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HBV杂志回顾 2013年5月1日 Christine M. Kukka [复制链接]

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发表于 2013-5-3 20:39 |只看该作者 |倒序浏览 |打印
HBV Journal Review
May 1, 2013, Vol 10, no 5
by Christine M. Kukka

EASL 2013 Edition


Antiviral Combination Used for HIV Appears Effective In "Immune Tolerant" Patients
A New Zealand researcher tried an antiviral drug combination used to treat HIV and found it very effective in temporarily reducing high viral loads in hepatitis B "e" antigen (HBeAg)-positive patients. However, the drug was effective only while patients took the tenofovir and emtricitabine (Truvada) combination.

Current medical guidelines do not recommend treating these "immune tolerant" patients, whose immune systems appear to tolerate high levels of the hepatitis B virus (HBV) without attacking the infected liver cells. Eventually, these patients' immune systems attack the HBV infection, but only after years of dangerously high viral loads.

After four years of treatment with the tenofovir-emtricitabine drug combination, 76% of 62 patients achieved nearly undetectable viral load without any signs of drug resistance. Only 55% of a similar immune-tolerant control group treated with just tenofovir (Viread) achieved undetectable viral load after four years, according to the report presented at the European Association for the Study of the Liver (EASL) conference held in Amsterdam in late April.

However, only five patients in the study lost HBeAg and only three of the five developed "e" antibodies, which usually results in a permanent lowering of viral load. None of the patients lost hepatitis B surface antigen (HBsAg) or developed surface antibodies— a sign of clearing the infection.

Half of the patients stopped treatment after the study concluded and all of them experienced a rebound in their viral loads to the same high levels as existed before treatment began.

While it appears an indefinite course of treatment would be needed in this "immune tolerant" population to suppress viral load, researchers suggest that doctors could selectively use the drug in patients with family histories of cirrhosis or liver cancer.

Despite Universal Care, Hepatitis B Care Is Inconsistent Across Canada
Despite accolades for its universal access to medical care, hepatitis B patients in Canada face inconsistent care across provinces, and even hepatitis B vaccination practices vary widely across the country, according to a March 2013 report entitled Liver Disease in Canada: A Crisis in the Making by the Canadian Liver Foundation.

Surprisingly, the country that delivers health care to all residents regardless of their ability to pay has different hepatitis B treatment guidelines and drug reimbursement rates from province to province. According to the report:

Inconsistent treatment: Each province has its own reimbursement policies and standards for when hepatitis B treatment is required, and which drug should be used. For example, several provinces allow the use of the antiviral entecavir (Baraclude) only when hepatitis B patients have developed cirrhosis. En-tecavir is one of two antivirals currently recommended for all first-line hepatitis B treatment by U.S. and European guidelines.

"Only in Quebec is the reimbursement policy in line with clinical practice guidelines," the report's authors wrote. "It is striking that there is no uniformity between provinces with regard to access to hepatitis B treatment," the report noted.

The inconsistent treatment guidelines also means that many people who require treatment won't get treatment simply because of the province they live in. Delaying hepatitis B treatment results in cirrhosis, liver cancer, and death.

Outdated treatment guidelines: Some of the guidelines also allow treatment only if alanine transaminase (ALT) levels are elevated, which often indicates liver damage is occurring. That assessment is outdated—numerous studies have shown that liver damage can be severe, due to long-term infection, even if current ALT levels are normal.

The report revealed that in 2009, 58% of hepatitis B patients covered by free, public health care received the antiviral lamivudine (Epivir-HBV). This outdated antiviral has an extremely high rate of drug resistance and is no longer recommended for use as a first-line treatment.

Meanwhile, the report revealed that 90% of affluent Canadians who were also covered by private health insurance policies were treated with more modern and effective antivirals other than lamivudine. This shows that even in Canada, people with high income and private insurance had access to superior hepatitis B treatment.

Record-keeping ineffective: Canada does not distinguish hepatitis B from hepatitis C in its death records, therefore tracking the infection's true impact cannot be documented. Additionally, deaths from cirrhosis and liver disease—though resulting from hepatitis B or C—are classified separately.

Only one province —Ontario —tracks hepatitis B deaths. Extrapolating from that data, the report estimates that 14,000 people die annually from hepatitis B in Canada, and that figure is expected to rise due to increases in hepatitis B cases through immigration from Asia and Africa.

Inconsistent immunization policies: Immunization schedules also vary between provinces. While British Columbia, New Brunswick, and Prince Edward Island guidelines recommend hepatitis B vaccination during infancy, the remaining provinces require immunizations later in childhood, during adolescence.

As a result, new hepatitis B cases are actually increasing during childhood in Canada because immunizations aren't occurring until adolescence.

Home Visits Key to Promoting Hepatitis B Screening Among Ethnic Groups
Educating Asian-Americans about their high risk of hepatitis B, and getting them screened, treated and vaccinated can be a cultural and medical challenge. Many immigrants and their children do not speak English, and many health care providers still do not follow medical guidelines and screen Asian-American patients for hepatitis B or offer translation services in their clinics.

A unique outreach program, conducted by lay health care workers in an Hmong community in Sacramento, proved to be highly effective in getting immigrants from mountainous areas in Laos and Vietnam screened for hepatitis B.

According to the report, authored by University of California-Davis Health System researchers and published in the April 23, 2013 issue of the journal Cancer Epidemiology, Biomarkers & Prevention, the Hmong have high rates of hepatitis B and liver cancer rates that are six- to seven-times that of white or Hispanic populations in the United States.

Because the Hmong know little about hepatitis B and rarely interact with local health care providers due to language and cultural barriers, HBV infection and liver cancer can be advanced when first diagnosed and patients often live for less than a year after a cancer diagnosis.

In the study, lay health care workers—many of whom were Hmong and knowledgeable about the culture and language—visited 260 Hmong residents in Sacramento. The residents were randomly assigned to two groups that received two home visits. During the visits residents received either hepatitis B and liver cancer education or nutrition and physical fitness information.

Six months later, 24% of the group that learned about hepatitis B had been screened at their doctors' clinic, compared to only 10% of the group that learned about nutrition and exercise.

By using Hmong lay educators recruited from two respected Hmong cultural organizations, the UC Davis researchers overcame cultural obstacles to HBV screening.

The participants were given a brochure in Hmong and English that they could use to request a hepatitis B screening during their next clinic visit, where translation services were often not available.

However, much of this effort would not be needed if doctors followed current practice recommendations for screening all Asian-Americans for hepatitis B, researchers noted.

Fibroscan Imaging Plus Blood Tests Could Replace Liver Biopsies
Researchers have been trying to develop new methods to assess patients' liver damage using blood tests or sonograms to avoid performing invasive and costly liver biopsies. One study, published in the April 2013 issue of the journal Alimentary Pharmacology and Therapeutics, found that two noninvasive tests come close to replacing liver biopsies in accurately measuring liver damage over a five year period.

The researchers used a Fibroscan to evaluate the degree of liver stiffness (also known as fibrosis or scarring). The Fibroscan uses a sonogram to measure the speed of sound waves through the liver to identify mild (fibrosis) to severe liver scarring (cirrhosis.) They also used a blood test called a Fibrotest that measures six elements in a blood sample to determine the degree of liver disease.

Researchers used these two diagnostic tools on 600 hepatitis B patients and followed them for nearly five years. Most of the patients were male, average age 42.5. Most had normal or moderately elevated ALT levels.

Doctors found that 94 (15.7%) had liver damage and liver biopsies were performed on 214 patients to test the accuracy of the noninvasive tests.

The researchers reported that the Fibroscan and Fibrotest together were very effective in assessing liver health and indicating when treatment was needed. In some cases, they reported that the two tests combined were more accurate than a liver biopsy.

"This information is of major importance, helping us to sharpen our various tools for the follow-up of our patients," they wrote. Using the two tests together..."could replace liver biopsy for the evaluation of the disease, whatever the stage of the disease."

Useful in patients with "inactive" liver disease: If proven accurate, these two diagnostic tools could prove critical for patients who are HBeAg-negative, have normal ALT levels, and have low viral loads (HBV DNA) under 20,000 IU/mL. Current medical guidelines do not recommend treatment for such patients.

However, in a study presented at EASL, Tunisian researchers performed liver biospsies on 80 HBeAg-negative patients with normal ALTs and low viral load and found that 40% of the patients had fibrosis or liver damage that required treatment. Having noninvasive tests available to evaluate the liver health in these seemingly asymptomatic patients could better identify who needs treatment and save lives.

However, the tests may miss mild fibrosis: A Romanian study presented at EASL confirmed that the two tests were accurate in..."confirming or excluding significant fibrosis, but they are not very accurate in staging (identifying) low grades of fibrosis."

Reports Mixed as to Whether Entecavir Lowers Cancer Risk in Cirrhotic Patients?
Korean researchers treated 220 patients with entecavir, 68% with moderate and 32% with severe (decompensated) cirrhosis, and followed them for five years to see if the antiviral reduced liver cancer in these high-risk patients.

They found the cancer rate was 28.5%. Older age (over 50), male gender and presence of diabetes increased the odds of liver cancer in these patients.

Patients who achieved low and undetectable viral loads had lower rates of liver cancer, according to the report presented at EASL. Researchers concluded that while antiviral treatment did not completely eradicate liver cancer risk in cirrhotic patients, those who responded had lower rates.

But a different EASL study that followed entecavir patients for five years appears to contradict those findings. Italian researchers followed 418 patients, most were in their 50s, male, HBeAg-negative and had fibrosis or cirrhosis.

By year 5, all patients had achieved undetectable viral load and one-third even lost HBsAg, with 13 stopping treatment due to the success. They reported that 93% achieved normal ALTs which would indicate no liver damage.

Despite clearing the virus, the lengthy HBV infections took their toll—over the study period 17 cirrhotic patients and five non-cirrhotic patients developed liver cancer.

"Entecavir efficiently suppressed HBV in patients with chronic hepatitis B," researchers noted, but it did not prevent liver cancer.

A third EASL study from Singapore also reported similar findings when entecavir or a combination of lamivudine and adefovir (Hepsera) was used to treat cirrhotic patients. While treatment lowered viral load, it rarely prevented progression of liver damage in hepatitis B patients.

Alcoholism and Smoking Increase Liver Cancer Risk in Younger Patients
A Taiwanese study presented at EASL found that HBV-infected people who drink heavily develop liver cancer more rapidly and at a younger age than hepatitis B patients who do not drink, or uninfected alcoholics.

Researchers followed 966 people with cirrhosis in the study: 132 had HBV infection and alcoholism, 632 had only hepatitis B, and 202 were alcoholics free of infection. Those who drank and had hepatitis B developed cirrhosis on average four earlier than HBV-infected people who did not drink.

When researchers looked at who developed liver cancer over the decade-long study period, they found:

    28.8% of patients with HBV and alcoholism developed liver cancer.
    15.8% of patients with just HBV infection developed liver cancer.
    And 10.4% of uninfected alcoholics developed cancer.

The annual incidence of liver cancer was 9.9%, 4.1%, and 2.1% respectively in the three groups.

Researchers also found that among all HBV-infected patients, higher viral load also increased liver cancer risk. Also, people with HBV genotype C had higher cancer rates than those with genotype B.

Smoking also increases risk: Another Taiwanese study presented at EASL followed 7,893 HBV-infected men and women age 20 and older between 1988 and 2006 to see what factors increased the risk of liver cancer, especially among younger patients. They reported that male gender, elevated ALT levels (greater than 80 IU/L) and years of smoking, "predispose HBV carriers to an earlier age of onset of liver cancer."

Inactive Infection and Older Age Increase HBsAg Clearance, as Do Unknown "Host" Factors
What enables some people to lose HBsAg while others continue to be actively infected with HBV for decades? French researchers followed 315 patients over nearly six years—109 of whom had inactive infection. Who lost HBsAg? Older patients with inactive infections were more likely to clear HBsAg.

Surprising, neither gender, race, treatment, body mass index, alcohol consumption, nor HBV DNA and ALT levels had an impact on who lost HBsAg, according to their report to EASL.

Patients with inactive infection had an annual HBsAg clearance rate of 23.4 cases per 1,000 persons-years, while treated HBeAg-positive patients had clearance rates of 20.7 and untreated HBeAg-negative patients had clearance rates of 10.1.

"The results of this study in a 'real-life' population of HBV carriers show that older age and the inactive HBsAg carrier state are independent predictive factors of HBsAg loss," researchers noted. Treatment only slightly increased the rate of HBsAg clearance. Other "host" factors, such as genotype or a patient's genetics or quality of life, appear to have more impact over HBsAg clearance.

These unknown host factors also appear to play a role in protecting HBV-infected Canadian Inuits from liver damage. Another EASL study found this population had low rates of liver damage over a 23-year-study period, despite their moderate viral loads.

The cause for the relatively benign infection among this community could be the HBV strain or genotype found in the Inuit (genotype B, subtype B6) or other host factors that have not yet been identified, researchers noted.

Dairy-Rich Diets Linked to Increase in Liver Cancer
Diets rich in milk and cheese are known to increase cancer rates in general, so a European team decided to see if a dairy-rich diet increased liver cancer risk in patients with viral hepatitis and found that it does.

While dairy foods are rich in calcium and vitamin D, "their increased consumption may also lead to higher circulating levels of IGF-1, a growth factor possibly related to increased risk of liver cancer," researchers reported to the EASL.

They followed 477,206 Europeans over 11 years and found higher liver cancer rates in those with higher dairy intake in both uninfected and HBV-infected individuals. "Higher circulating IGF-I level due to more dairy food intake may be a possible biologic explanation for these observations, but requires further study," they noted.


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发表于 2013-5-3 20:42 |只看该作者
用于艾滋病毒的抗病毒组合出现在“免疫耐受”的患者有效
一名新西兰的研究人员尝试了一种用于治疗艾滋病的抗病毒药物组合,并发现它暂时降低病毒载量高,在乙肝的“e”抗原(HBeAg)阳性的患者非常有效的。然而,药物是有效的,只有当患者服用替诺福韦和恩曲他滨(Truvada的)组合。

目前医学界指引不建议治疗这些“免疫耐受”的患者,其免疫系统出现容忍高水平的乙肝病毒(HBV),没有攻击感染的肝细胞。最终,这些患者的免疫系统攻击乙肝病毒感染,但只有经过多年的高危险病毒载量。

经过四年的替诺福韦,恩曲他滨药物组合治疗62例,76%达到近病毒载量检测不到的耐药性没有任何征兆。类似的免疫耐受治疗对照组只用替诺福韦(Viread的),只有55%的病毒载量检测不到四年后,根据晚在阿姆斯特丹举行的欧洲肝脏研究协会(EASL)会议提交的报告四月。

然而,只有五个患者在研究中HBeAg消失,只有三五个开发的“e”的抗体,这通常会导致在一个永久的病毒载量下降。没有患者失去了乙肝表面抗原(HBsAg),或开发表面抗体清除感染的标志。

一半的患者停止治疗后,该研究的结论,它们都经历过他们的病毒载量反弹存在治疗开始前同样的高层次。

虽然它出现一个将需要无限期疗程,这种“免疫耐受”的人群中抑制病毒载量,研究人员建议,医生可以选择性使用药物与肝硬化或肝癌家族史的患者。

尽管通用保健护理,B型肝炎是不一致的加拿大
尽管其普及医疗赞誉,乙肝患者在加拿大面对不一致的照顾跨省,甚至是B型肝炎疫苗接种的做法有很大的不同在全国范围内,根据到2013年3月的报告题为肝病加拿大:危机中制作加拿大肝脏基金会。

令人惊讶的是,提供医疗保健的所有居民,无论他们的支付能力的国家有不同的乙肝治疗指南和药品报销率能省就省。根据该报告:

不一致的处理:每个省都有自己的报销政策和标准,当乙肝治疗是必需的,应使用药物。例如,几个的省份允许使用的抗病毒药物恩替卡韦(博路定)仅当已经开发出乙型肝炎患者肝硬化。恩tecavir是两种抗病毒药物,目前推荐用于所有一线乙肝治疗的美国和欧洲的指引之一。

“只有在魁北克省的报销政策,符合临床实践指南”,该报告的作者写道。 “令人吃惊的是有没有访问乙肝治疗方面的省份之间的一致性,”该报告指出。

不一致的治疗指引也意味着需要治疗的人,很多人不能及时得到治疗,仅仅是因为他们住全省英寸延缓乙肝治疗导致肝硬化,肝癌,死亡。

过时的治疗准则:某些准则也允许治疗,只有当谷丙转氨酶(ALT)水平升高,这往往表明肝功能损害发生。评估过时的众多研究表明,可能是严重的肝功能损害,由于长期感染,即使目前的ALT水平正常。

该报告透露,2009年,58%的乙肝患者免费,公共医疗覆盖收到抗病毒药拉米夫定(拉米HBV)的。这种过时的抗病毒药物具有极高的耐药率,不再推荐使用作为第一线治疗。

同时,报告显示,90%的富裕加拿大人谁也涵盖了私人医疗保险政策进行治疗更加现代化和有效的抗病毒药物拉米夫定以外。这表明,即使在加拿大,人们有机会与高收入和私人保险以卓越的乙肝治疗。

记录保存无效:加拿大不区分B型肝炎C型肝炎在其死亡记录,因此跟踪感染的真实影响,不能记录。此外,肝硬化和肝癌的死亡疾病虽然产生B型肝炎或C型分别归类。

只有一个省份 - 安大略轨道乙肝死亡。从这些数据推断,该报告估计,14000人每年死于B型肝炎在加拿大,这一数字预计将上升由于通过增加B型肝炎病例来自亚洲和非洲的移民。

各省之间不一致的免疫政策:免疫接种时间表也各不相同。虽然不列颠哥伦比亚省,新不伦瑞克省和爱德华王子岛省的指引建议接种乙肝疫苗在婴儿期,其余省份都需要接种疫苗后在童年,在青春期。

因此,新的乙肝病例实际上是增加免疫接种,因为从小在加拿大期间没有发生,直到青春期。

家访促进B型肝炎筛检族群的关键
教育亚裔美国人对B型肝炎的高风险,让他们筛选,处理和接种疫苗,可以是一个文化和医疗的挑战。许多移民和他们的子女不会讲英语,许多卫生保健提供者仍然不遵循医疗指引和屏幕的亚裔美国人B型肝炎患者在其诊所或提供翻译服务。

一个独特的宣传方案,由非专业医护工作者在苗族社区在萨克拉门托进行,被证明是非常有效的,从老挝和越南的山区移民筛选乙型肝炎

根据该报告,大学加州大学戴维斯分校卫生系统的研究人员撰写并发表在2013年4月23日发行的杂志癌症流行病学,生物标记与预防,苗族有B型肝炎和肝脏的癌症发病率,高利率的六个七倍,在美国的白色或西班牙裔人口。

由于苗族关于乙肝知之甚少,很少与当地的卫生保健提供者,由于语言和文化障碍,HBV感染与肝癌可以提前首诊时,患者往往活不到一年后癌症诊断。

在这项研究中,打好医疗保健工作者,其中许多人是苗族和知识渊博的文化和语言走访了260苗族居民在萨克拉门托。居民被随机分配到两个组,分别接受两个家访。访问期间居民接受B型肝炎和肝癌的教育或营养和体能的信息。

6个月后,24%的组了解乙肝已在医生的诊所筛查,了解营养和运动组相比,只有10%。

通过使用苗族奠定教育从两个受人尊敬的苗族文化组织招募,加州大学戴维斯分校的研究人员克服文化障碍,以B型肝炎筛检。

学员们给出了一本小册子在苗族和英语,他们可能使用要求在他们的下一个诊所参观,翻译服务,往往没有B型肝炎筛检。

然而,很多这方面的努力将不会是必要的,如果医生按照现行做法的建议,检查所有亚裔美国人B型肝炎,研究人员指出。

Fibroscan的成像加血测试可以取代肝活检
研究人员一直在试图开发新的方法来评估患者的肝功能损害,使用验血或声像图,以避免执行侵入性和昂贵的肝活检。一项研究,发表在2013年4月发行的杂志上消化道药理学与治疗,发现两个非侵入性的测试来代替肝活检精确测量在五年期间肝功能损害。

研究人员使用了Fibroscan的评估肝脏硬度的程度(也被称为纤维化或疤痕)。肝纤维化扫描使用超音波检查来测量速度的声波通过肝脏识别轻度(纤维化),严重的肝脏结疤他们还使用验血(cirrhosis.)称为FibroTest的测量六个要素的程度来决定血液试样中的肝脏疾病。

研究人员使用这两个600 B型肝炎患者的诊断工具,跟着他们了将近五年。大多数的患者为男性,平均年龄42.5。大多数有正常或ALT中度升高水平。

医生发现,有94(15.7%)肝损伤和肝活检的214例患者进行非侵入性测试测试的准确性。

研究人员报告说,Fibroscan的FibroTest的一起是非常有效的评估肝脏的健康,并表示治疗时需要。在某些情况下,他们的报告,这两个组合的测试比肝活检更准确。

“这个信息是非常重要的,帮助我们提高我们的各种工具,为我们的患者的后续,”他们写道。一起使用的两个测试...“可以取代肝穿刺活检的评价的疾病,任何疾病的阶段。”

“无效”肝病患者有用:如果证明是准确的,这两种诊断工具可能被证明为HBeAg阴性,ALT水平正常,并有低病毒载量(HBV-DNA)在20,000 IU / mL的患者至关重要。目前医学界指引不建议对此类患者的治疗。

然而,突尼斯在EASL在一项研究中,研究人员进行肝biospsies对80例HBeAg阴性患者正常的低价竞标和低病毒载量,并发现,40%的患者有肝纤维化或肝功能损害,需要治疗。具有非侵入性测试,评估在这些看似无症状患者的肝脏健康,可以更好地确定谁需要治疗和拯救生命。

然而,测试可能会错过轻度纤维化:在EASL一名罗马尼亚的研究证实,这两个测试是准确的...“确认或排除明显的纤维化,但他们都不是很准确的分期(识别)低等级的纤维化。”

报告不一,无论是恩替卡韦在肝硬化患者,降低癌症风险?
韩国研究人员与恩替卡韦治疗的220例患者中,32%有严重肝硬化(失代偿期),68%,跟随了他们五年来看看,如果这些高危患者抗病毒药物的减少肝癌。

他们发现,癌症发病率是28.5%。在这些患者中,年龄较大(超过50),男性,有糖尿病的几率增加肝癌。

实现低,检测不到病毒负荷的患者肝癌率较低,根据在EASL提交的报告。研究人员得出结论,而抗病毒治疗不彻底根除肝癌的危险在肝硬化患者中,那些回应率较低。

但不同的欧洲肝脏研究学会(EASL)的研究显示恩替卡韦治疗的患者五年之后这些矛盾的结果。意大利研究人员跟踪调查了418例患者中,大多数是在50岁,男,HBeAg阴性,肝纤维化或肝硬化。

5年,所有患者已达到病毒载量检测不到三分之一甚至失去了乙肝表面抗原,13停止治疗,由于成功。他们报告说,93%取得了正常的低价竞标,这将表明无肝损害。

尽管清除病毒,冗长的HBV感染了他们的收费在研究期间,17例肝硬化患者和5个非肝硬化患者的肝癌。

“恩替卡韦能有效抑制HBV慢性乙型肝炎患者,”研究人员指出,但它并没有预防肝癌。

来自新加坡的第三个欧洲肝脏研究学会(EASL)的研究也报告了类似的结果,当恩替卡韦或拉米夫定和阿德福韦(阿德福韦酯)的组合被用来治疗肝硬化患者。虽然治疗降低病毒载量,它很少防止乙型肝炎患者的肝功能损害的进展。

在年轻患者的酗酒和吸烟增加肝癌风险
在EASL一位台湾研究发现,感染乙肝病毒的人谁喝大量更迅速地发展为肝癌,乙肝患者比不喝酒的人,或未受感染的酗酒有年轻化。

研究人员随访了966人在研究肝硬化:132有HBV感染者和酗酒,632只B型肝炎,和202是酗酒者无感染。开发那些谁喝得了乙肝肝硬化,平均四早于HBV感染的人,谁没喝过。

当研究人员观察了在长达十年的研究开发肝癌,他们发现:

    28.8%的乙肝患者和酗酒肝癌。
    只是乙肝病毒感染患者的15.8%,开发肝癌。
    和10.4%,未受感染的酗酒患上癌症。

肝癌的年发病率分别为9.9%,4.1%和2.1%,分别在三组。

研究人员还发现,在所有感染乙肝病毒的患者中,较高的病毒载量也增加肝癌的风险。此外,与HBV C基因型的人有较高的癌症发病率比B基因型

吸烟也增加了风险:另一位台商在EASL研究随访了7,893 HBV感染的男性和20岁以上的女性在1988年和2006年之间,看看有哪些因素增加肝癌的风险,尤其是年轻患者。他们的报告,男性,ALT水平升高(大于80 IU / L)和吸烟年,“乙肝病毒携带者易患肝癌的发病年龄较早。”

暂无感染和年龄增加HBsAg清除,未知因素“主机”
是什么让一些人失去乙肝表面抗原,而其他人继续积极与HBV感染了几十年吗?法国研究人员随访了315例患者近六年超过109人感染无效。谁失去了乙肝表面抗原?无效感染的老年患者,更容易清除HBsAg的。

令人惊讶的,无论性别,种族,治疗,身体质量指数,饮酒,也不HBV DNA和ALT水平,谁失去了乙肝表面抗原的影响,根据EASL他们的报告。

每年HBsAg清除率每1000人年为23.4例,无效感染患者治疗HBeAg阳性患者有20.7清除率和治疗HBeAg阴性患者的清除率10.1。

“人口的乙肝病毒携带者在”现实生活“这项研究结果显示,年龄和非活动性HBsAg携带状态是独立的预测因素,HBsAg消失,”研究人员指出。治疗HBsAg清除率只轻微上升。其他的“主机”的因素,如基因型或病人的遗传学或生活质量,似乎有更多的影响超过HBsAg清除。

这些未知的宿主因素似乎也发挥了作用,在保护HBV感染的肝损害加拿大因纽特人。另一个欧洲肝脏研究学会(EASL)的研究发现,这个人口有超过23年的研究期间,尽管其温和的病毒载量低利率肝损害。

这个社会之间相对良性的感染原因可能是乙肝病毒株或基因型发现因纽特人(B基因型,亚型B6)或其他主机尚未确定的因素,研究人员指出。

乳制品相关的丰富的饮食,以增加肝癌
饵料丰富牛奶和奶酪是已知会增加癌症发病率一般,所以一支欧洲球队如果富含乳制品的饮食中增加肝癌风险病毒性肝炎患者,发现它确实决定去看看。

虽然奶制品含有丰富的钙和维生素D,“他们的消费增加也可能导致更高的循环中IGF-1的水平可能与肝癌的风险增加,生长因子,研究人员报告EASL。

他们跟着477,206欧洲人超过11年,发现在那些具有较高的乳制品摄入量在未受感染和HBV感染的个人癌症发病率较高的肝。 “循环IGF-I的水平,由于更多的乳制品的食物摄入量较高可能是这些观察可能的生物学解释,但还需要进一步研究,”他们指出。

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发表于 2013-5-5 10:46 |只看该作者
如果不能阻止肝癌的发生,一切治疗又有神马意义呢,

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发表于 2013-5-5 10:49 |只看该作者
居然吃乳制品也会增加患肝癌的几率,真是没法活啦。

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发表于 2013-5-5 13:47 |只看该作者
哇,好清净的论坛,居然一个上午都没有一个人逛逛本版。

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发表于 2013-5-5 14:47 |只看该作者
乳制品会增加患肝癌的几率,以后不吃了。
抗病毒最好的方法,叶下珠+猪苓,联系服用一个月就有效果。可以从10三次方降到10二次方。

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才高八斗

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发表于 2013-5-5 18:08 |只看该作者
nationart 发表于 2013-5-5 14:47
乳制品会增加患肝癌的几率,以后不吃了。

关键字是"增加"进食乳制品.

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发表于 2013-5-5 22:04 |只看该作者
无论怎样,抗病毒总有好处的

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发表于 2013-5-14 12:23 |只看该作者
乳制品与肝癌不是这样研究的
也许吃乳制品会减少肝癌发生率,但乳制品超量的人可能脂肪肝导致肝癌。
欢迎收看肝胆卫士大型生活服务类节目《乙肝勿扰》,我们的目标是:普度众友,收获幸福。
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