Modeling lesion transition dynamics to clinically characterize patients with clade I mpox in the Democratic Republic of the Congo.

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Autori principali: Nishiyama, Takara, Miura, Fuminari, Jeong, Yong Dam, Nakamura, Naotoshi, Park, Hyeongki, Ishikane, Masahiro, Yamamoto, Shotaro, Iwamoto, Noriko, Suzuki, Michiyo, Sakurai, Ayana, Aihara, Kazuyuki, Watashi, Koichi, Hart, William S, Thompson, Robin N, Yasutomi, Yasuhiro, Ohmagari, Norio, Kingebeni, Placide Mbala, Huggins, John W, Iwami, Shingo, Pittman, Phillip R
Natura: Artículo científico
Lingua:en
Pubblicazione: Science translational medicine 2025
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author Nishiyama, Takara
Miura, Fuminari
Jeong, Yong Dam
Nakamura, Naotoshi
Park, Hyeongki
Ishikane, Masahiro
Yamamoto, Shotaro
Iwamoto, Noriko
Suzuki, Michiyo
Sakurai, Ayana
Aihara, Kazuyuki
Watashi, Koichi
Hart, William S
Thompson, Robin N
Yasutomi, Yasuhiro
Ohmagari, Norio
Kingebeni, Placide Mbala
Huggins, John W
Iwami, Shingo
Pittman, Phillip R
author_facet Nishiyama, Takara
Miura, Fuminari
Jeong, Yong Dam
Nakamura, Naotoshi
Park, Hyeongki
Ishikane, Masahiro
Yamamoto, Shotaro
Iwamoto, Noriko
Suzuki, Michiyo
Sakurai, Ayana
Aihara, Kazuyuki
Watashi, Koichi
Hart, William S
Thompson, Robin N
Yasutomi, Yasuhiro
Ohmagari, Norio
Kingebeni, Placide Mbala
Huggins, John W
Iwami, Shingo
Pittman, Phillip R
Nishiyama, Takara
Miura, Fuminari
Jeong, Yong Dam
Nakamura, Naotoshi
Park, Hyeongki
Ishikane, Masahiro
Yamamoto, Shotaro
Iwamoto, Noriko
Suzuki, Michiyo
Sakurai, Ayana
Aihara, Kazuyuki
Watashi, Koichi
Hart, William S
Thompson, Robin N
Yasutomi, Yasuhiro
Ohmagari, Norio
Kingebeni, Placide Mbala
Huggins, John W
Iwami, Shingo
Pittman, Phillip R
collection PubMed - marine biology
contents Modeling lesion transition dynamics to clinically characterize patients with clade I mpox in the Democratic Republic of the Congo. Nishiyama, Takara Miura, Fuminari Jeong, Yong Dam Nakamura, Naotoshi Park, Hyeongki Ishikane, Masahiro Yamamoto, Shotaro Iwamoto, Noriko Suzuki, Michiyo Sakurai, Ayana Aihara, Kazuyuki Watashi, Koichi Hart, William S Thompson, Robin N Yasutomi, Yasuhiro Ohmagari, Norio Kingebeni, Placide Mbala Huggins, John W Iwami, Shingo Pittman, Phillip R Humans Democratic Republic of the Congo Viral Load Male Mpox, Monkeypox Female Adult Middle Aged Models, Theoretical Disease Outbreaks Adolescent Coinciding with the global outbreak of clade IIb mpox virus (MPXV), the Democratic Republic of the Congo (DRC) recently experienced a rapid surge in mpox cases with clade I MPXV. On 14 August 2024, the World Health Organization declared the continued cross-border spread of this clade in Africa a public health emergency of international concern (PHEIC). Clade I MPXV is known to be more fatal than clade IIb, but its clinical characteristics and prognosis differ between patients. Here, we used mathematical modeling to quantify temporal changes in total lesion counts during clade I MPXV infections, using data from a large cohort of patients with mpox in the DRC from 2007 to 2011. We further analyzed individuals' clinical data to explore predictive biomarkers of high lesion counts. Our analysis indicates that patients with clade I mpox can be stratified into two groups according to lesion severity and that viral load in peripheral blood at symptom onset may serve as a predictor for this classification [area under the curve (AUC) = 0.70]. Our estimates also suggest substantial individual heterogeneity in the time period during which patients have lesions, ranging from 20 to 65 days. Understanding the severity and duration of lesions in different patients, as characterized by our approach, may contribute to more tailored treatment strategies and control measures in ongoing clade I mpox outbreaks.
format Artículo científico
id pubmed_40601777
institution PubMed
language en
publishDate 2025
publisher Science translational medicine
record_format pubmed
spellingShingle Modeling lesion transition dynamics to clinically characterize patients with clade I mpox in the Democratic Republic of the Congo.
Nishiyama, Takara
Miura, Fuminari
Jeong, Yong Dam
Nakamura, Naotoshi
Park, Hyeongki
Ishikane, Masahiro
Yamamoto, Shotaro
Iwamoto, Noriko
Suzuki, Michiyo
Sakurai, Ayana
Aihara, Kazuyuki
Watashi, Koichi
Hart, William S
Thompson, Robin N
Yasutomi, Yasuhiro
Ohmagari, Norio
Kingebeni, Placide Mbala
Huggins, John W
Iwami, Shingo
Pittman, Phillip R
Humans
Democratic Republic of the Congo
Viral Load
Male
Mpox, Monkeypox
Female
Adult
Middle Aged
Models, Theoretical
Disease Outbreaks
Adolescent
Modeling lesion transition dynamics to clinically characterize patients with clade I mpox in the Democratic Republic of the Congo. Nishiyama, Takara Miura, Fuminari Jeong, Yong Dam Nakamura, Naotoshi Park, Hyeongki Ishikane, Masahiro Yamamoto, Shotaro Iwamoto, Noriko Suzuki, Michiyo Sakurai, Ayana Aihara, Kazuyuki Watashi, Koichi Hart, William S Thompson, Robin N Yasutomi, Yasuhiro Ohmagari, Norio Kingebeni, Placide Mbala Huggins, John W Iwami, Shingo Pittman, Phillip R Humans Democratic Republic of the Congo Viral Load Male Mpox, Monkeypox Female Adult Middle Aged Models, Theoretical Disease Outbreaks Adolescent Coinciding with the global outbreak of clade IIb mpox virus (MPXV), the Democratic Republic of the Congo (DRC) recently experienced a rapid surge in mpox cases with clade I MPXV. On 14 August 2024, the World Health Organization declared the continued cross-border spread of this clade in Africa a public health emergency of international concern (PHEIC). Clade I MPXV is known to be more fatal than clade IIb, but its clinical characteristics and prognosis differ between patients. Here, we used mathematical modeling to quantify temporal changes in total lesion counts during clade I MPXV infections, using data from a large cohort of patients with mpox in the DRC from 2007 to 2011. We further analyzed individuals' clinical data to explore predictive biomarkers of high lesion counts. Our analysis indicates that patients with clade I mpox can be stratified into two groups according to lesion severity and that viral load in peripheral blood at symptom onset may serve as a predictor for this classification [area under the curve (AUC) = 0.70]. Our estimates also suggest substantial individual heterogeneity in the time period during which patients have lesions, ranging from 20 to 65 days. Understanding the severity and duration of lesions in different patients, as characterized by our approach, may contribute to more tailored treatment strategies and control measures in ongoing clade I mpox outbreaks.
title Modeling lesion transition dynamics to clinically characterize patients with clade I mpox in the Democratic Republic of the Congo.
topic Humans
Democratic Republic of the Congo
Viral Load
Male
Mpox, Monkeypox
Female
Adult
Middle Aged
Models, Theoretical
Disease Outbreaks
Adolescent
url https://pubmed.ncbi.nlm.nih.gov/40601777/