Black, White, Black and White: mixed race and health in Canada

Posted in Articles, Canada, Health/Medicine/Genetics, Media Archive, Social Science on 2017-04-12 00:00Z by Steven

Black, White, Black and White: mixed race and health in Canada

Ethnicity & Health
Published online: 2017-04-10
pages 1-12
DOI: 10.1080/13557858.2017.1315374

Gerry Veenstra, Professor of Sociology
University of British Columbia

  • Objectives: To document inequalities in hypertension, self-rated health, and self-rated mental health between Canadian adults who identify as Black, White, or Black and White and determine whether differences in educational attainment and household income explain them.
  • Design: The dataset was comprised of ten cycles (2001–2013) of the Canadian Community Health Survey. The health inequalities were examined by way of binary logistic regression modeling of hypertension and multinomial logistic regression modeling of self-rated health and self-rated mental health. Educational attainment and household income were investigated as potentially mediating factors using nested models and the Karlson-Holm-Breen decomposition technique.
  • Results: Black respondents were significantly more likely than White respondents to report hypertension, a disparity that was partly attributable to differences in income. White respondents reported the best and Black respondents reported the worst overall self-rated health, a disparity that was entirely attributable to income differences. Respondents who identified as both Black and White were significantly more likely than White respondents to report fair or poor mental health, a disparity that was partly attributable to income differences. After controlling for income, Black respondents were significantly less likely than White respondents to report fair or poor mental health. Educational attainment did not contribute to explaining any of these associations.
  • Conclusion: Canadians who identify as both Black and White fall between Black Canadians and White Canadians in regards to self-rated overall health, report the worst self-rated mental health of the three populations, and, with White Canadians, are the least likely to report hypertension. These heterogeneous findings are indicative of a range of diverse processes operative in the production of Black-White health inequalities in Canada.

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The Myth of Human Races, Second Edition

Posted in Books, Health/Medicine/Genetics, Media Archive, Monographs on 2017-04-11 00:12Z by Steven

The Myth of Human Races, Second Edition

Wheatmark
2016-07-25
288 pages
Paperback ISBN: 978-1627874175

Alain F. Corcos, Professor Emeritus of Botany and Plant Pathology
Michigan State University

The idea that human races exist is a socially constructed myth that has no grounding in science. Regardless of skin, hair, or eye color, stature or physiognomy, we are all of one race. Nonetheless, scientists, social scientists, and pseudoscientists have, for three centuries, tried vainly to prove that distinctive and separate “races” of humanity exist. These protagonists of race theory have based their flawed research on one or more of five specious assumptions:

  • humanity can be classified into groups using identifiable physical characteristics
  • human characteristics are transmitted “through the blood”
  • distinct human physical characteristics are inherited together
  • physical features can be linked to human behavior
  • human groups or “races” are by their very nature unequal and, therefore, they can be ranked in order of intellectual, moral, and cultural superiority

The Myth of Human Races systematically dispels these fallacies and unravels the web of flawed research that has been woven to demonstrate the superiority of one group of people over another.

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Genetic Determinism, Technology Optimism, and Race

Posted in Articles, Health/Medicine/Genetics, Media Archive, Politics/Public Policy, United States on 2017-04-10 00:44Z by Steven

Genetic Determinism, Technology Optimism, and Race

The ANNALS of the American Academy of Political and Social Science
Volume 661, Issue 1, 2015
pages 160-180
DOI: 10.1177/0002716215587875

Jennifer Hochschild, Henry LaBarre Jayne Professor of Government; Professor of African and African American Studies
Harvard University

Maya Sen, Assistant Professor of Public Policy
Harvard University

We begin with a typology of Americans’ understanding of the links between genetic inheritance and racial or ethnic groups. The typology has two dimensions: one running from genetic determinism to social construction, and the other from technology optimism to technology pessimism. Construing each dimension as a dichotomy enables four distinct political perspectives on the possibilities for reducing racial inequality in the United States through genomics. We then use a new public opinion survey to analyze Americans’ use of the typology. Survey respondents who perceive that some phenotypes are more prevalent in one group than another due to genetic factors are disproportionately technology optimists. Republicans and Democrats are equally likely to hold that set of views, as are self-identified blacks, whites, and Latinos. The article discusses the findings and speculates about alternative interpretations of the fact that partisanship and group identity do not differentiate Americans in their views of the links between genetic inheritance and racial inequality.

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[Interview] If only parents gave DNA samples when they put children up for adoption

Posted in Articles, Asian Diaspora, Health/Medicine/Genetics, Media Archive on 2017-04-09 21:41Z by Steven

[Interview] If only parents gave DNA samples when they put children up for adoption

The Hankyoreh
2017-04-04

Kang Sung-man, Senior Staff writer


Bella Siegel-Dalton is a mixed-race adoptee who returned to South Korea after 51 years to look for her biological mother’s family. The big Korean letters on her shirt say, “Back in South Korea, my mother’s country.” (by Kang Sung-man, senior staff writer)

More Korean adoptees are organizing to search for their birth parents through DNA testing

Bella Siegel-Dalton is back in South Korea for the first time since being adopted by a family in the Napa Valley of northern California in 1966. When Bella Siegel-Dalton, 56, met a Hankyoreh reporter in a coffee shop on the first floor of the Lotte Hotel in Seoul on Apr. 1, her face was pallid. Because of kidney trouble, she needs to receive a transplant within two years. She’s also receiving chemotherapy after being diagnosed with leukemia.

Seven years ago, Siegel-Dalton identified her biological father in the US through DNA testing, but he had already passed away. During this trip to South Korea she says she wants to find her biological mother. “My 17-day trip to South Korea is challenging, so I’m gritting my teeth and hanging on. But it’s not painful, because this visit is so important to me,” she said.

Siegel-Dalton is a mixed-race adoptee who was born in Dongducheon, Gyeonggi Province, in 1961, to a South Korean woman and an American soldier. Her birth name was Lee Ji-sun. “My adoptive parents were really good people. My mother was an English teacher with a Master’s degree, while my father was a researcher for Shell Oil. They would sometimes let me try kimchi and listen to ‘Arirang’ so that I wouldn’t forget my memories of Korea,” she said…

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Dr. Sandra Soo-Jin Lee: Toward a More Precise Genetics

Posted in Articles, Health/Medicine/Genetics, Interviews, Media Archive on 2017-03-25 20:30Z by Steven

Dr. Sandra Soo-Jin Lee: Toward a More Precise Genetics

Guernica / a magazine of global arts & politics
2017-02-27

Lynette Chiu
Brooklyn, New York

The medical anthropologist on the imperative to move beyond race in genetic research and the explanatory power of life experience and inequality.

For decades, the idea that excavating the genetic origins of disease could transform treatment of the body has lived in the sea of public imagination, buoyant but as yet unrealized. The Human Genome Project, a landmark initiative undertaken between 1990 and 2003, identified and analyzed all the genes found in humans, and sowed the potential for new understanding of major illnesses. It engendered hope of a future in which genetic makeup could be the primary factor in determining a person’s care. Researchers could make endless shapes out of a sandbox of data that was blind to race—that problematic and omnipresent variable in the biomedical sphere.

But it is not a simple thing to scrub race from human tissue samples or from the minds of the experts seeking answers, and it remains stubbornly inextricable from genetic research. Investigating the history, intricacies, and implications of this is Dr. Sandra Soo-Jin Lee, a medical anthropologist and senior research scholar at the Center for Biomedical Ethics at Stanford University, who has been studying the role of race in genomic science since the late 1990s. One of her principal interests is biobanks—the various repositories of samples that scientists turn to to test their hypotheses. She identifies them as chronicles of society’s evolving efforts to distinguish between groups; the sorting and labeling of their contents are a collision of the biological and the sociopolitical. The result is the physical matter of thousands upon thousands of individuals demarcated by an inconsistent jumble of terms such as “nationality,” “ethnicity,” and “skin color.”.

In her 2015 paper “The Biobank as Political Artifact: The Struggle Over Race in Categorizing Genetic Difference,” published in The Annals of the American Academy of Political and Social Science, Dr. Lee is forthright about the dangers of genetic studies built around samples identified by race. “The unqualified racial labeling of DNA that strips genes of the social context and experience of those who have donated these materials,” she writes, “allows for a pendulum shift in scientific discourse that racializes genes.” Race can end up standing in for factors, such as diet and environment, that go unaccounted for in gene-focused studies. The subsequent findings can then trickle down to affect how we explain differences in disease burden, create health policy, and progress toward eliminating health disparities between populations. With the term “precision medicine” on the rise, referring to a care model that translates insights around genetic variation into clinical practice, the need to inspect and augment how those insights come about has grown more urgent…

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Beyond black and white: Color and mortality in post-reconstruction era North Carolina

Posted in Articles, Census/Demographics, Economics, Health/Medicine/Genetics, History, Media Archive, Social Science, United States on 2017-03-19 21:35Z by Steven

Beyond black and white: Color and mortality in post-reconstruction era North Carolina

Explorations in Economic History
Volume 50, Issue 1, January 2013
pages 148–159
DOI: 10.1016/j.eeh.2012.06.002

Tiffany L. Green, Assistant Professor
Department of Healthcare Policy and Research
Virginia Commonwealth University, Richmond, Virginia

Tod G. Hamilton, Assistant Professor of Sociology
Department of Sociology and Office of Population Research
Princeton University, Princeton, New Jersey

A growing empirical literature in economics and sociology documents the existence of more favorable social and economic outcomes among mixed-race blacks compared to non-mixed race blacks. However, few researchers consider whether the advantages associated with mixed-race status extend to mortality. To address this gap in the literature, we employ unique data from the 1880 North Carolina Mortality Census records in conjunction with data from 1880 U.S. Census of Population for North Carolina to examine whether mulatto (mixed-race) blacks experienced mortality advantages over to their colored (non-mixed race) counterparts from June 1879 to May 1880. For men between the ages of 20 and 44, estimates demonstrate that all black males, both mulatto and colored, were more likely than whites to die during the survey period. Although our results indicate that there is no statistically significant difference in mortality between mulatto and colored black men, we find a substantial mortality advantage associated with mixed-race status among women.

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The Mixed Race Athlete’s ECG: Not So Black And White

Posted in Articles, Health/Medicine/Genetics, Media Archive, United Kingdom, United States on 2017-03-19 21:11Z by Steven

The Mixed Race Athlete’s ECG: Not So Black And White

Journal of the American College of Cardiology
Volume 69, Issue 11, Supplement
2017-03-21
pages 1416
DOI: 10.1016/S0735-1097(17)34805-2

Aneil Malhotra, Prashant Rao, Harshil Dhutia, Sabiha Gati, Tee Joo Yeo, Rajit Khosla, Vivek Prasad, Michael Papadakis, Sanjay Sharma
St. George’s University of London, London, United Kingdom

Non Invasive Imaging (Echocardiography, Nuclear, PET, MR and CT)

  • Background: The past 2 decades has seen a huge rise in the number of mixed race athletes with one white and one black parent. In fact this is the largest growing ethnic group in both the USA and UK. Little is known on the mixed race athlete’s EKG. This is the first study to analyse the EKGs of mixed race athletes (MAs) and compare them to white (WAs) and black (BAs) athletes.
  • Methods: The EKGs of 300 MAs professional soccer players were compared to 1,000 BA and 1,000 WA soccer players all of whom underwent mandatory preparticipation screening with EKG. All MAs had one white and one black parent. EKG characteristics were analysed independently by 2 cardiologists.
  • Results: The mean age of all athletes was 16.7 years. 95% were male. MAs had a higher prevalence of bradycardia (67%) vs. both WAs (44%) and BAs (46%; table 1). MAs had more left ventricular hypertrophy (30%) vs. BAs (17%). MAs revealed more atrial enlargement and left axis deviation than WAs, but not BAs. T wave inversion (TWI) was 4 times more common in MAs (8%) than WAs (2.3%) though less common than BAs (10.9%).
  • Conclusions: MAs demonstrate EKG changes similar to black athletes in terms of atrial enlargement and axis deviation which are borderline variants according to the refined criteria for EKG interpretation in athletes. MAs demonstrated a higher prevalence of TWI in all territories vs. WAs, though less than BAs. Mixed race athletes do indeed exhibit a “mixed” pattern of EKG characteristics though these tend to be more similar to black athletes’ EKG than white athletes.

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Loving v. Virginia as a Civil Rights Decision

Posted in Articles, Health/Medicine/Genetics, Law, Media Archive, United States on 2017-03-06 20:13Z by Steven

Loving v. Virginia as a Civil Rights Decision

New York Law School Law Review
Volume 59, Number 1 (2014/2015)
pages 175-209

Dorothy E. Roberts, George A. Weiss University Professor of Law and Sociology and the Raymond Pace and Sadie Tanner Mossell Alexander Professor of Civil Rights
University of Pennsylvania

Loving v. Virginia, the unanimous U.S. Supreme Court decision that invalidated state laws restricting interracial marriage, marked the tail end of the civil rights cases of the 1950s and ’60s. Loving was not issued until 1967, more than a decade after the Court’s decision in Brown v. Board of Education, holding racial segregation of public schools unconstitutional. At the time of the 1963 March on Washington, nineteen states still had laws prohibiting interracial marriage, and federal jurisprudence upholding these laws had remained the same since 1883.

Civil rights litigators waited so long to launch an attack on state anti-miscegenation statutes in federal court because interracial marriage seemed at once so trivial and so controversial. Trivial because it involved interpersonal relationships rather than the weighty public rights to equal education, voting, and employment. But challenging the marriage laws also struck at the bedrock of racism: Classifying human beings into supposedly biological races that should be kept apart. Some civil rights advocates, as well as justices on the Warren Court, feared that attacking anti-miscegenation too soon was doomed to fail and would threaten the implementation of recent civil rights victories because white Southerners’ loathing of racial intermingling was so basic to their dogma of racial separation. After all, a primary reason for segregated schooling was to foreclose the interracial intimacy that might be sparked in integrated classrooms. Moreover, prior to Loving, state control over marriage was absolute.

Loving was the capstone of the Court’s blow to the Jim Crow regime. As the Court stated, it struck down the Virginia law because it was a measure “designed to maintain White Supremacy.” Yet subsequent decades have faded the understanding of Loving as a civil rights decision. While Brown became the emblem of the end to de jure segregation, Loving fell into relative obscurity. In his recent book, The Civil Rights Revolution, constitutional law scholar Bruce Ackerman denies that Loving “deserves a central place in the civil rights canon.” The same-sex marriage movement revived the decision to stand for the right to marry the partner of one’s choice. In 2007, on the occasion of the fortieth anniversary of the Loving decision, Mildred Loving commented:

I am proud that Richard’s and my name is on a court case that can help reinforce the love, the commitment, the fairness, and the family that so many people, black or white, young or old, gay or straight seek in life. I support the freedom to marry for all. That’s what Loving, and loving, are all about.

Today, Loving is remembered more for protecting the right to marry than for toppling the final pillar of the de jure racial caste system in the United States. Moreover, to the extent that federal courts rely on Loving as a civil rights decision, they have largely distorted its reasoning, as well as its significance to the struggle to end racism and white domination.

This article aims to revive Loving as a civil rights decision, and to stress the continuing importance of its recognition of the relationship between racial classifications and white supremacy. Part I places the Lovings’ lawsuit in the context of the litigation agenda that helped institute the civil rights revolution. Jim Crow restrictions on marriage implemented the combined white supremacist and eugenicist ideologies of an innate racial hierarchy that called for racial separation. Both civil rights lawyers and U.S. Supreme Court justices delayed tackling state anti-miscegenation laws for strategic reasons. But they understood these laws as part of the Jim Crow segregationist system that the civil rights movement was dismantling and kept their abolition as an eventual goal.

Part II analyzes the Loving decision as a challenge to racism and white supremacy as much as the validation of marriage rights—and the entangled relationship between the two in the Court’s constitutional reasoning. Just as bans on interracial marriage were an essential part of the segregationist regime, eliminating them was an integral chapter in the series of civil rights decisions issued by the Warren Court. A central question in Loving was whether the Court would extend the holding in Brown from the realm of public education to state laws regulating marriage. By applying Brown’s prohibition of racial separation to the private sphere of marriage, formerly seen as the exclusive domain of states’ power, the Court radically confirmed a constitutional mandate for federal intervention in all aspects of the nation’s racial regime.

Part III evaluates how federal courts have interpreted the civil rights dimension of Loving in the decades that followed. I argue that key U.S. Supreme Court decisions have perverted the central lesson of Loving. Rather than link racial classifications to political subordination (as the Loving Court did), subsequent Court opinions have wrongly relied on Loving to do just the opposite. Loving has been misused to support a colorblind approach to the Fourteenth Amendment that treats the government’s use of race to eliminate the contemporary vestiges of Jim Crow as contemptible as the Jim Crow classifications designed to enforce white rule.

Finally, Part IV explains why the lessons of Loving as a civil rights decision are especially important in today’s supposedly “post-racial” society. A new biopolitics of race is resuscitating the notion of biological racial classifications underlying the anti-miscegenation laws that Loving struck down. Genomic science and gene-based biotechnologies are promoting race-consciousness at the molecular level at the very moment the Court and many policymakers believe race-consciousness is no longer necessary at the social level. I conclude that it is more urgent than ever to understand race as a political system that determines individuals’ status and welfare, and for federal courts to implement, uphold, and enforce strong race-conscious remedies for the lasting legacy of slavery that the Fourteenth Amendment was intended to abolish and civil rights activists fought to eradicate…

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What is Race? Just the Facts.

Posted in Articles, Health/Medicine/Genetics, Media Archive, Social Science on 2017-03-01 13:56Z by Steven

What is Race? Just the Facts.

The Nib
2017-02-24

Whit Taylor, cartoonist, writer, and educator from New Jersey

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My Mysterious Son: A Life-Changing Passage Between Schizophrenia and Shamanism

Posted in Africa, Books, Family/Parenting, Health/Medicine/Genetics, Media Archive, Monographs, Native Americans/First Nation on 2017-02-27 21:58Z by Steven

My Mysterious Son: A Life-Changing Passage Between Schizophrenia and Shamanism

Skyhorse Publishing
2014-11-18
432 pages
6.00 x 9.00 in.
Hardback ISBN: 9781629144870
eBook ISBN: 9781629149578

Dick Russell

What a father will do to fight the mental illness that has destroyed his son.

What does a father do when hope is gone that his only son can ever lead anything close to a “normal” life? That’s the question that haunted Dick Russell in the fall of 2011, when his son, Franklin, was thirty-two. At the age of seventeen, Franklin had been diagnosed with schizophrenia. For years he spent time in and out of various hospitals, and even went through periods of adamantly denying that Dick was actually his father.

A mixed-race child, Franklin was handsome, intelligent, and sensitive until his mental illness suddenly took control. After spending the ensuing years trying to build some semblance of a normal father-son relationship, Dick was invited with his son, out of the blue, to witness the annual wildlife migration on Africa’s Serengeti Plain. Seizing this potential opportunity to repair the damage that both had struggled with, after going through two perilous nights together in Tanzania, ultimately the two-week trip changed both of their lives.

Desperately seeking an alternative to the medical model’s medication regimen, the author introduces Franklin to a West African shaman in Jamaica. Dick discovers Franklin’s psychic capabilities behind the seemingly delusional thought patterns, as well as his artistic talents. Theirs becomes an ancestral quest, the journey finally taking them to the sacred lands of New Mexico and an indigenous healer. For those who understand the pain of mental illness as well the bond between a parent and a child, My Mysterious Son shares the intimate and beautiful story of a father who will do everything in his power to repair his relationship with a young man damaged by mental illness.

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