Jeffrey Carlson

Mr. Jeffrey Carlson


Research Focus & Metrics

Academic Career Length

8Years (2019-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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PLPatricia A. Janulewicz Lloyd
Patricia A. Janulewicz Lloyd
RSRatanesh Seth
Ratanesh Seth
JCJeffrey Carlson
Jeffrey Carlson
JAJoy Ajama
Joy Ajama
EQEmily Quinn
Emily Quinn
SCSaurabh Chatterjee
Saurabh Chatterjee
Gulf War Illness (GWI) is a chronic multi-symptom disorder affecting the central nervous system (CNS), immune and gastrointestinal (GI) systems of Gulf War veterans (GWV). We assessed the relationships between GWI, GI symptoms, gut microbiome and inflammatory markers in GWV from the Boston Gulf War Illness Consortium (GWIC). Three groups of GWIC veterans were recruited in this pilot study; GWV without GWI and no gastrointestinal symptoms (controls), GWV with GWI and no gastrointestinal symptoms (GWI-GI), GWV with GWI who reported gastrointestinal symptoms (GW+GI). Here we report on a subset of the first thirteen stool samples analyzed. Results showed significantly different gut microbiome patterns among the three groups and within the GWI +/−GI groups. Specifically, GW controls had a greater abundance of firmicutes and the GWI+GI group had a greater abundance of the phyla bacteroidetes, actinobacteria, euryarchaeota, and proteobacteria as well as higher abundances of the families Bacteroidaceae, Erysipelotrichaceae, and Bifidobacteriaceae. The GWI+GI group also showed greater plasma levels of the inflammatory cytokine TNF-RI and they endorsed significantly more chemical weapons exposure during the war and reported significantly greater chronic pain, fatigue and sleep difficulties than the other groups. Studies with larger samples sizes are needed to confirm these initial findings.

21 October 2022 in Environmental Research
Verified
Journal Article
Closed access
JCJeffrey Carlson
Jeffrey Carlson
AZAntonella Zanobetti
Antonella Zanobetti
SCStephanie Ettinger de Cuba
Stephanie Ettinger de Cuba
APAna P. Poblacion
Ana P. Poblacion
PFPatricia M. Fabian
Patricia M. Fabian
PJPatricia A. Janulewicz
Patricia A. Janulewicz

21 April 2022 in Environmental Science & Technology
Verified
Journal Article
Open access
JCJeffrey Carlson
Jeffrey Carlson
PJPatricia A. Janulewicz
Patricia A. Janulewicz
NKNicole Kleinstreuer
Nicole Kleinstreuer
WHWendy Heiger-Bernays
Wendy Heiger-Bernays
Chemical-induced alteration of maternal thyroid hormone levels may increase the risk of adverse neurodevelop-mental outcomes in offspring. US federal risk assessments relyalmost exclusively on apical endpoints in animal models forderiving points of departure (PODs). New approach method-ologies (NAMs) such as high-throughput screening (HTS) andmechanistically informative in vitro human cell-based systems,combined with in vitro to in vivo extrapolation (IVIVE),supplement in vivo studies and provide an alternative approachto calculate/determine PODs. We examine how parameterizationof IVIVE models impacts the comparison between IVIVE-derivedequivalent administered doses (EADs) from thyroid-relevant invitro assays and the POD values that serve as the basis for riskassessments. Pesticide chemicals with thyroid-based in vitro bioactivity data from the US Tox21 HTS program were included (n=45). Depending on the model structure used for IVIVE analysis, up to 35 chemicals produced EAD values lower than the POD. Atotal of 10 chemicals produced EAD values higher than the POD regardless of the model structure. The relationship between IVIVE-derived EAD values and the in vivo-derived POD values is highly dependent on model parameterization. Here, we derive a range of potentially thyroid-relevant doses that incorporate uncertainty in modeling choices and in vitro assay data.

AFAlexa Friedman
Alexa Friedman
PLPatricia A. Janulewicz Lloyd
Patricia A. Janulewicz Lloyd
JCJeffrey Carlson
Jeffrey Carlson
EQEmily Quinn
Emily Quinn
DKDylan Keating
Dylan Keating
Kimberly SullivanKimberly Sullivan
Kimberly Sullivan
Reproductive outcomes, such as preterm birth, miscarriage/stillbirth, and pre-eclampsia, are understudied in veterans, particularly among Gulf War veterans (GWVs). During deployment, women GWVs were exposed to toxicant and nontoxicant exposures that may be associated with adverse reproductive and developmental outcomes. The data come from a survey of 239 participants from northeastern and southern U.S. cohorts of women veterans. The questionnaire collected information about the service history, current and past general health, reproductive and family health, demographic information, and deployment exposures. Odds ratios were computed with 95% confidence intervals between exposures in theater and reproductive/children’s health outcomes. GWVs experienced adverse reproductive outcomes: 25% had difficulty conceiving, and 31% had a pregnancy that ended in a miscarriage or stillbirth. Pregnancy complications were common among GWVs: 23% had a high-risk pregnancy, and 16% were diagnosed with pre-eclampsia. About a third of GWVs reported their children (38%) had a developmental disorder. Use of pesticide cream during deployment was associated with higher odds of all reproductive and developmental outcomes. The results demonstrate that GWVs experienced reproductive and children’s health outcomes at potentially high rates, and exploratory analyses suggest pesticide exposure as associated with higher odds of adverse reproductive outcomes. Future longitudinal studies of women veterans should prioritize examining reproductive and children’s health outcomes.

30 August 2023 in Research Square
Verified
Preprint
Open access
PDF file
JCJeffrey Carlson
Jeffrey Carlson
RSRegina M Simeone
Regina M Simeone
BWBailey Wallace
Bailey Wallace
SESascha Ellington
Sascha Ellington
SSSharon Saydah
Sharon Saydah
VTVan Tong
Van Tong
This study describes the frequency of post-COVID conditions and other co-occurring health outcomes at the delivery hospitalization. PCC diagnoses occurred in 0.02% of delivery hospitalizations and were more frequent in pregnant people who were White, had private health insurance, and delivered preterm.