. Orlando, J. Palmquist, M. Phillips, L. Ponder, S. Prahalad, M. Punaro, D. Puplava, S. Quinn, A. Quintero, C. Rabinovich, A. Reed, C. Reed, S. Ringold, M. Riordan, S. Roberson, A. Robinson, J. Rosette, D. Rothman, D. Russo, N. Ruth, K. Schikler, (A) Sestak, (B) Shaham, Y. Sherman, M. Simmons, N. Singer, S. Spalding, H. Stapp, R. Syed, E. Thomas, K. Torok, D. Trejo, J. Tress, W. Upton, R. Vehe, E. von Scheven, L. Walters, J. Weiss, P. Weiss, N. Welnick, A. White, J. Woo, J. Wootton, A. Yalcindag, C. Zapp, L. Zemel, and A. Zhu. The authors thank the following CARRA Registry site principal investigators, sub-investigators and research coordinators: K. Abulaban, A. Adams, C. Aguiar Lapsia, A. Akinsete, S. Akoghlanian, M. Al Manaa, A. AlBijadi, E. Allenspach, (A) Almutairi, R. Alperin, G. Amarilyo, M. Amir, M. Amoruso, S. Angeles-Han, S. Ardoin, S. Armendariz, M. Asad, L. Asfaw, I. Balboni, S. Ballinger, F. Barbar-Smiley, L. Barillas-Arias, M. Basiaga, K. Baszis, S. Baxter, E. Behrens, S. Benseler, L. Bermudez-Santiago, W. Bernal, T. Bigley, (B) Binstadt, (C) Black, M. Blakley, J. Bohnsack, A. Boneparth, H. Bradfield, J. Bridges, E. Brooks, M. Brothers, H. Brunner, Mary Buckley, Meredith Buckley, H. Bukulmez, D. Bullock, L. Cannon, S. Canny, V. Cartwright, E. Cassidy, E. Chalom, Joyce Chang, M. Chang, Johanna Chang, A. Chang-Hoftman, V. Chauhan, A. Chen, P. Chiraseveenuprapund, K. Ciaglia, D. Co, E. Cohen, H. Conlon, R. Connor, A. Cooper, J. Cooper, C. Correll, R. Cron, M. Curry, A. Dalrymple, T. Davis, D. De Ranieri, J. Dean, C. DeCoste, F. Dedeoglu, M. DeGuzman, N. Delnay, E. DeSantis, M. Dhalla, A. Dhanrajani, D. Dissanayake, J. Drew, K. Driest, Q. Du, K. Dunnock, D. Durkee, J. Dvergsten, (A) Eberhard, K. Ede, C. Edens, T. El Tal, M. Elder, Y. Elzaki, S. Fadrhonc, C. Failing, D. Fair, (B) Feldman, I. Ferguson, P. Ferguson, E. Flanagan, T. Klausmeier, L. Fogel, E. Fox, M. Fox, L. Franklin, R. Fuhlbrigge, J. Fuller, S. Gagne, T. Garcia, D. Gerstbacher, M. Gilbert, (A) Gilbert, I. Goh, D. Goldsmith, K. Gonzales, S. Gorry, N. Goswami, (B) Gottlieb, T. Graham, T. Griffin, J. Olson, M. Guevara, T. Hahn, O. Halyabar, E. Hammelev, L. Harel, S. Savani, J. Harris, O. Harry, A. Hay, K. Hayward, L. Henderson, C. Bacha, M. Henrickson, A. Hersh, K. Hickey, L. Hiraki, M. Hiskey, P. Hobday, C. Hoffart, M. Holland, M. Hollander, S. Hong, M. Horwitz, J. Hsu, A. Huber, A. Huberts, J. Huggins, L. Huie, J. Hui-Yuen, M. Ibarra, A. Imlay, L. Imundo, C. Inman, (A) Jackson, K. James, G. Janow, S. Jared, L. Nicole Johnson, Nicole Johnson, J. Jones, D. Kafisheh, P. Kahn, N. Karan, R. Kaur, E. Kessler, (B) Kienzle, S. Kim, Y. Kimura, D. Kingsbury, M. Kitcharoensakkul, K. Klein, M. Klein-Gitelman, (A) Knight, L. Kovalick, S. Kramer, C. Kremer, T. LaFlam, (B) Lang, L. Tate, S. Lapidus, A. Lasky, C. Lawler, E. Lawson, R. Laxer, Pui Lee, Patricia Lee, T. Lee, A. Lee, E. Leisinger, L. Lentini, M. Lerman, D. Levy, S. Li, S. Lieberman, L. Lim, E. Limenis, C. Lin, N. Ling, A. Brown, M. Lloyd, M. Lo, A. Long, M. Lopez-Peña, D. Lovell, N. Luca, S. Lvovich, A. Lytch, M. Ma, J. MacMahon, J. Madison, (A) White, M. Mannion, C. Manos, L. Mansfield, C. Mariani, (B) Marston, V. Gennaro, T. Mason, L. McAllister, J. McColl, D. McCurdy, K. McDaniels, J. McDonald, E. Meidan, E. Mellins, L. Michalowski, M. Miller, D. Milojevic, R. Mitacek, R. Modica, S. Mohan, T. Moore, K. Moore, L. Moorthy, E. Morgan, (A) Moyer, (B) Murante, E. Muscal, O. Mwizerwa, K. Nanda, N. Nasah, L. Nassi, S. Nativ, M. Natter, K. Nearanz, J. Neely, L. Newhall, P. Nigrovic, J. Nocton, B. Nolan, K. Nowicki, R. Oakes, E. Oberle, E. Ogbu, M. Oliver, R. Olveda, K. Onel, M. Orlando, P. O’Rourke, J. Padam, A. Paller, K. Schmidt, N. Pan, J. Pandya, S. Panupattanapong, P. Patel, J. Patel, S. Patrizi, S. Paul, J. Perfetto, M. Perron, K. Phillippi, C. Plasterer, L. Ponder, R. Pooni, S. Prahalad, M. Quinlan-Waters, C. Rabinovich, J. Rafko, H. Rahimi, A. Rakestraw, K. Rampone, S. Ramsey, L. Ray, Ann Reed, Annelle Reed, H. Reid, D. Reiff, S. Richins, M. Riebschleger, M. Riordan, M. Riskalla, L. Robinson, (A) Robinson, M. Rodriquez, D. Rogers, T. Ronis, M. Rosenkranz, N. Rosenwasser, (B) Rosolowski, H. Rothermel, D. Rothman, E. Rothschild, E. Roth-Wojcicki, K. Rouster - Stevens, T. Rubinstein, J. Harrison, J. Rupp, W. Ambler, J. Fennell, N. Ruth, S. Sabbagh, R. Sadun, (C) Sandborg, L. Santiago, V. Saper, A. Sarkissian, L. Scalzi, J. Schahn, L. Schanberg, K. Schikler, A. Schlefman, W. Stewart, H. Schmeling, E. Schmitt, R. Schneider, G. Schulert, K. Schultz, C. Schutt, C. Seper, R. Sheets, A. Shehab, S. Shenoi, J. Shirley, A. Shuster, N. Singer, V. Sivaraman, E. Sloan, C. Smith, J. Smith, E. Smitherman, J. Soep, M. Son, D. Sosna, L. Spiegel, J. Spitznagle, H. Srinivasalu, H. Stapp, K. Steigerwald, (A) Stephens, Y. Sterba Rakovchik, S. Stern, (B) Stevens, R. Stevenson, K. Stewart, (C) Stingl, M. Stoll, E. Stringer, R. Rivas-Chacon, S. Sule, J. Sullivan, R. Sundel, M. Sutter, R. Syed, G. Syverson, A. Szymanski, S. Taber, A. Tambralli, A. Taneja, T. Tanner, S. Tarvin, A. Taxter, J. Taylor, M. Tesher, (A) Thatayatikom, (B) Thomas, N. Thomas, T. Ting, D. Toib, K. Torok, H. Tory, M. Toth, (C) Tsao, S. 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Funding

This study was supported by the Childhood Arthritis and Rheumatology Research Alliance/ Arthritis Foundation Fellow Grant. Dr. Rubinstein’s research is supported by the Childhood Arthritis and Rheumatology Research Alliance/ Arthritis Foundation Career Development Award and the National Institute of Arthritis and Musculoskeletal and Skin Diseases of the National Institutes of Health (K23AR080803). The CARRA Legacy Registry was supported by a grant from National Institute of Arthritis and Musculoskeletal and Skin Diseases of the National Institute of Health (RC2AR058934). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health and the Childhood Arthritis and Rheumatology Research Alliance.

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Authors and Affiliations

  1. Division of Pediatric Rheumatology, Department of Pediatrics, Albert Einstein College of Medicine, Bronx, NY, USA

    Tamara I. Tanner, Dawn M. Wahezi & Tamar B. Rubinstein

  2. Division of Pediatric Rheumatology, Children’s Hospital at Montefiore, Bronx, NY, USA

    Tamara I. Tanner, Dawn M. Wahezi & Tamar B. Rubinstein

  3. Department of Epidemiology & Population Health, Albert Einstein College of Medicine, Bronx, NY, USA

    Ilir Agalliu

  4. Department of Psychiatry & Behavioral Sciences, Albert Einstein College of Medicine, Bronx, NY, USA

    Tamar B. Rubinstein

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  1. Tamara I. Tanner
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  2. Ilir Agalliu
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Contributions

Drs. Tanner and Rubinstein conceived of the study; Drs. Tanner, Rubinstein, Agalliu, and Wahezi developed the study design; the CARRA Registry Investigators were responsible for the acquisition of data; Drs. Agalliu was primarily responsible for the data analysis with contributions from Drs. Rubinstein and Tanner; Drs. Tanner, Agalliu, Rubinstein, and Wahezi contributed to the interpretation of the results; Dr. Tanner drafted the manuscript; all authors contributed to the revision and final approval of the manuscript.

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Correspondence to Tamar B. Rubinstein.

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Tanner, T.I., Agalliu, I., Wahezi, D.M. et al. Relationship of regional ultraviolet index data with rash and systemic disease activity in youth with childhood-onset systemic lupus: results from the Childhood Arthritis and Rheumatology Research Alliance Registry. Pediatr Rheumatol 22, 54 (2024). https://doi.org/10.1186/s12969-024-00973-5

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Keywords

Pediatric Rheumatology

ISSN: 1546-0096