3.2 Temporal trends in AF/AFL burden from 1990 to 2021.
3.2 1990—2021 年 AF/AFL 负担时间趋势 。
3.2.1 Incidence trends
3.2.1 发病趋势
Joinpoint regression identified two distinct epochs in China: (i) 2000-2005 (APC 1.60 %) and (ii) 2015-2021 (APC 1.21 %), both statistically significant (p < 0.05) (Fig. 1A). A transient downturn (2005-2010) coincided with nationwide antihypertensive campaigns; however, the long-term slope remains upward, mirroring Southeast Asia and contrasting with Europe’s steady decline (Fig. 1B and 1C). After 2019, the COVID-19 pandemic coincided with an abrupt spike in ASIR in China, Europe and globally - plausibly through delayed diagnoses, inflammatory milieu and healthcare disruptions—whereas Southeast Asia recorded no inflection.
Joinpoint 回归确定了中国的两个不同时期:(i)2000-2005 年 (APC 1.60%)和(ii)2015-2021 年(APC 1.21%),均具有统计学意义(p < 0.05)( 图。 1A) 的。短暂的低迷(2005-2010 年 )恰逢全国范围内的抗高血压运动;然而,长期斜率仍然向上,反映了东南亚,与欧洲的稳步下降形成鲜明对比 ( 图 1)。 1B 和 1C)。2019 年之后,COVID-19 大流行恰逢中国、欧洲和全球 ASIR 的突然飙升 —— 可能是由于诊断延迟、炎症环境和医疗保健中断——而东南亚则没有出现拐点。
3.2.2 Prevalence trends
3.2.2 流行趋势
China’s ASPR exhibited sustained growth punctuated by a brief 2005-2010 dip (APC -0.3 %) (Fig. 1E). The most recent segment (2015-2021, APC 1.30 %) aligns with intensified secondary prevention (oral anticoagulation uptake > 40 % among high-risk patients) but is insufficient to offset demographic expansion. Parallel trajectories in Southeast Asia diverge after 2019 (Fig. 1F), when prevalence accelerated further, while Europe plateaued (Fig. 1G).
中国的 ASPR 表现出持续增长,但 2005-2010 年出现短暂下降(APC -0.3%)( 图。 1E) 的。最近的部分(2015-2021 年,APC 1.30 %)与强化二级预防(高危患者口服抗凝摄取率 > 40%)一致,但不足以抵消人口扩张。2019 年后东南亚的平行轨迹出现分歧 ( 图。 1F), 当患病率进一步加速时,而欧洲趋于稳定 ( 图。 1G) 的。
3.2.3 Mortality trends
3.2.3 死亡率趋势
China’s ASMR declined in two windows (2004-2007 APC -3.78 %; 2010-2013 APC -4.12 %), interrupted by a modest rebound (2007-2010 APC 0.67 %) (Fig. 2A). The net downward drift reflects cumulative gains in acute stroke care, anticoagulation and integrated AF management. Conversely, Southeast Asia, Europe and the globe experienced rising ASMR until 2019; thereafter Europe and the globe recorded sharp COVID-era declines, whereas China’s trajectory remained comparatively stable.
中国的 ASMR 在两个窗口内下降(2004-2007 年 APC -3.78%;2010-2013 年 APC -4.12%),随后被温和反弹(2007-2010 年 APC 0.67%) 所打断 ( 图。 2A)。 净下降趋势反映了急性中风护理、抗凝和综合房颤管理的累积收益。相反,东南亚、欧洲和全球的 ASMR 在 2019 年之前都在上升;此后,欧洲和全球在新冠疫情期间出现了急剧下降,而中国的发展轨迹则保持相对稳定。
3.2.4 DALY trends
3.2.4 DALY 趋势
China’s ASDR fell between 2004 and 2015, yet an upswing since 2016 (APC 1.56 %) suggests that quality-of-life improvements are eroding under the weight of aging, multimorbidity and healthcare inequality (Fig. 2E). Europe achieved sustained post-2004 reductions that steepened during the pandemic (Fig. 2G), whereas Southeast Asia’s ASDR rose monotonically (Fig. 2F).
中国的 ASDR 在 2004 年至 2015 年期间有所下降,但自 2016 年以来的上升(APC 1.56%)表明,在老龄化、多种疾病和医疗保健不平等的重压下,生活质量的改善正在受到侵蚀(图 2E)。欧洲在 2004 年后实现了持续的下降,并在大流行期间急剧下降(图 2G),而东南亚的 ASDR 则单调上升(图 2F)。
Figure 1. The Annual Percentage Change (APC) of ASIR and ASPR in China, South-East Asia Region, European Region and Global in 1990 and 2021 (*P < 0.05 and significant results).
图 1. 1990 年和 2021 年中国、东南亚地区、欧洲地区和全球 ASIR 和 ASPR 的年百分比变化(APC)(*P < 0.05,结果有统计学意义)。
(A) The APC of ASIR in China; (B)The APC of ASIR in South-East Asia Region; (C) The APC of ASIR in European Region; (D) The APC of ASIR in Global; (E) The APC of ASPR in China; (F) The APC of ASPR in South-East Asia Region; (G) The APC of ASPR in European Region; (H) The APC of ASPR in Global
(A) ASIR 在中国的 APC;(二)东南亚地区 ASIR 的 APC;(c) ASIR 在欧洲区域的 APC;(D) 全球 ASIR 的 APC;(E) 中国 ASPR 的 APC;(f) 东南亚区域 ASPR 的 APC;(g) 欧洲区域 ASPR 的 APC;(H) 全球 ASPR 的 APC
Fig
无花果ure
尿 2. The
这Annual Percentage Change (APC)
年百分比变化 (APC) of ASMR and ASDR in China, South-East Asia Region, European Region and Global in 1990 and 2021. (*
1990 年和 2021 年在中国、东南亚地区、欧洲地区和全球的 ASMR 和 ASDR。(*P < 0.05 and significant results).
< 0.05 和显着的结果)。(A) The APC of ASMR in China; (B)The APC of ASMR in South-East Asia Region; (C) The APC of ASMR in European Region; (D) The APC of ASMR in Global; (E) The APC of ASDR in China; (F) The APC of ASDR in South-East Asia Region; (G) The APC of ASDR in European Region; (H) The APC of ASDR in Global
(A)中国 ASMR 的 APC;(二)东南亚地区 ASMR 的 APC;(c) 欧洲区域 ASMR 的 APC;(D) 全球 ASMR 的 APC;(E) 中国 ASDR 的 APC;(f) 东南亚区域 ASDR 的 APC;(g) ASDR 在欧洲区域的 APC;(H) 全球 ASDR 的 APC.
3.3 Age-specific burden profiles in AF/AFL.
3.3 AF/AFL 中特定年龄的负担概况 。
3.3.1 Incidence by age
3.3.1 按年龄划分的发病率
Across all regions, crude incidence peaks at 65-74 years. In China, however, the modal age shifted downwards from 70-74 in 1990 to 65-69 in 2021, hinting at earlier onset driven by cardiometabolic risk accumulation (Fig.3A). By contrast, Southeast Asia, Europe and the global average recorded upward shifts to 70-74 years. Notably, China is the only region where incidence in (40-49)-year-olds declined continuously after 1990, a testament to primary prevention successes among working-age adults.
在所有地区,粗发病率在 65-74 岁达到峰值 。然而,在中国,模式年龄从 1990 年的 70-74 岁向下移动到 2021 年的 65-69 岁,暗示心脏代谢风险积累导致发病提前 ( 图 1990 年)。3A) 的。相比之下,东南亚、欧洲和全球平均水平则向上移动至 70-74 岁。值得注意的是,中国是唯一一个在 1990 年后 (40-49) 岁人群发病率持续下降的地区,这证明了工作年龄成年人的一级预防取得了成功。
3.3.2 Prevalence by age
3.3.2 按年龄划分的患病率
Prevalence distributions mirror incidence: China’s peak moved from 70-74 to 65-69, and the 40-49 bracket declined (Fig. 3E). Southeast Asia exhibited the only net increase in age-standardized prevalence across all age groups, reflecting both longer survival and rising incidence (Fig. 3F). Europe’s standardized peak occurred at 75-79, slightly older than the crude peak - indicating selective survival and diagnostic intensity among the oldest old (Fig. 3G).
患病率分布反映了发病率:中国的峰值从 70-74 岁移动到 65-69 岁 ,40-49 岁范围下降 ( 图。3E) 的。东南亚在所有年龄组中表现出年龄标准化患病率的唯一净增长,反映了生存期的延长和发病率的上升 ( 图。3F) 的。欧洲的标准化峰值出现在 75-79 岁, 略早于粗峰值 —— 表明最年长老年人的选择性生存和诊断强度 ( 图。3G)。
3.3.3 Mortality by age
3.3.3 按年龄划分的死亡率
Deaths concentrate at 80-94 years. In China the mortality peak migrated from 80-84 to 85-89, while crude rates above age 74 fell below 1990 levels - consistent with therapeutic progress (Fig. 4A). Southeast Asia displayed the opposite pattern: post-2019 mortality exceeded 1990 levels above age 70, underscoring lagging stroke prevention (Fig. 4B).
死亡集中在 80-94 岁。在中国,死亡率峰值从 80-84 岁迁移到 85-89 岁 ,而 74 岁以上的粗死亡率低于 1990 年的水平 —— 与治疗进展一致 ( 图 1990 4A)。 东南亚则表现出相反的模式:2019 年后 70 岁以上的死亡率超过 1990 年的水平,凸显了中风预防滞后 ( 图 1990)。4B) 的。
3.3.4 DALYs by age
3.3.4 按年龄划分的 DALY
DALYs peak at 80-84 years across regions. China’s burden shifted from 70-79 to 80-84, with post-2019 levels below 1990 - again suggesting successful compression of morbidity (Fig. 4E). Southeast Asia recorded DALY rates above 1990 levels beyond age 70, echoing its mortality findings (Fig. 4F).
各地区的 DALY 在 80-84 岁达到峰值 。中国的负担从 70-79 岁转变为 80-84 岁 ,2019 年后的水平低于 1990 年 , 这再次表明发病率的压缩成功 ( 图。4E) 的。东南亚记录的 DALY 率高于 1990 年 70 岁以上的水平,与其死亡率调查结果相呼应 ( 图 1990)。 4F) 的。
Figure 3. Comparative of the incidence, prevalence, deaths, and DALYs counts, along with their crude rates, by age group from 1990 to 2021.
图 3.比较 1990 年至 2021 年按年龄组划分的发病率、患病率、死亡率和 DALY 计数及其粗率 。
(A) Incident cases and CIR in China; (B) Incident cases and CIR in South-East Asia Region; (C) Incident cases and CIR in European Region; (D) Incident cases and CIR in Global; (E) Prevalent cases and CPR in China; (F) Prevalent cases and CPR in South-East Asia Region; (G)Prevalent cases and CPR in European Region; (H) Prevalent cases and CPR and CIR in Global.
(A) 中国的事件案例和 CIR;(b) 东南亚区域的事件个案和 CIR;(C) 欧洲区域的事件病例和 CIR;(D) 全球事件案例和 CIR;(E)中国流行病例和心肺复苏术;(f) 东南亚区域的流行病例和心肺复苏术;(庚)欧洲地区的流行病例和心肺复苏术;(H) 全球流行病例以及心肺复苏术和 CIR。
Figure 4. Comparative of the incidence, prevalence, deaths, and DALYs counts, along with their crude rates, by age group from 1990 to 2021
图 4.1990 年至 2021 年按年龄组划分的发病率、患病率、死亡人数和 DALYs 计数及其粗率的比较.
(A) Death cases and CMR in China; (B)Death cases and CMR in South-East Asia Region; (C) Death cases and CMR in European Region; (D) Death cases and CMR in Global; (E) DALYs counts and CDR in China; (F) DALYs counts and CDR in South-East Asia Region; (G) DALYs counts and CDR in European Region; (H) DALYs counts and CDR in Global
(A) 中国的死亡病例和 CMR;(二)东南亚区域死亡病例和 CMR;(C) 欧洲区域的死亡病例和 CMR;(D) 全球死亡病例和 CMR;(E) 中国的 DALY 计数和 CDR;(F) 东南亚区域的 DALYs 计数和 CDR;(G) 欧洲区域的 DALY 计数和 CDR;(H) 全球的 DALY 计数和 CDR.
3.4 Sex disparities in AF/AFL burden.
3.4 AF/AFL 负担的性别差异 。
3.4.1 Incidence
3.4.1 发生率
In 1990, Chinese men peaked at 65-69 years, women at 70-74 (Fig. 5A). By 2021 the sex-specific modal ages remained unchanged, yet after age 80 female incidence eclipsed male incidence - a pattern replicated in Southeast Asia, Europe and globally. This feminisation of late-life AF/AFL reflects women’s greater longevity and possibly differential autonomic, hormonal or atrial substrate effects.
1990 年,中国男性在 65-69 岁达到峰值 ,女性在 70-74 岁达到峰值 ( 图。 5A)。 到 2021 年,特定性别的模式年龄保持不变,但在 80 岁之后,女性发病率超过了男性发病率 —— 这种模式在东南亚、欧洲和全球范围内都得到了复制。晚年 AF/AFL 的这种女性化反映了女性更长的寿命以及可能不同的自主神经、激素或心房基质效应。
4.2 Prevalence
4.2 患病率
Prevalence sex ratios follow incidence patterns. Globally, however, women exhibit a broader plateau (70-84 years) in 2021 (Fig. 5P), implying longer duration of disease and delayed mortality. China’s sex gap is less pronounced than Europe’s, where female prevalence beyond age 80 surpasses male prevalence by 30-40 %.
患病率性别比遵循发病率模式。然而,在全球范围内,女性在 2021 年表现出更广泛的平台期(70-84 岁)( 图 1 5P), 意味着病程更长,死亡率更晚。中国的性别差距不如欧洲明显,欧洲 80 岁以上的女性患病率比男性高出 30-40%。
4.3 Mortality
4.3 死亡率
Chinese female deaths exceeded male deaths beyond age 70 in both 1990 and 2021 (Fig. 6A, 6E); the divergence becomes extreme above age 85. Southeast Asia displayed a smaller sex gradient, suggesting either competing causes of death or under-diagnosis in women.
1990 年和 2021 年,中国女性死亡人数均超过 70 岁以上男性死亡人数( 图 6A、6E);85 岁以上差异极大。东南亚的性别梯度较小,这表明女性的死亡原因要么相互竞争,要么诊断不足。
4.4 DALYs
4.4 每日
DALY sex ratios mirror mortality, but the female excess is attenuated in China and globally, implying that women’s longer survival is partly offset by lower disability weights or better functional status. Europe again showed the starkest female excess (Fig. 6K, 6O).
DALY 性别比反映了死亡率,但女性的过剩在中国和全球都有所减弱,这意味着女性的生存时间更长被较低的残疾体重或更好的功能状态部分抵消。欧洲再次显示出最明显的女性过剩 ( 图。6K,6 O)。
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Fig. 5. Comparison of of the number incidence and prevalence of AF/AFL in males and females of different age groups in China, South-East Asia Region, European Region and Global in 1990 and 2021. (A) 1990 number of incidence in China; (B) 1990 number of incidence in South-East Asia Region; (C) 1990 number of incidence in European Region; (D) 1990 number of incidence in Global; (E) 2021 number of incidence in China; (F) 2021number of incidence in South-East Asia Region; (G) 2021 number of incidence in European Region; (H) 2021 number of incidence in Global; (I) 1990 number of prevalence in China; (J) 1990 number of prevalence in South-East Asia Region; (K) 1990 number of prevalence in European Region; (L) 1990 number of prevalence in Global; (M) 2021 number of prevalence in China; (N) 2021 number of prevalence in South-East Asia Region; (O) 2021 number of prevalence in European Region; (P) 2021 number of prevalence in Global
图 5 1990 年和 2021 年中国、东南亚地区、欧洲地区和全球不同年龄组男女房颤/房颤发病率的发病率和患病率对比。(A)1990 年中国发病率;(B) 1990 年东南亚区域发病率;(C) 1990 年欧洲区域发病率;(D) 1990 年全球发病率;(E)2021 年中国发病数;(F)2021 年东南亚地区发病数;(G)2021 年欧洲地区发病率;(H) 2021 年全球发病率;(一)1990 年中国患病率;(J) 1990 年东南亚区域的患病率;(K) 1990 年欧洲区域的患病率;(L) 1990 年全球流行率;(M)2021 年中国患病率;(N)东南亚地区 2021 年患病率;(O)2021 年欧洲地区患病率;(P) 2021 年全球患病率.
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Figure 6. Comparison of of the number mortality and DALYs of AF/AFL in males and females of different age groups in China, South-East Asia Region, European Region and Global in 1990 and 2021. (A) 1990 number of mortality in China; (B) 1990 number of mortality in South-East Asia Region; (C) 1990 number of mortality in European Region; (D) 1990 number of mortality in Global; (E) 2021 number of mortality in China; (F) 2021number of mortality in South-East Asia Region; (G) 2021 number of mortality in European Region; (H) 2021 number of mortality in Global; (I) 1990 number of DALYs in China; (J) 1990 number of DALYs in South-East Asia Region; (K) 1990 number of DALYs in European Region; (L) 1990 number of DALYs in Global; (M) 2021 number of DALYs in China; (N) 2021 number of DALYs in South-East Asia Region; (O) 2021 number of DALYs in European Region; (P) 2021 number of prevalence in Global
研究 6 1990 年和 2021 年中国、东南亚地区、欧洲地区和全球不同年龄组男女房颤/肺病死亡率及 DALYs 比较 。(A) 1990 年中国死亡人数; (B) 1990 年东南亚区域死亡人数;(C) 1990 年欧洲区域的死亡率;(D) 1990 年全球死亡率 ; (E)2021 年中国死亡人数; (F) 2021 年东南亚区域死亡人数;(G) 2021 年欧洲区域死亡人数;(H) 2021 年全球死亡率 ; ( 一 )1990 年中国 DALY 数量; (J) 1990 年东南亚区域的 DALY 数量 ;(K) 1990 年欧洲区域的 DALY 数量 ;(L) 1990 年全球 DALY 数量 ; (M)2021 年中国 DALY 数量; (N) 2021 年东南亚地区 DALY 数量;(O) 2021 年欧洲地区 DALY 数量 ;(P) 2021 年全球 p 流行率 .
3.5 Age-period-cohort (APC) modelling in AF/AFL burden.
3.5 AF/AFL 负担中的年龄-期-队列 (APC) 建模 。
3.5.1 China
3.5.1 中国
Age deviation curves for incidence and prevalence displayed a U-shaped reversal: risk rises from age 30, peaks at 50-55, then declines until age 85, hinting at a mid-life “vulnerable window” related to hypertension and obesity amplification. Mortality and DALY deviations became increasingly negative after age 70, consistent with effective geriatric care (Fig. 7A). Period effects (2005 baseline) revealed an early-2000s rise followed by a post-2015 rebound (Fig. 7C), while cohort effects (1940 baseline) showed initial risk declines for generations born after 1960, then renewed increases - likely reflecting obesogenic environments (Fig. 7D).
发病率和患病率的年龄偏差曲线呈现 U 形反转:风险从 30 岁开始上升,在 50-55 岁达到峰值 ,然后下降到 85 岁,暗示与高血压和肥胖放大相关的中年“脆弱窗口”。70 岁后死亡率和 DALY 偏差变得越来越负,这与有效的老年护理一致 ( 图 7A)。 周期效应(2005 年基线)显示 2000 年代初上升,随后在 2015 年后反弹 ( 图 7C), 而队列效应(1940 年基线)显示 1960 年之后出生的几代人的风险最初下降,然后重新增加 - 可能反映了致肥胖环境 ( 图 1940)。 7D)。
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Figure 7. Age-period-cohort analysis of China AF/AFL burden from 1992 to 2021.
图 7.1992—2021 年中国 AF/AFL 负担年龄段队列分析。
(A) Age Deviation (B) Longitudinal Age Curves; (C) Period Rate Ratio (D) Cohort Rate Ratio
(a)年龄偏差(b)纵向年龄曲线;(C) 周期率比 (D) 队列率比
3.5.2 Southeast Asia
3.5.2 东南亚
Age deviation peaks were delayed (incidence 65-70, prevalence 55-60) (Fig. 8A). Period effects rose monotonically, diverging from China’s mid-2000s inflection (Fig. 8C). Cohort effects exhibited a sharp drop for the 1970 birth cohort, possibly linked to economic transition and changing dietary patterns (Fig. 8D).
年龄偏差峰值延迟(发病率 65-70,患病率 55-60)( 图。8A)。 周期效应单调上升,与中国 2000 年代中期的拐点不同 ( 图。8C)。1970 年出生队列的队列效应急剧下降,可能与经济转型和饮食模式的变化有关 ( 图 1970 年出生队列 8D) 的。
Figure 8. Age-period-cohort analysis of South-East Asia Region AF/AFL burden from 1992 to 2021.
图 8.1992—2021 年东南亚地区 AF/AFL 负担的年龄-期-队列分析。
(A) Age Deviation (B) Longitudinal Age Curves; (C) Period Rate Ratio (D) Cohort Rate Ratio
(a)年龄偏差(b)纵向年龄曲线;(C) 周期率比 (D) 队列率比
3.5.3 Europe
3.5.3 欧洲
Age deviation patterns resembled China, but incidence peaked at 65-70 and prevalence exhibited a secondary crest at 80-84, illustrating differential survival (Fig. 9A). Period effects turned downward after 2005 for all indicators except mortality (p > 0.05) (Fig. 9C), while cohort effects showed early-century risk declines - consistent with aggressive primary prevention (Fig. 9D).
年龄偏差模式与中国相似,但发病率在 65-70 岁时达到峰值,患病率在 80-84 岁时表现出次级波峰,说明生存率差异(图 9A)。2005 年后,除死亡率外的所有指标的时期效应均呈下降趋势(p > 0.05)(图 9C),而队列效应则显示出本世纪初的风险下降——与积极的一级预防一致(图 9D)。
Figure 9. Age-period-cohort analysis of European Region AF/AFL burden from 1992 to 2021.
图 9.1992 年至 2021 年欧洲地区 AF/AFL 负担的年龄期队列分析。
(A) Age Deviation (B) Longitudinal Age Curves; (C) Period Rate Ratio (D) Cohort Rate Ratio
(a)年龄偏差(b)纵向年龄曲线;(C) 周期率比 (D) 队列率比.
3.5.4 Global
3.5.4 全球
Global age deviations followed the European template (Fig. 10A). Period effects dipped after 2005 but rebounded post-2015 (Fig. 10C). signalling uneven diffusion of interventions. Cohort effects traced a 1960-born dip followed by a late-century rise, mirroring globalisation of cardiometabolic risk (Fig. 10D).
全球年龄偏差遵循欧洲模板 ( 图。10A)。 周期效应在 2005 年之后下降,但在 2015 年之后反弹 ( 图。10C)。 表明干预措施的传播不均匀。队列效应追溯了 1960 年出生的下降,然后是本世纪末的上升,反映了心脏代谢风险的全球化 ( 图 196010D)。
Figure 10. Age-period-cohort analysis of Global AF/AFL burden from 1992 to 2021.
图 10.1992 年至 2021 年全球 AF/AFL 负担的年龄期队列分析。
(A) Age Deviation (B) Longitudinal Age Curves; (C) Period Rate Ratio (D) Cohort Rate Ratio
(a)年龄偏差(b)纵向年龄曲线;(C) 周期率比 (D) 队列率比.
3.6 Forecasting of AF/AFL burden from 2022 to 2050.
3.6 2022-20 年 AF/AFL 负担预测 5 0.
3.6.1 China
3.6.1 中国
Nationwide ASIR and ASPR are projected to rise modestly (≈ 5-7 % by 2050) (Fig. 11A and 11B). with minimal sex divergence. ASMR will continue to decline (≈ -10 %) (Fig. 11C). while ASDR remains flat-indicating that ageing-related incident cases will be counterbalanced by survival gains (Fig. 11D).
全国范围内的 ASIR 和 ASPR 预计将小幅上升( 到 2050 年≈ 5-7%)( 图 1 图 11A 和 11B)。 性别差异最小。ASMR 将继续下降(≈-10%)( 图。11C)。 而 ASDR 保持持平 ,表明与衰老相关的事件病例将被生存率的提高所抵消 ( 图 11D)。
3.6.2 Southeast Asia
3.6.2 东南亚
Both ASIR and ASPR are forecast to fall markedly (≈ -15 %) (Fig. 11E and 11F). driven by demographic stabilisation and accelerating risk-factor control. ASMR and ASDR will also decline, narrowing the gap with China (Fig. 11G and 11H).
预计 ASIR 和 ASPR 都将显着下降(≈-15%)( 图。11E 和 11F)。 在人口稳定和加速风险因素控制的推动下。ASMR 和 ASDR 也将下降,缩小与中国的差距 ( 图。11G 和 11H)。
3.6.3 Europe
3.6.3 欧洲
ASIR and ASPR will edge upward (≈ 3 %) (Fig. 12A and 12B). but ASMR is predicted to fall heterogeneously - female ASMR declining faster than male, reflecting sex-specific uptake of novel oral anticoagulants (NOACs) and catheter ablation (Fig. 12C).
ASIR 和 ASPR 将小幅上升(≈3%)( 图。12A 和 12B)。 但预计 ASMR 将异质性下降 - 女性 ASMR 下降速度快于男性,反映了新型口服抗凝剂 (NOAC) 和导管消融的性别特异性吸收 ( 图 112C) 的。
3.6.4 Global
3.6.4 全球
Global ASIR and ASPR will increase slightly, propelled by low- and middle-income countries (LMICs) (Fig. 12E and 12F). Female ASIR/ASPR growth will outpace male, yet female ASMR/ASDR will decline more steeply, suggesting an emerging gender paradox of better risk-factor management in women (Fig. 12G and 12H).
在中低收入人口 (LMIC) 的推动下,全球 ASIR 和 ASPR 将略有上升 ( 图。12E 和 12F)。 女性 ASIR/ASPR 的增长速度将超过男性,但女性 ASMR/ASDR 的下降幅度更大 , 这表明女性中存在更好的风险因素管理的新性别悖论 (图 112G 和 12H)。
Figure 11. Predictions of AF/AFL trends was projected by BAPC-INLA model
图 11.通过 BAPC-INLA 模型预测 AF/AFL 趋势的预测.
The projected ASRs of incidence (A), prevalence (B), death (C), and DALYs (D) for AF/AFL by sex from in China form 1990 to 2050. The projected ASRs of incidence (E), prevalence (F), death (G), and DALYs (H) for AF/AFL by sex from in South-East Asia Region form 1990 to 2050,. The dots represent the observed values, and the fan shape represent the predictive distribution between the 2.5 and 97.5 % quantiles. The solid line represents the predicted ASRs during 2020-2050.
1990—2050 年中国按性别划分的房颤/房颤发病发病率(A)、患病率(B)、死亡率(C)和 DALYs(D)的预测 ASR。1990 年至 2050 年东南亚地区按性别划分的 AF/AFL 发病率 (E)、患病率 (F)、死亡率 (G) 和 DALY (H) 的预测 ASR。点代表观测值,扇形代表 2.5% 和 97.5 % 分位数之间的预测分布。实线代表 2020-2050 年预测的 ASR。
Figure 12. Predictions of AF/AFL trends was projected by BAPC-INLA model
图 12.通过 BAPC-INLA 模型预测 AF/AFL 趋势的预测.
The projected ASRs of incidence (A), prevalence (B), death (C), and DALYs (D) for AF/AFL by sex from in European Region form 1990 to 2050. The projected ASRs of incidence (E), prevalence (F), death (G), and DALYs (H) for AF/AFL by sex from in Global form 1990 to 2050,. The dots represent the observed values, and the fan shape represent the predictive distribution between the 2.5 and 97.5 % quantiles. The solid line represents the predicted ASRs during 2020–2050.
1990 年至 2050 年欧洲地区按性别划分的 AF/AFL 发病率 (A)、患病率 (B)、死亡率 (C) 和 DALY (D) 的预测 ASR。1990 年至 2050 年按性别划分的 AF/AFL 发病率 (E)、患病率 (F)、死亡率 (G) 和 DALY (H) 的预测 ASR。点代表观测值,扇形代表 2.5% 和 97.5 % 分位数之间的预测分布。实线代表 2020-2050 年期间预测的 ASR。
3.7 Decomposition analysis in AF/AFL burden from 1990 to 2021.
3.7 1990—2021 年 AF/AFL 负荷分解分析 。
Between 1990 and 2021, population growth accounted for 68 % of the increase in incident cases in China; aging contributed 24 % and epidemiological change -8 %. The same pattern held for prevalence. For mortality, population growth contributed 52 %, ageing 48 %, but epidemiological change contributed -35 %, attesting to the life-saving impact of anticoagulation, rate control and integrated stroke systems. Globally, population growth dominated incidence and prevalence increases, while Europe experienced the largest epidemiological dividend in mortality (-42 %), plausibly through widespread NOAC adoption and AF catheter ablation programmes (Fig. 13).
1990 年至 2021 年间,人口增长占中国发病病例增长的 68%;老龄化占 24%,流行病学变化占-8%。同样的模式也适用于流行。死亡率方面,人口增长贡献了 52%,老龄化贡献了 48%,但流行病学变化贡献了 -35%,证明了抗凝、心率控制和综合中风系统的挽救生命的影响。在全球范围内,人口增长主导了发病率和患病率的增加,而欧洲的死亡率在流行病学方面取得了最大的红利(-42%),这可能是通过广泛的 NOAC 采用和 AF 导管消融计划( 图 1999 年)。13) 的。
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Figure 13. Impact of Aging, Epidemiological Shifts, and Population Growth on AF/AFL Burden (1990-2021) in China, South-East Asia Region, European Region and Global
图 13.老龄化、流行病学变化和人口增长对中国、东南亚地区、欧洲地区和全球 AF/AFL 负担的影响(1990-2021 年).
(A)Incidence (B)Prevalence (C)Death (D)DALYs
(一)发病率 (B)患病率 (C)死亡 (D)DALYs.
3.8 Frontier analysis in AF/AFL burden base on SDI index from 1990 to 2021.
3.8 基于 1990—2021 年 SDI 指数的 AF/AFL 负荷前沿分析 。
Using data-envelopment analysis with 100-bootstrap iterations, we constructed efficiency frontiers linking Socio-demographic Index (SDI) to ASMR and ASDR for 200+ countries, 1980-2021. In 2021 China (orange) lay markedly closer to the frontier than in 2019 (blue), outperforming many high-SDI European nations (purple), which drifted rightward - indicating rising mortality despite affluence. Singapore (green) remained on the frontier across high SDI values, exemplifying optimal AF care. Frontier convergence accelerated with SDI, yet dispersion widened post-2015 among high-income countries, signalling that income alone does not guarantee efficiency. China’s trajectory suggests that policy-driven improvement (national stroke screening, tiered diagnosis, universal NOAC reimbursement) can yield outsized mortality reductions even at moderate SDI levels.
使用具有 100 次引导迭代的数据包络分析,我们构建了 1980-2021 年 200+ 个国家的社会人口指数 (SDI) 与 ASMR 和 ASDR 联系起来的效率前沿 。2021 年,中国(橙色)明显比 2019 年(蓝色)更接近边境,优于许多向右偏移的高 SDI 欧洲国家(紫色 ), 表明尽管富裕,但死亡率仍在上升。新加坡 (绿色)在高 SDI 值方面仍然处于前沿,体现了最佳的 AF 护理。随着 SDI 的加速,前沿趋同加速,但 2015 年后,高收入国家之间的分散扩大,这表明仅靠收入并不能保证效率。中国的发展轨迹表明,即使在中等 SDI 水平下,政策驱动的改进(全国中风筛查、分层诊断、普遍 NOAC 报销)也可以大幅降低死亡率。
Taken together, these findings portray China as a region where demographic momentum and mid-life risk-factor surges inflate incidence and prevalence, yet aggressive downstream management compresses mortality and disability. Southeast Asia faces an earlier-stage transition, Europe confronts plateauing incidence but persistent late-life mortality, and the global average reflects a mosaic of unmet need and emerging success stories (Fig. 14 and Fig. 15).
综上所述,这些发现将中国描绘成一个人口势头和中年风险因素激增导致发病率和患病率上升的地区,但积极的下游管理却压缩了死亡率和残疾。东南亚面临早期转型,欧洲发病率趋于稳定,但晚年或期持续存在 ,全球平均水平反映了未满足的需求和新兴成功案例的马赛克 (图。14 和图 1。15)。
Figure 14. Frontier analysis of ASMR for AF/AFLbased on the SDI from 1990 to 2021.
图 14.1990—2021 年基于 SDI 的 AF/AFLASMR 前沿分析
(A) Global Mortality Patterns by SDI. ASMR for AF/AFL vs. SDI values across countries. Points colored red indicate ASMR increased since 2019, blue indicates decreased. China (orange-red), European (purple), and Southeast Asian (green) countries are highlighted. (B) Spatiotemporal dynamic distribution of ASMR. Color gradient (light to dark blue) denotes year progression (1990 to 2020).
(A) 按 SDI 分列的全球死亡率模式。AF/AFL 与不同国家/地区 SDI 值的 ASMR。红色点表示 ASMR 自 2019 年以来有所增加,蓝色表示有所下降。突出显示了中国(橙红色)、欧洲(紫色)和东南亚(绿色)国家。(B)ASMR 的时空动态分布。颜色渐变(浅蓝色到深蓝色)表示年份递进(1990 年至 2020 年)。
Figure 15. Frontier analysis of ASDR for AF/AFL based on the SDI from 1990 to 2021.
图 15.1990—2021 年基于 SDI 的 AF/AFLASDR 前沿分析
(A) Global DALYs Patterns by SDI. ASDR for AF/AFL vs. SDI values across countries. Points colored red indicate ASDR increased since 2019, blue indicates decreased. China (orange-red), European (purple), and Southeast Asian (green) countries are highlighted. (B) Spatiotemporal dynamic distribution of ASDR. Color gradient (light to dark blue) denotes year progression (1990 to 2020).
(A) SDI 的全球 DALY 模式。AF/AFL 与 SDI 值的 ASDR 跨国家/地区。红色点表示 ASDR 自 2019 年以来有所增加,蓝色表示有所下降。突出显示了中国(橙红色)、欧洲(紫色)和东南亚(绿色)国家。(B)ASDR 的时空动态分布。颜色渐变(浅蓝色到深蓝色)表示年份递进(1990 年至 2020 年)。
Discussion
讨论
AF/AFL have emerged as dominant contributors to global cardiovascular morbidity, and the GBD 1990-2021 repository now allows us to trace their footprint with unprecedented precision. Worldwide, 52.6 million people lived with AF/AFL in 2021, 4.5 million were newly diagnosed, 8.36 million DALYs were accrued, and 340 000 deaths were recorded. China alone accounted for 10.8 million prevalent cases, 0.91 million incident cases, 165,000 DALYs and 60,000 deaths-figures that dwarf those of entire continents. Yet the age-standardised mortality rate in China has fallen by 2.3 % per year since 2005, while Europe, despite lower absolute numbers, now records the highest regional ASMR. This divergence underscores that disease burden is a compound of demography, biology and health-system architecture; headline statistics, while sobering, can obscure the more nuanced story of who dies, when, and why.
AF/AFL 已成为全球心血管发病率的主要贡献者,GBD 1990-2021 存储库现在使我们能够以前所未有的精度追踪它们的足迹。2021 年,全球有 5260 万人患有 AF/AFL,450 万人新诊断,累积 836 万 DALY,记录了 34 万人死亡。仅中国就占了 1080 万例流行病例、91 万例发病病例、165000 例 DALY 和 60000 例死亡 —— 这些数字使整个大陆相形见绌。然而,自 2005 年以来,中国的年龄标准化死亡率每年下降 2.3%,而欧洲尽管绝对数字较低,但目前是地区 ASMR 最高的国家。这种差异强调,疾病负担是人口学、生物学和卫生系统结构的复合体;头条新闻虽然发人深省,但可能会掩盖谁死、何时死以及为什么死的更微妙的故事。
Joinpoint regression reveals a synchronised upward inflection in incidence and prevalence after 2019, coinciding with the COVID-19 pandemic. SARS-CoV-2 triggers atrial injury through ACE-2 down-regulation, cytokine storm and autonomic imbalance23,24; population-level data from Sweden and the United States already show a 15-20 % relative rise in new AF within thirty days of infection25. China’s strict containment measures and universal vaccination appear to have blunted this surge, allowing ASMR to continue its secular decline, whereas Europe experienced a transient but sharp drop in deaths that more likely reflects differential COVID-19 mortality than improved arrhythmia care. The episode illustrates how exogenous shocks can masquerade as therapeutic success, and why disentangling period effects from genuine health-system gains remains essential26
Joinpoint 回归显示,2019 年之后发病率和患病率同步上升,与 COVID-19 大流行同时发生。SARS-CoV-2 通过 ACE-2 下调、细胞因子风暴和自主神经失衡引发心房损伤 23,24;瑞典和美国的人口水平数据已经显示 , 在感染后 30 天内,新发房颤的相对增加 15-20%25。中国严格的遏制措施和全民疫苗接种似乎减缓了这一激增,使 ASMR 继续长期下降,而欧洲的死亡人数经历了短暂但急剧下降,这更可能反映了 COVID-19 死亡率的差异,而不是心律失常护理的改善。这一事件说明了外源性休克如何伪装成治疗成功,以及为什么将经期影响与真正的卫生系统收益分开仍然至关重要 26.
Age-period-cohort (APC) modelling provides a nuanced understanding of AF/AFL burden across regions, revealing critical disparities that demand tailored interventions. Globally, relative risk follows an inverted U-shape, peaking at 60–74 years, but regional variations are stark, with a trend toward younger onset driven by modern lifestyle shifts such as fast-food culture in China and Southeast Asia, which exacerbate abdominal obesity and circadian rhythm disruptions, alongside genetic predispositions like MYBPC3 variants in European populations that heighten cardiomyopathy risks. Crucially, mid-life vulnerability (50–55 years) is amplified by comorbid metabolic disorders, particularly obstructive sleep apnea (OSA), whose pathological mechanisms involve intermittent hypoxia-induced oxidative stress and sustained sympathetic-adrenal axis activation; this increases vascular permeability, stimulates atrial β1-receptors, elevates autonomic tone, and shortens effective refractory periods, directly promoting atrial remodeling and AF initiation—underscoring OSA as a critically underestimated risk factor in recent studies.In China, age deviation curves exhibit a distinct U-shaped reversal, with risk rising sharply from age 30 to peak at 50–55 years—reflecting this "vulnerable window"—and declining post-85 due to effective geriatric care; Period effects diverge more starkly: China shows rising incidence but falling mortality since 2005, consistent with the third phase of the obesity-diabetes-AF transition in which acute cardiovascular care outpaces primary prevention27; while cohort effects (1940 baseline) indicate initial declines for post-1960 births followed by increases mirroring cardiometabolic risk accumulation.Conversely. Southeast Asia displays delayed peaks (incidence at 65–70 years, prevalence at 55–60 years) and exhibits uniformly adverse period trends, reflecting widening rural–urban disparities and fragile primary-care systems28. These patterns caution against one-size-fits-all policies: the same birth cohort may carry different risk trajectories across geographies, demanding age-specific and context-specific interventions29,30. To address this in China, interventions must be age-stratified and context-specific, beginning with intensified early identification for 40–70-year-olds through AI-driven targeted screening (e.g., leveraging existing clinical data to enhance asymptomatic case detection, as supported by recent AI models that boost efficacy by 20–30% in community settings), combined with mobile ECG deployments in rural areas to bridge healthcare gaps; simultaneously, mid-life high-risk groups (50–55 years) require integrated metabolic management, such as OSA-pathway incorporation (e.g., routine polysomnography in primary care) and obesity control programs in urban hubs, while elderly-focused strategies must expand NOAC reimbursement and sex-specific approaches for women over 70 (who show higher mortality) to harness projected ASMR declines. Furthermore, policy enhancements should build on China's "Healthy China 2030" initiatives—which narrowed rural–urban divides through AF center networks and NOAC/LAAC coverage—by embedding multidisciplinary comorbidity management (e.g., diabetes–AF integrated clinics) and adopting APHRS's "ABC pathway" for holistic age-tailored care, ultimately mitigating burden amplification from aging and urbanization through precision public health.
年龄段队列 (APC) 模型提供了对各地区 AF/AFL 负担的细致入微的了解,揭示了需要量身定制干预措施的关键差异。在全球范围内,相对风险呈倒 U 形,在 60-74 岁达到峰值,但地区差异明显,现代生活方式的转变推动了年轻发病的趋势,例如中国和东南亚的快餐文化,加剧了腹部肥胖和昼夜节律紊乱,以及欧洲人群中的 MYBPC3 变异等遗传易感性,增加了心肌病风险。 至关重要的是,中年脆弱性(50-55 岁)会因合并代谢紊乱而放大,特别是阻塞性睡眠呼吸暂停 (OSA),其病理机制涉及间歇性缺氧诱导的氧化应激和持续的交感神经-肾上腺轴激活;这增加了血管通透性,刺激心房 β1 受体,提高了自主神经张力,并缩短了有效的不应期,直接促进了心房重塑和 AF 的启动——这突显了 OSA 在最近的研究中是一个被严重低估的风险因素。在中国,年龄偏差曲线呈现出明显的 U 形反转,风险从 30 岁急剧上升到 50-55 岁达到峰值——反映了这个“脆弱窗口”——而 85 岁后则由于有效的老年护理而下降; 经期效应差异更为明显:自 2005 年以来,中国的发病率上升,但死亡率下降,与肥胖-糖尿病-房颤过渡的第三阶段一致,其中急性心血管护理超过了一级预防 27;而队列效应(1940 年基线)表明 1960 年后出生的最初下降,随后增加,反映了心脏代谢风险的积累。相反。 东南亚出现延迟高峰(发病率为 65-70 岁,患病率为 55-60 岁),并表现出一致的不利时期趋势,反映出城乡差距的扩大和初级保健系统的脆弱性 28 这些模式警告不要采取一刀切的政策:同一出生队列可能在不同地区携带不同的风险轨迹,需要针对特定年龄和特定环境的干预措施 29,30 为了在中国解决这个问题,干预措施必须按年龄分层和针对具体情况进行,首先是通过人工智能驱动的靶向筛查(例如,利用现有临床数据加强无症状病例检测,最近的人工智能模型支持,在社区环境中将疗效提高 20-30%),结合在农村地区部署移动心电图以弥合医疗保健差距;同时,中年高危人群(50-55 岁)需要综合代谢管理,例如 OSA 通路纳入(例如,初级保健中的常规多导睡眠图)和城市中心的肥胖控制计划,而以老年人为中心的战略必须扩大 NOAC 报销和针对 70 岁以上女性(死亡率较高)的性别特定方法,以利用预计的 ASMR 下降。 此外,政策的加强应以中国的“健康中国 2030”倡议为基础,通过 AF 中心网络和 NOAC/LAAC 覆盖范围缩小城乡差距,嵌入多学科合并症管理(例如,糖尿病-AF 综合诊所)并采用 APHRS 的“ABC 途径”进行全面的年龄定制护理,最终通过精准公共卫生减轻老龄化和城市化带来的负担放大。
Decomposition attributes 70 % of China’s increased prevalent cases to population growth and ageing, 22 % to worsening metabolic risk, and 8 % to improved survival. Europe, by contrast, sees demography contribute only 42 %, with the remainder driven by persistent obesity and hypertension. The arithmetic is sobering: without aggressive metabolic risk reduction, China could add another 1.9 million prevalent cases by 2035 even if incidence rates remain constant. Conversely, a five percent population-level reduction in BMI could avert 190 000 incident cases, underlining the outsized leverage of primordial prevention.
分解将中国 70% 的患病病例增加归因于人口增长和老龄化,22% 归因于代谢风险恶化,8% 归因于生存率的提高。相比之下,欧洲的人口结构仅占 42%, 其余由持续肥胖和高血压驱动。这个算术发人深省:如果不积极降低代谢风险,即使发病率保持不变,到 2035 年,中国可能会再增加 190 万例流行病例。相反,BMI 在人口水平上降低 5% 可以避免 190,000 例事件,这凸显了原始预防的巨大影响力。
Gender analysis challenges canonical narratives. While Framingham and ARIC report male predominance until the ninth decade, GBD data show the female-to-male ratio for DALYs and deaths exceeds unity after age 75 in China, Southeast Asia and Europe31. Biology contributes: oestrogen suppresses atrial fibrosis until menopause, after which abrupt withdrawal accelerates structural remodelling; X-chromosome loci such as paired-like homeodomain transcription factor 2 (PITX2) exhibit stronger effect sizes in women32. Social constructs magnify the gap: restrictive gender norms in Southeast Asia curtail outdoor activity and healthcare access, amplifying psychosocial stress. Encouragingly, China’s EAPC model projects a steeper ASMR decline in women (-3.1 % per year) than in men (-1.9 %), plausibly linked to sex-specific gains: the CHA₂DS₂-VASc score assigns an extra point to women, driving anticoagulation rates from 18 % in 2010 to 41 % in 2020, while 2017 national reimbursement drug list (NRDL) reimbursement for NOACs disproportionately benefited women by circumventing warfarin-related intracranial bleeding risk33. The lesson is that targeted strategies—frailty-adjusted anticoagulation in elderly women, rhythm-control prioritisation in symptomatic females—can narrow the gender gap without compromising efficacy.
性别分析挑战规范叙事。虽然弗雷明汉和 ARIC 报告称,直到第九个十年,男性占主导地位,但 GBD 数据显示,在中国、东南亚和欧洲,75 岁后 DALY 和死亡人数的男女比例超过了统一 31。生物学有助于:雌激素抑制心房纤维化直至绝经,之后突然戒断加速结构重塑;X 染色体位点,例如成对同源结构域转录因子 2 (PITX2), 在女性中表现出更强的效应大小 32。社会结构扩大了差距:东南亚的限制性性别规范限制了户外活动和医疗保健的获取,放大了社会心理压力。令人鼓舞的是,中国的 EAPC 模型预测,女性的 ASMR 下降幅度更大( 每年 -3.1%),低于男性(-1.9%),这似乎与性别特异性增长有关:CHA₂DS₂-VASc 评分为女性加分,将抗凝率从 2010 年的 18%提高到 2020 年的 41%,而 2017 年国家报销率 (NRDL)NOAC 的报销通过规避与华法林相关的颅内出血风险,使妇女受益匪浅 33.教训是,有针对性的策略——对老年女性进行虚弱调整抗凝治疗,对有症状的女性进行节律控制优先排序——可以在不影响疗效的情况下缩小性别差距。
Frontier efficiency analysis positions China above its SDI production frontier, outperforming 82 % of nations including several high-SDI counterparts such as Belgium and Portugal. Key inflection points include the 2016 launch of 1,200 certified AF centres with standardised catheter-ablation pathways, integration of opportunistic screening into the Basic Public Health Service package, and tiered reimbursement that covers 70-90 % of NOAC cost34. Yet rural western provinces still report ablation volume one-tenth that of eastern megacities; telemedicine and mobile ECG devices offer scalable solutions35, as demonstrated by the Shanghai “Know-AF” programme which increased case-finding by 27 %36
前沿效率分析显示,中国高于其 SDI 生产前沿,表现优于 82%的国家,包括比利时和葡萄牙等几个高 SDI 国家。关键的转折点包括 2016 年启动 1,200 个经过认证的 AF 中心,该中心具有标准化的导管消融途径,将机会性筛查纳入基本公共卫生服务计划,以及涵盖 NOAC 费用 70-90% 的分层报销 34。然而,西部农村省份报告的消融量仍然是东部特大城市的十分之一;远程医疗和移动心电图设备提供了可扩展的解决方案 35,上海的“Know-AF”计划证明了这一点,该计划将病例发现提高了 27 %36.
Looking forward, a paradigm shift-from reactive treatment of complications to proactive, sex-specific and age-stratified prevention-is now imperative. China’s commitment to eliminating urban-rural health disparities, prioritizing middle-aged women’s care, integrating obstructive sleep apnea and obesity management into atrial fibrillation (AF) pathways, and advancing AI-guided screening will play a pivotal role in enabling the nation—and the global community—to curb the projected surge of AF-related stroke, heart failure, and premature mortality by 205037-39
展望未来,范式转变 —— 从并发症的反应性治疗到主动的、针对性别的和年龄分层的预防 —— 现在势在必行 。 中国致力于消除城乡健康差距,优先考虑中年妇女护理,将阻塞性睡眠呼吸暂停和肥胖管理纳入心房颤动(AF)途径,并推进人工智能引导的筛查,这将在使国家和国际社会能够遏制预计到 2050 年房颤相关中风、心力衰竭和过早死亡的激增方面发挥关键作用 37-39.
Nevertheless, we must acknowledge that this study still has limitations. Firstly, the database primarily relies on statistical modeling rather than original case registration information. Although its estimation methods provide a benchmark framework for cross-country comparisons, some regions (especially underdeveloped areas with weak grassroots medical data) may have systematic biases, which could affect the precise assessment of the multidimensional epidemiological characteristics of AF/AFL40. Secondly, the existing disease classification system has not refined the clinical diversity of AF/AFL. Differences in outcomes due to various electrophysiological subtypes (such as paroxysmal vs. persistent) and comorbidity combinations (beyond hypertension and diabetes, factors of metabolic syndrome such as obesity and chronic kidney disease) have not been fully incorporated into the model, potentially leading to insufficiently comprehensive predictions of complication risks and healthcare needs41,42. Lastly, the dynamic assessment of disease progression has inherent delays. The current model uses fixed weight coefficients to assess health losses, failing to adequately reflect treatment changes such as the application of new anticoagulants and the promotion of catheter ablation technology, as well as significant differences in healthcare resource accessibility between eastern and western regions. This simplification of temporal and spatial dimensions may weaken the regional guiding value of the research results. It should be noted that despite these methodological limitations, this study, through a systematic integration of multiple health indicators, can still provide important reference for policymakers to understand the evolution of the disease spectrum of atrial fibrillation/atrial flutter in China, while promoting the construction of precise prevention and control measures and optimizing the allocation of healthcare resources, thereby effectively controlling the complex damage to health caused by cardiovascular events induced by AF/AFL.
尽管如此,我们必须承认这项研究仍然存在局限性。首先,该数据库主要依赖于统计建模,而不是原始病例登记信息。尽管其估计方法为跨国比较提供了基准框架,但一些地区(尤其是基层医疗数据较弱的欠发达地区)可能存在系统偏差,这可能影响 AF/AFL 40 多维流行病学特征的精确评估 。其次,现有疾病分类体系未细化 AF/AFL 的临床多样性。由于各种电生理亚型(例如阵发性与持续性)和合并症组合(除了高血压和糖尿病、肥胖和慢性肾脏病等代谢综合征因素)导致的结果差异尚未完全纳入模型中,可能导致对并发症风险和医疗保健需求的预测不够全面 41,42.最后,疾病进展的动态评估具有固有的延迟。目前的模型使用固定的权重系数来评估健康损失,未能充分反映治疗变化,如新型抗凝剂的应用和导管消融技术的推广,以及东西部地区医疗资源可及性的显著差异。这种时空维度的简化可能会削弱研究成果的区域指导价值。 需要注意的是,尽管存在这些方法学局限性,但本研究通过系统整合多个健康指标,仍可为政策制定者了解我国心房颤动/心房扑动疾病谱的演变提供重要参考,同时推动精准防控措施建设,优化医疗资源配置, 从而有效控制 AF/AFL 诱发的心血管事件对健康造成的复杂损害。
In conclusion, this study underscores the increasing burden of atrial fibrillation/flutter across various regions, emphasizing the importance of targeted interventions and ongoing monitoring to enhance patient care and reduce healthcare costs. The findings reveal significant regional disparities in disease incidence and mortality, necessitating tailored healthcare strategies to address the unique challenges faced by different populations. Future research should focus on elucidating the underlying mechanisms and risk factors contributing to these trends, thereby informing public health policies and optimizing resource allocation in managing AF/AFL effectively.
总之,这项研究强调了各个地区心房颤动/扑动负担的增加,强调了有针对性的干预措施和持续监测对于加强患者护理和降低医疗成本的重要性。研究结果揭示了疾病发病率和死亡率的显着地区差异,需要量身定制的医疗保健策略来应对不同人群面临的独特挑战。未来的研究应侧重于阐明导致这些趋势的潜在机制和风险因素,从而为公共卫生政策提供信息并优化有效管理 AF/AFL 的资源分配。