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	<title>nativity &#8211; Science</title>
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	<title>nativity &#8211; Science</title>
	<link>https://scienmag.com</link>
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		<title>HPV Vaccination Gaps in New York City Track Closely with Where People Were Born</title>
		<link>https://scienmag.com/hpv-vaccination-gaps-in-new-york-city-track-closely-with-where-people-were-born/</link>
		
		<dc:creator><![CDATA[Phoebe Ingram]]></dc:creator>
		<pubDate>Tue, 13 Oct 2026 00:01:51 +0000</pubDate>
				<category><![CDATA[Cancer]]></category>
		<category><![CDATA[cancer prevention]]></category>
		<category><![CDATA[community health]]></category>
		<category><![CDATA[community-based health survey in NYC]]></category>
		<category><![CDATA[data disaggregation]]></category>
		<category><![CDATA[Health disparities]]></category>
		<category><![CDATA[health inequities in HPV vaccine distribution]]></category>
		<category><![CDATA[HPV vaccination]]></category>
		<category><![CDATA[HPV vaccination disparities in New York City]]></category>
		<category><![CDATA[HPV vaccine coverage among young adults]]></category>
		<category><![CDATA[immigrant health disparities and HPV vaccination]]></category>
		<category><![CDATA[immigrants]]></category>
		<category><![CDATA[immunization]]></category>
		<category><![CDATA[impact of country of birth on vaccine uptake]]></category>
		<category><![CDATA[influence of ethnicity and birthplace on preventive healthcare]]></category>
		<category><![CDATA[multiethnic population health study]]></category>
		<category><![CDATA[multinomial logistic regression]]></category>
		<category><![CDATA[nativity]]></category>
		<category><![CDATA[New York City]]></category>
		<category><![CDATA[NYC Cancer Community Needs Assessment]]></category>
		<category><![CDATA[Public health]]></category>
		<category><![CDATA[public health gaps in urban cancer prevention]]></category>
		<category><![CDATA[racial and ethnic influences on HPV vaccination]]></category>
		<category><![CDATA[social determinants of HPV vaccination]]></category>
		<category><![CDATA[SWANA]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=266383</guid>

					<description><![CDATA[A community-based study of 1,278 New York City adults finds that foreign-born residents across several racial and ethnic groups have significantly lower odds of HPV vaccination than US-born White individuals, with foreign-born SWANA respondents showing the steepest deficits.]]></description>
										<content:encoded><![CDATA[<p>Human papillomavirus vaccination remains one of the most powerful tools in cancer prevention, yet its benefits are not distributed evenly across urban populations. A new study conducted in New York City reveals that a person&#8217;s country of birth, combined with their race and ethnicity, shapes their odds of having received the vaccine far more than either factor alone. The research, led by Perla Chebli of the Department of Population Health at NYU Grossman School of Medicine and colleagues, was published in BMC Cancer and draws on a large community-based survey designed to capture groups that are usually invisible in standard public health statistics.</p>
<p>The investigation used data from the 2021 to 2022 Cancer Community Health Resources and Needs Assessment, an effort organized by the NYU Langone Health Perlmutter Cancer Center together with 23 community partner organizations. This collaborative design allowed the researchers to reach a genuinely multiethnic adult population across the city. The analytic sample included 1,278 adults between the ages of 18 and 45, a demographic window that matters because the HPV vaccine is licensed and recommended for catch-up vaccination in young adults even though routine recommendation begins in adolescence.</p>
<p>What distinguishes this study methodologically is its refusal to collapse racial and ethnic groups into broad, aggregated categories. Instead of treating Asian, Black, Hispanic, or White residents as monolithic blocks, the team analyzed six distinct groups: White, Hispanic, Black, Southwest Asian and North African (often abbreviated SWANA), Asian, and an Other category that included American Indian and Alaskan Native, Central Asian, mixed-race, Native Hawaiian and Pacific Islander, and unknown responses. This disaggregation is critical because national surveys frequently lump together populations with vastly different migration histories, languages, healthcare access patterns, and cultural attitudes toward vaccination.</p>
<p>The statistical approach centered on multinomial logistic regression, a technique suited to outcomes with more than two unordered categories. Here the outcome had four levels: receiving no doses of the HPV vaccine, receiving one dose, receiving more than one dose, or having an unknown vaccination status. The researchers tested an interaction term between race and ethnicity on one side and nativity, meaning US-born versus foreign-born status, on the other. That interaction term was statistically significant at a threshold of p less than 0.01 and was retained in the final models, which were additionally adjusted for sociodemographic covariates. In practical terms, the interaction means the effect of being foreign-born on vaccination differed depending on a person&#8217;s racial and ethnic group, and vice versa.</p>
<p>The descriptive picture of the sample already tells a striking story. Respondents were predominantly female, at 61 percent, and a substantial majority, 65 percent, were born outside the United States. About 73 percent reported having health insurance, leaving more than a quarter uninsured. Most sobering was the vaccination picture: over half of respondents, 53 percent, had never received any dose of the HPV vaccine, and another 23 percent did not know their own vaccination status. Taken together, fewer than one in four participants could be confidently counted as having initiated the vaccine series, a figure that underscores how much work remains even in a city with dense healthcare infrastructure.</p>
<p>The regression results sharpened the pattern around nativity. Compared with US-born White individuals, the reference category in the models, foreign-born SWANA individuals had markedly lower odds of having received one dose versus no doses, with an odds ratio of 0.21 and a 95 percent confidence interval of 0.06 to 0.74. Foreign-born White individuals also showed reduced odds of a single dose, with an odds ratio of 0.35 and a confidence interval of 0.12 to 0.96. Because these confidence intervals exclude one, the findings are statistically significant, and the magnitude of the SWANA estimate, roughly a 79 percent reduction in odds, is substantial by any epidemiological standard.</p>
<p>For the more demanding outcome of receiving more than one dose, which reflects series initiation beyond a first injection, the disparities widened. Foreign-born Asian individuals had an odds ratio of 0.34 (95 percent CI: 0.17 to 0.71) relative to US-born White individuals, and foreign-born Black individuals had an odds ratio of 0.39 (95 percent CI: 0.16 to 0.95). The steepest deficits appeared among foreign-born SWANA respondents, with an odds ratio of 0.07 (95 percent CI: 0.02 to 0.34), and foreign-born White respondents, with an odds ratio of 0.08 (95 percent CI: 0.02 to 0.30). These estimates indicate that, after adjustment, being born outside the United States was associated with dramatically lower completion of multiple doses across several groups, including among White residents, a finding that would have been masked entirely if nativity had not been modeled separately.</p>
<p>One of the most intriguing results concerns uncertainty itself. Foreign-born Asian individuals had higher odds of reporting unknown vaccination status rather than no doses, with an odds ratio of 2.82 (95 percent CI: 1.16 to 6.83) compared with US-born White individuals. This is more than a data-quality footnote. Unknown status may reflect fragmented medical records across countries, vaccination received abroad that is not documented in US systems, language barriers during clinical encounters, or lower familiarity with one&#8217;s own immunization history. From a surveillance standpoint, a quarter of the entire sample not knowing their status means that measured uptake gaps could be either underestimated or overestimated, and that interventions to consolidate vaccination records could meaningfully improve both care and measurement.</p>
<p>The biological rationale for closing these gaps is well established. HPV is a sexually transmitted virus whose persistent infection with high-risk genotypes drives cervical, anal, oropharyngeal, penile, vaginal, and vulvar cancers. The vaccine targets the most oncogenic types, and vaccination at a young age produces the strongest immune responses and greatest protection because it precedes any exposure. Adults in the 18 to 45 range represent a catch-up population in whom even partial series initiation confers benefit, which is why the distinction between one dose and more than one dose in this study carries real clinical weight rather than being a mere statistical convenience.</p>
<p>The authors conclude that their findings highlight the importance of disaggregated data for developing effective programs to improve HPV vaccination uptake. The implication for public health practice is concrete: city-level vaccination campaigns that target race and ethnicity alone will miss the foreign-born residents within nearly every group who face the largest deficits, and outreach that treats all immigrants as a single category will miss the especially low uptake among SWANA populations, a group rarely broken out in US health statistics. Community-partnered data collection of the kind used here, built through organizations embedded in the neighborhoods they serve, offers a template for identifying precisely where the gaps lie. The research was supported by the National Cancer Institute, the Centers for Disease Control and Prevention, and the Dune Road Foundation, and it was approved by the NYU Langone Health Institutional Review Board, with informed consent obtained from all participants.</p>
<p><strong>Subject of Research:</strong> HPV vaccine uptake by race, ethnicity, and nativity among adults in New York City</p>
<p><strong>Article Title:</strong> HPV vaccination in New York City: variation by population characteristics and nativity</p>
<p><strong>Article References:</strong> Chebli, P., Nakra, N. M., Wyatt, L., Kwon, S. C., Trinh-Shevrin, C., &amp; LeCroy, M. N. (2026). HPV vaccination in New York City: variation by population characteristics and nativity. <em>BMC Cancer</em>. <a href="https://doi.org/10.1186/s12885-026-16819-0" rel="noopener noreferrer">https://doi.org/10.1186/s12885-026-16819-0</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1186/s12885-026-16819-0" rel="noopener noreferrer">10.1186/s12885-026-16819-0</a></p>
<p><strong>Keywords:</strong> HPV vaccination, New York City, nativity, immigrants, health disparities, cancer prevention, SWANA, data disaggregation, multinomial logistic regression, public health, immunization, community health</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">266383</post-id>	</item>
		<item>
		<title>New Maps Reveal Where Americans Move—and Who Stays Put</title>
		<link>https://scienmag.com/new-maps-reveal-where-americans-move-and-who-stays-put/</link>
		
		<dc:creator><![CDATA[Courtney Benton]]></dc:creator>
		<pubDate>Sat, 12 Sep 2026 12:33:17 +0000</pubDate>
				<category><![CDATA[Social Science]]></category>
		<category><![CDATA[American Community Survey]]></category>
		<category><![CDATA[American internal migration patterns]]></category>
		<category><![CDATA[census data analysis of migration]]></category>
		<category><![CDATA[demographic factors influencing migration]]></category>
		<category><![CDATA[demographic heterogeneity]]></category>
		<category><![CDATA[geographic mobility in the United States]]></category>
		<category><![CDATA[impact of migration slowdown on population distribution]]></category>
		<category><![CDATA[individual-level migration modeling]]></category>
		<category><![CDATA[internal migration]]></category>
		<category><![CDATA[LISA]]></category>
		<category><![CDATA[logistic regression]]></category>
		<category><![CDATA[long-term trends in American mobility]]></category>
		<category><![CDATA[migration slowdown]]></category>
		<category><![CDATA[nativity]]></category>
		<category><![CDATA[nativity and migration trends]]></category>
		<category><![CDATA[policy implications of migration patterns]]></category>
		<category><![CDATA[population redistribution]]></category>
		<category><![CDATA[race and ethnicity]]></category>
		<category><![CDATA[racial and ethnic disparities in migration]]></category>
		<category><![CDATA[regional population concentration]]></category>
		<category><![CDATA[spatial clustering]]></category>
		<category><![CDATA[spatial demography]]></category>
		<category><![CDATA[spatial statistics in population research]]></category>
		<category><![CDATA[United States]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=194219</guid>

					<description><![CDATA[A twenty-year analysis of U.S. census data shows that internal migration clusters differ sharply by race, ethnicity, and nativity, and that regional concentration does not necessarily match individual mobility.]]></description>
										<content:encoded><![CDATA[<p>Americans are famously mobile, but a sweeping new analysis of two decades of census data shows that movement within the United States is far from random. Instead, it follows deeply etched geographic patterns that differ sharply across racial, ethnic, and nativity groups, and that have persisted even as overall mobility has declined to historic lows. The study, published in the Journal of Population Research, combines spatial statistics with individual-level modeling to paint one of the most detailed portraits yet of who moves, where they cluster, and how those two stories diverge.</p>
<p>Ernesto F. L. Amaral and Nereyda Y. Ortiz Osejo de Lemus of Texas A&amp;M University analyzed American Community Survey data spanning 2005 to 2024, covering adults aged eighteen and older across the entire country. Their central question was deceptively simple: are the places where migration rates run high the same for everyone, and do the groups with the strongest regional concentrations also have the highest individual likelihood of moving? The answer, they found, is frequently no—a discrepancy with significant implications for how researchers and policymakers understand population redistribution in America.</p>
<p>The backdrop to the study is what demographers have called the Great American Migration Slowdown. Between 1968 and 2009, annual interstate migration rates fell from 3.6 percent to just 1.6 percent, and between 1982 and 2015, moves across state and county lines dropped by roughly half. The new analysis confirms this trajectory continued into recent years: overall migration rates bottomed out at 4.57 percent in 2012, recovered modestly through 2019, dipped during the COVID-19 pandemic, and settled back down to 4.58 percent by 2024. The decline is pronounced compared with other developed countries and is thought to reflect reduced responsiveness to regional economic differences, growing place attachment, and shifts in job mobility.</p>
<p>But the aggregate numbers conceal enormous variation. Hispanic, non-Hispanic African American, and non-Hispanic Native American populations consistently showed lower migration rates than non-Hispanic whites and non-Hispanic Asians throughout the two decades studied, with foreign-born Hispanics recording the lowest rates of any group. Foreign-born individuals of all backgrounds moved less often than their U.S.-born counterparts, reflecting differences in settlement histories, social networks, and access to information about destinations. When the researchers modeled individual migration odds statistically, controlling for age, education, income, marital status, children, homeownership, employment, and region of residence, these group differences persisted rather than disappearing.</p>
<p>The spatial half of the analysis used a technique called Local Indicators of Spatial Association, or LISA, which identifies statistically significant clusters of high or low values across neighboring geographic areas. Applied to Migration Public Use Microdata Areas—the finest geography available in the public census microdata—the method revealed striking regional signatures. In 2019, hotspots of high internal migration appeared across parts of the West, including northern California, Nevada, Utah, southern Idaho, and northwestern Wyoming, along with central Texas and northern Florida. By 2024, most of the western hotspots had faded, while Texas and Florida concentrations endured. A long corridor of low migration, stretching from Texas through the Midwest to the Northeast, remained stable across the entire period and even expanded into California and New Mexico.</p>
<p>Those patterns, however, look very different depending on which demographic group is mapped. Non-Hispanic African Americans showed pronounced high-migration clusters across southeastern regions, alongside widespread low-migration zones in the Midwest, Northeast, and West. Hispanic clustering concentrated in California, the Mountain West, Texas, and Florida. Non-Hispanic Native Americans displayed high-migration clusters in the Northwest, Southwest, and parts of the Great Plains, including Arizona, Utah, New Mexico, Colorado, Oklahoma, and Alaska—areas where Indigenous populations are geographically concentrated. Non-Hispanic Asians, by contrast, were characterized mainly by low-migration clusters in southern and Midwestern regions, with some expansion into the Northwest by 2024.</p>
<p>Nativity proved to be a crucial modifier of these spatial patterns. U.S.-born Hispanics showed broad high-migration clustering across western and southern areas, while foreign-born Hispanics displayed far fewer hotspots, concentrated primarily in Texas and Florida by 2024. The contrast was equally stark for African Americans: U.S.-born Black migrants exhibited a broad southeastern pattern, whereas foreign-born Black migrants showed tightly localized clusters in eastern metropolitan areas, including Florida, Atlanta, and Washington, DC—patterns likely reflecting distinct immigrant origins, settlement networks, and labor market incorporation. Foreign-born whites, meanwhile, were marked predominantly by low-migration clusters across central regions of the country.</p>
<p>Perhaps the study&#8217;s most striking finding is that regional concentration and individual mobility are genuinely distinct dimensions of migration. Non-Hispanic African Americans and Hispanics both showed lower individual odds of moving than non-Hispanic whites after adjustment, yet both groups displayed strong, persistent regional hotspots. Conversely, non-Hispanic Asians showed relatively high individual mobility despite maps dominated by low-migration clusters. A group can be regionally concentrated precisely because most of its members who do move go to the same places, or because past settlement histories anchor its geography, without its members being frequent movers overall. The authors are careful to note that their LISA maps describe spatial clustering at selected points in time and cannot disentangle the cumulative flows, network effects, and historical settlement processes that may have produced them.</p>
<p>The research also has limitations that the authors acknowledge candidly. The analysis is associational rather than causal, and the logistic regression models do not formally account for spatial autocorrelation, which could lead to underestimated standard errors. The aggregated geographic units limit the ability to study very local dynamics, and detailed subgroup-specific flow analysis at the county level would require restricted Census data. The 2020 ACS, disrupted by pandemic data-collection problems, was tested in robustness checks and found not to alter the main results. Still, the authors argue the two-pronged approach—descriptive spatial clustering paired with adjusted individual-level models—offers a descriptive framework that previous single-lens studies could not provide.</p>
<p>What emerges is a compelling guide for future research. The findings point directly to places and populations where localized studies could uncover the mechanisms behind the patterns: Hispanic migration in Texas and Florida, African American migration in the Southeast, foreign-born African American settlement in Atlanta and Washington, DC, and Native American migration across the Southwest, Great Plains, and Alaska. The authors suggest combining administrative county-to-county flow data with survey microdata, and applying spatially explicit methods such as geographically weighted regression, to test whether the relationships they identify vary across places. As the United States continues to grow more demographically diverse while its residents grow more rooted, understanding precisely where and how different communities redistribute themselves—and why geography and mobility do not always move in tandem—has become an essential question for demographers, economists, and anyone concerned with regional inequality.</p>
<p><strong>Subject of Research:</strong> Spatial patterns and demographic heterogeneity of internal migration in the United States by nativity and race/ethnicity</p>
<p><strong>Article Title:</strong> Internal migration, demographic heterogeneity, and spatial patterns in the United States</p>
<p><strong>Article References:</strong> Internal migration, demographic heterogeneity, and spatial patterns in the United States. (n.d.). <a href="https://doi.org/10.1007/s12546-026-09434-0" rel="noopener noreferrer">https://doi.org/10.1007/s12546-026-09434-0</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1007/s12546-026-09434-0" rel="noopener noreferrer">10.1007/s12546-026-09434-0</a></p>
<p><strong>Keywords:</strong> internal migration, demographic heterogeneity, spatial clustering, LISA, nativity, race and ethnicity, American Community Survey, population redistribution, spatial demography, United States, logistic regression, migration slowdown</p>
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